Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*68:01-B*39:01-C*07:02-DRB1*16:02-DQA1*05:05-DQB1*03:01 | Brazil Puyanawa | 0.33 | 150 | 10_52_S_53_5_W |
2 | A*01:01-B*39:01-C*07:02-DRB1*16:02-DQB1*03:01 | USA Hispanic pop 2 | 0.05 | 1,999 | 44_58_N_93_15_W |
3 | A*02:01-B*39:01-C*07:02-DRB1*16:02-DQB1*03:01 | USA Hispanic pop 2 | 0.05 | 1,999 | 44_58_N_93_15_W |
4 | A*24:02-B*39:01-C*07:02-DRB1*16:02-DQB1*05:02 | USA Asian pop 2 | 0.04 | 1,772 | 44_58_N_93_15_W |
5 | A*11:01-B*39:01-C*07:02-DRB1*16:02 | Germany DKMS - China minority | 0.04 | 1,282 | 48_31_N_9_3_E |
6 | A*11:02-B*39:01-C*07:02-DRB1*16:02 | Germany DKMS - China minority | 0.04 | 1,282 | 48_31_N_9_3_E |
7 | A*24:02-B*39:01-C*07:02-DRB1*16:02-DQB1*05:02 | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.03 | 4,335 | 41_22_N_2_11_E |
8 | A*30:01:01-B*39:01:01-C*07:02:01-DRB1*16:02:01-DQB1*05:02:01 | China Zhejiang Han | 0.03 | 1,734 | 27_2_N_118_1_E |
9 | A*11:01:01-B*39:01:01-C*07:02:01-DRB1*16:02:01-DPB1*05:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.03 | 5,266 | 22_25_N_114_17_E |
10 | A*02:01-B*39:01-C*07:02-DRB1*16:02 | Hong Kong Chinese BMDR | 0.02 | 7,595 | 22_15_N_114_10_E |
11 | A*24:02:01-B*39:01:01-C*07:02:01-DRB1*16:02:01-DPB1*05:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
12 | A*26:01-B*39:01-C*07:02-DRB1*16:02 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
13 | A*02:01:01-B*39:01:01-C*07:02:01-DRB1*16:02:01-DPB1*05:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
14 | A*11:02:01-B*39:01:01-C*07:02:01-DRB1*16:02:01-DPB1*13:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
15 | A*02:01-B*39:01-C*07:02-DRB1*16:02 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |