Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11326 |
|---|---|
| ensemblid | ENSG00000155659.15 |
| hgncid | 17032 |
| symbol | VSIG4 |
| name | V-set and immunoglobulin domain containing 4 |
| refseq_nuc | NM_007268.3 |
| refseq_prot | NP_009199.1 |
| ensembl_nuc | ENST00000374737.9 |
| ensembl_prot | ENSP00000363869.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 66021738 |
| end | 66040080 |
| strand | - |
| ver | v1.2 |
| region | chrX:66021738-66040080 |
| region5000 | chrX:66016738-66045080 |
| regionname0 | VSIG4_chrX_66021738_66040080 |
| regionname5000 | VSIG4_chrX_66016738_66045080 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 206 | 40 | 40 | 83 | 11 | 30 | 63 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0002 | 0/0 | 399 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0003 | 0/0 | 399 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0004 | 0/0 | 399 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0005 | 0/0 | 70 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0006 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0007 | 0/0 | 399 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0008 | 0/0 | 189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1200 | 203 | 39 | 38 | 83 | 11 | 30 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0002 | 0/0 | 1200 | 4 | 2 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0003 | 0/0 | 1200 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0004 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0005 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0006 | 0/0 | 1199 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0007 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0008 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0009 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| c0010 | 0/0 | 1201 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 608 | 195 | 34 | 41 | 78 | 10 | 30 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| t0002 | 0/0 | 608 | 7 | 6 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| t0003 | 0/0 | 608 | 7 | 0 | 0 | 7 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| t0004 | 0/0 | 608 | 5 | 0 | 4 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| t0005 | 0/0 | 608 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| t0006 | 0/0 | 608 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| t0007 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 9 | 0 | 0 | 6 | 0 | 3 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0002 | 0/0 | 7 | 0 | 0 | 3 | 0 | 4 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1200 | 203 | 39 | 38 | 83 | 11 | 30 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0004 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0008 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0002c0002 | 0/0 | 1200 | 4 | 2 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0003c0005 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0004c0003 | 0/0 | 1200 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0005c0010 | 0/0 | 1201 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0006c0009 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0007c0007 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0008c0006 | 0/0 | 1199 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1807 | 180 | 30 | 34 | 76 | 10 | 28 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0001t0002 | 0/0 | 1807 | 7 | 6 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0001t0003 | 0/0 | 1807 | 7 | 0 | 0 | 7 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0001t0004 | 0/0 | 1807 | 5 | 0 | 4 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0001t0005 | 0/0 | 1807 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0001t0006 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0001t0007 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0004t0001 | 0/0 | 1807 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0001c0008t0001 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0002c0002t0001 | 0/0 | 1807 | 4 | 2 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0003c0005t0001 | 0/0 | 1807 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0004c0003t0001 | 0/0 | 1807 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0005c0010t0001 | 0/0 | 1808 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0006c0009t0001 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0007c0007t0001 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| a0008c0006t0001 | 0/0 | 1806 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | copy fasta | chrX | 66016738 | 66045080 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 6 | 0 | 3 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 3 | 0 | 4 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0003c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0003c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0004c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0005c0010t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0006c0009t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0007c0007t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0008c0006t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00733 | hp2 | a0003 | c0005 | t0001 | g0053 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01168 | hp2 | a0003 | c0005 | t0001 | g0054 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02004 | hp2 | a0008 | c0006 | t0001 | g0029 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02647 | hp1 | a0001 | c0008 | t0001 | g0162 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0119 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03130 | hp1 | a0007 | c0007 | t0001 | g0063 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03704 | hp2 | a0004 | c0003 | t0001 | g0015 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03831 | hp2 | a0004 | c0003 | t0001 | g0015 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18957 | hp1 | a0006 | c0009 | t0001 | g0121 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | LWK | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19057 | hp2 | a0005 | c0010 | t0001 | g0085 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | GIH | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0139 | REF | REF | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:66022315
|
G | A | 1 | a0003 | 2 | HG00733.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.1148C>T | p.Thr383Ile | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 1230/1807 | 1148/1200 | 383/399 | chrX | 66022315 | ||
| chrX:66025057
|
T | C | 1 | a0002 | 4 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.908A>G | p.Tyr303Cys | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/8 | 990/1807 | 908/1200 | 303/399 | chrX | 66025057 | ||
| chrX:66025129
|
C | T | 1 | a0004 | 2 | HG03704.hp2 HG03831.hp2 |
missense_variant&splice_region_variant | MODERATE | c.836G>A | p.Gly279Glu | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/8 | 918/1807 | 836/1200 | 279/399 | chrX | 66025129 | ||
| chrX:66032581
|
C | T | 1 | a0007 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.581G>A | p.Ser194Asn | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/8 | 663/1807 | 581/1200 | 194/399 | chrX | 66032581 | ||
| chrX:66032665
|
TG | T | 1 | a0008 | 1 | HG02004.hp2 | frameshift_variant | HIGH | c.496delC | p.Gln166fs | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/8 | 578/1807 | 496/1200 | 166/399 | chrX | 66032665 | ||
| chrX:66033513
|
C | A | 1 | a0006 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.373G>T | p.Val125Phe | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/8 | 455/1807 | 373/1200 | 125/399 | chrX | 66033513 | ||
| chrX:66033612
|
C | A | 1 | a0003 | 2 | HG00733.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.274G>T | p.Val92Phe | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/8 | 356/1807 | 274/1200 | 92/399 | chrX | 66033612 | ||
| chrX:66033740
|
T | TA | 1 | a0005 | 1 | NA19057.hp2 | frameshift_variant | HIGH | c.145dupT | p.Tyr49fs | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/8 | 227/1807 | 145/1200 | 49/399 | chrX | 66033740 |
| 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:66022389
|
A | T | 1 | a0001c0004 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1074T>A | p.Ser358Ser | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 1156/1807 | 1074/1200 | 358/399 | chrX | 66022389 | ||
| chrX:66032559
|
C | T | 1 | a0001c0008 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.603G>A | p.Ala201Ala | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/8 | 685/1807 | 603/1200 | 201/399 | chrX | 66032559 |
| 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:66021884
|
G | A | 1 | a0001c0001t0004 | 5 | HG00735.hp2 HG01109.hp1 HG01346.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*379C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 379 | chrX | 66021884 | |||||
| chrX:66021926
|
G | T | 1 | a0001c0001t0003 | 7 | HG00621.hp1 HG02132.hp1 NA18747.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*337C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 337 | chrX | 66021926 | |||||
| chrX:66022026
|
G | T | 1 | a0001c0001t0007 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*237C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 237 | chrX | 66022026 | |||||
| chrX:66022116
|
C | T | 1 | a0001c0001t0006 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 147 | chrX | 66022116 | |||||
| chrX:66022135
|
C | A | 1 | a0001c0001t0005 | 2 | HG02615.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*128G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 128 | chrX | 66022135 | |||||
| chrX:66040051
|
C | T | 1 | a0001c0001t0002 | 7 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/8 | 53 | chrX | 66040051 |
| 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:66022509
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.963-9G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 7/7 | chrX | 66022509 | ||||||
| chrX:66022650
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0049 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.963-150G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 7/7 | chrX | 66022650 | ||||||
| chrX:66022667
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.963-167G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 7/7 | chrX | 66022667 | ||||||
| chrX:66023112
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.941-250C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023112 | ||||||
| chrX:66023282
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.941-420G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023282 | ||||||
| chrX:66023421
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.941-559T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023421 | ||||||
| chrX:66023483
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.941-621C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023483 | ||||||
| chrX:66023484
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.941-622G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023484 | ||||||
| chrX:66023880
|
G | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.941-1018C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023880 | ||||||
| chrX:66024093
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0150 | 3 | NA18975.hp2 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.940+932C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024093 | ||||||
| chrX:66024220
|
T | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(36): Show | 44 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.940+805A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024220 | ||||||
| chrX:66024590
|
C | G | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.940+435G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024590 | ||||||
| chrX:66024749
|
G | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.940+276C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024749 | ||||||
| chrX:66024808
|
A | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0070a0001c0001t0001g0086others(4): Show | 8 | NA18947.hp1 NA18954.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.940+217T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024808 | ||||||
| chrX:66025263
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.836-134G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66025263 | ||||||
| chrX:66025940
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.836-811T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66025940 | ||||||
| chrX:66026027
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.836-898G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026027 | ||||||
| chrX:66026359
|
CT | C | 1 | a0001c0001t0001g0094 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.835+1089delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026359 | ||||||
| chrX:66026520
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+929C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026520 | ||||||
| chrX:66026663
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.835+786G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026663 | ||||||
| chrX:66026715
|
A | ATTTAATT others(140): Show |
1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.835+733_835+734ins others(147): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026715 | ||||||
| chrX:66026730
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.835+719C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026730 | ||||||
| chrX:66026857
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.835+592T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026857 | ||||||
| chrX:66026933
|
T | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.835+516A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026933 | ||||||
| chrX:66027252
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.835+197C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66027252 | ||||||
| chrX:66027259
|
T | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(50): Show | 60 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.835+190A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66027259 | ||||||
| chrX:66027414
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.835+35T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66027414 | ||||||
| chrX:66027567
|
T | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(47): Show | 56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.758-41A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027567 | ||||||
| chrX:66027727
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.758-201A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027727 | ||||||
| chrX:66027776
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.758-250T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027776 | ||||||
| chrX:66027860
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.757+190C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027860 | ||||||
| chrX:66027968
|
CCATGGCA others(7): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.757+68_757+81delAT others(12): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027968 | ||||||
| chrX:66028151
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-39G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028151 | ||||||
| chrX:66028193
|
G | A | 3 | a0002c0002t0001g0018a0002c0002t0001g0147a0002c0002t0001g0148 | 4 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-81C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028193 | ||||||
| chrX:66028326
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.695-214C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028326 | ||||||
| chrX:66028363
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-251G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028363 | ||||||
| chrX:66028377
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.695-265A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028377 | ||||||
| chrX:66028378
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.695-266T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028378 | ||||||
| chrX:66028438
|
TG | T | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-327delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028438 | ||||||
| chrX:66028514
|
CT | C | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-403delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028514 | ||||||
| chrX:66028550
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(36): Show | 44 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.695-438C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028550 | ||||||
| chrX:66028558
|
C | CT | 10 | a0001c0001t0001g0067a0001c0001t0001g0100a0001c0001t0001g0103others(7): Show | 10 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-447dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | ||||||
| chrX:66028558
|
C | CTT | 5 | a0001c0001t0001g0066a0001c0001t0001g0118a0001c0001t0001g0126others(2): Show | 5 | HG02055.hp1 HG02074.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-448_695-447dup others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | ||||||
| chrX:66028558
|
CT | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0035others(42): Show | 50 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.695-447delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | ||||||
| chrX:66028558
|
CTT | C | 10 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0140others(7): Show | 11 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.695-448_695-447del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | ||||||
| chrX:66028558
|
CTTT | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0170 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.695-449_695-447del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | ||||||
| chrX:66028589
|
T | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.695-477A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028589 | ||||||
| chrX:66028616
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.695-504G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028616 | ||||||
| chrX:66028647
|
TC | T | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-536delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028647 | ||||||
| chrX:66028656
|
TG | T | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-545delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028656 | ||||||
| chrX:66028695
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG01361.hp2 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-583A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028695 | ||||||
| chrX:66028740
|
AC | A | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-629delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028740 | ||||||
| chrX:66028763
|
A | AG | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-652dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028763 | ||||||
| chrX:66029023
|
TG | T | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695-912delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029023 | ||||||
| chrX:66029097
|
T | C | 50 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(47): Show | 56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.695-985A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029097 | ||||||
| chrX:66029104
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.695-992G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029104 | ||||||
| chrX:66029132
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-1020C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029132 | ||||||
| chrX:66029146
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0110 | 5 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-1034C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029146 | ||||||
| chrX:66029260
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.695-1148C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029260 | ||||||
| chrX:66029469
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.695-1357T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029469 | ||||||
| chrX:66029538
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695-1426C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029538 | ||||||
| chrX:66029590
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.695-1478T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029590 | ||||||
| chrX:66029593
|
T | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-1481A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029593 | ||||||
| chrX:66029762
|
A | G | 50 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(47): Show | 56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.695-1650T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029762 | ||||||
| chrX:66029809
|
G | A | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG00738.hp1 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-1697C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029809 | ||||||
| chrX:66029884
|
G | GA | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.695-1773dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029884 | ||||||
| chrX:66029890
|
AT | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.695-1779delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029890 | ||||||
| chrX:66029891
|
T | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(48): Show | 58 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.695-1779A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029891 | ||||||
| chrX:66030346
|
T | C | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+2122A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030346 | ||||||
| chrX:66030360
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.694+2108C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030360 | ||||||
| chrX:66030383
|
ACATATAT others(6): Show |
A | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.694+2072_694+2084d others(15): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030383 | ||||||
| chrX:66030483
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.694+1985C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030483 | ||||||
| chrX:66030589
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.694+1879T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030589 | ||||||
| chrX:66030740
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+1728T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030740 | ||||||
| chrX:66030839
|
C | T | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG00738.hp1 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.694+1629G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030839 | ||||||
| chrX:66030894
|
A | G | 26 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(23): Show | 28 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.694+1574T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030894 | ||||||
| chrX:66030953
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+1515C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030953 | ||||||
| chrX:66031208
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.694+1260G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031208 | ||||||
| chrX:66031295
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.694+1173G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031295 | ||||||
| chrX:66031306
|
C | T | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.694+1162G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031306 | ||||||
| chrX:66031322
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.694+1146A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031322 | ||||||
| chrX:66031369
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.694+1099C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031369 | ||||||
| chrX:66031582
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.694+886A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031582 | ||||||
| chrX:66031992
|
G | A | 1 | a0006c0009t0001g0121 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.694+476C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031992 | ||||||
| chrX:66032126
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0046 | 5 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+342G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032126 | ||||||
| chrX:66032209
|
T | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+259A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032209 | ||||||
| chrX:66032236
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+232G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032236 | ||||||
| chrX:66032244
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.694+224A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032244 | ||||||
| chrX:66032325
|
GT | G | 1 | a0001c0001t0001g0133 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.694+142delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032325 | ||||||
| chrX:66032373
|
T | TCTCCCAA others(6): Show |
1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.694+82_694+94dupGA others(11): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032373 | ||||||
| chrX:66032386
|
CT | C | 1 | a0008c0006t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.694+81delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032386 | ||||||
| chrX:66032759
|
A | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02071.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.413-10T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032759 | ||||||
| chrX:66032837
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG01361.hp2 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-88G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032837 | ||||||
| chrX:66032857
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.413-108C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032857 | ||||||
| chrX:66032891
|
A | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-142T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032891 | ||||||
| chrX:66033012
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.413-263C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033012 | ||||||
| chrX:66033111
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0143 | 2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.413-362G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033111 | ||||||
| chrX:66033156
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.412+318G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033156 | ||||||
| chrX:66033204
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0125 | 2 | NA18947.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.412+270C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033204 | ||||||
| chrX:66033369
|
G | A | 1 | a0001c0008t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412+105C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033369 | ||||||
| chrX:66033389
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.412+85G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033389 | ||||||
| chrX:66033841
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0007g0091 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.56-11C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033841 | ||||||
| chrX:66033842
|
G | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-12C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033842 | ||||||
| chrX:66033879
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.56-49G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033879 | ||||||
| chrX:66033927
|
T | C | 50 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(47): Show | 56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.56-97A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033927 | ||||||
| chrX:66033954
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(29): Show | 37 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.56-124A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033954 | ||||||
| chrX:66034005
|
AC | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-176delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034005 | ||||||
| chrX:66034035
|
T | TG | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-206dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034035 | ||||||
| chrX:66034187
|
A | AT | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-358dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034187 | ||||||
| chrX:66034220
|
CT | C | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-391delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034220 | ||||||
| chrX:66034293
|
TA | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-464delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034293 | ||||||
| chrX:66034488
|
GT | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-659delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034488 | ||||||
| chrX:66034516
|
AT | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-687delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034516 | ||||||
| chrX:66034526
|
T | A | 1 | a0001c0001t0001g0004 | 4 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-696A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034526 | ||||||
| chrX:66034538
|
AC | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-709delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034538 | ||||||
| chrX:66034663
|
GA | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-834delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034663 | ||||||
| chrX:66034692
|
G | GA | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-863_56-862insT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034692 | ||||||
| chrX:66034704
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.56-874C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034704 | ||||||
| chrX:66034763
|
G | GA | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-934_56-933insT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034763 | ||||||
| chrX:66034766
|
T | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-936A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034766 | ||||||
| chrX:66034766
|
T | TG | 15 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0037others(12): Show | 17 | HG01346.hp2 HG01516.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.56-937dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034766 | ||||||
| chrX:66034766
|
TG | T | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.56-937delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034766 | ||||||
| chrX:66034770
|
GGT | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(36): Show | 46 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.56-942_56-941delAC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034770 | ||||||
| chrX:66034771
|
GT | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0038others(32): Show | 41 | HG00438.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.56-942delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034771 | ||||||
| chrX:66034772
|
T | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 72 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.56-942A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034772 | ||||||
| chrX:66034777
|
G | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.56-947C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034777 | ||||||
| chrX:66034855
|
A | AT | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1026dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034855 | ||||||
| chrX:66034874
|
TG | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1045delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034874 | ||||||
| chrX:66034888
|
TG | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1059delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034888 | ||||||
| chrX:66034991
|
TC | T | 1 | a0008c0006t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.56-1162delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034991 | ||||||
| chrX:66035126
|
G | GC | 1 | a0001c0001t0002g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-1297dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035126 | ||||||
| chrX:66035161
|
AT | A | 1 | a0001c0001t0002g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-1332delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035161 | ||||||
| chrX:66035228
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.56-1398G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035228 | ||||||
| chrX:66035251
|
G | GA | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1422dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035251 | ||||||
| chrX:66035305
|
AT | A | 1 | a0001c0001t0002g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-1476delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035305 | ||||||
| chrX:66035311
|
GT | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1482delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035311 | ||||||
| chrX:66035360
|
CT | C | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1531delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035360 | ||||||
| chrX:66035466
|
TG | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1637delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035466 | ||||||
| chrX:66035522
|
T | C | 1 | a0001c0001t0001g0004 | 4 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-1692A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035522 | ||||||
| chrX:66035528
|
AT | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1699delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035528 | ||||||
| chrX:66035623
|
C | A | 4 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-1793G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035623 | ||||||
| chrX:66035759
|
TC | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1930delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035759 | ||||||
| chrX:66035771
|
TC | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1942delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035771 | ||||||
| chrX:66035806
|
GA | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-1977delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035806 | ||||||
| chrX:66036100
|
TC | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2271delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036100 | ||||||
| chrX:66036120
|
T | TC | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.56-2291dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036120 | ||||||
| chrX:66036130
|
CT | C | 1 | a0001c0001t0001g0057 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.56-2301delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036130 | ||||||
| chrX:66036139
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-2309A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036139 | ||||||
| chrX:66036148
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56-2318A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036148 | ||||||
| chrX:66036157
|
CT | C | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2328delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036157 | ||||||
| chrX:66036191
|
C | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.56-2361G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036191 | ||||||
| chrX:66036214
|
CT | C | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2385delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036214 | ||||||
| chrX:66036238
|
TC | T | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.56-2409delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036238 | ||||||
| chrX:66036274
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-2444C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036274 | ||||||
| chrX:66036295
|
C | CA | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2466dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036295 | ||||||
| chrX:66036318
|
TC | T | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.56-2489delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036318 | ||||||
| chrX:66036336
|
TC | T | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.56-2507delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036336 | ||||||
| chrX:66036338
|
CA | C | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2509delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036338 | ||||||
| chrX:66036394
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(35): Show | 43 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.56-2564A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036394 | ||||||
| chrX:66036493
|
T | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2663A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036493 | ||||||
| chrX:66036519
|
TG | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2690delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036519 | ||||||
| chrX:66036520
|
G | C | 3 | a0002c0002t0001g0018a0002c0002t0001g0147a0002c0002t0001g0148 | 4 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-2690C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036520 | ||||||
| chrX:66036542
|
GA | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2713delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036542 | ||||||
| chrX:66036573
|
TA | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2744delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036573 | ||||||
| chrX:66036584
|
GA | G | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2755delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036584 | ||||||
| chrX:66036596
|
TA | T | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2767delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036596 | ||||||
| chrX:66036621
|
ATATT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2795_56-2792del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036621 | ||||||
| chrX:66036623
|
AT | A | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2794delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036623 | ||||||
| chrX:66036635
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2805C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036635 | ||||||
| chrX:66036638
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2808T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036638 | ||||||
| chrX:66036641
|
ATTT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2814_56-2812del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036641 | ||||||
| chrX:66036654
|
AAT | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-2826_56-2825del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036654 | ||||||
| chrX:66036657
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2827T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036657 | ||||||
| chrX:66036661
|
A | AAAAT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2832_56-2831ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036661 | ||||||
| chrX:66036662
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2832T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036662 | ||||||
| chrX:66036667
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0002g0022 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2837T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036667 | ||||||
| chrX:66036668
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2838A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036668 | ||||||
| chrX:66036671
|
AAT | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.56-2843_56-2842del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036671 | ||||||
| chrX:66036672
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2842T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036672 | ||||||
| chrX:66036674
|
AT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2845delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036674 | ||||||
| chrX:66036678
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2848T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036678 | ||||||
| chrX:66036680
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2850T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036680 | ||||||
| chrX:66036681
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2851T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036681 | ||||||
| chrX:66036682
|
TACG | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2855_56-2853del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036682 | ||||||
| chrX:66036684
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0002g0022others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-2854G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036684 | ||||||
| chrX:66036685
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2855C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036685 | ||||||
| chrX:66036691
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0022 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2861A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036691 | ||||||
| chrX:66036692
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2862A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036692 | ||||||
| chrX:66036693
|
AT | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2864delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036693 | ||||||
| chrX:66036694
|
T | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(44): Show | 54 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.56-2864A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036694 | ||||||
| chrX:66036694
|
T | TA | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2865_56-2864ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036694 | ||||||
| chrX:66036697
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0002g0022 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2867T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036697 | ||||||
| chrX:66036703
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2873A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036703 | ||||||
| chrX:66036703
|
T | G | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2873A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036703 | ||||||
| chrX:66036706
|
A | AT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2877_56-2876ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036706 | ||||||
| chrX:66036709
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2879A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036709 | ||||||
| chrX:66036714
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2884T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036714 | ||||||
| chrX:66036714
|
AAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2886_56-2885del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036714 | ||||||
| chrX:66036718
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2888A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036718 | ||||||
| chrX:66036719
|
A | AT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2890dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036719 | ||||||
| chrX:66036725
|
T | TATATAAT others(41): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-2896_56-2895ins others(48): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036725 | ||||||
| chrX:66036730
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2900T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036730 | ||||||
| chrX:66036731
|
AT | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2902delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036731 | ||||||
| chrX:66036732
|
T | TTAA | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2903_56-2902ins others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036732 | ||||||
| chrX:66036741
|
AT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2912delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036741 | ||||||
| chrX:66036743
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2913A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036743 | ||||||
| chrX:66036744
|
A | AT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2915_56-2914ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036744 | ||||||
| chrX:66036746
|
TA | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2917delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036746 | ||||||
| chrX:66036747
|
AAT | A | 1 | a0001c0001t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.56-2919_56-2918del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036747 | ||||||
| chrX:66036749
|
T | TATATA | 1 | a0002c0002t0001g0018 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.56-2924_56-2920dup others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036749 | ||||||
| chrX:66036749
|
TATATA | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0151 | 2 | NA19007.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.56-2924_56-2920del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036749 | ||||||
| chrX:66036754
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2924T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036754 | ||||||
| chrX:66036754
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2924T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036754 | ||||||
| chrX:66036759
|
A | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-2929T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036759 | ||||||
| chrX:66036761
|
T | TA | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2932dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036761 | ||||||
| chrX:66036766
|
T | TA | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.56-2937dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036766 | ||||||
| chrX:66036766
|
T | TATATAAT others(3): Show |
1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2937_56-2936ins others(10): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036766 | ||||||
| chrX:66036768
|
T | TATATTAT others(32): Show |
1 | a0001c0001t0002g0027 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.56-2977_56-2939dup others(39): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036768 | ||||||
| chrX:66036770
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2940A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036770 | ||||||
| chrX:66036771
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2941T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036771 | ||||||
| chrX:66036772
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2942A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036772 | ||||||
| chrX:66036772
|
T | TATTA | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2943_56-2942ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036772 | ||||||
| chrX:66036773
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2943A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036773 | ||||||
| chrX:66036775
|
T | TA | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2946dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036775 | ||||||
| chrX:66036777
|
T | TTATATTA others(32): Show |
1 | a0001c0001t0002g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56-2948_56-2947ins others(39): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036777 | ||||||
| chrX:66036778
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2948A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036778 | ||||||
| chrX:66036782
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2952A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036782 | ||||||
| chrX:66036783
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0022 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2953A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036783 | ||||||
| chrX:66036785
|
TATA | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2958_56-2956del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036785 | ||||||
| chrX:66036785
|
TATATA | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.56-2960_56-2956del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036785 | ||||||
| chrX:66036787
|
T | TTA | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2958_56-2957ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036787 | ||||||
| chrX:66036790
|
A | AATATAAT others(24): Show |
1 | a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.56-2961_56-2960ins others(31): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036790 | ||||||
| chrX:66036792
|
TA | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0046 | 5 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-2963delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036792 | ||||||
| chrX:66036793
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2963T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036793 | ||||||
| chrX:66036795
|
A | AT | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2966_56-2965ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036795 | ||||||
| chrX:66036796
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2966T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036796 | ||||||
| chrX:66036797
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2967A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036797 | ||||||
| chrX:66036797
|
T | TA | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2968dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036797 | ||||||
| chrX:66036801
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2971A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036801 | ||||||
| chrX:66036802
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2972A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036802 | ||||||
| chrX:66036806
|
TA | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2977delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036806 | ||||||
| chrX:66036807
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2977T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036807 | ||||||
