Listed here are the human Y-chromosome DNA haplogroups found in various ethnic groups and populations from North Africa and the Sahel (Tuaregs).
Population | Language (if specified) | n | A/B | E(xE1b1b) | E-M215 | G | I | J | R1a | R1b | Other | Study |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Algerians | 377 | 0.3 | 13.0 | 54.6 | 19.9 | 12.2 | Bekada et al. (2015) [1] | |||||
Amazighs (Algeria - Aurès) | AA (Tamazight) | 218 | 0 | 4.6 | 84.4 | 0 | 0.5 | 5.5 | 2.3 | 0 | 1.7 | Abdeli and Benhassine (2019) [2] |
Amazighs (Algeria - Mzab) | AA (Tamazight) | 67 | 0 | 4.5 | 89.6 | 1.5 | 0 | 1.5 | 0 | 3 | 0 | Dugoujon et al. (2009) [3] |
Amazighs (Algeria - Mzab) | AA (Tamazight) | 20 | 0 | 10 | 80 | 0 | 0 | 0 | 0 | 10 | 0 | Bekada et al. (2015) [1] |
Amazighs (Algeria - Tizi Ouzou) | AA (Tamazight) | 16 | 0 | 0 | 47.3 | 0 | 0 | 15.7 | 0 | 15.7 | 0 | Arredi et al. (2004) [4] |
Amazighs (Algeria - Tuat) | AA (Tamazight) | 35 | 0 | 25.6 | 51.4 | 0 | 0 | 11.4 | 0 | 8.5 | 0 | Bekada et al. (2014) [1] |
Amazighs (Egypt - Siwa) | AA (Tamazight) | 93 | 28 | 6.5 | 12 | 3.2 | 0 | 14 | 0 | 28 | 8.3 | Dugoujon et al. (2009) [3] |
Amazighs (Libya) | AA (Tamazight) | 83 | 1.3 | 38.5 | 53 | 0 | 0 | 0 | 0 | 0 | 0 | Bekada et al. (2013) [5] |
Amazighs (Morocco) | AA (Tamazight) | 64 | 0 | 6.3 | 79.6 | 0 | 0 | 0 | 0 | 0 | 14.1 | Semino et al. (2004) [6] |
Amazighs (Morocco - Amizmiz) | AA (Tamazight) | 33 | 3 | 6.1 | 90.8 | 0 | 0 | 0 | 0 | 0 | 0 | Alvarez et al. (2009) |
Amazighs (Morocco - Asni) | AA (Tamazight) | 54 | 0 | 9.3 | 85.2 | 0 | 0 | 1.9 | 0 | 1.9 | 1.9 | Dugoujon et al. (2009) [3] |
Amazighs (Morocco - Bouhria) | AA (Tamazight) | 67 | 0 | 7.5 | 79.1 | 6 | 0 | 3 | 4.5 | 0 | 0 | Dugoujon et al. (2009) [3] |
Amazighs (Morocco - Middle Atlas) | AA (Tamazight) | 69 | 2.9 | 5.7 | 81.1 | 4.3 | 0 | 5.8 | 0 | 0 | 0 | Dugoujon et al. (2009) [3] |
Amazighs (Morocco - North) | AA (Tamazight) | 55 | 0 | 12.7 | 65.1 | 0 | 0 | 0 | 0 | 0 | 12.7 | Semino et al. (2004) [6] |
Amazighs (Morocco - South) | AA (Tamazight) | 35 | 0 | 2.5 | 85 | 0 | 0 | 0 | 0 | 0 | 12.5 | Semino et al. (2004) [6] |
Amazighs (Tunisia - Bou Omrane) | AA (Tamazight) | 40 | 0 | 5 | 92.5 | 0 | 0 | 0 | 0 | 0 | 0 | Ennafaa et al. (2011) [7] |
Amazighs (Tunisia - Bou Saad) | AA (Tamazight) | 40 | 0 | 0 | 92.5 | 0 | 0 | 5 | 0 | 0 | 2.5 | Ennafaa et al. (2011) [7] |
Amazighs (Tunisia - Chenini–Douiret) | AA (Tamazight) | 27 | 0 | 0 | 100 | 0 | 0 | 0 | 0 | 0 | 0 | Fadhlaoui-Zid et al. (2011) [8] |
