Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7504 |
| ensemblid | ENSG00000047597.7 |
| hgncid | 12811 |
| symbol | XK |
| name | X-linked Kx blood group antigen, Kell and VPS13A binding protein |
| refseq_nuc | NM_021083.4 |
| refseq_prot | NP_066569.1 |
| ensembl_nuc | ENST00000378616.5 |
| ensembl_prot | ENSP00000367879.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 37685791 |
| end | 37732130 |
| strand | + |
| ver | v1.2 |
| region | chrX:37685791-37732130 |
| region5000 | chrX:37680791-37737130 |
| regionname0 | XK_chrX_37685791_37732130 |
| regionname5000 | XK_chrX_37680791_37737130 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1332 | 210 | 59 | 37 | 80 | 5 | 27 | XK_chrX_37680791_37737130 | XK | ATGAA others(1327): Show |
chrX | 37680791 | 37737130 | ||
| a0001c0002 | 0/0 | 1332 | 7 | 7 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | ATGAA others(1327): Show |
chrX | 37680791 | 37737130 | ||
| a0001c0003 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | ATGAA others(1327): Show |
chrX | 37680791 | 37737130 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5174 | 130 | 8 | 24 | 72 | 5 | 19 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0002 | 0/0 | 5174 | 30 | 10 | 8 | 5 | 0 | 7 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0003 | 0/0 | 5174 | 15 | 15 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0004 | 0/0 | 5174 | 10 | 7 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0005 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0006 | 0/0 | 5174 | 4 | 4 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0008 | 0/0 | 5174 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0009 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0011 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0012 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0013 | 0/0 | 5174 | 2 | 1 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0014 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0015 | 0/0 | 5174 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0016 | 0/0 | 5174 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0017 | 0/0 | 5174 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0018 | 0/0 | 5174 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0019 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0021 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0001t0022 | 0/0 | 5174 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0002t0005 | 0/0 | 5174 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0002t0007 | 0/0 | 5174 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0002t0020 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| a0001c0003t0010 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | AGAGC others(5169): Show |
chrX | 37680791 | 37737130 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 12 | 1 | 1 | 7 | 0 | 2 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0004g0003 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0008g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0011g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0013g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0013g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0015g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0016g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0021g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0002t0020g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| a0001c0003t0010g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01192 | hp1 | a0001 | c0001 | t0022 | g0001 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0161 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02055 | hp1 | a0001 | c0002 | t0020 | g0037 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02132 | hp1 | a0001 | c0001 | t0016 | g0101 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0066 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02615 | hp2 | a0001 | c0002 | t0007 | g0134 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02622 | hp1 | a0001 | c0003 | t0010 | g0023 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0136 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0160 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0132 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02897 | hp1 | a0001 | c0002 | t0007 | g0133 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0115 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0027 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0025 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0127 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0004 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0137 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0162 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0135 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18906 | hp2 | a0001 | c0003 | t0010 | g0023 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18944 | hp1 | a0001 | c0001 | t0018 | g0058 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | LWK | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19056 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ASW | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | ASW | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | USA | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | USA | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37686111 | C | T | 1 | a0001c0002 | 7 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.150C>T | p.Leu50Leu | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/3 | 321/5174 | 150/1335 | 50/444 | chrX | 37686111 | |||
| chrX:37727892 | C | G | 1 | a0001c0003 | 2 | HG02622.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.765C>G | p.Leu255Leu | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 936/5174 | 765/1335 | 255/444 | chrX | 37727892 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37685814 | C | A | 1 | a0001c0001t0014 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/3 | 148 | chrX | 37685814 | ||||||
| chrX:37728551 | A | T | 1 | a0001c0001t0002 | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*89A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 89 | chrX | 37728551 | ||||||
| chrX:37728952 | G | A | 1 | a0001c0001t0015 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 490 | chrX | 37728952 | ||||||
| chrX:37729365 | T | C | 1 | a0001c0002t0007 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*903T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 903 | chrX | 37729365 | ||||||
| chrX:37729392 | A | G | 1 | a0001c0001t0022 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 930 | chrX | 37729392 | ||||||
| chrX:37729399 | G | A | 4 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0009 others(1): Show |
23 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 937 | chrX | 37729399 | ||||||
| chrX:37729464 | C | T | 1 | a0001c0003t0010 | 2 | HG02622.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1002C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1002 | chrX | 37729464 | ||||||
| chrX:37729566 | T | A | 1 | a0001c0001t0011 | 2 | HG02630.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1104T>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1104 | chrX | 37729566 | ||||||
| chrX:37729835 | C | A | 1 | a0001c0001t0016 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1373 | chrX | 37729835 | ||||||
| chrX:37729845 | G | A | 1 | a0001c0002t0007 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1383G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1383 | chrX | 37729845 | ||||||
| chrX:37729860 | T | C | 1 | a0001c0001t0006 | 4 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1398T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1398 | chrX | 37729860 | ||||||
| chrX:37729930 | G | A | 3 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0014 |
13 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1468G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1468 | chrX | 37729930 | ||||||
| chrX:37730297 | A | G | 2 | a0001c0001t0013 a0001c0001t0021 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1835A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1835 | chrX | 37730297 | ||||||
| chrX:37730347 | C | T | 1 | a0001c0002t0020 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1885C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1885 | chrX | 37730347 | ||||||
| chrX:37730348 | G | A | 1 | a0001c0001t0021 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1886G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1886 | chrX | 37730348 | ||||||
| chrX:37730426 | C | T | 5 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0019 others(2): Show |
9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1964C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1964 | chrX | 37730426 | ||||||
| chrX:37730605 | G | T | 1 | a0001c0001t0018 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 2143 | chrX | 37730605 | ||||||
| chrX:37730985 | T | C | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(2): Show |
46 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2523T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 2523 | chrX | 37730985 | ||||||
| chrX:37731355 | C | A | 2 | a0001c0001t0005 a0001c0002t0005 |
5 | HG02809.hp1 HG03516.hp1 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2893C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 2893 | chrX | 37731355 | ||||||
| chrX:37731656 | G | A | 2 | a0001c0001t0009 a0001c0003t0010 |
4 | HG02622.hp1 HG03471.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3194G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3194 | chrX | 37731656 | ||||||
| chrX:37731812 | A | T | 1 | a0001c0001t0002 | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3350A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3350 | chrX | 37731812 | ||||||
| chrX:37731829 | A | G | 1 | a0001c0001t0017 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3367A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3367 | chrX | 37731829 | ||||||
| chrX:37732044 | G | A | 1 | a0001c0001t0012 | 2 | HG02451.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3582G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3582 | chrX | 37732044 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:37686554 | G | T | 4 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0163 others(1): Show |
9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.245+348G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37686554 | |||||||
| chrX:37687108 | G | T | 3 | a0001c0001t0013g0161 a0001c0001t0013g0162 a0001c0001t0021g0160 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.245+902G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687108 | |||||||
| chrX:37687115 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.245+909A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687115 | |||||||
| chrX:37687158 | A | ATC | 6 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0026 others(3): Show |
11 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+972_245+973dup others(2): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687158 | ||||||
| chrX:37687158 | ATC | A | 3 | a0001c0001t0003g0157 a0001c0001t0009g0158 a0001c0003t0010g0023 |
4 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+972_245+973del others(2): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687158 | ||||||
| chrX:37687170 | CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0002g0008 | 3 | HG00639.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245+974_245+983del others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687170 | ||||||
| chrX:37687194 | T | TAC | 26 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(23): Show |
35 | HG00280.hp1 HG00735.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.245+1019_245+1020d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | ||||||
| chrX:37687194 | T | TACAC | 2 | a0001c0001t0014g0025 a0001c0001t0019g0027 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.245+1017_245+1020d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | ||||||
| chrX:37687194 | TAC | T | 32 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0154 others(29): Show |
38 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.245+1019_245+1020d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | ||||||
| chrX:37687226 | C | CACAT | 2 | a0001c0001t0006g0011 a0001c0001t0006g0028 |
3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.245+1020_245+1021i others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687226 | |||||||
| chrX:37687233 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.245+1027A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687233 | |||||||
| chrX:37687263 | A | T | 1 | a0001c0001t0013g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.245+1057A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687263 | |||||||
| chrX:37687324 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.245+1118G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687324 | |||||||
| chrX:37687339 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245+1133C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687339 | |||||||
| chrX:37687366 | C | T | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.245+1160C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687366 | |||||||
| chrX:37687488 | A | G | 8 | a0001c0001t0003g0013 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
9 | HG01891.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+1282A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687488 | |||||||
| chrX:37687675 | C | T | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.245+1469C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687675 | |||||||
| chrX:37687953 | G | C | 3 | a0001c0001t0003g0157 a0001c0001t0009g0158 a0001c0003t0010g0023 |
4 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+1747G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687953 | |||||||
| chrX:37688027 | A | ATTTC | 21 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(18): Show |
28 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+1853_245+1856d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688027 | ||||||
| chrX:37688027 | ATTTC | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0159 a0001c0002t0020g0037 |
3 | HG02055.hp1 HG03834.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.245+1853_245+1856d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688027 | ||||||
| chrX:37688035 | C | A | 1 | a0001c0001t0011g0127 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.245+1829C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688035 | |||||||
| chrX:37688048 | TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0155 |
2 | HG00639.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.245+1845_245+1855d others(13): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688048 | ||||||
| chrX:37688049 | TTCTTTCT others(3): Show |
T | 23 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(20): Show |
28 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+1845_245+1854d others(12): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688049 | ||||||
| chrX:37688051 | CTTTCTTT others(4): Show |
C | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
10 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.245+1849_245+1859d others(13): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688051 | ||||||
