Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*02:01:01-B*15:11:01-C*03:03:01-DRB1*15:01:01-DQB1*06:02:01 | China Zhejiang Han | 0.06 | 1,734 | 27_2_N_118_1_E |
2 | A*02:06-B*15:11-C*03:03-DRB1*15:01-DQB1*05:02-DPB1*04:01 | Russia Karelia | 0.06 | 1,075 | 63_9_N_32_59_E |
3 | A*02:06-B*15:11-C*03:03-DRB1*15:01 | Germany DKMS - China minority | 0.04 | 1,282 | 48_31_N_9_3_E |
4 | A*01:01-B*15:11-C*03:03-DRB1*15:01 | Germany DKMS - China minority | 0.04 | 1,282 | 48_31_N_9_3_E |
5 | A*11:01-B*15:11-C*03:03-DRB1*15:01 | Germany DKMS - China minority | 0.04 | 1,282 | 48_31_N_9_3_E |
6 | A*02:01-B*15:11-C*03:03-DRB1*15:01 | Japan pop 16 | 0.03 | 18,604 | 35_41_N_139_46_E |
7 | A*02:01:01-B*15:11:01-C*03:03:01-DRB1*15:01:01-DQB1*03:02:01 | China Zhejiang Han | 0.03 | 1,734 | 27_2_N_118_1_E |
8 | A*24:02-B*15:11-C*03:03-DRB1*15:01 | Japan pop 16 | 0.03 | 18,604 | 35_41_N_139_46_E |
9 | A*02:01-B*15:11-C*03:03-DRB1*15:01 | Hong Kong Chinese BMDR | 0.03 | 7,595 | 22_15_N_114_10_E |
10 | A*02:06-B*15:11-C*03:03-DRB1*15:01 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
11 | A*31:01:02-B*15:11:01-C*03:03:01-DRB1*15:01:01-DPB1*02:01:02 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
12 | A*11:01:01-B*15:11:01-C*03:03:01-DRB1*15:01:01-DPB1*03:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
13 | A*24:02-B*15:11-C*03:03-DRB1*15:01 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
14 | A*33:03-B*15:11-C*03:03-DRB1*15:01 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
15 | A*02:06-B*15:11-C*03:03-DRB1*15:01 | Hong Kong Chinese BMDR | 0.00 | 7,595 | 22_15_N_114_10_E |