Amazighs (Tunisia - Djerba) | AA (Tamazight) | 46 | 2.2 | 0 | 80.4 | 0 | 0 | 10.9 | 4.3 | 2.2 | 0 | Manni et al. (2005) [9] |
Amazighs (Tunisia - Kesra) | AA (Tamazight) | 23 | 8.7 | 0 | 91.3 | 0 | 0 | 0 | 0 | 0 | 0 | Cherni et al. (2005) [10] |
Amazighs (Tunisia - Tekrouna) | AA (Tamazight) | 19 | 0 | 0 | 100 | 0 | 0 | 0 | 0 | 0 | 0 | Frigi, S. et al. (2006) [11] |
Amazighs (Tunisia - Sejenane) | AA (Tamazight) | 47 | 4.3 | 2.1 | 51.1 | 2.1 | 2.1 | 36.1 | 0 | 0 | 2.2 | Frigi, S. et al. (2006) [12] |
Amazighs (Tunisia - Jradou) | AA (Semitic) | 32 | 0 | 0 | 100 | 0 | 0 | 0 | 0 | 0 | 0 | Fadhlaoui-Zid et al. (2011) [8] |
Amazighs (Tunisia - Sened) | AA (Tamazight) | 35 | 0 | 0 | 65.7 | 0 | 0 | 31.4 | 0 | 0 | 0 | Fadhlaoui-Zid et al. (2011) [8] |
Andalusians (Tunisia - Qalaat Al-Andalus) | AA (Arabic) | 19 | 0 | 0 | 89.5 | 0 | 0 | 10.5 | 0 | 0 | 0 | Cherni et al. (2005) [13] |
Andalusians (Tunisia - Testour) | AA (Arabic) | 48 | 2.1 | 2.1 | 68.7 | 0 | 0 | 25.0 | 2.1 | 0 | 0 | Cherni et al. (2005) [13] |
Andalusians (Tunisia - Esslouguia) | AA (Arabic) | 22 | 0 | 0 | 59.1 | 0 | 0 | 18.2 | 13.6 | 4.6 | 4.5 | Cherni et al. (2005) [13] |
Andalusians (Tunisia - El Alia) | AA (Arabic) | 43 | 0 | 0 | 44.2 | 4.7 | 2.3 | 34.9 | 0 | 9.3 | 4.6 | Cherni et al. (2005) [13] |
Arabs (Algeria - Algiers) | AA (Semitic) | 35 | 0 | 2.9 | 54.3 | 0 | 0 | 28.6 | 0 | 0 | 0 | Arredi et al. (2004) [4] |
Arabs (Algeria - Algiers) | AA (Semitic) | 26 | 0 | 3.8 | 69.2 | 0 | 0 | 19.2 | 0 | 0 | 0 | Bekada et al. (2014) [1] |
Arabs (Algeria - Oran) | AA (Semitic) | 102 | 0 | 7.9 | 51 | 0 | 0 | 27.4 | 1 | 11.8 | 1 | Robino et al. (2008) [14] |
Arabs (Algeria - Oran) | AA (Semitic) | 80 | 1.2 | 11.2 | 47.5 | 0 | 0 | 23.7 | 0 | 7.5 | 0 | Bekada et al. (2014) [1] |
Arabs (Algeria - Sahara) | AA (Semitic) | 60 | 0 | 3.3 | 85 | 0 | 0 | 10 | 0 | 0 | 0 | Bekada et al. (2014) [1] |
Lower Egyptians (Egypt) | AA (Semitic) | 370 | 1.4 | 3.0 | 43.8 | 5.7 | 0.5 | 27.6 | 2.2 | 5.9 | 10 | Bekada et al. (2013) [5] |
Lower Egyptians(Egypt) | AA (Semitic) | 147 | 2.7 | 2.7 | 36.1 | 9.5 | 0 | 31.9 | 3.4 | 4.1 | 2.1 | Luis et al. (2004) [15] |
Delta Egyptians (Egypt - North) | AA (Semitic) | 44 | 2.3 | 0 | 52.3 | 0 | 0 | 18.2 | 2.3 | 9.9 | 6.8 | Arredi et al. (2004) [4] |
Upper Egyptians (Egypt - South) | AA (Semitic) | 29 | 0 | 0 | 31 | 0 | 3.4 | 24.1 | 0 | 13.8 | 0 | Arredi et al. (2004) [4] |
Bedouins (Egypt - Western Desert) | AA (Semitic) | 35 | 0 | 5.7 | 62.9 | 0 | 0 | 31.4 | 0 | 0 | 0 | Kujanová et al. (2009) [16] |
Libyans | AA (Semitic) | 215 | 0 | 1.4 | 49.3 | 5.1 | 0 | 41.4 | 0.5 | 2.3 | 0 | Fadhlaoui-Zid et al. (2013) [17] |
Arabs (Mauritania) | AA (Semitic) | 189 | 0.5 | 12.7 | 66.6 | 0 | 0 | 13.2 | 0 | 7.4 | 0.1 | Bekada et al. (2013) [5] |
Arabs (Morocco) | AA (Semitic) | 49 | 0 | 0 | 75.5 | 0 | 0 | 20.4 | 0 | 0 | 0 | Semino et al. (2004) [6] |
Arabs (Morocco) | AA (Semitic) | 44 | 0 | 0 | 63.7 | 0 | 0 | 15.9 | 0 | 0 | 0 | Semino et al. (2004) [6] |
Arabs (Morocco - Sahara) | AA (Semitic) | 89 | 0 | 20.2 | 59.6 | 0 | 0 | 20.2 | 0 | 0 | 0 | Fregel et al. (2009) [18] |
Arabs (Tunisia - Kairouan) | AA (Semitic) | 49 | 2 | 0 | 83.8 | 2 | 0 | 10.2 | 0 | 0 | 2.0 | Elkamel et al. (2021) [19] |
Arabs (Tunisia - Oueslatia) | AA (Semitic) | 46 | 0 | 0 | 23.9 | 0 | 0 | 54.4 | 0 | 4.3 | 17.4 | Elkamel et al. (2021) [20] |
Arabs (Tunisia - Djerba) | AA (Semitic) | 47 | 0 | 0 | 93.6 | 0 | 0 | 4.3 | 0 | 0 | 2.1 | Manni et al. (2005) [9] |
Arabs (Tunisia - Djerba) | AA (Semitic) | 47 | 0 | 0 | 75 | 0 | 0 | 11.7 | 0 | 0 | 0 | Ennafaa et al. (2011) [7] |
Arabs (Tunisia - Sousse) | AA (Semitic) | 220 | 0.5 | 2.3 | 54.6 | 0.5 | 0 | 34.1 | 0.5 | 0.9 | 6.8 | Fadhlaoui-Zid et al. (2015) [21] |
Arabs (Tunisia - Tunis) | AA (Semitic) | 33 | 0 | 0 | 66.5 | 0 | 0 | 24.2 | 0 | 0 | 0 | Fadhlaoui-Zid et al. (2011) [8] |
Arabs (Tunisia - Tunis) | AA (Semitic) | 148 | 0 | 2 | 49.3 | 0 | 0 | 35.8 | 0.7 | 6.1 | 0.7 | Arredi et al. (2004) [4] |
Arabs (Tunisia - Zaghouan) | AA (Semitic) | 32 | 0 | 9.4 | 43.7 | 0 | 0 | 46.9 | 0 | 0 | 0 | Fadhlaoui-Zid et al. (2011) [8] |
Arabs (Tunisia - Zriba) | AA (Semitic) | 31 | 0 | 0 | 100 | 0 | 0 | 0 | 0 | 0 | 0 | Cherni et al. (2005) [13] |
Copts of Sudan | AA (Egyptian) | 100 | 0 | 74 | 0 | 7 | 0 | 1 | 0 | 0 | 15 | Crubézy2010 [22] |
Jews (Tunisia - Djerba) | AA (Semitic) | 34 | 0 | 0 | 0 | 0 | 0 | 100 | 0 | 0 | 0 | Manni et al. (2005) [9] |
Libyans | 175 | 0.6 | 0.6 | 44.6 | 1.1 | 1.1 | 34.3 | 1.7 | 5.1 | 10.9 | Triki-Fendri et al. (2015) [23] | |
Moroccans | 760 | 0.9 | 6 | 79 | 0.6 | 0.1 | 7.6 | 0 | 4.4 | 0 | Bekada et al. (2013) [5] | |
Moroccans | 316 | 0 | 0 | 52.5 | 0 | 0 | 1.2 | 0 | 3.4 | 42.9 | Zalloua et al. (2008) [24] | |
Moroccans | 221 | 0 | 6.4 | 75.9 | 0.9 | 0.5 | 9.1 | 0 | 4.1 | 0 | Fregel et al. (2009) [18] | |
Moroccans | 176 | 0 | 6.3 | 66.7 | 0 | 0 | 13.6 | 0 | 2.8 | 0 | Bosch et al. (2001) [25] | |
Moroccans | 51 | 3.9 | 5.9 | 54.9 | 0 | 0 | 19.6 | 0 | 3.9 | 0 | Onofri et al. (2008) [26] | |
Moroccans (Central) | 87 | 0 | 9.8 | 62.2 | 0 | 0 | 28 | 0 | 0 | 0 | Fadhlaoui-Zid et al. (2013) [17] | |
Spaniards (Canary Islands) | IE (Romance) | 652 | 0 | 1.4 | 14.1 | 4 | 9.7 | 13.9 | 2.8 | 50.6 | 0 | Fregel et al. (2009) [18] |
Subsaharans (Tunisia - Djerba) | 42 | 0 | 33.3 | 11.9 | 0 | 11.9 | 2.4 | 2.4 | 35.7 | 2.4 | Khodjet-El-Khil, H. et al. (2005) [27] | |
Tuaregs (Libya) | AA (Tamazight) | 47 | 0 | 42.5 | 48.9 | 0 | 0 | 0 | 0 | 6.4 | 2.1 | Ottoni et al. (2011) [28] |
Tunisians | 601 | 0.1 | 1.1 | 71.7 | 0.1 | 0.1 | 17.9 | 0.5 | 2.1 | 3.7 | Bekada et al. (2013) [5] | |
Tunisians | 62 | 0 | 0 | 82.3 | 0 | 0 | 8 | 0 | 0 | 9.7 | Zalloua et al. (2008) [24] | |
Tunisians (immigrants to Italy) | 52 | 0 | 0 | 57.7 | 0 | 0 | 38.4 | 0 | 0 | 0 | Onofri et al. (2008) [26] |
This section relies largely or entirely on a single source .(May 2023) |
Samples over-represent the smaller populations which are usually the subject of genetic studies [29]
Country [5] | n | A | B | E-M33 | E-M2 | E-M35* | E-M78* | E-V12 | E-V32 | E-V13 | E-V22 | E-V65 | E-M81 | E-M34 | F | G | I | J1 | J2 | K | L | O | P,R | Q | R1a | R1b-V88 | R1b-M269 | R2 | T |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Mauritania/Western Sahara | 189 | - | 0.53 | 5.29 | 6.88 | - | - | - | - | - | - | - | 55.56 | 11.11 | - | - | - | 13.23 | - | - | - | - | - | - | - | 6.88 | 0.53 | - | - |
Morocco | 760 | 0.26 | 0.66 | 2.76 | 3.29 | 4.21 | 0.79 | 0.26 | - | 0.26 | 1.84 | 3.68 | 67.37 | 0.66 | 0.26 | 0.66 | 0.13 | 6.32 | 1.32 | 0.53 | - | - | 0.26 | - | - | 0.92 | 3.55 | - | - |
Algeria | 156 | - | - | 0.64 | 5.13 | 0.64 | 1.92 | 0.64 | - | 0.64 | 1.28 | 1.92 | 44.23 | 1.28 | 3.85 | - | - | 21.79 | 4.49 | 0.64 | - | - | - | 0.64 | 0.64 | 2.56 | 7.04 | - | - |
Tunisia | 601 | - | 0.17 | 0.5 | 0.67 | 1.66 | - | - | - | - | 3 | 3.16 | 62.73 | 1.16 | 2.66 | 0.17 | 0.17 | 16.64 | 2.83 | 0.33 | - | - | 0.33 | - | 0.5 | 1.83 | 0.33 | - | 1.16 |
Libya | 83 | - | - | - | 38.55 | - | - | - | - | 2.41 | - | 4.82 | 45.78 | - | - | - | - | - | - | - | - | - | 2.41 | - | - | 6.02 | - | - | - |
Egypt | 370 | 1.35 | - | 0.54 | 2.43 | 3.24 | 0.81 | 7.03 | 1.62 | 0.81 | 9.19 | 2.43 | 11.89 | 6.76 | 1.08 | 5.68 | 0.54 | 20.81 | 6.75 | 0.27 | 0.81 | 0.27 | 0.54 | 0.27 | 2.16 | 2.97 | 2.97 | 0.54 | 6.22 |
This section relies largely or entirely on a single source .(May 2023) |
