Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*03:01-B*47:01-C*06:02-DRB1*03:01-DQA1*05:01-DQB1*02:01-DPB1*15:01 | South Africa Worcester | 1.60 | 159 | 33_39_S_19_27_E |
2 | A*01:01-B*37:01-C*06:02-DRB1*03:01-DQB1*02:01-DPB1*15:01 | Tanzania Maasai | 0.64 | 336 | 3_11_S_37_4_E |
3 | A*25:01:01-B*18:01-C*07:01:01-DRB1*15:01:01-DQA1*01:02:01-DQB1*02:01:01-DPA1*01:03:01-DPB1*15:01:01 | Russian Federation Vologda Region | 0.42 | 119 | 59_13_N_39_54_E |
4 | A*68:02-B*41:01-C*17:01-DRB1*03:01-DQB1*02:01-DPB1*15:01 | Tanzania Maasai | 0.32 | 336 | 3_11_S_37_4_E |
5 | A*03:01:01-B*57:01:01-C*07:02:01-DRB1*03:01:01-DQB1*02:01:01-DPA1*01:03:01-DPB1*15:01:01 | Brazil Barra Mansa Rio State Caucasian | 0.31 | 405 | 22_32_S_44_10_W |
6 | DRB1*07:01-DQB1*02:01-DPB1*15:01 | Gambia pop 3 | 0.22 | 939 | 13_0_N_16_0_W |
7 | DRB1*03:01-DQB1*02:01-DPB1*15:01 | Gambia pop 3 | 0.07 | 939 | 13_0_N_16_0_W |
8 | DRB1*09:01-DQB1*02:01-DPB1*15:01 | Gambia pop 3 | 0.07 | 939 | 13_0_N_16_0_W |
9 | A*02:01-B*40:01-C*03:04-DRB1*07:01-DQB1*02:01-DPB1*15:01 | Russia Karelia | 0.06 | 1,075 | 63_9_N_32_59_E |
10 | A*03:01-B*47:01-C*06:02-DRB1*07:01-DQB1*02:01-DPB1*15:01 | Germany DKMS - German donors | 0.05 | 3,456,066 | 48_31_N_9_3_E |
11 | A*30:01-B*08:01-C*15:05-DRB1*14:141-DQA1*05:01-DQB1*02:01-DPA1*02:02-DPB1*15:01 | United Arab Emirates Pop 1 | 0.05 | 570 | 24_42_N_54_82_E |
12 | A*33:03-B*08:01-C*05:31-DRB1*03:01-DQA1*05:01-DQB1*02:01-DPA1*01:04-DPB1*15:01 | United Arab Emirates Pop 1 | 0.05 | 570 | 24_42_N_54_82_E |
13 | A*01:01-B*08:01-C*07:01-DRB1*03:01-DQB1*02:01-DPB1*15:01 | Germany DKMS - German donors | 0.02 | 3,456,066 | 48_31_N_9_3_E |
14 | A*01:01-B*08:01-C*07:01-DRB1*07:01-DQB1*02:01-DPB1*15:01 | Germany DKMS - German donors | 0.01 | 3,456,066 | 48_31_N_9_3_E |