| chrX:37688051 | CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0003g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.245+1849_245+1860d others(14): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688051 | ||||||
| chrX:37688055 | CTTTCTT | C | 10 | a0001c0001t0003g0121 a0001c0001t0003g0157 a0001c0001t0006g0011 others(7): Show |
12 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.245+1853_245+1858d others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688055 | ||||||
| chrX:37688057 | TTC | T | 5 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0163 others(2): Show |
10 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.245+1853_245+1854d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688057 | ||||||
| chrX:37688059 | C | CT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(2): Show |
5 | HG02738.hp1 HG03688.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.245+1872dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | ||||||
| chrX:37688059 | CTT | C | 6 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(3): Show |
6 | HG01255.hp1 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+1871_245+1872d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | ||||||
| chrX:37688067 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.245+1861T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688067 | |||||||
| chrX:37688188 | G | C | 3 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 |
3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.245+1982G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688188 | |||||||
| chrX:37688301 | C | T | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+2095C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688301 | |||||||
| chrX:37688318 | G | A | 1 | a0001c0001t0004g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.245+2112G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688318 | |||||||
| chrX:37688422 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.245+2216A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688422 | |||||||
| chrX:37688759 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.245+2553G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688759 | |||||||
| chrX:37688778 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.245+2572A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688778 | |||||||
| chrX:37689535 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0130 a0001c0001t0002g0131 |
5 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+3329G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37689535 | |||||||
| chrX:37689597 | A | G | 60 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(57): Show |
75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.245+3391A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37689597 | |||||||
| chrX:37690204 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+3998A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690204 | |||||||
| chrX:37690222 | T | A | 1 | a0001c0001t0002g0140 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.245+4016T>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690222 | |||||||
| chrX:37690415 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.246-3871A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690415 | |||||||
| chrX:37690739 | G | C | 82 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0044 others(79): Show |
98 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.246-3547G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690739 | |||||||
| chrX:37690934 | T | C | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-3352T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690934 | |||||||
| chrX:37690999 | G | A | 6 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(3): Show |
6 | HG01255.hp1 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-3287G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690999 | |||||||
| chrX:37691214 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0021 others(8): Show |
20 | HG00621.hp1 HG01109.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.246-3072C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37691214 | |||||||
| chrX:37691294 | T | C | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-2992T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37691294 | |||||||
| chrX:37691301 | G | A | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.246-2985G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37691301 | |||||||
| chrX:37692519 | G | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-1767G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692519 | |||||||
| chrX:37692804 | G | T | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.246-1482G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692804 | |||||||
| chrX:37692889 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.246-1397G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692889 | |||||||
| chrX:37692950 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.246-1336G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692950 | |||||||
| chrX:37692971 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.246-1315C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692971 | |||||||
| chrX:37693148 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.246-1138C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693148 | |||||||
| chrX:37693306 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
8 | NA18944.hp1 NA18953.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-980A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693306 | |||||||
| chrX:37693476 | C | CGTGTGTG others(1): Show |
3 | a0001c0002t0005g0136 a0001c0002t0005g0137 a0001c0002t0020g0037 |
3 | HG02055.hp1 HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.246-791_246-784dup others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(3): Show |
3 | a0001c0001t0001g0018 a0001c0001t0002g0141 a0001c0001t0006g0028 |
4 | HG02083.hp1 HG02818.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-793_246-784dup others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(5): Show |
28 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0045 others(25): Show |
38 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.246-795_246-784dup others(12): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(7): Show |
26 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0034 others(23): Show |
32 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.246-797_246-784dup others(14): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(11): Show |
12 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0096 others(9): Show |
12 | HG02027.hp1 HG02970.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.246-801_246-784dup others(18): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(13): Show |
9 | a0001c0001t0001g0057 a0001c0001t0001g0100 a0001c0001t0001g0102 others(6): Show |
9 | HG01891.hp1 HG02040.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.246-803_246-784dup others(20): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(15): Show |
2 | a0001c0001t0001g0071 a0001c0001t0001g0103 |
2 | HG02135.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.246-805_246-784dup others(22): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693476 | C | CGTGTGTG others(17): Show |
1 | a0001c0001t0005g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246-807_246-784dup others(24): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | ||||||
| chrX:37693503 | A | G | 4 | a0001c0002t0005g0135 a0001c0002t0005g0136 a0001c0002t0005g0137 others(1): Show |
4 | HG02055.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-783A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693503 | |||||||
| chrX:37693667 | T | C | 1 | a0001c0001t0004g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.246-619T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693667 | |||||||
| chrX:37693738 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.246-548G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693738 | |||||||
| chrX:37693962 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-324G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693962 | |||||||
| chrX:37693966 | C | T | 1 | a0001c0001t0004g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246-320C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693966 | |||||||
| chrX:37693996 | G | T | 1 | a0001c0001t0003g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.246-290G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693996 | |||||||
| chrX:37694061 | A | C | 1 | a0001c0001t0006g0011 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.246-225A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37694061 | |||||||
| chrX:37694230 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.246-56G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37694230 | |||||||
| chrX:37694765 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0056 |
3 | HG02683.hp1 NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.508+217T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37694765 | |||||||
| chrX:37694998 | A | G | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+450A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37694998 | |||||||
| chrX:37695357 | A | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0115 |
3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+809A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695357 | |||||||
| chrX:37695438 | T | TA | 6 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(3): Show |
6 | HG01255.hp1 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+902dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37695438 | ||||||
| chrX:37695438 | TA | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0113 others(5): Show |
10 | HG01358.hp1 HG01884.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+902delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37695438 | ||||||
| chrX:37695661 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0068 others(2): Show |
6 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+1113C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695661 | |||||||
| chrX:37695835 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.508+1287A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695835 | |||||||
| chrX:37695857 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.508+1309C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695857 | |||||||
| chrX:37696326 | C | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+1778C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696326 | |||||||
| chrX:37696409 | A | T | 4 | a0001c0002t0005g0135 a0001c0002t0005g0136 a0001c0002t0005g0137 others(1): Show |
4 | HG02055.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+1861A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696409 | |||||||
| chrX:37696448 | A | T | 4 | a0001c0001t0003g0121 a0001c0001t0006g0011 a0001c0001t0006g0028 others(1): Show |
5 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+1900A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696448 | |||||||
| chrX:37696679 | G | C | 60 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(57): Show |
75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.508+2131G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696679 | |||||||
| chrX:37697184 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.508+2636A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37697184 | |||||||
| chrX:37698511 | G | A | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(22): Show |
30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.508+3963G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698511 | |||||||
| chrX:37698543 | C | CA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(35): Show |
51 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.508+4021dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | ||||||
| chrX:37698543 | C | CAA | 5 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0003g0123 others(2): Show |
5 | HG03139.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+4020_508+4021d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | ||||||
| chrX:37698543 | CA | C | 39 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0073 others(36): Show |
45 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.508+4021delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | ||||||
| chrX:37698587 | T | C | 3 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0143 |
3 | HG02683.hp2 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.508+4039T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698587 | |||||||
| chrX:37698592 | G | A | 33 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(30): Show |
44 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.508+4044G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698592 | |||||||
| chrX:37698760 | C | T | 1 | a0001c0001t0003g0013 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.508+4212C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698760 | |||||||
| chrX:37698845 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.508+4297T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698845 | |||||||
| chrX:37698964 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.508+4416C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698964 | |||||||
| chrX:37699180 | G | A | 1 | a0001c0001t0002g0152 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508+4632G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37699180 | |||||||
| chrX:37700279 | G | C | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+5731G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700279 | |||||||
| chrX:37700301 | G | A | 3 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 |
3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+5753G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700301 | |||||||
| chrX:37700752 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.508+6204C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700752 | |||||||
| chrX:37700770 | C | T | 1 | a0001c0001t0013g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.508+6222C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700770 | |||||||
| chrX:37701203 | G | T | 3 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 |
3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+6655G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701203 | |||||||
| chrX:37701452 | G | C | 1 | a0001c0001t0009g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508+6904G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701452 | |||||||
| chrX:37701553 | TCAC | T | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+7009_508+7011d others(5): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37701553 | ||||||
| chrX:37701675 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.508+7127G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701675 | |||||||
| chrX:37701755 | G | A | 1 | a0001c0003t0010g0023 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+7207G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701755 | |||||||
| chrX:37701835 | TGGAGAGA others(1): Show |
T | 18 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(15): Show |
22 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.508+7288_508+7295d others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701835 | |||||||
| chrX:37701888 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508+7340G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701888 | |||||||
| chrX:37701984 | C | T | 31 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(28): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.508+7436C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701984 | |||||||
| chrX:37702313 | G | C | 3 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 |
3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+7765G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37702313 | |||||||
| chrX:37702943 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.508+8395T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37702943 | |||||||
| chrX:37702967 | A | G | 1 | a0001c0001t0005g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.508+8419A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37702967 | |||||||
| chrX:37703258 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.508+8710G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703258 | |||||||
| chrX:37703339 | C | T | 1 | a0001c0001t0006g0011 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.508+8791C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703339 | |||||||
| chrX:37703374 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.508+8826G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703374 | |||||||
| chrX:37703858 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.508+9310A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703858 | |||||||
| chrX:37703863 | A | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0115 |
3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+9315A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703863 | |||||||
| chrX:37704399 | T | C | 3 | a0001c0001t0013g0161 a0001c0001t0013g0162 a0001c0001t0021g0160 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.508+9851T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704399 | |||||||
| chrX:37704503 | C | G | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(22): Show |
30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.508+9955C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704503 | |||||||
| chrX:37704558 | G | A | 29 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(26): Show |
35 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.508+10010G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704558 | |||||||
| chrX:37704749 | C | T | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+10201C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704749 | |||||||
| chrX:37704783 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+10235C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704783 | |||||||
| chrX:37704791 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0084 |
2 | HG03834.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.508+10243C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704791 | |||||||
| chrX:37705029 | A | T | 2 | a0001c0001t0011g0127 a0001c0001t0011g0128 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+10481A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705029 | |||||||
| chrX:37705183 | C | T | 67 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(64): Show |
82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+10635C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705183 | |||||||
| chrX:37705212 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.508+10664A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705212 | |||||||
| chrX:37705217 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508+10669G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705217 | |||||||
| chrX:37705241 | C | G | 1 | a0001c0001t0003g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.508+10693C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705241 | |||||||
| chrX:37705242 | A | G | 3 | a0001c0001t0001g0059 a0001c0001t0003g0121 a0001c0001t0014g0025 |
3 | HG03195.hp1 HG03516.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.508+10694A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705242 | |||||||
| chrX:37705289 | CA | C | 29 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(26): Show |
35 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.508+10754delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705289 | ||||||
| chrX:37705377 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.508+10829G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705377 | |||||||
| chrX:37705383 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0070 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.508+10835T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705383 | |||||||
| chrX:37705408 | C | T | 4 | a0001c0001t0003g0121 a0001c0001t0006g0011 a0001c0001t0006g0028 others(1): Show |
5 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+10860C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705408 | |||||||
| chrX:37705416 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.508+10868G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705416 | |||||||
| chrX:37705426 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.508+10878T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705426 | |||||||
| chrX:37705430 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0096 |
3 | NA18945.hp1 NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.508+10882T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705430 | |||||||
| chrX:37705433 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0096 |
3 | NA18945.hp1 NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.508+10885A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705433 | |||||||
| chrX:37705439 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.508+10891G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705439 | |||||||
| chrX:37705451 | C | CA | 28 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0096 others(25): Show |
34 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.508+10917dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705451 | ||||||
| chrX:37705631 | A | G | 1 | a0001c0001t0012g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508+11083A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705631 | |||||||
| chrX:37705830 | G | A | 5 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0163 others(2): Show |
10 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+11282G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705830 | |||||||
| chrX:37705919 | A | AT | 49 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0002g0007 others(46): Show |
58 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.508+11386dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705919 | ||||||
| chrX:37706217 | T | A | 1 | a0001c0001t0011g0127 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.508+11669T>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706217 | |||||||
| chrX:37706332 | A | T | 1 | a0001c0001t0018g0058 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.508+11784A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706332 | |||||||
| chrX:37706573 | G | A | 10 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0026 others(7): Show |
16 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+12025G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706573 | |||||||
| chrX:37706603 | C | CT | 57 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(54): Show |
72 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.508+12064dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37706603 | ||||||
| chrX:37706603 | C | CTT | 6 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 others(3): Show |
