Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Distribution¹ |
1 | A*25:01-B*39:01-C*12:03-DRB1*11:01-DQA1*05:01-DQB1*03:01-DPB1*04:01 | | USA San Diego | 0.5210 | | 496 |
|
2 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*04:02:01-DQA1*03:01:01-DQB1*03:02-DPA1*02:01:01-DPB1*11:01:01 | | Russia Belgorod region | 0.3268 | | 153 |
|
3 | A*25:01-B*39:01-C*12:03-DRB1*16:01-DQB1*05:02 | | Italy pop 5 | 0.2900 | | 975 |
|
4 | A*25:01-B*39:01-C*12:03 | | Italy pop 5 | 0.2700 | | 975 |
|
5 | A*25:01-B*39:01-C*12:03-DRB1*07:01:01-DQB1*02:01 | | England North West | 0.2000 | | 298 |
|
6 | A*25:01-B*39:01-C*12:03-DRB1*07:01 | | Germany DKMS - United Kingdom minority | 0.1440 | | 1,043 |
|
7 | A*25:01-B*39:01-C*12:03-DRB1*16:01 | | Germany DKMS - France minority | 0.1070 | | 1,406 |
|
8 | A*25:01-B*39:01-C*12:03-DRB1*16:01 | | Italy pop 5 | 0.1000 | | 975 |
|
9 | A*25:01-B*39:01-C*12:03-DRB1*11:01 | | Germany DKMS - Greece minority | 0.0530 | | 1,894 |
|
10 | A*25:01-B*39:01-C*12:03-DRB1*16:01 | | Germany DKMS - Croatia minority | 0.0490 | | 2,057 |
|
11 | A*25:01-B*39:01-C*12:03-DRB1*11:01 | | Germany DKMS - United Kingdom minority | 0.0480 | | 1,043 |
|
12 | A*25:01-B*39:01-C*12:03-DRB1*16:01-DQB1*05:02 | | USA Hispanic pop 2 | 0.0470 | | 1,999 |
|
13 | A*25:01-B*39:01-C*12:03-DRB1*11:01-DQB1*03:01 | | Germany DKMS - Italy minority | 0.0430 | | 1,159 |
|
14 | A*25:01-B*39:01-C*12:03-DRB1*12:01 | | Germany DKMS - Romania minority | 0.0410 | | 1,234 |
|
15 | A*25:01-B*39:01-C*12:03-DRB1*16:01 | | Germany DKMS - Romania minority | 0.0410 | | 1,234 |
|
16 | A*25:01-B*39:01-C*12:03-DRB1*01:01-DQB1*05:01 | | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.0340 | | 4,335 |
|
17 | A*25:01-B*39:01-C*12:03-DRB1*11:01-DQB1*03:01 | | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.0340 | | 4,335 |
|
18 | A*25:01-B*39:01-C*12:03-DRB1*16:01-DQB1*05:02 | | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.0340 | | 4,335 |
|
19 | A*25:01:01-B*39:01:01-C*12:03:01:01-DRB1*09:01:02-DQB1*03:03:02 | | Russia Nizhny Novgorod, Russians | 0.0331 | | 1,510 |
|
20 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*16:01:01-DQB1*05:02:01 | | Poland BMR | 0.0267 | | 23,595 |
|
21 | A*25:01-B*39:01-C*12:03-DRB1*01:01 | | Germany DKMS - Croatia minority | 0.0240 | | 2,057 |
|
22 | A*25:01-B*39:01-C*12:03-DRB1*16:01 | | Poland DKMS | 0.0152 | | 20,653 |
|
23 | A*25:01-B*39:01-C*12:03-DRB1*11:01 | | Poland DKMS | 0.0121 | | 20,653 |
|
24 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*11:01:01-DQB1*03:01:01 | | Poland BMR | 0.0121 | | 23,595 |
|
25 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*12:01:01-DQB1*03:01:01 | | Poland BMR | 0.0097 | | 23,595 |
|
26 | A*25:01-B*39:01-C*12:03-DRB1*13:02 | | Poland DKMS | 0.0047 | | 20,653 |
|
27 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*11:01:01-DQB1*06:02:01 | | Poland BMR | 0.0042 | | 23,595 |
|
28 | A*25:01-B*39:01-C*12:03-DRB1*04:03 | | Poland DKMS | 0.0028 | | 20,653 |
|
29 | A*25:01-B*39:01-C*12:03-DRB1*15:01 | | Poland DKMS | 0.0028 | | 20,653 |
|
30 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*04:01:01-DQB1*03:01:01 | | Poland BMR | 0.0024 | | 23,595 |
|
31 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*01:01:01-DQB1*05:01:01 | | Poland BMR | 0.0022 | | 23,595 |
|
32 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*11:01:01-DQB1*05:02:01 | | Poland BMR | 0.0021 | | 23,595 |
|
33 | A*25:01:01-B*39:01:01-C*12:03:01-DRB1*15:01:01-DQB1*06:02:01 | | Poland BMR | 0.0020 | | 23,595 |
|
* 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).