Haplogroup F (mtDNA)
{{Short description|Human mitochondrial DNA haplogroup}}
{{About|the human mtDNA haplogroup|the human Y-DNA haplogroup|Haplogroup F-M89}}
{{cs1 config|name-list-style=vanc|display-authors=6}}
{{Infobox haplogroup
|name=F
|map=Peopling of eurasia.jpg
|origin-place = Asia
|ancestor=R9
|descendants= F1, F2, F3, F4
}}
Haplogroup F is a human mitochondrial DNA (mtDNA) haplogroup. The clade is most common in East Asia and Southeast Asia. It has not been found among Native Americans.[http://www.ianlogan.co.uk/discussion/hap_F.htm Haplogroup F.]
It is a primary branch of haplogroup R9.
Distribution
The F haplogroup is fairly common in East Asia. High frequencies of the clade are found among the Lahu from Yunnan (33% - 77%, average 52%), Nicobar Islands (50%), Shors from Kemerovo Oblast of Siberia (41%), and Arunachal Pradesh, India (31%).{{cite journal | vauthors = Derenko M, Malyarchuk B, Grzybowski T, Denisova G, Dambueva I, Perkova M, Dorzhu C, Luzina F, Lee HK, Vanecek T, Villems R, Zakharov I | title = Phylogeographic analysis of mitochondrial DNA in northern Asian populations | journal = American Journal of Human Genetics | volume = 81 | issue = 5 | pages = 1025–1041 | date = November 2007 | pmid = 17924343 | pmc = 2265662 | doi = 10.1086/522933 }} There is also an important frequency in Taiwanese aborigines, Khakas, Kets, Han Chinese (and, thus, nearly all of China), Lombok, Sumba, Thailand, and Vietnam. Its distribution extends with low frequency to the Tharu of southern Nepal and the Bashkirs of the southern Urals.M. A. Bermisheva, K. Tambets, R. Villems, and E. K. Khusnutdinova, "Diversity of Mitochondrial DNA Haplogroups in Ethnic Populations of the Volga–Ural Region", Molecular Biology Vol. 36, No. 6, 2002, pp. 802–812. Translated from Molekulyarnaya Biologiya, Vol. 36, No. 6, 2002, pp. 990–1001.{{cite journal | vauthors = Fornarino S, Pala M, Battaglia V, Maranta R, Achilli A, Modiano G, Torroni A, Semino O, Santachiara-Benerecetti SA | title = Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation | journal = BMC Evolutionary Biology | volume = 9 | issue = 1 | pages = 154 | date = July 2009 | pmid = 19573232 | pmc = 2720951 | doi = 10.1186/1471-2148-9-154 | bibcode = 2009BMCEE...9..154F | doi-access = free }}{{cite journal | vauthors = Pimenoff VN, Comas D, Palo JU, Vershubsky G, Kozlov A, Sajantila A | title = Northwest Siberian Khanty and Mansi in the junction of West and East Eurasian gene pools as revealed by uniparental markers | journal = European Journal of Human Genetics | volume = 16 | issue = 10 | pages = 1254–1264 | date = October 2008 | pmid = 18506205 | doi = 10.1038/ejhg.2008.101 | s2cid = 19488203 | doi-access = free }}
Haplogroup F also occurs at low frequencies on the Comoros Islands (<10%).{{cite journal | vauthors = Msaidie S, Ducourneau A, Boetsch G, Longepied G, Papa K, Allibert C, Yahaya AA, Chiaroni J, Mitchell MJ | title = Genetic diversity on the Comoros Islands shows early seafaring as major determinant of human biocultural evolution in the Western Indian Ocean | journal = European Journal of Human Genetics | volume = 19 | issue = 1 | pages = 89–94 | date = January 2011 | pmid = 20700146 | pmc = 3039498 | doi = 10.1038/ejhg.2010.128 }}
It is also found at low frequencies on the Hvar island in Croatia (8.3%).
Subclades
F1a clearly predominates among the representatives of haplogroup F in Southeast Asia, but subclades of this haplogroup have been found in populations as far north as the Buryats and Ulchi of Siberia.
F1b tends to become more frequent as a fraction of total F in populations of the northern parts of East Asia and Central Asia, such as Mongols, Kazakhs, Uyghurs, and Japanese. It also has been found among the Yi people. There are odd exclaves of F1b in Gaininsk Bashkirs of Perm Oblast and Croats of Hvar Island.{{cite journal | vauthors = Tolk HV, Barac L, Pericic M, Klaric IM, Janicijevic B, Campbell H, Rudan I, Kivisild T, Villems R, Rudan P | title = The evidence of mtDNA haplogroup F in a European population and its ethnohistoric implications | journal = European Journal of Human Genetics | volume = 9 | issue = 9 | pages = 717–723 | date = September 2001 | pmid = 11571562 | doi = 10.1038/sj.ejhg.5200709 | doi-access = free }}
F1d is the second most frequent sub-clade in Newar (Nepal). Haplogroup F1d reaches the greatest proportion in Newar (11.97%) of Nepal and Kshatriya (16%) of North India.{{cite journal |vauthors=Basnet R, Rai N, Tamang R, Awasthi NP, Pradhan I, Parajuli P, Kashyap D, Reddy AG, Chaubey G, Das Manandhar K, Shrestha TR, Thangaraj K |date=February 2023 |title=The matrilineal ancestry of Nepali populations |journal=Human Genetics |volume=142 |issue=2 |pages=167–180 |doi=10.1007/s00439-022-02488-z |pmid=36242641 |s2cid=252904281}}
F2 has been found mainly in the form of F2a, which has been observed in more than 10% of a couple samples of Nu and Lisu from Gongshan, Yunnan.{{cite journal |vauthors=Wen B, Xie X, Gao S, Li H, Shi H, Song X, Qian T, Xiao C, Jin J, Su B, Lu D, Chakraborty R, Jin L |date=May 2004 |title=Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans |journal=American Journal of Human Genetics |volume=74 |issue=5 |pages=856–865 |doi=10.1086/386292 |pmc=1181980 |pmid=15042512}} F2 has been found with frequencies exceeding 5% in several other populations of Southwest China, Guangxi, and Hainan, including the Han majority population. Outside of southwestern China, F2 has been found with frequency greater than 5% in a sample of Oirat Mongols from Xinjiang and a sample of Khakas from Khakassia, with the former population boasting particularly high diversity within this clade.
F3 is especially common among Austronesian peoples of Taiwan and the Malay Archipelago, but it also has been found in many populations of Southwest China and South-Central China, and in a sample of Hans from Xinjiang.
F4 has been found mainly in aboriginal populations of Taiwan and Hainan, with some representatives among samples of Filipinos from Luzon, Indonesians from Sumatra, and Hans and Uzbeks from Xinjiang.
=Tree=
This phylogenetic tree of haplogroup F subclades is based on the paper by Mannis van Oven and Manfred Kayser Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation and subsequent published research.
- F
- F* – China, KoreaHwan Young Lee, Ji-Eun Yoo, Myung Jin Park, Ukhee Chung, Chong-Youl Kim, and Kyoung-Jin Shin, "East Asian mtDNA haplogroup determination in Koreans: Haplogroup-level coding region SNP analysis and subhaplogroup-level control region sequence analysis." Electrophoresis (2006). DOI 10.1002/elps.200600151.
- F1
- F1a'c'f – Thailand (Kaleun in Nakhon Phanom ProvinceWibhu Kutanan, Jatupol Kampuansai, Metawee Srikummool, Daoroong Kangwanpong, Silvia Ghirotto, Andrea Brunelli, and Mark Stoneking, "Complete mitochondrial genomes of Thai and Lao populations indicate an ancient origin of Austroasiatic groups and demic diffusion in the spread of Tai–Kadai languages." Hum Genet 2016 DOI 10.1007/s00439-016-1742-y.), China, Korea, Kazakhstan
- F1a – China, Korea, Uyghur, Thailand, Mongolia
- F1a1'4 – Thailand (Khon Mueang in Chiang Rai Province), China (Ma'an site, Wuxi, Majiabang culture)
- F1a1 – Japan, Korea, China, Ulchi, Uyghur, Vietnam (incl. Cờ Lao), Laos, Thailand, Indonesia, Mexico
- F1a1a – Thailand, Laos, Vietnam, China (Zhanjiang, etc.), Tibet, Indonesia
- F1a1a1 – Vietnam, Laos, Thailand, Cambodia, Nicobar Islands, Malaysia, Indonesia, China, Uyghur
- F1a1b – Japan, Korea
- F1a1c – Zhuang (Bama), Thailand, Tibet, Buryats (Inner Mongolia and Irkutsk Oblast), Japan
- F1a1c1 – Moken
- F1a1c2 – Japan, Xibo, China (Shanghai)
- F1a1d – Thailand, China, Taiwanese Aborigines (Tsou, Bunun, Rukai), Philippines
- F1a1d1 – Tao (Orchid Island)
- F1a4
- F1a4a – Thailand, Han Chinese (Denver), Ulchi
- F1a4a1 – Taiwanese Aborigines (Tsou, Makatao, Bunun, Ami, etc.), Philippines (Ivatan, Ibaloi, Abaknon, Bugkalot, Kalangoya, Dulag, etc.), Guam, Malaysia (Kelantan Malay), Sumatra, Vietnam (Dao), Thailand (Khon Mueang in Mae Hong Son Province and Chiang Mai Province), South Africa
- F1a4b – China
- F1a2 – Thailand, Vietnam (Hmong), China (Guizhou)
- F1a2a – Thailand (Phutai in Sakon Nakhon Province, Nyaw in Nakhon Phanom Province, Mon in Lopburi Province), China (Han in Zhanjiang, Dong, etc.)
- F1a3
- F1a3a – Philippines (Lipa City, Abaknon, Batak from Palawan Island, Aeta from Bataan), Taiwan, Indonesia
- F1a3a1 – Taiwan (Bunun, Puyuma, etc.)
- F1a3a1a – Japan, Korea
- F1a3a2 – Philippines (Ivatan)
- F1a3a3 – Taiwanese Aborigines (Tsou, Bunun, Makatao, Thao), Philippines (Ivatan)
- F1a3a7 - Philippines, Malaysia, Indonesia
- F1a3a8 - Philippines
- F1a3b - China (Hunan Han, etc.), Taiwan (Minnan from Kaohsiung, etc.), Kazakhstan (Jetisu)
- F1a3c (C10223T) - Thailand (Khmer, etc.), China (Han)
- F1a3e (C11860T) - Thailand, China (Uyghurs)
- F1c – Japan
- F1c1 – Japan
- F1c1a – Korea, Xinjiang, Tibet, Jammu and Kashmir, Thailand (Palaung in Chiang Mai Province, Khmu in Nan Province, Khon Mueang in Lampang Province)
- F1c1a1 – Russia, China (Qingdao, etc.), Evenk (New Barag Left Banner), Oroqen, Zhuang (Bama), Taiwan (Minnan)
- F1c1a1a – Tibet (Shannan, Sherpa, etc.), Yi
- F1c1a1b – China
- F1c1a2 – Tibet, Thailand, China (Chongqing), India
- F1f – Thailand, China, Lahu, Myanmar, Tibet, Cambodia, Vietnam (Hmong)
- F1-T16189C!
- F1b - Korea, Japan, Mongolia,{{cite journal | vauthors = Cardinali I, Bodner M, Capodiferro MR, Amory C, Rambaldi Migliore N, Gomez EJ, Myagmar E, Dashzeveg T, Carano F, Woodward SR, Parson W, Perego UA, Lancioni H, Achilli A | title = Mitochondrial DNA Footprints from Western Eurasia in Modern Mongolia | journal = Frontiers in Genetics | volume = 12 | pages = 819337 | date = 2022 | pmid = 35069708 | doi = 10.3389/fgene.2021.819337 | doi-access = free | pmc = 8773455 }} China (North China)
- F1b1 – China, Tibet (Shigatse, etc.), Ladakh, Uyghur (Artux, etc.), Kyrgyz, Azeri, Kurd (Iran), Armenian, Turkey, Russia, Croatia
- F1b1a – Japan, Korea, Uyghur
- F1b1a1 – Japan, Korea
- F1b1a1a – Japan, Korea, USA (African American)Rebecca S Just, Melissa K Scheible, Spence A Fast, et al., "Full mtGenome reference data: development and characterization of 588 forensic-quality haplotypes representing three U.S. populations." Forensic Sci Int Genet. 2015 Jan;14:141-55. doi: 10.1016/j.fsigen.2014.09.021. Epub 2014 Oct 5.
