Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*33:03-B*40:03-C*03:04-DRB1*14:05 | Japan pop 16 | 0.07 | 18,604 | 35_41_N_139_46_E |
2 | A*24:02:01-B*40:03:01-C*03:04:01-DRB1*14:05:01-DQB1*05:03:01 | China Zhejiang Han | 0.07 | 1,734 | 27_2_N_118_1_E |
3 | A*02:01-B*40:03-C*03:04-DRB1*14:05 | Germany DKMS - China minority | 0.06 | 1,282 | 48_31_N_9_3_E |
4 | A*11:01-B*40:03-C*03:04-DRB1*14:05 | Germany DKMS - China minority | 0.06 | 1,282 | 48_31_N_9_3_E |
5 | A*11:01:01-B*40:03:01-C*03:04:01-DRB1*14:05:01-DQB1*05:03:01 | China Zhejiang Han | 0.05 | 1,734 | 27_2_N_118_1_E |
6 | A*24:02-B*40:03-C*03:04-DRB1*14:05 | Japan pop 16 | 0.04 | 18,604 | 35_41_N_139_46_E |
7 | A*24:02:01:01-B*40:03-C*03:04:01-DRB1*14:05:01-DQB1*02:02 | Russia Nizhny Novgorod, Russians | 0.03 | 1,510 | 56_19_N_43_59_E |
8 | A*02:01-B*40:03-C*03:04-DRB1*14:05 | Japan pop 16 | 0.03 | 18,604 | 35_41_N_139_46_E |
9 | A*33:03-B*40:03-C*03:04-DRB1*14:05-DQA1*01:04-DQB1*05:03-DPA1*02:02-DPB1*05:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
10 | A*31:01-B*40:03-C*03:04-DRB1*14:05 | Japan pop 16 | 0.02 | 18,604 | 35_41_N_139_46_E |
11 | A*24:02:01-B*40:03:01-C*03:04:01-DRB1*14:05:01-DPB1*05:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.02 | 5,266 | 22_25_N_114_17_E |
12 | A*02:01-B*40:03-C*03:04-DRB1*14:05 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
13 | A*11:01-B*40:03-C*03:04-DRB1*14:05 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
14 | A*24:02:01-B*40:03:01-C*03:04:01-DRB1*14:05:01-DPB1*02:01:02 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
15 | A*33:03:01-B*40:03:01-C*03:04:01-DRB1*14:05:01-DPB1*05:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
16 | A*11:01-B*40:03-C*03:04-DRB1*14:05 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |