Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*30:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01-DPB1*01:01:01 | South African Black | 2.47 | 142 | 29_9_S_24_39_E |
2 | A*30:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01 | Costa Rica African -Caribbean (G) | 1.47 | 102 | 9_59_N_83_1_W |
3 | A*02:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01 | Costa Rica African -Caribbean (G) | 0.98 | 102 | 9_59_N_83_1_W |
4 | A*68:02:01-B*42:01:01-C*17:01:01-DRB1*03:02:01 | Costa Rica African -Caribbean (G) | 0.49 | 102 | 9_59_N_83_1_W |
5 | A*02:05:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01-DPB1*105:01:01 | South African Black | 0.35 | 142 | 29_9_S_24_39_E |
6 | A*03:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*03:19:01-DPB1*131:01 | South African Black | 0.35 | 142 | 29_9_S_24_39_E |
7 | A*29:02:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01-DPB1*01:01:01 | South African Black | 0.35 | 142 | 29_9_S_24_39_E |
8 | A*30:02:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01-DPB1*02:01:02 | South African Black | 0.35 | 142 | 29_9_S_24_39_E |
9 | A*68:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*02:02:01-DPB1*02:01:02 | South African Black | 0.35 | 142 | 29_9_S_24_39_E |
10 | A*68:02:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01-DPB1*01:01:01 | South African Black | 0.35 | 142 | 29_9_S_24_39_E |
11 | A*30:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01-DPA1*02:02:02-DPB1*01:01:01 | Brazil Barra Mansa Rio State Caucasian | 0.31 | 405 | 22_32_S_44_10_W |
12 | A*30:01:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*06:02:01-DPA1*01:03:01-DPB1*01:01:02 | Brazil Rio de Janeiro Caucasian | 0.19 | 521 | 22_54_S_43_12_W |
13 | A*68:01:01:02-B*42:01:01-C*17:01:01:02-DRB1*03:02:01-DQB1*04:02:01 | Russia Nizhny Novgorod, Russians | 0.03 | 1,510 | 56_19_N_43_59_E |
14 | A*24:02:01-B*42:01:01-C*17:01:01-DRB1*03:02:01-DQB1*04:02:01 | Poland BMR | 0.01 | 23,595 | 52_0_N_19_22_E |