- F1b1a1a1 – Japan, Korea
- F1b1a1a1a – Japan
- F1b1a1a2 – Japan, Korea
- F1b1a1a3 – Japan
- F1b1a2 – Japan, Korea
- F1b1b – Yakut, Uyghur, Kyrgyz, Turk, Even (Sakkyryyr, Tompo), Korea
- F1b1c – China, Yi, Buryat
- F1b1d – Japan, Korea
- F1b1e – Uyghur, Kyrgyz, Buryat, Oroqen, Russian (Sverdlovsk Oblast)
- F1b1e1 – Yakut
- F1b1f – China, Uyghur, Buryat (Buryat Republic), Yakut (Namsky District), Evenk (Stony Tunguska River basin), Hungary (ancient Avars)
- F1d – China (Hunan, Zhejiang, Jiangsu, Beijing, Liaoning, Korean from Antu County, Hezhen, Minnan, Lhasa, etc.), Thailand (Mon in Kanchanaburi Province), South Korea, Japan, Kyrgyz (Artux, Ak-Say), ancient Scythian
- F1d1 – Tibet, Nepal (Tharu), Newar of Nepal (12%), Myanmar, Thailand (Mon in Kanchanaburi Province), China, Japan, South Africa
- F1e
- F1e1 – China (North China), Mongolia
- F1e1a – Japan
- F1e2 – China, Kyrgyz (Tashkurgan)
- F1e3 – China (Guangdong, etc.), Laos (Lao in Vientiane), Thailand (Phuan in Lopburi Province and Phichit Province), Sumatra, Vietnam (Kinh)
- F1g – Tibet, Thailand (Phuan in Lopburi Province, Sukhothai Province, and Phichit Province), China, Kyrgyz (Tashkurgan)
- F1g1 – China (Yunnan, etc.), Vietnam (Hmong, Dao), Nepal (Newar, 2.4%)
- F2
- F2* – Laos (Lao in Vientiane), China, Hong Kong, Uyghur (Artux)
- F2a'b'g
- F2a – China (Han from Beijing, Xinjiang, etc.), Taiwan (Makatao), Korea, Japan, Kazakhstan
- F2a1 – China (Han from Shandong), Naxi, Bai, Nu, Tu (Monguor),Kong, Q.P., Yao, Y.G., Sun, C., Zhu, C.L., Zhong, L., Wang, C.Y., Cai, W.W., Xu, X.M., Xu, A.L. and Zhang, Y.P., 2004. Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic. Journal of human genetics, 49(8), p.414. Yi, Tibetan
- F2a2 – China (Han from Zhanjiang, etc.), Miao (Guizhou), Kinh (Guangxi), Dai and Lisu (Yunnan)
- F2a3 – China (Han from Xinjiang, Yunnan, Qinghai, and Shandong), Tu, Hui, Mongols in Inner Mongolia
- F2b – China (Han from Qingdao), Taiwan (Hakka)
- F2b1 – Thailand (Lao Isan in Roi Et Province and Chaiyaphum Province, Khon Mueang in Lampang Province), China (Han from Beijing, Xinjiang, etc.), Buryat (Irkutsk Oblast), Yakut, Even (NE Sakha Republic), Yukaghir (NE Sakha Republic),Sardana A Fedorova, Maere Reidla, Ene Metspalu, et al., "Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia." BMC Evolutionary Biology 2013, 13:127. http://www.biomedcentral.com/1471-2148/13/127 Nepal (Newar, 1.1%)
- F2g – China, Ladakh
- F2c – China
- F2c1 – China (Shantou, etc.), Japan
- F2c2 – China (Han from Beijing), Kyrgyzstan (Kyrgyz)
- F2d – China, Uyghur, Thailand (Khon Mueang in Chiang Mai Province and Lamphun Province), Singapore, Japan, Kazakhstan
- F2e – China, Thailand (Tai Yuan in Uttaradit Province, Phuan in Phrae Province and Lopburi Province, Khon Mueang in Chiang Mai Province), Vietnam (Dao)
- F2e1 – China, Barghut (Hulun Buir)
- F2f – Japan, Korea, China, Pakistan (Hazara), Azerbaijan (Astara),{{fact|date=February 2021}} Bashkortostan (Bashkir), Poland
- F2h'i – China
- F2h – China, Tibet (Lhasa), Taiwan, Thailand (Tai Dam in Kanchanaburi Province)
- F2i – China, Taiwan (Makatao), Korea
- F3 (formerly R9a)
- F3a – China (Han from Ili, etc.), Uyghur, Thailand
- F3a1 – China (Han from Yunnan, Guizhou, Shantou, Lanzhou,Hongbin Yao, Mengge Wang, Xing Zou, et al., "New insights into the fine-scale history of western-eastern admixture of the northwestern Chinese population in the Hexi Corridor via genome-wide genetic legacy." Mol Genet Genomics 2021 Mar 1. doi: 10.1007/s00438-021-01767-0.
etc.), Kyrgyz (Tashkurgan), Taiwan (Hakka, etc.), Thailand (Phuan in Suphan Buri Province, Shan in Mae Hong Son Province, Khon Mueang in Chiang Rai Province, Mae Hong Son Province, Chiang Mai Province, Lamphun Province, and Lampang Province), Vietnam (Hmong, Dao)
- F3b – Thailand, Japan, Korea, China (Han from Qijiang), Yi
- F3b1 – Philippines, Comoros (Comorian from Grande Comore), USA
- F3b1a – Taiwan (Rukai, Puyuma, Paiwan, Tsou, Makatao, Bunun, Ami, etc.), Philippines (Maranao)
- F3b1a1 – Philippines (Bugkalot), Indonesia
- F3b1a2 – Taiwan (Puyuma, Bunun, Paiwan, etc.)
