Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Distribution¹ |
1 | A*31:01-B*35:01-C*07:02-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Mexico Tixcacaltuyub Maya | 1.4925 | | 67 |
|
2 | A*68:03-B*35:43-C*01:02-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Mexico Tixcacaltuyub Maya | 1.4925 | | 67 |
|
3 | A*02:06-B*35:01-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Mexico Chichen Itza Maya (prehispanic) | 1.0638 | | 47 |
|
4 | A*24:02-B*35:17-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Mexico Chichen Itza Maya (prehispanic) | 1.0638 | | 47 |
|
5 | A*02:01-B*35:08-C*05:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | United Arab Emirates Abu Dhabi | 0.9600 | | 52 |
|
6 | A*01:01-B*35:02-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Kosovo | 0.8060 | | 124 |
|
7 | A*24:02-B*35:20-C*03:05-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Mexico Tixcacaltuyub Maya | 0.7463 | | 67 |
|
8 | A*30:01-B*35:03-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Brazil Puyanawa | 0.6667 | | 150 |
|
9 | A*02:06-B*35:01-C*07:02-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*04:02 | | Mexico Chiapas Lacandon Mayans | 0.4587 | | 218 |
|
10 | A*02:01-B*35:03-C*06:02-E*01:01:01-F*01:03:01-G*01:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Portugal Azores Terceira Island | 0.4386 | | 130 |
|
11 | A*68:03-B*35:43-C*01:02-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPB1*04:02 | | Nicaragua Managua | 0.4329 | | 339 |
|
12 | A*11:01-B*35:01-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Kosovo | 0.4030 | | 124 |
|
13 | A*32:01-B*35:08-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Kosovo | 0.4030 | | 124 |
|
14 | A*68:03-B*35:01-C*07:02-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*04:02 | | Mexico Chiapas Lacandon Mayans | 0.2294 | | 218 |
|
15 | A*32:01-B*35:01-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPB1*02:01 | | Nicaragua Managua | 0.2165 | | 339 |
|
16 | A*68:01-B*35:43-C*01:02-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPB1*04:02 | | Nicaragua Managua | 0.2165 | | 339 |
|
17 | A*26:03-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*02:01 | | Japan pop 17 | 0.1000 | | 3,078 |
|
18 | A*26:03-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*03:01 | | Japan pop 17 | 0.1000 | | 3,078 |
|
19 | A*11-B*35-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Brazil Paraná Caucasian | 0.0780 | | 641 |
|
20 | A*69-B*35-DRB1*04:03-DQA1*03:01-DQB1*03:02 | | Brazil Paraná Caucasian | 0.0780 | | 641 |
|
21 | A*31:01-B*35:03-C*04:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPB1*05:01 | | Sri Lanka Colombo | 0.0700 | | 714 |
|
22 | A*02:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*02:01 | | Japan pop 17 | 0.0700 | | 3,078 |
|
23 | A*02:06-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*03:01 | | Japan pop 17 | 0.0700 | | 3,078 |
|
24 | A*26:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*02:01 | | Japan pop 17 | 0.0700 | | 3,078 |
|
25 | A*26:01-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0700 | | 3,078 |
|
26 | A*33:03-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0700 | | 3,078 |
|
27 | A*02:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
28 | A*02:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*09:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
29 | A*02:01-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
30 | A*02:06-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
31 | A*02:06-B*35:01-C*03:04-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*02:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
32 | A*02:06-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
33 | A*02:06-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
34 | A*02:07-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
35 | A*11:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
36 | A*24:02-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*02:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
37 | A*24:02-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
38 | A*24:02-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
39 | A*24:02-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
40 | A*24:02-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*03:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
41 | A*24:02-B*35:01-C*08:01-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
42 | A*26:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*03:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
43 | A*26:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
44 | A*26:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:01-DPB1*13:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
45 | A*26:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*03:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
46 | A*26:03-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*04:02 | | Japan pop 17 | 0.0300 | | 3,078 |
|
47 | A*31:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*01:03-DPB1*04:02 | | Japan pop 17 | 0.0300 | | 3,078 |
|
48 | A*31:01-B*35:01-C*03:03-DRB1*04:03-DQA1*03:01-DQB1*03:02-DPA1*02:02-DPB1*05:01 | | Japan pop 17 | 0.0300 | | 3,078 |
|
* 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).