Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Distribution¹ |
1 | A*01:01-B*58:02-C*06:02-DRB1*11:14-DQA1*05:05-DQB1*06:02-DPB1*105:01 |  | South Africa Worcester | 0.3000 |  | 159 |
 |
2 | A*23:01-B*07:05-C*02:02-DRB1*11:14-DQA1*05:01-DQB1*03:01-DPB1*04:02 |  | South Africa Worcester | 0.3000 |  | 159 |
 |
3 | A*24:02-B*57:02-C*07:01-DRB1*11:14-DQA1*05:05-DQB1*03:01-DPB1*11:01 |  | South Africa Worcester | 0.3000 |  | 159 |
 |
4 | A*74:01-B*15:03-C*02:10-DRB1*11:14-DQA1*01:02-DQB1*06:02-DPB1*01:01 |  | South Africa Worcester | 0.3000 |  | 159 |
 |
5 | A*32:01-B*15:01-C*03:03-DRB1*11:14 |  | Germany DKMS - Netherlands minority | 0.0730 |  | 1,374 |
 |
6 | A*01:01-B*58:01-C*07:01-DRB1*11:14 |  | Germany DKMS - Portugal minority | 0.0430 |  | 1,176 |
 |
7 | A*01:01-B*44:03-C*04:01-DRB1*11:14 |  | Germany DKMS - France minority | 0.0360 |  | 1,406 |
 |
8 | A*02:01-B*51:01-C*15:04-DRB1*11:14 |  | Germany DKMS - France minority | 0.0360 |  | 1,406 |
 |
9 | A*24:02-B*51:01-C*05:01-DRB1*11:14 |  | Germany DKMS - Netherlands minority | 0.0360 |  | 1,374 |
 |
10 | A*30:02-B*49:01-C*07:01-DRB1*11:14 |  | Germany DKMS - France minority | 0.0360 |  | 1,406 |
 |
11 | A*01:01-B*40:01-C*07:01-DRB1*11:14-DQB1*05:03 |  | Colombia Bogotá Cord Blood | 0.0342 |  | 1,463 |
 |
12 | A*02:05-B*50:01-C*06:02-DRB1*11:14-DQB1*03:01 |  | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.0340 |  | 4,335 |
 |
13 | A*26:01-B*35:03-C*16:02-DRB1*11:143-DQB1*03:01 |  | India Tamil Nadu | 0.0201 |  | 2,492 |
 |
14 | A*24-B*35-DRB1*11:146 |  | Chile Santiago | 0.0181 |  | 920 |
 |
15 | A*01-B*38-DRB1*11:146 |  | Chile Santiago | 0.0148 |  | 920 |
 |
16 | A*23-B*44-DRB1*11:146 |  | Chile Santiago | 0.0136 |  | 920 |
 |
17 | A*03:02-B*51:01-C*15:02-DRB1*11:140-DQB1*03:01 |  | India North UCBB | 0.0085 |  | 5,849 |
 |
18 | A*29-B*51-DRB1*11:142 |  | Chile Santiago | 0.0078 |  | 920 |
 |
19 | A*01-B*57-DRB1*11:140 |  | Chile Santiago | 0.0068 |  | 920 |
 |
20 | A*01-B*57-DRB1*11:141 |  | Chile Santiago | 0.0068 |  | 920 |
 |
21 | A*02-B*47-DRB1*11:140 |  | Chile Santiago | 0.0068 |  | 920 |
 |
22 | A*02-B*47-DRB1*11:141 |  | Chile Santiago | 0.0068 |  | 920 |
 |
23 | A*02-B*35-DRB1*11:140 |  | Chile Santiago | 0.0060 |  | 920 |
 |
24 | A*02-B*35-DRB1*11:141 |  | Chile Santiago | 0.0060 |  | 920 |
 |
25 | A*02-B*35-DRB1*11:147 |  | Chile Santiago | 0.0060 |  | 920 |
 |
26 | A*02-B*18-DRB1*11:140 |  | Chile Santiago | 0.0054 |  | 920 |
 |
27 | A*02-B*18-DRB1*11:141 |  | Chile Santiago | 0.0054 |  | 920 |
 |
28 | A*02-B*18-DRB1*11:144 |  | Chile Santiago | 0.0054 |  | 920 |
 |
29 | A*69-B*55-DRB1*11:140 |  | Chile Santiago | 0.0054 |  | 920 |
 |
30 | A*69-B*55-DRB1*11:141 |  | Chile Santiago | 0.0054 |  | 920 |
 |
31 | A*69-B*55-DRB1*11:144 |  | Chile Santiago | 0.0054 |  | 920 |
 |
32 | A*02:01-B*45:01-DRB1*11:14 |  | Israel Ashkenazi Jews pop 3 | 0.0054 |  | 4,625 |
 |
33 | A*02-B*15-DRB1*11:140 |  | Chile Santiago | 0.0045 |  | 920 |
 |
34 | A*02-B*15-DRB1*11:141 |  | Chile Santiago | 0.0045 |  | 920 |
 |
35 | A*02-B*15-DRB1*11:143 |  | Chile Santiago | 0.0045 |  | 920 |
 |
36 | A*02-B*15-DRB1*11:144 |  | Chile Santiago | 0.0045 |  | 920 |
 |
37 | A*02-B*15-DRB1*11:147 |  | Chile Santiago | 0.0045 |  | 920 |
 |
38 | A*02:01-B*39:01-C*07:02-DRB1*11:14-DQB1*03:01 |  | Belgium | 0.0041 |  | 31,412 |
 |
39 | A*31:01-B*27:05-C*15:02-DRB1*11:14-DQB1*03:01 |  | Belgium | 0.0041 |  | 31,412 |
 |
40 | A*01-B*35-DRB1*11:146 |  | Chile Santiago | 0.0033 |  | 920 |
 |
41 | A*03:01-B*35:01-C*04:01-DRB1*11:14 |  | Poland DKMS | 0.0024 |  | 20,653 |
 |
42 | A*03:01-B*27:05-C*15:02-DRB1*11:14-DQB1*03:01 |  | Belgium | 0.0020 |  | 31,412 |
 |
43 | A*29:02-B*51:01-C*02:02-DRB1*11:14-DQB1*03:01 |  | Belgium | 0.0020 |  | 31,412 |
 |
* Haplotype Frequencies: Total number of copies of the haplotype in the population sample (Haplotypes / 2n) shown in percentages (%).
: This field has been expanded to two decimals to better represent frequencies of large datasets (e.g. where sample size > 1000 individuals)
¹ Distribution - Shows the geographic distribution in overlaid maps of the complete haplotype (left icon) or the input alleles if low level resolution was entered (right icon).