- F3b1b – Madagascar, Sumatra, Philippines (Batak from Palawan Island)
- F3b1b1 – Philippines (Ibaloi, Kankanaey, Ifugao), Spain, Denmark
- F4
- F4a – Thailand/Laos, China, Taiwan, Korea
- F4a1
- F4a1a – Japan, China (Han from Lanzhou, She), Taiwan
- F4a1b – China, Japan
- F4a2 – China, Laos (Lao in Vientiane and Luang Prabang), Thailand (Phuan in Lopburi Province, Nyah Kur in Chaiyaphum Province, Khon Mueang in Lamphun Province)
- F4b – China (Han from Beijing), Thailand (Khon Mueang in Mae Hong Son Province, Lao Isan in Roi Et Province)
- F4b1 – China, Taiwan (Atayal, Bunun, Saisiyat, Thao, Tsou, Ami, Makatao, etc.), Philippines, Madagascar
Table of frequencies by ethnic group
{{refimprove|section|date=February 2024}}
class="wikitable" style="float: right;"
! align="center" style="background:#c63;"|Population ! align="center" style="background:#f96;"|Frequency ! align="center" style="background:#f96;"|Count ! align="center" style="background:#f96;"|Source ! align="center" style="background:#f96;"|Subtypes | ||||
Lahu (Lancang, Yunnan) | 0.771 | 35 | F1a=18, F(xF1a, F1b, F1c, F2a)=9 | |
Senoi (Malaysia) | 0.442 | 52 | {{cite journal |vauthors=Hill C, Soares P, Mormina M, Macaulay V, Meehan W, Blackburn J, Clarke D, Raja JM, Ismail P, Bulbeck D, Oppenheimer S, Richards M |date=December 2006 |title=Phylogeography and ethnogenesis of aboriginal Southeast Asians |journal=Molecular Biology and Evolution |volume=23 |issue=12 |pages=2480–2491 |doi=10.1093/molbev/msl124 |pmid=16982817 |doi-access=free |hdl-access=free |hdl=1885/23220}} | F1a1a=23 |
Tujia (Yongshun, Hunan) | 0.433 | 30 | F(xF1a, F1b, F1c, F2a)=6, F1a=4, F1c=2, F1b=1 | |
Shor (Kemerovo) | 0.415 | 82 | F1=33, F2a=1 | |
Lahu (Simao, Yunnan) | 0.344 | 32 | F1a=10, F2a=1 | |
Lahu (Xishuangbanna, Yunnan) | 0.333 | 15 | F1a=3, F1b=1, F1c=1 | |
Pan Yao (Tianlin, Guangxi) | 0.313 | 32 | {{cite journal |vauthors=Wen B, Li H, Gao S, Mao X, Gao Y, Li F, Zhang F, He Y, Dong Y, Zhang Y, Huang W, Jin J, Xiao C, Lu D, Chakraborty R, Su B, Deka R, Jin L |date=March 2005 |title=Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages |journal=Molecular Biology and Evolution |volume=22 |issue=3 |pages=725–734 |doi=10.1093/molbev/msi055 |pmid=15548747 |doi-access=free}} | F3=2, F1b=2, F1a1a=2, F1a1(xF1a1a)=2, F1a(xF1a1)=1, F1c=1 |
Yi (Hezhang County, Guizhou) | 0.300 | 20 | {{fact|date=March 2021}} | F1b=4, F1a=2 |
Lingao (Hainan) | 0.290 | 31 | {{fact|date=March 2021}} | F(xF1, F2, F3, F4)=2, F2=2, F1(xF1a)=1, F1a1(xF1a1a)=1, F1a1a=1, F3=1, F4=1 |
Lowland Yao (Fuchuan, Guangxi) | 0.286 | 42 | F2a=4, F1a1(xF1a1a)=2, F1a(xF1a1)=2, F1b=1, F1c=1, F1(xF1a, F1b, F1c)=1, F3=1 | |
Xiban Yao (Fangcheng, Guangxi) | 0.273 | 11 | F1b=1, F1a(xF1a1)=1, F(xF1, F2a, F3)=1 | |
Lanten Yao (Tianlin, Guangxi) | 0.269 | 26 | F1a(xF1a1)=5, F1a1(xF1a1a)=1, F(xF1, F2a, F3)=1 | |
Bai (Xishuangbanna, Yunnan) | 0.263 | 19 | F1a=2, F1b=2, F(xF1a, F1b, F1c, F2a)=1 | |
Huatou Yao (Fangcheng, Guangxi) | 0.263 | 19 | F1a1a=2, F1a1(xF1a1a)=1, F1a(xF1a1)=1, F(xF1, F2a, F3)=1 | |
Vietnamese | 0.262 | 42 | {{fact|date=March 2021}} | F1a=10, F(xF1a, F1b, F1c, F2)=1 |
Taiwan (aborigines) | 0.253 | 640 | {{fact|date=March 2021}} | F4=72, F3=54, F1a1(xF1a1a)=21, F1a(xF1a1)=14, F2=1 |
Bai (Dali, Yunnan) | 0.250 | 68 | F1a=6, F1c=4, F2a=4, F1b=2, F(xF1a, F1b, F1c, F2a)=1 | |
Indonesian (Mataram, Lombok) | 0.250 | 44 | F1a1a=4, F1a(xF1a1, F1a3, F1a4, F1a5)=4, F1a3=1, F1a4=1, F(xF1a, F1b, F2, F3a, F3b, F4)=1 | |
Uyghur (Uzbekistan/Kyrgyzstan) | 0.250 | 16 | {{cite journal |vauthors=Comas D, Plaza S, Wells RS, Yuldaseva N, Lao O, Calafell F, Bertranpetit J |date=June 2004 |title=Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages |journal=European Journal of Human Genetics |volume=12 |issue=6 |pages=495–504 |doi=10.1038/sj.ejhg.5201160 |pmid=14872198 |doi-access=free}} | F=4 |
Yi (Xishuangbanna, Yunnan) | 0.250 | 16 | F1b=2, F1a=1, F2a=1 | |
Khakassian (Khakassia) | 0.246 | 57 | F1=11, F2a=3 | |
Naxi (Lijiang, Yunnan) | 0.244 | 45 | F1a=8, F1b=2, F2a=1 | |
Bunu (Dahua & Tianlin, Guangxi) | 0.240 | 25 | F1b=2, F(xF1, F2a, F3)=1, F1a1(xF1a1a)=1, F1a1a=1, F3=1 | |
Ket | 0.237 | 38 | {{cite journal |vauthors=Starikovskaya EB, Sukernik RI, Derbeneva OA, Volodko NV, Ruiz-Pesini E, Torroni A, Brown MD, Lott MT, Hosseini SH, Huoponen K, Wallace DC |date=January 2005 |title=Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups |journal=Annals of Human Genetics |volume=69 |issue=Pt 1 |pages=67–89 |doi=10.1046/j.1529-8817.2003.00127.x |pmc=3905771 |pmid=15638829}} | F=9 |
Han (Beijing) | 0.225 | 40 | {{fact|date=March 2021}} | F1a=4, F(xF1a, F1b, F1c, F2)=3, F1b=2 |
Taiwanese (Taipei, Taiwan) | 0.220 | 91 | {{fact|date=March 2021}} | F=20 |
Han (Southwest China; pool of 44 Sichuan, 34 Chongqing, 33 Yunnan, & 26 Guizhou) | 0.219 | 137 | {{fact|date=March 2021}} | F1a=15, F2=8, F3=7 |
Hani (Xishuangbanna, Yunnan) | 0.212 | 33 | F1a=6, F1b=1 | |
Tibetan (Shigatse, Tibet) | 0.207 | 29 | {{fact|date=March 2021}} | F1a=5, F1b=1 |
Tujia (Yanhe County, Guizhou) | 0.207 | 29 | {{fact|date=March 2021}} | F1a=2, F1c=1, F2a3=1, F2b=1, F(xF1, F2)=1 |
Bapai Yao (Liannan, Guangdong) | 0.200 | 35 | F1b=3, F3=2, F1a1a=1, F1a(xF1a1)=1 | |
Indonesian (Waingapu, Sumba) | 0.200 | 50 | F1a4=3, F1a3=2, F1a1a=2, F1a(xF1a1, F1a3, F1a4, F1a5)=1, F1a1(xF1a1a)=1, F3b=1 | |
Manchurian | 0.200 | 40 | {{fact|date=March 2021}} | F(xF1a, F1b, F1c, F2)=3, F1a=2, F1b=2, F1c=1 |
Thai | 0.200 | 40 | {{fact|date=March 2021}} | F1b=8 |
Li (Hainan) | 0.197 | 346 | {{fact|date=March 2021}} | F1a1(xF1a1a)=30, F2=20, F1(xF1a)=4, F1a(xF1a1)=4, F1a1a=3, F3=3, F4=3, F(xF1, F2, F3, F4)=1 |
Han (Xinjiang) | 0.191 | 47 | {{fact|date=March 2021}} | F1a=2, F3=2, F1b=1, F1c=1, F2a2=1, F2a3=1, F4=1 |
Thailand | 0.190 | 105 | Supannee Kaewsutthi, Nopasak Phasukkijwatana, Yutthana Joyjinda et al., "Mitochondrial Haplogroup Background May Influence Southeast Asian G11778A Leber Hereditary Optic Neuropathy", Investigative Ophthalmology & Visual Science, June 2011, Vol. 52, No. 7 | F1=18, F(xF1)=2 |
Lisu (Gongshan, Yunnan) | 0.189 | 37 | F2a=4, F1b=2, F1a=1 | |
Han (southern California) | 0.187 | 390 | {{fact|date=March 2021}} | F=73 |
Oirat Mongol (Xinjiang) | 0.184 | 49 | {{fact|date=March 2021}} | F2(xF2a2, F2a3, F2b)=3, F1b=3, F1a=2, F2b=1 |
Dong (Tianzhu County, Guizhou) | 0.179 | 28 | {{fact|date=March 2021}} | F1a=4, F1b=1 |
Han (Taiwan) | 0.175 | 1117 | {{fact|date=March 2021}} | F=196 |
CHB (Han from Beijing Normal University) | 0.174 | 121 | {{fact|date=March 2021}} | F=21 |
Jino (Xishuangbanna, Yunnan) | 0.167 | 18 | F1a=2, F1b=1 | |
Nu (Gongshan, Yunnan) | 0.167 | 30 | F2a=5 | |
Gelao (Daozhen County, Guizhou) | 0.161 | 31 | {{fact|date=March 2021}} | F1a=3, F1(xF1a, F1b, F1c)=1, F(xF1, F2)=1 |
Nepal (Newar)
|0.155 | |F1c1a = 2.4%, F1d = 12%, F1g = 2.4%, F2b1 = 1.1% | ||||
CHD (Han from Denver) | 0.151 | 73 | {{fact|date=March 2021}} | F=11 |
Filipino (Palawan) | 0.150 | 20 | {{fact|date=March 2021}} | F3b2=3 |
Indonesian (52 Pekanbaru, 42 Medan, 34 Bangka, 28 Palembang, & 24 Padang) | 0.150 | 180 | F1a1a=9, F1a(xF1a1, F1a3, F1a4, F1a5)=8, F1a5=3, F4=3, F1a3=2, F1a4=2 | |
Kyrgyz (Uzbekistan/Kyrgyzstan) | 0.150 | 20 | F=3 | |
Yi (Shuangbai, Yunnan) | 0.150 | 40 | F(xF1a, F1b, F1c, F2a)=2, F1a=2, F1b=2 | |
Mongolian (Ulan Bator) | 0.149 | 47 | {{fact|date=March 2021}} | F1a=3, F1b=3, F2a=1 |
Borneo (89 Banjarmasin & 68 Kota Kinabalu) | 0.146 | 157 | F3b=9, F(xF1a, F1b, F2, F3a, F3b, F4)=4, F1a3=3, F1a4=3, F1a1(xF1a1a)=2, F1a(xF1a1, F1a3, F1a4, F1a5)=1, F1a1a=1 | |
Indonesian (Bali) | 0.146 | 82 | F1a(xF1a1, F1a3, F1a4, F1a5)=5, F1a1(xF1a1a)=4, F1a1a=2, F(xF1a, F1b, F2, F3a, F3b, F4)=1 | |
Hmong (Jishou, Hunan) | 0.146 | 103 | F1a1(xF1a1a)=4, F1a1a=3, F(xF1, F2a, F3)=3, F1a(xF1a1)=2, F1b=2, F3=1 | |
Aini (Xishuangbanna, Yunnan) | 0.140 | 50 | F1a=6, F(xF1a, F1b, F1c, F2a)=1 | |
Indonesian (Ambon) | 0.140 | 43 | F1a3=3, F1a4=2, F1a1a=1 | |
Cun (Hainan) | 0.133 | 30 | {{fact|date=March 2021}} | F4=3, F1a1(xF1a1a)=1 |
Hui (Xinjiang) | 0.133 | 45 | {{fact|date=March 2021}} | F1b=2, F1c=2, F1a=1, F2a3=1 |
Batak (Palawan) | 0.129 | 31 | {{fact|date=March 2021}} | F1a3=3, F3b2=1 |
Yi (Luxi, Yunnan) | 0.129 | 31 | F1b=3, F(xF1a, F1b, F1c, F2a)=1 | |
Mongolian (Khovd Province)
|0.128 |429 |F(xF1e1a)=7, F1=3, F1a=2, F1a1=4, F1a1a(xF1a1a1)=4, F1a2=2, F1b=2, F1b1(xF1b1b)=5, F2=1, F2a=14, F2b1=4, F4a=7 | ||||
Guoshan Yao (Jianghua, Hunan) | 0.125 | 24 | F1a(xF1a1)=1, F1b=1, F3=1 | |
Tu Yao (Hezhou, Guangxi) | 0.122 | 41 | F1a1a=4, F1a(xF1a1)=1 | |
Gelao (Daozhen County, Guizhou) | 0.118 | 102 | {{fact|date=March 2021}} | F1a(xF1a1)=4, F1b=3, F2(xF2a, F2b)=2, F3a=2, F3(xF3a)=1 |
Tibetan (Nagchu, Tibet) | 0.114 | 35 | {{fact|date=March 2021}} | F=4 |
Tibetan (Lhasa, Tibet) | 0.114 | 44 | {{fact|date=March 2021}} | F1a=2, F2=2, F1b=1 |
Filipino (Luzon) | 0.113 | 177 | {{cite journal |vauthors=Tabbada KA, Trejaut J, Loo JH, Chen YM, Lin M, Mirazón-Lahr M, Kivisild T, De Ungria MC |date=January 2010 |title=Philippine mitochondrial DNA diversity: a populated viaduct between Taiwan and Indonesia? |journal=Molecular Biology and Evolution |volume=27 |issue=1 |pages=21–31 |doi=10.1093/molbev/msp215 |pmid=19755666 |doi-access=free}} | F1a3=6, F1a4=6, F3b=5, F4b=2, F1a1a=1 |
Indonesian (Alor) | 0.111 | 45 | F1a4=3, F1a1a=1, F1a(xF1a1, F1a3, F1a4, F1a5)=1 | |
Indonesian (Sulawesi, incl. 89 Manado, 64 Toraja, 46 Ujung Padang, & 38 Palu) | 0.110 | 237 | F1a4=12, F1a3=4, F1a(xF1a1, F1a3, F1a4, F1a5)=4, F1a1a=3, F1a1(xF1a1a)=1, F1a5=1, F1b=1 | |
Tujia (western Hunan) | 0.109 | 64 | F(xF1a, F1b, F1c, F2a)=2, F1a=2, F1b=2, F1c=1 | |
Cham (Bình Thuận, Vietnam) | 0.107 | 168 | {{cite journal |vauthors=Peng MS, Quang HH, Dang KP, Trieu AV, Wang HW, Yao YG, Kong QP, Zhang YP |date=October 2010 |title=Tracing the Austronesian footprint in Mainland Southeast Asia: a perspective from mitochondrial DNA |journal=Molecular Biology and Evolution |volume=27 |issue=10 |pages=2417–2430 |doi=10.1093/molbev/msq131 |pmid=20513740 |doi-access=free}} | F1a1a=10, F1(xF1a)=3, F1a(xF1a1)=3, F1a1(xF1a1a)=2 |
Tibetan (Shannan, Tibet) | 0.105 | 19 | {{fact|date=March 2021}} | F=2 |
Altai Kizhi (Altai Republic)
|0.102 |324 |F1=25, F2=8 | ||||
Dingban Yao (Mengla, Yunnan) | 0.100 | 10 | F1a(xF1a1)=1 | |
Filipino (Visayas) | 0.098 | 112 | F1a4=7, F1a3=3, F3b=1 | |
Korean (South Korea) | 0.097 | 185 | {{fact|date=March 2021}} | F1a=8, F1b=8, F2(xF2a)=2 |
Korean (Seoul National University Hospital)
|0.097 |1365 |F=132 | ||||
Filipino | 0.094 | 64 | F1a3=3, F1a4=3 | |
Mien (Shangsi, Guangxi) | 0.094 | 32 | F1a1(xF1a1a)=2, F1a1a=1 | |
Tibetan (Tibet) | 0.093 | 216 | {{fact|date=March 2021}} | F1a=13, F1b=4, F2=3 |
Mongolian (Mongolia)
|0.092 |2420 |F1a=55, F1b=71, F1c=13, F1(xF1d, F1e1)=33, F2=44, F3a=2, F4a=7 | ||||
CHS (Han from Hunan & Fujian) | 0.091 | 55 | {{fact|date=March 2021}} | F=5 |
Altai (Altai Republic)
|0.091 |110 |F=10 | ||||
Mongolian (Khentii Province)
|0.091 |132 |F1=1, F1a=3, F1b=5, F1c=2, F2b=1 | ||||
Buryat | 0.087 | 126 | {{fact|date=March 2021}} | F1b=6, F1a=3, F(xF1a, F1b, F1c, F2a)=2 |
Tofalar | 0.087 | 46 | F1b=4 | |
Uzbek (Xinjiang) | 0.086 | 58 | {{fact|date=March 2021}} | F2a3=2, F4=2, F1b=1 |
Tuvinian (Tuva) | 0.086 | 105 | F1=8, F2a=1 | |
Korean (South Korea)
|0.083 |850 |F1a(xF1a3)=7, F1a1=17, F1b1=19, F1(xF1c, F1d)=11, F2=14, F3a=2, F4a1a=1 | ||||
Japanese (Tōhoku) | 0.083 | 336 | {{fact|date=March 2021}} | F=28 |
Mongol (New Barag Left Banner) | 0.083 | 48 | {{fact|date=March 2021}} | F1a=2, F1c=1, F2a=1 |
Pumi (Ninglang, Yunnan) | 0.083 | 36 | F2a=2, F1b=1 | |
Tibetan (Diqing, Yunnan) | 0.083 | 24 | F1a=1, F1b=1 | |
Korean (South Korea)
|0.080 |593 |F=3, F1=7, F1ac=2, F1a=12, F1c=2, F1b=16, F2a=3 | ||||
Korean (Ulsan)
|0.079 |1094 |F=86 | ||||
Korean (northern China) | 0.078 | 51 | {{fact|date=March 2021}} | F(xF1a, F1b, F1c, F2)=1, F1a=1, F1b=1, F1c=1 |
Daur (Hulunbuir)
|0.076 |209 |F1a=2, F1a1(xF1a1a)=4, F1a1a1=1, F1b1(xF1b1b)=2, F1c1a=1, F2(xF2d)=5, F4a1b=1 | ||||
JPT (Japanese from Tokyo) | 0.076 | 118 | {{fact|date=March 2021}} | F=9 |
Kazakh (Xinjiang) | 0.075 | 53 | {{fact|date=March 2021}} | F1b=3, F2(xF2a2, F2a3, F2b)=1 |
Chinese (Shenyang, Liaoning) | 0.075 | 160 | {{fact|date=March 2021}} | F=12 |
Danga (Hainan) | 0.075 | 40 | {{fact|date=March 2021}} | F1a1(xF1a1a)=1, F2=1, F3=1 |
Japanese (northern Kyūshū) | 0.074 | 256 | {{fact|date=March 2021}} | F=19 |
Tibetan (Nyingchi, Tibet) | 0.074 | 54 | {{fact|date=March 2021}} | F1a=2, F1b=2 |
Mongolian (Sükhbaatar Province)
|0.073 |246 |F=1, F1a=5, F1b=8, F1c=3, F2i=1 | ||||
Uyghur | 0.073 | 55 | {{fact|date=March 2021}} | F1b=2, F1a=1, F1c=1 |
Filipino (Mindanao) | 0.071 | 70 | F3b=2, F1a4=2, F1a3=1 | |
Korean (Seoul & Daejeon, South Korea) | 0.069 | 261 | {{fact|date=March 2021}} | F1=12, F(xF1)=6 |
Tibetan (Chamdo, Tibet) | 0.069 | 29 | {{fact|date=March 2021}} | F1a=2 |
Semelai (Malaysia) | 0.066 | 61 | F1a1a=4 | |
Japanese (Hokkaidō) | 0.065 | 217 | {{harvnb|Asari|2007}} | F=14 |
Mongolian (Dornod Province)
|0.065 |370 |F1(xF1c, F1d)=6, F1a=7, F1b=7, F2=4 | ||||
Wuzhou Yao (Fuchuan, Guangxi) | 0.065 | 31 | F1a1(xF1a1a)=1, F3=1 | |
Korean (South Korea) | 0.064 | 203 | {{fact|date=March 2021}} | F=13 |
Mongolian (Ulan Bator) | 0.064 | 47 | F1=3 | |
Uyghur (Xinjiang) | 0.064 | 47 | {{fact|date=March 2021}} | F1b=2, F1a=1 |
Bashkir (Beloretsky, Sterlibashevsky, Ilishevsky, & Perm) | 0.063 | 221 | F=14 | |
Dungan (Uzbekistan/Kyrgyzstan) | 0.063 | 16 | F=1 | |
Japanese (Miyazaki) | 0.060 | 100 | {{cite journal |vauthors=Taketo U, Rinnosuke H, Kenshi S, Kazuhiko I, Kazumasa S, Kentaro K |year=2007 |title=Mitochondrial DNA Sequence Variation and Phylogenetic Analysis in Japanese Individuals from Miyazaki Prefecture |journal=Japanese Journal of Forensic Science and Technology |volume=12 |issue=1 |pages=83–96 |doi=10.3408/jafst.12.83 |doi-access=free}} | F1b=3, F1a=2, F2a=1 |
Kazakh (Zhetysu)
|0.060 |200 |F1=11, F2=1 | ||||
Tharu (Chitwan, Nepal) | 0.060 | 133 | F1c=7, F1(xF1c, F1d)=1 | |
Japanese (Gifu) | 0.059 | 1617 | {{cite journal |vauthors=Fuku N, Park KS, Yamada Y, Nishigaki Y, Cho YM, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Nozawa Y, Lee HK, Tanaka M |date=March 2007 |title=Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians |journal=American Journal of Human Genetics |volume=80 |issue=3 |pages=407–415 |doi=10.1086/512202 |pmc=1821119 |pmid=17273962}} | F=96 |
Japanese (Tōkai) | 0.057 | 282 | {{fact|date=March 2021}} | F=16 |
Teleut (Kemerovo) | 0.057 | 53 | F1=3 | |
Altai Kizhi | 0.056 | 90 | F1=3, F2a=2 | |
Kalmyk (Kalmykia) | 0.055 | 110 | F1=6 | |
Tibetan (Shannan, Tibet) | 0.055 | 55 | {{fact|date=March 2021}} | F1a=2, F2=1 |
Tibetan (Qinghai) | 0.054 | 56 | F1c=2, F1a=1 | |
Japanese | 0.052 | 211 | {{cite journal |vauthors=Maruyama S, Minaguchi K, Saitou N |date=August 2003 |title=Sequence polymorphisms of the mitochondrial DNA control region and phylogenetic analysis of mtDNA lineages in the Japanese population |journal=International Journal of Legal Medicine |volume=117 |issue=4 |pages=218–225 |doi=10.1007/s00414-003-0379-2 |pmid=12845447 |s2cid=1224295}} | F1b=9, F1a=2 |
Hmong (Wenshan, Yunnan) | 0.051 | 39 | F1b=1, F3=1 | |
Kazakh (Kosh-Agach, Altai Republic) | 0.051 | 98 | {{cite journal |vauthors=Derenko M, Malyarchuk B, Denisova G, Perkova M, Rogalla U, Grzybowski T, Khusnutdinova E, Dambueva I, Zakharov I |year=2012 |title=Complete mitochondrial DNA analysis of eastern Eurasian haplogroups rarely found in populations of northern Asia and eastern Europe |journal=PLOS ONE |volume=7 |issue=2 |pages=e32179 |bibcode=2012PLoSO...732179D |doi=10.1371/journal.pone.0032179 |pmc=3283723 |pmid=22363811 |doi-access=free}} | F1=5 |
Karakalpak (Uzbekistan/Kyrgyzstan) | 0.050 | 20 | F=1 | |
Tharu (Morang, Nepal) | 0.050 | 40 | F1c=1, F1d=1 | |
Turkmen (Uzbekistan/Kyrgyzstan) | 0.050 | 20 | F=1 | |
Korean (South Korea) | 0.049 | 103 | F1=5 | |
Oroqen (Oroqen Autonomous Banner) | 0.045 | 44 | {{fact|date=March 2021}} | F1b=2 |
Yakut | 0.043 | 117 | {{fact|date=March 2021}} | F2a=3, F1b=2 |
Tuvan | 0.042 | 95 | F(xF1b)=3, F1b=1 | |
Kyrgyz (Talas) | 0.042 | 48 | {{fact|date=March 2021}} | F1a=1, F1b=1 |
Tibetan (Nyingchi, Tibet) | 0.042 | 24 | {{fact|date=March 2021}} | F=1 |
Khamnigan (Buryatia) | 0.040 | 99 | F1=4 | |
Iu Mien (Mengla, Yunnan) | 0.037 | 27 | F(xF1, F2a, F3)=1 | |
Kazakh | 0.036 | 55 | {{fact|date=March 2021}} | F1b=2 |
Barghut (Hulunbuir) | 0.034 | 149 | F1=4, F2=1 | |
Buryat (Buryatia) | 0.031 | 295 | F1=7, F2a=2 | |
Ulch people
|0.031 |160 |{{fact|date=March 2021}} |F1a=5 | ||||
Tibetan (Zhongdian, Yunnan) | 0.029 | 35 | F2a=1 | |
Kim Mun (Malipo, Yunnan) | 0.025 | 40 | F1a1(xF1a1a)=1 | |
Uzbek (Uzbekistan/Kyrgyzstan) | 0.025 | 40 | F=1 | |
Okinawa | 0.025 | 326 | {{fact|date=March 2021}} | F=8 |
Evenk (New Barag Left Banner) | 0.021 | 47 | {{fact|date=March 2021}} | F1c=1 |
Ainu | 0.020 | 51 | {{fact|date=March 2021}} | F1b=1 |
Evenk (53 Stony Tunguska basin & 18 Tugur-Chumikan) | 0.014 | 71 | F1b=1 | |
Telenghit (Altai Republic) | 0.014 | 71 | F1=1 | |
Tubalar | 0.014 | 72 | F1b=1 | |
Evenk (Krasnoyarsk) | 0.014 | 73 | F1=1 | |
Ulchi (Old & New Bulava, Ulchsky, Khabarovsk) | 0.011 | 87 | F(xF1b)=1 | |
Mansi | 0.010 | 98 | F=1 | |
Khanty | 0.009 | 106 | F1=1 | |
Chukchi (Anadyr) | 0.000 | 15 | - | |
Bukharan Arab (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |
Crimean Tatar (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |
Iranian (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |
Kazakh (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |
Tajik (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |
Hindu (Chitwan, Nepal) | 0.000 | 24 | - | |
Nganasan | 0.000 | 24 | - | |
Buryat (Kushun, Nizhneudinsk, Irkutsk Oblast) | 0.000 | 25 | - | |
Kurd (northwestern Iran) | 0.000 | 25 | - | |
Andhra Pradesh (tribal) | 0.000 | 29 | - | |
Batek (Malaysia) | 0.000 | 29 | - | |
Mendriq (Malaysia) | 0.000 | 32 | - | |
Negidal | 0.000 | 33 | - | |
Temuan (Malaysia) | 0.000 | 33 | - | |
Yakut (Yakutia) | 0.000 | 36 | - | |
Tibetan (Deqin, Yunnan) | 0.000 | 40 | - | |
Tajik (Tajikistan) | 0.000 | 44 | - | |
Daur (Evenk Autonomous Banner) | 0.000 | 45 | {{fact|date=March 2021}} | - |
Evenk (Buryatia) | 0.000 | 45 | - | |
Udege (Gvasiugi, Imeni Lazo, Khabarovsk) | 0.000 | 46 | - | |
Itelmen | 0.000 | 47 | - | |
Kyrgyz (Sary-Tash) | 0.000 | 47 | {{fact|date=March 2021}} | - |
Korean (Arun Banner) | 0.000 | 48 | {{fact|date=March 2021}} | - |
Jahai (Malaysia) | 0.000 | 51 | - | |
Nivkh (northern Sakhalin) | 0.000 | 56 | - | |
Mansi | 0.000 | 63 | - | |
Chukchi | 0.000 | 66 | {{fact|date=March 2021}} | - |
Siberian Eskimo | 0.000 | 79 | - | |
Persian (eastern Iran) | 0.000 | 82 | - | |
Koryak | 0.000 | 155 | - |
{{Clear}}
See also
References
{{Reflist}}
Sources
- {{cite journal | last1 = Asari | first1 = M | display-authors = etal | year = 2007 | title = Utility of haplogroup determination for forensic mtDNA analysis in the Japanese population | journal = Leg Med | volume = 9| issue = 5| pages = 237–240| doi = 10.1016/j.legalmed.2007.01.007 | pmid = 17467322 }}
External links
{{Commons category|Haplogroup F (mtDNA)}}
- General
- Ian Logan's [http://www.ianlogan.co.uk/sequences_by_group/haplogroup_select.htm Mitochondrial DNA Site]
- Mannis van Oven's [http://www.phylotree.org Phylotree]
- Haplogroup F
- YFull MTree's [https://www.yfull.com/mtree/F/ Haplogroup F]
- MITOMAP's [https://mitomap.org/cgi-bin/haplo_distribution?hg=F Haplogroup F]
- FamilyTreeDNA's mtDNA Haplotree: [https://www.familytreedna.com/public/mt-dna-haplotree/F Haplogroup F]
- [https://web.archive.org/web/20060320200143/https://www3.nationalgeographic.com/genographic/atlas.html?card=mm017 Spread of Haplogroup F], from National Geographic
{{MtDNA}}
{{DEFAULTSORT:Haplogroup F (Mtdna)}}