Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Location |
1 | A*33:03-B*44:03-C*14:03-DRB1*15:01 | Japan pop 16 | 0.11 | 18,604 | 35_41_N_139_46_E |
2 | A*33:03-B*44:03-C*14:03-DRB1*15:01-DQA1*01:02-DQB1*06:02-DPA1*01:03-DPB1*02:01 | Japan pop 17 | 0.07 | 3,078 | 37_36_N_138_2_E |
3 | A*02:07-B*44:03-C*14:03-DRB1*15:01-DQA1*01:02-DQB1*06:02-DPA1*02:02-DPB1*05:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
4 | A*33:03-B*44:03-C*14:03-DRB1*15:01-DQA1*01:02-DQB1*06:02-DPA1*02:01-DPB1*13:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
5 | A*33:03-B*44:03-C*14:03-DRB1*15:01-DQA1*01:02-DQB1*06:02-DPA1*02:02-DPB1*05:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
6 | A*02:01-B*44:03-C*14:03-DRB1*15:01 | Germany DKMS - Greece minority | 0.03 | 1,894 | 48_31_N_9_3_E |
7 | A*26:01-B*44:03-C*14:03-DRB1*15:01-DQB1*06:02 | Germany DKMS - Turkey minority | 0.02 | 4,856 | 48_31_N_9_3_E |
8 | A*33:03-B*44:03-C*14:03-DRB1*15:01 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
9 | A*02:07-B*44:03-C*14:03-DRB1*15:01 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
10 | A*26:01-B*44:03-C*14:03-DRB1*15:01 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
11 | A*02:01:01-B*44:03:01-C*14:03-DRB1*15:01:01-DQB1*05:02:01 | Poland BMR | 0.00 | 23,595 | 52_0_N_19_22_E |