Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6741 |
| ensemblid | ENSG00000138385.16 |
| hgncid | 11316 |
| symbol | SSB |
| name | small RNA binding exonuclease protection factor La |
| refseq_nuc | NM_003142.5 |
| refseq_prot | NP_003133.1 |
| ensembl_nuc | ENST00000260956.9 |
| ensembl_prot | ENSP00000260956.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 169798871 |
| end | 169812064 |
| strand | + |
| ver | v1.2 |
| region | chr2:169798871-169812064 |
| region5000 | chr2:169793871-169817064 |
| regionname0 | SSB_chr2_169798871_169812064 |
| regionname5000 | SSB_chr2_169793871_169817064 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 408 | 422 | 93 | 74 | 193 | 14 | 46 | 147 | SSB_chr2_169793871_169817064 | SSB | MAENG others(403): Show |
chr2 | 169793871 | 169817064 |
| a0002 | 0/0 | 408 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | MAENG others(403): Show |
chr2 | 169793871 | 169817064 |
| a0003 | 0/0 | 408 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | MAENG others(403): Show |
chr2 | 169793871 | 169817064 |
| a0004 | 0/0 | 408 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | MAENG others(403): Show |
chr2 | 169793871 | 169817064 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1224 | 412 | 92 | 73 | 190 | 14 | 41 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 | ||
| a0001c0002 | 0/0 | 1224 | 7 | 0 | 0 | 3 | 0 | 4 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 | ||
| a0001c0003 | 0/0 | 1224 | 2 | 1 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 | ||
| a0001c0005 | 0/0 | 1224 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 | ||
| a0002c0004 | 0/0 | 1224 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 | ||
| a0003c0006 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 | ||
| a0004c0007 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATGGC others(1219): Show |
chr2 | 169793871 | 169817064 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1650 | 389 | 75 | 70 | 187 | 14 | 41 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0001t0002 | 0/0 | 1650 | 19 | 14 | 3 | 2 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0001t0003 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0001t0004 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0001t0006 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0002t0001 | 0/0 | 1650 | 7 | 0 | 0 | 3 | 0 | 4 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0003t0001 | 0/0 | 1650 | 2 | 1 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0001c0005t0005 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0002c0004t0002 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0003c0006t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| a0004c0007t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | ATCTT others(1645): Show |
chr2 | 169793871 | 169817064 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 62 | 6 | 7 | 40 | 1 | 8 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0002 | 0/0 | 36 | 1 | 4 | 29 | 0 | 2 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0003 | 0/0 | 19 | 1 | 3 | 7 | 3 | 5 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0004 | 0/0 | 15 | 3 | 4 | 4 | 1 | 3 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0005 | 0/0 | 10 | 3 | 2 | 5 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0007 | 0/0 | 9 | 4 | 1 | 2 | 1 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0008 | 0/0 | 8 | 4 | 0 | 3 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0014 | 0/1 | 5 | 0 | 1 | 0 | 3 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0034 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0049 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0002t0001g0010 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0001c0005t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0002c0004t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0002c0004t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0003c0006t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| a0004c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01884 | hp1 | a0002 | c0004 | t0002 | g0012 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02809 | hp2 | a0002 | c0004 | t0002 | g0130 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03710 | hp2 | a0001 | c0005 | t0005 | g0118 | SAS | PJL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | STU | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18522 | hp2 | a0003 | c0006 | t0001 | g0067 | AFR | YRI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18950 | hp2 | a0004 | c0007 | t0001 | g0057 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | LWK | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | GIH | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | USA | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | USA | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0014 | REF | REF | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0034 | REF | REF | SSB_chr2_169793871_169817064 | SSB | chr2 | 169793871 | 169817064 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169807028 | C | T | 1 | a0004 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.511C>T | p.Pro171Ser | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/12 | 626/1650 | 511/1227 | 171/408 | chr2 | 169807028 | |||
| chr2:169808883 | T | C | 1 | a0002 | 2 | HG01884.hp1 HG02809.hp2 |
missense_variant | MODERATE | c.650T>C | p.Leu217Ser | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/12 | 765/1650 | 650/1227 | 217/408 | chr2 | 169808883 | |||
| chr2:169810289 | C | G | 1 | a0003 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.676C>G | p.Leu226Val | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 9/12 | 791/1650 | 676/1227 | 226/408 | chr2 | 169810289 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169800972 | T | C | 1 | a0001c0003 | 2 | HG01261.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.12T>C | p.Asn4Asn | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/12 | 127/1650 | 12/1227 | 4/408 | chr2 | 169800972 | |||
| chr2:169810303 | T | C | 1 | a0001c0002 | 7 | HG02015.hp1 HG03239.hp2 HG03654.hp2 others(4): Show |
synonymous_variant | LOW | c.690T>C | p.Ile230Ile | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 9/12 | 805/1650 | 690/1227 | 230/408 | chr2 | 169810303 | |||
| chr2:169810405 | C | T | 1 | a0001c0005 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.792C>T | p.Phe264Phe | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 9/12 | 907/1650 | 792/1227 | 264/408 | chr2 | 169810405 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169798909 | G | A | 1 | a0001c0001t0004 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/12 | 2052 | chr2 | 169798909 | ||||||
| chr2:169811812 | C | T | 1 | a0001c0001t0003 | 2 | HG02451.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*56C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 12/12 | 56 | chr2 | 169811812 | ||||||
| chr2:169811835 | A | T | 1 | a0001c0001t0006 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 12/12 | 79 | chr2 | 169811835 | ||||||
| chr2:169811981 | C | A | 2 | a0001c0001t0002 a0002c0004t0002 |
21 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 12/12 | 225 | chr2 | 169811981 | ||||||
| chr2:169812039 | T | G | 1 | a0001c0005t0005 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 12/12 | 283 | chr2 | 169812039 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169799126 | C | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(20): Show |
44 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10+150C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799126 | |||||||
| chr2:169799197 | G | A | 2 | a0001c0001t0001g0066 a0003c0006t0001g0067 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-10+221G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799197 | |||||||
| chr2:169799278 | C | CT | 44 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(41): Show |
81 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-10+324dupT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169799278 | ||||||
| chr2:169799278 | C | CTT | 14 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(11): Show |
20 | HG00642.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+323_-10+324dup others(2): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169799278 | ||||||
| chr2:169799278 | C | CTTT | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(48): Show |
146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.-10+322_-10+324dup others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169799278 | ||||||
| chr2:169799278 | C | CTTTT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0173 others(5): Show |
12 | HG01192.hp2 HG02602.hp2 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+321_-10+324dup others(4): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169799278 | ||||||
| chr2:169799278 | CTTT | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(21): Show |
50 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10+322_-10+324del others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169799278 | ||||||
| chr2:169799419 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-10+443C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799419 | |||||||
| chr2:169799433 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0127 a0001c0001t0001g0137 others(2): Show |
8 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+457G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799433 | |||||||
| chr2:169799487 | A | G | 2 | a0001c0001t0003g0097 a0001c0001t0003g0126 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-10+511A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799487 | |||||||
| chr2:169799745 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
22 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10+769C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799745 | |||||||
| chr2:169799765 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0095 |
3 | HG02258.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-10+789A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799765 | |||||||
| chr2:169799844 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-10+868T>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799844 | |||||||
| chr2:169799869 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+893C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799869 | |||||||
| chr2:169799894 | TAC | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0125 others(1): Show |
12 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+920_-10+921del others(2): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169799894 | ||||||
| chr2:169799948 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10+972A>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799948 | |||||||
| chr2:169799993 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG00673.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-9-959T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169799993 | |||||||
| chr2:169800027 | A | G | 1 | a0001c0001t0001g0025 | 3 | HG02922.hp2 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-9-925A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800027 | |||||||
| chr2:169800238 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0064 |
3 | NA18906.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-9-714A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800238 | |||||||
| chr2:169800269 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.-9-683A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800269 | |||||||
| chr2:169800337 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.-9-615T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800337 | |||||||
| chr2:169800512 | C | T | 2 | a0001c0002t0001g0010 a0001c0002t0001g0068 |
7 | HG02015.hp1 HG03239.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-440C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800512 | |||||||
| chr2:169800534 | C | CA | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
118 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-9-399dupA | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0092 others(6): Show |
11 | HG02451.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-400_-9-399dupAA | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAA | 9 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0050 others(6): Show |
13 | HG01256.hp2 HG02559.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9-402_-9-399dupAA others(2): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAA | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
139 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-9-403_-9-399dupAA others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0076 others(5): Show |
13 | HG00408.hp1 HG01081.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-404_-9-399dupAA others(4): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0098 others(8): Show |
17 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-405_-9-399dupAA others(5): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(1): Show |
13 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0096 others(10): Show |
29 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9-406_-9-399dupAA others(6): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02523.hp2 HG03209.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-407_-9-399dupAA others(7): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(3): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0022 others(16): Show |
36 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9-408_-9-399dupAA others(8): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
10 | HG01175.hp2 HG02145.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-409_-9-399dupAA others(9): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0104 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-9-415_-9-399dupAA others(15): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(12): Show |
1 | a0001c0003t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9-417_-9-399dupAA others(17): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(13): Show |
1 | a0001c0003t0001g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-9-399_-9-398insAA others(18): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0103 a0001c0001t0001g0128 |
4 | HG01099.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-399_-9-398insAA others(19): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9-399_-9-398insAA others(20): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(23): Show |
2 | a0001c0001t0002g0037 a0001c0001t0002g0073 |
3 | HG01070.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-9-399_-9-398insAA others(28): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0002g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-9-399_-9-398insAA others(29): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | C | CAAAAAAA others(28): Show |
2 | a0001c0001t0001g0100 a0001c0001t0002g0101 |
2 | NA18943.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-9-399_-9-398insAA others(33): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800534 | CAAAAAA | C | 2 | a0001c0002t0001g0010 a0001c0002t0001g0068 |
7 | HG02015.hp1 HG03239.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-404_-9-399delAA others(4): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169800534 | ||||||
| chr2:169800608 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-9-344A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800608 | |||||||
| chr2:169800626 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-9-326C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800626 | |||||||
| chr2:169800692 | T | G | 13 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0078 others(10): Show |
15 | HG01255.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-260T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800692 | |||||||
| chr2:169800755 | T | A | 2 | a0001c0003t0001g0134 a0001c0003t0001g0135 |
2 | HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-9-197T>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800755 | |||||||
| chr2:169800851 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9-101T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800851 | |||||||
| chr2:169800864 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0125 others(1): Show |
12 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-88C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 1/11 | chr2 | 169800864 | |||||||
| chr2:169801153 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.66+127A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801153 | |||||||
| chr2:169801227 | ATAAAC | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0123 others(2): Show |
8 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+204_66+208delAA others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169801227 | ||||||
| chr2:169801342 | G | A | 11 | a0001c0001t0001g0041 a0001c0001t0001g0078 a0001c0001t0001g0092 others(8): Show |
12 | HG01255.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+316G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801342 | |||||||
| chr2:169801404 | T | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
121 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.66+378T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801404 | |||||||
| chr2:169801509 | G | GT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(28): Show |
51 | HG00621.hp1 HG00733.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.66+506dupT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169801509 | ||||||
| chr2:169801509 | G | GTT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0032 others(2): Show |
15 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+505_66+506dupTT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169801509 | ||||||
| chr2:169801509 | G | GTTT | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0125 others(1): Show |
6 | HG03225.hp1 HG03471.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+504_66+506dupTT others(1): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169801509 | ||||||
| chr2:169801509 | GT | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
160 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.66+506delT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169801509 | ||||||
| chr2:169801509 | GTT | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.66+505_66+506delTT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169801509 | ||||||
| chr2:169801512 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+486T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801512 | |||||||
| chr2:169801545 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.66+519C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801545 | |||||||
| chr2:169801600 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.66+574A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801600 | |||||||
| chr2:169801935 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.66+909C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169801935 | |||||||
| chr2:169802049 | T | TA | 4 | a0001c0001t0001g0023 a0001c0001t0001g0079 a0001c0001t0001g0087 others(1): Show |
6 | HG02523.hp1 NA18976.hp1 NA19072.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+1024dupA | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169802049 | ||||||
| chr2:169802065 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.66+1039G>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802065 | |||||||
| chr2:169802130 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.66+1104G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802130 | |||||||
| chr2:169802134 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.66+1108T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802134 | |||||||
| chr2:169802155 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(22): Show |
46 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+1129G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802155 | |||||||
| chr2:169802204 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66+1178T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802204 | |||||||
| chr2:169802270 | A | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.66+1244A>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802270 | |||||||
| chr2:169802293 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+1267C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802293 | |||||||
| chr2:169802313 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.66+1287G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802313 | |||||||
| chr2:169802315 | TA | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(20): Show |
44 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.66+1291delA | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169802315 | ||||||
| chr2:169802366 | C | G | 2 | a0001c0001t0001g0066 a0003c0006t0001g0067 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.66+1340C>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802366 | |||||||
| chr2:169802440 | G | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.66+1414G>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802440 | |||||||
| chr2:169802521 | T | G | 2 | a0001c0001t0001g0066 a0003c0006t0001g0067 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.66+1495T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802521 | |||||||
| chr2:169802791 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.66+1765A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169802791 | |||||||
| chr2:169803003 | C | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
7 | HG00733.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+1977C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803003 | |||||||
| chr2:169803040 | A | C | 1 | a0001c0001t0001g0043 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.66+2014A>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803040 | |||||||
| chr2:169803278 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67-2196A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803278 | |||||||
| chr2:169803314 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.67-2160G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803314 | |||||||
| chr2:169803358 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.67-2116A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803358 | |||||||
| chr2:169803484 | G | A | 1 | a0002c0004t0002g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.67-1990G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803484 | |||||||
| chr2:169803487 | T | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0103 a0001c0001t0001g0128 |
4 | HG01099.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1987T>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803487 | |||||||
| chr2:169803561 | A | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0125 others(1): Show |
12 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-1913A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803561 | |||||||
| chr2:169803587 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.67-1887A>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803587 | |||||||
| chr2:169803966 | T | C | 1 | a0001c0001t0001g0027 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.67-1508T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169803966 | |||||||
| chr2:169804015 | G | A | 10 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-1459G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804015 | |||||||
| chr2:169804175 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.67-1299G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804175 | |||||||
| chr2:169804240 | C | CT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.67-1212dupT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169804240 | ||||||
| chr2:169804240 | C | CTT | 33 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(30): Show |
59 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.67-1213_67-1212dup others(2): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169804240 | ||||||
| chr2:169804240 | C | CTTT | 12 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0053 others(9): Show |
14 | HG02145.hp2 HG02258.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-1214_67-1212dup others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169804240 | ||||||
| chr2:169804443 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.67-1031G>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804443 | |||||||
| chr2:169804490 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.67-984A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804490 | |||||||
| chr2:169804632 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0103 a0001c0001t0001g0128 |
4 | HG01099.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-842G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804632 | |||||||
| chr2:169804649 | G | T | 1 | a0001c0001t0001g0027 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.67-825G>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804649 | |||||||
| chr2:169804689 | G | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0155 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.67-785G>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804689 | |||||||
| chr2:169804735 | G | A | 1 | a0001c0005t0005g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.67-739G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804735 | |||||||
| chr2:169804823 | C | CT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.67-651_67-650insT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804823 | |||||||
| chr2:169804914 | G | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0019 others(8): Show |
28 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.67-560G>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804914 | |||||||
| chr2:169804936 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.67-538A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804936 | |||||||
| chr2:169804983 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.67-491C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169804983 | |||||||
| chr2:169805070 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18990.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.67-404C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805070 | |||||||
| chr2:169805120 | ACT | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(20): Show |
44 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.67-351_67-350delCT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169805120 | ||||||
| chr2:169805179 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.67-295A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805179 | |||||||
| chr2:169805183 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
9 | HG02145.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-291A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805183 | |||||||
| chr2:169805289 | T | C | 2 | a0001c0001t0001g0066 a0003c0006t0001g0067 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.67-185T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805289 | |||||||
| chr2:169805355 | G | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0089 |
4 | NA18940.hp1 NA18962.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-119G>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805355 | |||||||
| chr2:169805402 | T | C | 2 | a0001c0002t0001g0010 a0001c0002t0001g0068 |
7 | HG02015.hp1 HG03239.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-72T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805402 | |||||||
| chr2:169805420 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.67-54G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 2/11 | chr2 | 169805420 | |||||||
| chr2:169805906 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
22 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.345+67G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169805906 | |||||||
| chr2:169805974 | T | C | 1 | a0001c0001t0001g0027 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.345+135T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169805974 | |||||||
| chr2:169806011 | C | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0123 others(2): Show |
8 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+172C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806011 | |||||||
| chr2:169806124 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(26): Show |
110 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.345+285C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806124 | |||||||
| chr2:169806221 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.345+382T>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806221 | |||||||
| chr2:169806335 | A | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
16 | HG02015.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.346-450A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806335 | |||||||
| chr2:169806436 | T | C | 2 | a0001c0001t0003g0097 a0001c0001t0003g0126 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.346-349T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806436 | |||||||
| chr2:169806464 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346-321C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806464 | |||||||
| chr2:169806634 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.346-151A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 4/11 | chr2 | 169806634 | |||||||
| chr2:169807219 | A | G | 1 | a0004c0007t0001g0057 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.554+148A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807219 | |||||||
| chr2:169807290 | C | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.554+219C>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807290 | |||||||
| chr2:169807348 | G | T | 1 | a0001c0001t0001g0041 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.554+277G>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807348 | |||||||
| chr2:169807404 | T | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.554+333T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807404 | |||||||
| chr2:169807409 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02129.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.554+338C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807409 | |||||||
| chr2:169807531 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.554+460C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807531 | |||||||
| chr2:169807538 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.554+467C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807538 | |||||||
| chr2:169807549 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.554+478A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807549 | |||||||
| chr2:169807568 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.554+497C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807568 | |||||||
| chr2:169807703 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.554+632G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807703 | |||||||
| chr2:169807716 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.554+645T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807716 | |||||||
| chr2:169807737 | C | CT | 17 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0043 others(14): Show |
26 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.554+689dupT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | C | CTT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0078 others(6): Show |
17 | HG01123.hp2 HG01255.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.554+688_554+689dup others(2): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | C | CTTT | 25 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0051 others(22): Show |
45 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.554+687_554+689dup others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | C | CTTTT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0027 others(19): Show |
69 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.554+686_554+689dup others(4): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | C | CTTTTT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(18): Show |
58 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.554+685_554+689dup others(5): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | C | CTTTTTT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0147 a0001c0001t0001g0153 others(5): Show |
11 | HG00099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+684_554+689dup others(6): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | CTTTTTT | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0125 others(1): Show |
12 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.554+684_554+689del others(6): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807737 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0066 a0003c0006t0001g0067 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.554+678_554+689del others(12): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807737 | ||||||
| chr2:169807760 | T | TTTA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0029 others(7): Show |
25 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.554+689_554+690ins others(3): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807760 | |||||||
| chr2:169807760 | T | TTTTA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(11): Show |
26 | HG01192.hp1 HG01255.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.554+689_554+690ins others(4): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169807760 | |||||||
| chr2:169807806 | GTGTC | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
155 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.555-670_555-667del others(4): Show |
SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169807806 | ||||||
| chr2:169808002 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(23): Show |
105 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.555-480A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808002 | |||||||
| chr2:169808055 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0095 |
3 | HG02258.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.555-427G>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808055 | |||||||
| chr2:169808120 | C | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
22 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.555-362C>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808120 | |||||||
| chr2:169808249 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18943.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.555-233C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808249 | |||||||
| chr2:169808422 | A | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0123 others(2): Show |
8 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-60A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808422 | |||||||
| chr2:169808470 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.555-12T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808470 | |||||||
| chr2:169808473 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0125 others(1): Show |
12 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.555-9G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 6/11 | chr2 | 169808473 | |||||||
| chr2:169808598 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.626+45G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 7/11 | chr2 | 169808598 | |||||||
| chr2:169808908 | T | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
22 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.669+6T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169808908 | |||||||
| chr2:169808911 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0123 others(4): Show |
10 | HG01261.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+9A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169808911 | |||||||
| chr2:169808925 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0125 others(1): Show |
12 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+23T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169808925 | |||||||
| chr2:169808954 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.669+52A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169808954 | |||||||
| chr2:169809060 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.669+158A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809060 | |||||||
| chr2:169809254 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.669+352G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809254 | |||||||
| chr2:169809255 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.669+353C>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809255 | |||||||
| chr2:169809533 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0129 |
2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.669+631C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809533 | |||||||
| chr2:169809613 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.670-670A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809613 | |||||||
| chr2:169809673 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.670-610C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809673 | |||||||
| chr2:169809700 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.670-583C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809700 | |||||||
| chr2:169809788 | A | AT | 3 | a0001c0001t0001g0078 a0001c0002t0001g0010 a0001c0002t0001g0068 |
8 | HG01255.hp2 HG02015.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-486dupT | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 169809788 | ||||||
| chr2:169809789 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.670-494T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809789 | |||||||
| chr2:169809826 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0168 a0001c0001t0001g0175 |
4 | HG00735.hp2 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-457C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809826 | |||||||
| chr2:169809859 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0062 |
6 | HG02135.hp2 NA18948.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-424G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809859 | |||||||
| chr2:169809994 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.670-289A>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169809994 | |||||||
| chr2:169810149 | C | T | 1 | a0001c0001t0001g0025 | 3 | HG02922.hp2 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.670-134C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169810149 | |||||||
| chr2:169810157 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(20): Show |
44 | HG00438.hp1 HG00621.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.670-126G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 8/11 | chr2 | 169810157 | |||||||
| chr2:169810607 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
22 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.810+184A>G | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 9/11 | chr2 | 169810607 | |||||||
| chr2:169811401 | T | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
22 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1138+78T>C | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 11/11 | chr2 | 169811401 | |||||||
| chr2:169811510 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1139-158C>T | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 11/11 | chr2 | 169811510 | |||||||
| chr2:169811596 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1139-72G>A | SSB | ENSG00000138385.16 | transcript | ENST00000260956.9 | protein_coding | 11/11 | chr2 | 169811596 |