6 | HG02809.hp1 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+12063_508+1206 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37706603 | ||||||
| chrX:37706631 | A | T | 4 | a0001c0001t0001g0093 a0001c0001t0004g0024 a0001c0001t0004g0163 others(1): Show |
5 | HG02451.hp2 HG02723.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+12083A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706631 | |||||||
| chrX:37706980 | CAGA | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0050 others(5): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.508+12437_508+1243 others(7): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37706980 | ||||||
| chrX:37707243 | G | A | 6 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 others(3): Show |
6 | HG02809.hp1 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+12695G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707243 | |||||||
| chrX:37707255 | G | A | 6 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 others(3): Show |
6 | HG02809.hp1 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+12707G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707255 | |||||||
| chrX:37707289 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.508+12741C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707289 | |||||||
| chrX:37707302 | G | A | 3 | a0001c0002t0007g0132 a0001c0002t0007g0133 a0001c0002t0007g0134 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.508+12754G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707302 | |||||||
| chrX:37707342 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0002g0140 |
2 | HG03704.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.508+12794C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707342 | |||||||
| chrX:37707343 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.508+12795G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707343 | |||||||
| chrX:37707414 | TGGCTGCC others(33): Show |
T | 2 | a0001c0001t0008g0022 a0001c0001t0008g0115 |
3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+12919_508+1295 others(44): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37707414 | ||||||
| chrX:37707449 | C | T | 1 | a0001c0001t0006g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508+12901C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707449 | |||||||
| chrX:37707489 | C | T | 3 | a0001c0001t0013g0161 a0001c0001t0013g0162 a0001c0001t0021g0160 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.508+12941C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707489 | |||||||
| chrX:37707509 | AGGGCTCC others(33): Show |
A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0068 others(1): Show |
5 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+12990_508+1302 others(44): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37707509 | ||||||
| chrX:37707529 | C | T | 1 | a0001c0001t0004g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.508+12981C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707529 | |||||||
| chrX:37707534 | C | T | 5 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0163 others(2): Show |
10 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+12986C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707534 | |||||||
| chrX:37707535 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0150 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.508+12987G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707535 | |||||||
| chrX:37707589 | G | A | 9 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(6): Show |
9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+13041G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707589 | |||||||
| chrX:37707612 | A | G | 67 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(64): Show |
82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+13064A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707612 | |||||||
| chrX:37707614 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.508+13066C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707614 | |||||||
| chrX:37707625 | C | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0001c0001t0001g0078 others(4): Show |
7 | HG01255.hp1 HG02809.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.508+13077C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707625 | |||||||
| chrX:37707744 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.508+13196T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707744 | |||||||
| chrX:37707803 | T | C | 8 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0026 others(5): Show |
13 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.508+13255T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707803 | |||||||
| chrX:37707888 | C | T | 10 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0026 others(7): Show |
16 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+13340C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707888 | |||||||
| chrX:37707891 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0094 |
2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.508+13343G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707891 | |||||||
| chrX:37707897 | G | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+13349G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707897 | |||||||
| chrX:37707915 | C | A | 23 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(20): Show |
28 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.508+13367C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707915 | |||||||
| chrX:37708033 | A | G | 2 | a0001c0001t0002g0149 a0001c0001t0002g0152 |
2 | NA18974.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+13485A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37708033 | |||||||
| chrX:37708586 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.508+14038A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37708586 | |||||||
| chrX:37709021 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+14473G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709021 | |||||||
| chrX:37709154 | T | C | 10 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0026 others(7): Show |
16 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+14606T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709154 | |||||||
| chrX:37709238 | A | G | 63 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(60): Show |
78 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.508+14690A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709238 | |||||||
| chrX:37709435 | G | T | 63 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(60): Show |
78 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.508+14887G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709435 | |||||||
| chrX:37709657 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.508+15109C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709657 | |||||||
| chrX:37709661 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.508+15113C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709661 | |||||||
| chrX:37710080 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+15532C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710080 | |||||||
| chrX:37710177 | G | A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0040 |
2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.508+15629G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710177 | |||||||
| chrX:37710593 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+16045C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710593 | |||||||
| chrX:37710897 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.508+16349G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710897 | |||||||
| chrX:37711001 | A | G | 2 | a0001c0001t0006g0028 a0001c0001t0006g0119 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508+16453A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711001 | |||||||
| chrX:37711326 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509-16310G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711326 | |||||||
| chrX:37711579 | T | C | 9 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(6): Show |
9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-16057T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711579 | |||||||
| chrX:37711853 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.509-15783G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711853 | |||||||
| chrX:37712233 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.509-15403C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712233 | |||||||
| chrX:37712257 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0112 |
3 | HG00621.hp1 NA18952.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.509-15379C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712257 | |||||||
| chrX:37712290 | C | G | 44 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(41): Show |
53 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.509-15346C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712290 | |||||||
| chrX:37712318 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509-15318C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712318 | |||||||
| chrX:37713408 | A | G | 1 | a0001c0002t0005g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509-14228A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713408 | |||||||
| chrX:37713445 | A | G | 15 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(12): Show |
18 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.509-14191A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713445 | |||||||
| chrX:37713458 | T | C | 3 | a0001c0001t0009g0118 a0001c0001t0009g0158 a0001c0003t0010g0023 |
4 | HG02622.hp1 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-14178T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713458 | |||||||
| chrX:37713532 | C | T | 1 | a0001c0003t0010g0023 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-14104C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713532 | |||||||
| chrX:37713602 | C | CT | 8 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0026 others(5): Show |
13 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.509-14021dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37713602 | ||||||
| chrX:37713699 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0072 a0001c0001t0001g0075 others(3): Show |
6 | NA18986.hp1 NA19005.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-13937C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713699 | |||||||
| chrX:37713700 | G | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-13936G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713700 | |||||||
| chrX:37714319 | T | C | 9 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(6): Show |
9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-13317T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714319 | |||||||
| chrX:37714454 | A | C | 1 | a0001c0002t0020g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.509-13182A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714454 | |||||||
| chrX:37714461 | A | G | 1 | a0001c0002t0005g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509-13175A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714461 | |||||||
| chrX:37714590 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.509-13046T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714590 | |||||||
| chrX:37714922 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.509-12714A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714922 | |||||||
| chrX:37714941 | A | T | 1 | a0001c0003t0010g0023 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-12695A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714941 | |||||||
| chrX:37715015 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.509-12621A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715015 | |||||||
| chrX:37715024 | G | GTA | 4 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0163 others(1): Show |
9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-12598_509-1259 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37715024 | ||||||
| chrX:37715279 | T | C | 4 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0163 others(1): Show |
9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-12357T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715279 | |||||||
| chrX:37715671 | C | A | 6 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0157 others(3): Show |
7 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-11965C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715671 | |||||||
| chrX:37715823 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509-11813T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715823 | |||||||
| chrX:37715851 | A | C | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-11785A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715851 | |||||||
| chrX:37716015 | C | T | 1 | a0001c0001t0002g0008 | 3 | HG00639.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.509-11621C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37716015 | |||||||
| chrX:37716294 | T | G | 3 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0019g0027 |
3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.509-11342T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37716294 | |||||||
| chrX:37716724 | T | C | 1 | a0001c0001t0003g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509-10912T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37716724 | |||||||
| chrX:37717003 | G | C | 3 | a0001c0002t0007g0132 a0001c0002t0007g0133 a0001c0002t0007g0134 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.509-10633G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717003 | |||||||
| chrX:37717070 | G | A | 4 | a0001c0001t0003g0157 a0001c0001t0009g0118 a0001c0001t0009g0158 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-10566G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717070 | |||||||
| chrX:37717123 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.509-10513C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717123 | |||||||
| chrX:37717743 | A | G | 9 | a0001c0001t0005g0029 a0001c0001t0005g0062 a0001c0001t0013g0161 others(6): Show |
9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-9893A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717743 | |||||||
| chrX:37717838 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.509-9798G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717838 | |||||||
| chrX:37718850 | G | C | 3 | a0001c0001t0013g0161 a0001c0001t0013g0162 a0001c0001t0021g0160 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509-8786G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37718850 | |||||||
| chrX:37718914 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.509-8722A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37718914 | |||||||
| chrX:37719158 | A | G | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(22): Show |
30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.509-8478A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719158 | |||||||
| chrX:37719249 | G | T | 3 | a0001c0001t0003g0039 a0001c0001t0003g0041 a0001c0001t0003g0042 |
3 | HG02922.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.509-8387G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719249 | |||||||
| chrX:37719696 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0068 others(1): Show |
5 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-7940A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719696 | |||||||
| chrX:37719797 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509-7839T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719797 | |||||||
| chrX:37719973 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509-7663C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719973 | |||||||
| chrX:37720020 | C | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0115 |
3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-7616C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720020 | |||||||
| chrX:37720169 | A | G | 1 | a0001c0001t0009g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509-7467A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720169 | |||||||
| chrX:37720351 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.509-7285A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720351 | |||||||
| chrX:37720462 | C | G | 1 | a0001c0003t0010g0023 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-7174C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720462 | |||||||
| chrX:37720760 | A | C | 2 | a0001c0001t0008g0022 a0001c0001t0008g0115 |
3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-6876A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720760 | |||||||
| chrX:37720965 | C | T | 1 | a0001c0002t0007g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.509-6671C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720965 | |||||||
| chrX:37721260 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.509-6376T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721260 | |||||||
| chrX:37721534 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.509-6102A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721534 | |||||||
| chrX:37721579 | G | T | 3 | a0001c0001t0013g0161 a0001c0001t0013g0162 a0001c0001t0021g0160 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509-6057G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721579 | |||||||
| chrX:37721588 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.509-6048A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721588 | |||||||
| chrX:37721669 | G | A | 1 | a0001c0002t0020g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.509-5967G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721669 | |||||||
| chrX:37721984 | C | G | 1 | a0001c0003t0010g0023 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-5652C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721984 | |||||||
| chrX:37722117 | G | A | 1 | a0001c0002t0020g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.509-5519G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722117 | |||||||
| chrX:37722153 | A | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0115 |
3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-5483A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722153 | |||||||
| chrX:37722204 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.509-5432T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722204 | |||||||
| chrX:37722433 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-5203G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722433 | |||||||
| chrX:37722455 | G | A | 4 | a0001c0001t0003g0157 a0001c0001t0009g0118 a0001c0001t0009g0158 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-5181G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722455 | |||||||
| chrX:37722490 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0016g0101 |
2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.509-5146A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722490 | |||||||
| chrX:37722786 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG00609.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.509-4850T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722786 | |||||||
| chrX:37723467 | A | G | 67 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(64): Show |
82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.509-4169A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723467 | |||||||
| chrX:37723708 | A | G | 9 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(6): Show |
11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-3928A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723708 | |||||||
| chrX:37723774 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.509-3862C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723774 | |||||||
| chrX:37723934 | A | C | 1 | a0001c0001t0011g0127 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509-3702A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723934 | |||||||
| chrX:37724231 | G | A | 3 | a0001c0001t0013g0161 a0001c0001t0013g0162 a0001c0001t0021g0160 |
3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509-3405G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37724231 | |||||||
| chrX:37724273 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0073 |
3 | HG00140.hp1 HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.509-3363G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37724273 | |||||||
| chrX:37724375 | T | G | 67 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0116 others(64): Show |
82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.509-3261T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37724375 | |||||||
| chrX:37725124 | C | G | 1 | a0001c0003t0010g0023 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-2512C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725124 | |||||||
| chrX:37725568 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.509-2068C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725568 | |||||||
| chrX:37725588 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
13 | HG01123.hp2 HG01884.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.509-2048A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725588 | |||||||
| chrX:37725596 | G | T | 4 | a0001c0001t0003g0157 a0001c0001t0009g0118 a0001c0001t0009g0158 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-2040G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725596 | |||||||
| chrX:37726217 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1419G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726217 | |||||||
| chrX:37726218 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1418T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726218 | |||||||
| chrX:37726219 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1417G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726219 | |||||||
| chrX:37726297 | A | C | 1 | a0001c0001t0003g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.509-1339A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726297 | |||||||
| chrX:37726409 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.509-1227T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726409 | |||||||
| chrX:37726458 | A | T | 4 | a0001c0001t0003g0157 a0001c0001t0009g0118 a0001c0001t0009g0158 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1178A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726458 | |||||||
| chrX:37726686 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.509-950T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726686 | |||||||
| chrX:37726928 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.509-708T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726928 | |||||||
| chrX:37727058 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0070 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.509-578A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37727058 | |||||||
| chrX:37727256 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.509-380G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37727256 |