Component [30] | Morocco (n=760) | Algeria (n=156) | Tunisia (n=601) | Mauritania/Western Sahara (189) | Egypt (370) |
---|---|---|---|---|---|
North Africa | 79% | 62.5% | 71.7% | 66.6% | 43.7% |
Middle East | 7.6% | 26.2% | 19.4% | 13.2% | 27.5% |
Europe | 4.4% | 9.5% | 2.1% | 7.4% | 5.9% |
West Africa | 6% | 5.7% | 1.1% | 12.1% | 2.9% |
East Africa | 0.9% | 0% | 0.1% | 0.5% | 1.3% |
Tunisia's population was estimated to be around 12.04 million in 2022. In the generally youthful African continent, Tunisia's population is among the most mature. This is because the government has supported a successful family planning program that has reduced the population growth rate to just over 1% per annum, contributing to Tunisia's economic and social stability.
In human genetics, Haplogroup J-M172 or J2 is a Y-chromosome haplogroup which is a subclade (branch) of haplogroup J-M304. Haplogroup J-M172 is common in modern populations in Western Asia, Central Asia, South Asia, Southern Europe, Northwestern Iran and North Africa. It is thought that J-M172 may have originated in the Caucasus, Anatolia and/or Western Iran.
Haplogroup J-M304, also known as J, is a human Y-chromosome DNA haplogroup. It is believed to have evolved in Western Asia. The clade spread from there during the Neolithic, primarily into North Africa, the Horn of Africa, the Socotra Archipelago, the Caucasus, Europe, Anatolia, Central Asia, South Asia, and Southeast Asia.
Haplogroup K or K-M9 is a genetic lineage within human Y-chromosome DNA haplogroup. A sublineage of haplogroup IJK, K-M9, and its descendant clades represent a geographically widespread and diverse haplogroup. The lineages have long been found among males on every continent except Antarctica.
Haplogroup J-M267, also commonly known as Haplogroup J1, is a subclade (branch) of Y-DNA haplogroup J-P209 along with its sibling clade haplogroup J-M172.
Haplogroup T-M184, also known as Haplogroup T, is a human Y-chromosome DNA haplogroup. The unique-event polymorphism that defines this clade is the single-nucleotide polymorphism known as M184.
The various ethnolinguistic groups found in the Caucasus, Central Asia, Europe, the Middle East, North Africa and/or South Asia demonstrate differing rates of particular Y-DNA haplogroups.
Haplogroup E-M75 is a human Y-chromosome DNA haplogroup. Along with haplogroup E-P147, it is one of the two main branches of the older haplogroup E-M96.
