Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*24:02-B*15:07-C*03:03-DRB1*09:01 | Japan pop 16 | 0.04 | 18,604 | 35_41_N_139_46_E |
2 | A*24:02-B*15:07-C*03:03-DRB1*09:01-DQB1*02:01 | Colombia Bogotá Cord Blood | 0.03 | 1,463 | 4_39_N_73_52_W |
3 | A*02:01-B*15:07-C*03:03-DRB1*09:01-DQA1*03:02-DQB1*03:03-DPA1*02:02-DPB1*05:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
4 | A*24:02-B*15:07-C*03:03-DRB1*09:01-DQA1*03:02-DQB1*03:03-DPA1*01:03-DPB1*02:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
5 | A*24:02-B*15:07-C*03:03-DRB1*09:01-DQA1*03:02-DQB1*03:03-DPA1*01:03-DPB1*02:02 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
6 | A*24:02:01-B*15:07:01-C*03:03:01-DRB1*09:01:02-DQB1*03:01:01 | China Zhejiang Han | 0.03 | 1,734 | 27_2_N_118_1_E |
7 | A*24:02:01-B*15:07:01-C*03:03:01-DRB1*09:01:02-DPB1*02:01:02 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
8 | A*02:01-B*15:07-C*03:03-DRB1*09:01 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
9 | A*11:01-B*15:07-C*03:03-DRB1*09:01 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |