Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Distribution¹ |
1 | DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Ireland South | 1.0000 | | 250 |
|
2 | A*03:01:01-B*15:18:01-C*07:04:01-DRB1*13:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Rio de Janeiro Parda | 0.5882 | | 170 |
|
3 | A*02:01:01-B*15:18:01-C*07:04:01-DRB1*13:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Rio de Janeiro Caucasian | 0.5837 | | 521 |
|
4 | A*03:01:01-B*07:02:01-C*07:02:01-DRB1*15:01:01-DQA1*04:01:01-DQB1*06:03-DPA1*02:01:01-DPB1*03:01:01 | | Russian Federation Vologda Region | 0.4202 | | 119 |
|
5 | A*32:01:01-B*41:02:01-C*17:03:01-DRB1*13:03:01-DQA1*05:05:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01 | | Russian Federation Vologda Region | 0.4202 | | 119 |
|
6 | DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Gambia pop 3 | 0.3347 | | 939 |
|
7 | A*02:01-B*38:01-C*12:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.3280 | | 1,075 |
|
8 | A*02:01:01-B*38:01:01-C*12:03:01-DRB1*13:01:01-DQA1*01:02:01-DQB1*06:03-DPA1*01:03:01-DPB1*03:01:01 | | Russia Belgorod region | 0.3268 | | 153 |
|
9 | A*02:01:01-B*38:01:01-C*12:03:01-DRB1*13:01:01-DQA1*01:03:01-DQB1*06:03-DPA1*01:03:01-DPB1*03:01:01 | | Russia Belgorod region | 0.3268 | | 153 |
|
10 | A*31:01:02-B*15:08-C*01:02:01-DRB1*13:01:01-DQB1*06:03:01-DPB1*03:01:01 | | Saudi Arabia pop 6 (G) | 0.3141 | | 28,927 |
|
11 | A*01:01:01-B*15:18:01-C*07:04:01-DRB1*13:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Barra Mansa Rio State Caucasian | 0.3125 | | 405 |
|
12 | A*11:01:01-B*14:02:01-C*07:02:01-DRB1*08:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Barra Mansa Rio State Caucasian | 0.3125 | | 405 |
|
13 | A*01:01-B*15:01-C*03:03-DRB1*15:01-DQA1*01:02-DQB1*06:03-DPB1*03:01 | | USA San Diego | 0.2600 | | 496 |
|
14 | A*30:01-B*15:01-C*03:03-DRB1*07:01-DQA1*01:03-DQB1*06:03-DPB1*03:01 | | USA San Diego | 0.2600 | | 496 |
|
15 | A*23:01:01-B*44:03:01-C*04:01:01-DRB1*13:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Rio de Janeiro Caucasian | 0.1946 | | 521 |
|
16 | A*24:02:01-B*35:08:01-C*16:01:01-DRB1*13:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Rio de Janeiro Caucasian | 0.1946 | | 521 |
|
17 | A*32:01:01-B*40:02:01-C*02:02:02-DRB1*13:01:01-DQB1*06:03:01-DPA1*01:03:01-DPB1*03:01:01 | | Brazil Rio de Janeiro Caucasian | 0.1946 | | 521 |
|
18 | A*30:02-B*27:03-C*02:02-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Panama | 0.1900 | | 462 |
|
19 | A*31:01:02-B*51:01:01-C*15:02:01-DRB1*13:01:01-DQB1*06:03:01-DPB1*03:01:01 | | Saudi Arabia pop 6 (G) | 0.1250 | | 28,927 |
|
20 | A*02:01-B*51:01-C*07:01-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.1129 | | 1,075 |
|
21 | A*02:01-B*15:01-C*03:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.1003 | | 1,075 |
|
22 | A*31:01-B*40:06-C*15:02-DRB1*13:01-DQA1*01:03-DQB1*06:03-DPB1*03:01 | | Sri Lanka Colombo | 0.0700 | | 714 |
|
23 | A*26:01-B*38:01-C*12:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.0643 | | 1,075 |
|
24 | A*02:01-B*38:01-C*12:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0600 | | 3,456,066 |
|
25 | DRB1*13:01-DQA1*01:03-DQB1*06:03-DPA1*01:03-DPB1*03:01 | | China Zhejiang Han pop 2 | 0.0600 | | 833 |
|
26 | A*31:01-B*51:01-C*05:01-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.0565 | | 1,075 |
|
27 | A*26:01-B*44:02-C*05:01-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.0565 | | 1,075 |
|
28 | A*02:01-B*44:02-C*07:04-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.0564 | | 1,075 |
|
29 | A*24:02-B*40:02-C*02:02-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Russia Karelia | 0.0556 | | 1,075 |
|
30 | A*24:02-B*15:01-C*03:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0511 | | 3,456,066 |
|
31 | A*02:01-B*44:02-C*05:01-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0504 | | 3,456,066 |
|
32 | A*02:01-B*15:01-C*03:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0444 | | 3,456,066 |
|
33 | A*02:30-B*38:01-C*12:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0336 | | 3,456,066 |
|
34 | A*11:01-B*44:02-C*05:01-DRB1*13:01-DQA1*01:03-DQB1*06:03-DPA1*01:03-DPB1*03:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
35 | A*24:02-B*50:01-C*06:02-DRB1*13:01-DQA1*01:03-DQB1*06:03-DPA1*01:03-DPB1*03:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
36 | A*03:01-B*07:02-C*07:02-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0238 | | 3,456,066 |
|
37 | A*02:01-B*51:01-C*14:02-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0230 | | 3,456,066 |
|
38 | A*01:01-B*08:01-C*07:01-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0196 | | 3,456,066 |
|
39 | A*26:01-B*38:01-C*12:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0147 | | 3,456,066 |
|
40 | A*01:01-B*57:01-C*06:02-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0131 | | 3,456,066 |
|
41 | A*03:01-B*15:01-C*03:03-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0129 | | 3,456,066 |
|
42 | A*02:01-B*40:01-C*03:04-DRB1*13:01-DQB1*06:03-DPB1*03:01 | | Germany DKMS - German donors | 0.0127 | | 3,456,066 |
|
* 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).