Haplogroup E-V68, also known as E1b1b1a, is a major human Y-chromosome DNA haplogroup found in North Africa, the Horn of Africa, Western Asia and Europe. It is a subclade of the larger and older haplogroup, known as E1b1b or E-M215. The E1b1b1a lineage is identified by the presence of a single nucleotide polymorphism (SNP) mutation on the Y chromosome, which is known as V68. It is a subject of discussion and study in genetics as well as genetic genealogy, archaeology, and historical linguistics.
Y-DNA haplogroups in populations of Europe are haplogroups of the male Y-chromosome found in European populations.
Listed here are notable ethnic groups and populations from Western Asia, Egypt and South Caucasus by human Y-chromosome DNA haplogroups based on relevant studies. The samples are taken from individuals identified with the ethnic and linguistic designations in the first two columns, the third column gives the sample size studied, and the other columns give the percentage of the particular haplogroup. Some old studies conducted in the early 2000s regarded several haplogroups as one haplogroup, e.g. I, G and sometimes J were haplogroup 2, so conversion sometimes may lead to unsubstantial frequencies below.
Y-DNA haplogroups in populations of South Asia are haplogroups of the male Y-chromosome found in South Asian populations.
The genetic history of North Africa encompasses the genetic history of the people of North Africa. The most important source of gene flow to North Africa from the Neolithic Era onwards was from Western Asia, while the Sahara desert to the south and the Mediterranean Sea to the North were also important barriers to gene flow from sub-Saharan Africa and parts of Europe in prehistory. However, North Africa is connected to Western Asia via the Isthmus of Suez and the Sinai peninsula, while at the Straits of Gibraltar, North Africa and Europe are separated by only 15 km (9 mi), similarly Malta, Sicily, Canary Islands, Lampedusa and Crete are close to the coasts of North Africa.
E-Z827, also known as E1b1b1b, is a major human Y-chromosome DNA haplogroup. It is the parent lineage to the E-Z830 and E-V257 subclades, and defines their common phylogeny. The former is predominantly found in the Middle East; the latter is most frequently observed in North Africa, with its E-M81 subclade observed among the ancient Guanche natives of the Canary Islands. E-Z827 is also found at lower frequencies in Europe, and in isolated parts of Southeast Africa.
In human genetics, Y Haplogroup E-M123 is a Y-chromosome haplogroup, and defined by the single nucleotide polymorphism (SNP) mutation M123. Like its closest relatives within the larger E-M215 haplogroup, E-M123 is found in Asia, Europe and Africa.
Moroccan genetics encompasses the genetic history of the people of Morocco, and the genetic influence of this ancestry on world populations. It has been heavily influenced by geography.
Haplogroup K2b (P331), also known as MPS is a human y-chromosome haplogroup that is thought to be less than 3,000 years younger than K, and less than 10,000 years younger than F, meaning it probably is around 50,000 years old, according to the age estimates of Tatiana Karafet et al. 2014.
Haplogroup T-L206, also known as haplogroup T1, is a human Y-chromosome DNA haplogroup. The SNP that defines the T1 clade is L206. The haplogroup is one of two primary branches of T (T-M184), the other subclade being T2 (T-PH110).
Haplogroup R-M269 is the sub-clade of human Y-chromosome haplogroup R1b that is defined by the SNP marker M269. According to ISOGG 2020 it is phylogenetically classified as R1b1a1b. It underwent intensive research and was previously classified as R1b1a2, R1b1c, R1b1b2 and R1b1a1a2.
Haplogroup E-M2, also known as E1b1a1-M2, is a human Y-chromosome DNA haplogroup. E-M2 is primarily distributed within Africa followed by West Asia. More specifically, E-M2 is the predominant subclade in West Africa, Central Africa, Southern Africa, and the region of the African Great Lakes; it also occurs at moderate frequencies in North Africa, and the Middle East. E-M2 has several subclades, but many of these subhaplogroups are included in either E-L485 or E-U175. E-M2 is especially common among indigenous Africans who speak Niger-Congo languages, and was spread to Southern Africa and East Africa through the Bantu expansion.