| chrX:66036807
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2977T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036807 | ||||||
| chrX:66036810
|
AT | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2981delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036810 | ||||||
| chrX:66036812
|
T | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0157a0001c0001t0002g0022 | 3 | HG01358.hp1 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.56-2982A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036812 | ||||||
| chrX:66036813
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2983T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036813 | ||||||
| chrX:66036817
|
AT | A | 3 | a0001c0001t0002g0022a0001c0001t0005g0033a0001c0001t0005g0034 | 3 | HG02572.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.56-2988delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036817 | ||||||
| chrX:66036817
|
ATT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2989_56-2988del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036817 | ||||||
| chrX:66036818
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2988A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036818 | ||||||
| chrX:66036820
|
A | AT | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2991dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036820 | ||||||
| chrX:66036822
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2992A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036822 | ||||||
| chrX:66036823
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2993T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036823 | ||||||
| chrX:66036823
|
ATAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2996_56-2994del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036823 | ||||||
| chrX:66036826
|
T | TG | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2997_56-2996ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036826 | ||||||
| chrX:66036827
|
AT | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2998delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036827 | ||||||
| chrX:66036829
|
A | AT | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-3000dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036829 | ||||||
| chrX:66036832
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3002T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036832 | ||||||
| chrX:66036834
|
ATGT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-3007_56-3005del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036834 | ||||||
| chrX:66036836
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-3006C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036836 | ||||||
| chrX:66036836
|
G | GT | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3007dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036836 | ||||||
| chrX:66036837
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3007A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036837 | ||||||
| chrX:66036838
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3008A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036838 | ||||||
| chrX:66036842
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-3012A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036842 | ||||||
| chrX:66036842
|
T | TA | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-3013dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036842 | ||||||
| chrX:66036843
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3013T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036843 | ||||||
| chrX:66036843
|
A | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0099 | 3 | HG03041.hp2 HG03195.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-3013T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036843 | ||||||
| chrX:66036844
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3014T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036844 | ||||||
| chrX:66036845
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3015A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036845 | ||||||
| chrX:66036845
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.56-3015A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036845 | ||||||
| chrX:66036846
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3016T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036846 | ||||||
| chrX:66036849
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3019A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036849 | ||||||
| chrX:66036850
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3020A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036850 | ||||||
| chrX:66036853
|
A | ATAT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3026_56-3024dup others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036853 | ||||||
| chrX:66036854
|
T | TA | 2 | a0001c0001t0001g0066a0001c0001t0001g0172 | 2 | HG02004.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.56-3025dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036854 | ||||||
| chrX:66036855
|
AT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-3026delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036855 | ||||||
| chrX:66036858
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3028A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036858 | ||||||
| chrX:66036859
|
A | AATAATAT others(34): Show |
1 | a0001c0001t0003g0134 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.55+3044_56-3030dup others(41): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036859 | ||||||
| chrX:66036859
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3029T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036859 | ||||||
| chrX:66036862
|
A | ATATC | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3033_56-3032ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036862 | ||||||
| chrX:66036868
|
T | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0002g0022 | 3 | HG02055.hp1 HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-3038A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036868 | ||||||
| chrX:66036869
|
T | A | 14 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0051others(11): Show | 15 | HG00733.hp2 HG01168.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.56-3039A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036869 | ||||||
| chrX:66036870
|
ATAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-3043_56-3041del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036870 | ||||||
| chrX:66036873
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3043A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036873 | ||||||
| chrX:66036874
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3044A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036874 | ||||||
| chrX:66036874
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3044A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036874 | ||||||
| chrX:66036874
|
T | TATATATT others(22): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+3041_56-3045dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036874 | ||||||
| chrX:66036878
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3048A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036878 | ||||||
| chrX:66036880
|
T | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-3050A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036880 | ||||||
| chrX:66036882
|
AT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-3053delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036882 | ||||||
| chrX:66036885
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3055A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036885 | ||||||
| chrX:66036885
|
T | TATAA | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3056_56-3055ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036885 | ||||||
| chrX:66036886
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3056A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036886 | ||||||
| chrX:66036891
|
AT | A | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+3052delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036891 | ||||||
| chrX:66036892
|
T | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02055.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3052A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036892 | ||||||
| chrX:66036893
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3051A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036893 | ||||||
| chrX:66036894
|
T | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0099others(1): Show | 4 | HG02572.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3050A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036894 | ||||||
| chrX:66036894
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3050A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036894 | ||||||
| chrX:66036896
|
AT | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3047delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036896 | ||||||
| chrX:66036896
|
ATT | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3046_55+3047del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036896 | ||||||
| chrX:66036897
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3047A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036897 | ||||||
| chrX:66036898
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3046A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036898 | ||||||
| chrX:66036904
|
ATATATTA others(10): Show |
A | 38 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(35): Show | 43 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.55+3023_55+3039del others(17): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036904 | ||||||
| chrX:66036906
|
ATAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3035_55+3037del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036906 | ||||||
| chrX:66036909
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0022 | 3 | HG02572.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3035A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036909 | ||||||
| chrX:66036910
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3034A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036910 | ||||||
| chrX:66036912
|
T | TA | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3031dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036912 | ||||||
| chrX:66036914
|
TG | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3029delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036914 | ||||||
| chrX:66036915
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3029C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036915 | ||||||
| chrX:66036915
|
G | GCA | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3028_55+3029ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036915 | ||||||
| chrX:66036915
|
G | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0099others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3029C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036915 | ||||||
| chrX:66036918
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3026T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036918 | ||||||
| chrX:66036921
|
T | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0099others(1): Show | 4 | HG03041.hp2 HG03195.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3023A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036921 | ||||||
| chrX:66036921
|
TTATATTA others(5): Show |
T | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.55+3011_55+3022del others(12): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036921 | ||||||
| chrX:66036922
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3022A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036922 | ||||||
| chrX:66036923
|
AT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3020delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036923 | ||||||
| chrX:66036924
|
T | TA | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3019dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036924 | ||||||
| chrX:66036925
|
A | ATT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+3017_55+3018dup others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036925 | ||||||
| chrX:66036926
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3018A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036926 | ||||||
| chrX:66036926
|
T | TAATAATA others(3): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3017_55+3018ins others(10): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036926 | ||||||
| chrX:66036927
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3017A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036927 | ||||||
| chrX:66036927
|
T | G | 3 | a0001c0001t0003g0159a0001c0001t0004g0006a0001c0001t0004g0011 | 6 | HG00735.hp2 HG01109.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+3017A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036927 | ||||||
| chrX:66036932
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0022 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.55+3012C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036932 | ||||||
| chrX:66036932
|
G | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3012C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036932 | ||||||
| chrX:66036935
|
ATAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3006_55+3008del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036935 | ||||||
| chrX:66036937
|
AT | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3006delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036937 | ||||||
| chrX:66036938
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0002g0022 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+3006A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036938 | ||||||
| chrX:66036944
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0002g0022 | 3 | HG02055.hp1 HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.55+3000C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036944 | ||||||
| chrX:66036944
|
G | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0101 | 3 | HG03041.hp2 HG03195.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.55+3000C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036944 | ||||||
| chrX:66036945
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2999T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036945 | ||||||
| chrX:66036946
|
T | TATA | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2995_55+2997dup others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036946 | ||||||
| chrX:66036947
|
AT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2996delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036947 | ||||||
| chrX:66036950
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2994A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036950 | ||||||
| chrX:66036951
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0002g0022 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2993A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036951 | ||||||
| chrX:66036954
|
AT | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2989delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036954 | ||||||
| chrX:66036955
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2989A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036955 | ||||||
| chrX:66036955
|
T | TTATATGA | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.55+2988_55+2989ins others(7): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036955 | ||||||
| chrX:66036956
|
T | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0001g0101 | 3 | HG02055.hp1 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.55+2988A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036956 | ||||||
| chrX:66036958
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.55+2986A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036958 | ||||||
| chrX:66036961
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0101 | 2 | HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.55+2983A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036961 | ||||||
| chrX:66036961
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2983A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036961 | ||||||
| chrX:66036961
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+2983A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036961 | ||||||
| chrX:66036963
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2981A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036963 | ||||||
| chrX:66036965
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2979A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036965 | ||||||
| chrX:66036966
|
A | AAAAT | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2977_55+2978ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036966 | ||||||
| chrX:66036966
|
A | ATT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2977_55+2978ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036966 | ||||||
| chrX:66036966
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0127 | 2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.55+2978T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036966 | ||||||
| chrX:66036967
|
A | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2977T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036967 | ||||||
| chrX:66036971
|
AT | A | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2972delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036971 | ||||||
| chrX:66036973
|
A | AATATAAT others(22): Show |
3 | a0001c0001t0001g0103a0001c0001t0004g0006a0001c0001t0004g0011 | 6 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2942_55+2970dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036973 | ||||||
| chrX:66036973
|
A | C | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0005g0033others(1): Show | 4 | HG00639.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2971T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036973 | ||||||
| chrX:66036973
|
A | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0099others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2971T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036973 | ||||||
| chrX:66036974
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2970T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036974 | ||||||
| chrX:66036977
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2967A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036977 | ||||||
| chrX:66036978
|
A | ATATAAT | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2965_55+2966ins others(6): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036978 | ||||||
| chrX:66036978
|
A | ATATT | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2965_55+2966ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036978 | ||||||
| chrX:66036978
|
A | ATT | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2965_55+2966ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036978 | ||||||
| chrX:66036979
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2965T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036979 | ||||||
| chrX:66036980
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2964A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036980 | ||||||
| chrX:66036981
|
ATATCAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2957_55+2962del others(6): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036981 | ||||||
| chrX:66036985
|
C | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2959G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036985 | ||||||
| chrX:66036985
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2959G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036985 | ||||||
| chrX:66036985
|
CATATA | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(36): Show | 44 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.55+2954_55+2958del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036985 | ||||||
| chrX:66036991
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2953T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036991 | ||||||
| chrX:66036992
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2952A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036992 | ||||||
| chrX:66036992
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2952A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036992 | ||||||
| chrX:66036997
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2947A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036997 | ||||||
| chrX:66036999
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2945A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036999 | ||||||
| chrX:66037001
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0002g0022 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2943A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037001 | ||||||
| chrX:66037001
|
TC | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2942delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037001 | ||||||
| chrX:66037002
|
C | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038others(29): Show | 33 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.55+2942G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037002 | ||||||
| chrX:66037002
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0002g0022 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2942G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037002 | ||||||
| chrX:66037003
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2941T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037003 | ||||||
| chrX:66037007
|
A | G | 8 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0047others(5): Show | 8 | HG00735.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+2937T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037007 | ||||||
| chrX:66037008
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2936T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037008 | ||||||
| chrX:66037009
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2935A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037009 | ||||||
| chrX:66037010
|
AT | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2933delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037010 | ||||||
| chrX:66037011
|
T | TAC | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2932_55+2933ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037011 | ||||||
| chrX:66037011
|
TATC | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2930_55+2932del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037011 | ||||||
| chrX:66037012
|
ATCAT | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2928_55+2931del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037012 | ||||||
| chrX:66037014
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0002g0022 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2930G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037014 | ||||||
| chrX:66037016
|
T | TATA | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2925_55+2927dup others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037016 | ||||||
| chrX:66037021
|
T | TA | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2922dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037021 | ||||||
| chrX:66037021
|
TATA | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2920_55+2922del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037021 | ||||||
| chrX:66037030
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2914A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037030 | ||||||
| chrX:66037030
|
TA | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2913delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037030 | ||||||
| chrX:66037031
|
A | T | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2913T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037031 | ||||||
| chrX:66037032
|
A | ATATACAT others(520): Show |
1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2911_55+2912ins others(527): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037032 | ||||||
| chrX:66037032
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2912T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037032 | ||||||
| chrX:66037034
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2910C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037034 | ||||||
| chrX:66037035
|
TA | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2908delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037035 | ||||||
| chrX:66037038
|
T | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2906A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037038 | ||||||
| chrX:66037038
|
TATAA | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2902_55+2905del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037038 | ||||||
| chrX:66037041
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2903T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037041 | ||||||
| chrX:66037043
|
TATATC | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0146 | 3 | HG01192.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.55+2896_55+2900del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037043 | ||||||
| chrX:66037045
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2899A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037045 | ||||||
| chrX:66037047
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0022 | 3 | HG02572.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2897A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037047 | ||||||
| chrX:66037047
|
T | TAATA | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2896_55+2897ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037047 | ||||||
| chrX:66037048
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2896G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037048 | ||||||
| chrX:66037048
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0022 | 3 | HG02572.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2896G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037048 | ||||||
| chrX:66037049
|
A | C | 1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+2895T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037049 | ||||||
| chrX:66037052
|
T | TG | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.55+2891_55+2892ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037052 | ||||||
| chrX:66037053
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2891T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037053 | ||||||
| chrX:66037054
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2890T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037054 | ||||||
| chrX:66037056
|
A | AAT | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2887_55+2888ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037056 | ||||||
| chrX:66037061
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2883A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037061 | ||||||
| chrX:66037061
|
TTA | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2881_55+2882del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037061 | ||||||
| chrX:66037062
|
T | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG02622.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2882A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037062 | ||||||
| chrX:66037063
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2881T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037063 | ||||||
| chrX:66037064
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2880A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037064 | ||||||
| chrX:66037064
|
T | TATAATAA others(570): Show |
2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2879_55+2880ins others(577): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037064 | ||||||
| chrX:66037066
|
TA | T | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2877delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037066 | ||||||
| chrX:66037070
|
A | AT | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2873_55+2874ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037070 | ||||||
| chrX:66037074
|
TA | T | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.55+2869delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037074 | ||||||
| chrX:66037075
|
A | AT | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2868_55+2869ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037075 | ||||||
| chrX:66037075
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2869T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037075 | ||||||
| chrX:66037077
|
TATATC | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2862_55+2866del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037077 | ||||||
| chrX:66037081
|
T | A | 4 | a0001c0001t0001g0099a0001c0001t0002g0022a0001c0001t0005g0033others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2863A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037081 | ||||||
| chrX:66037081
|
T | TTA | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2862_55+2863ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037081 | ||||||
| chrX:66037082
|
C | T | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0099others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+2862G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037082 | ||||||
| chrX:66037090
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2854T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037090 | ||||||
| chrX:66037091
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2853A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037091 | ||||||
| chrX:66037093
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2851A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037093 | ||||||
| chrX:66037099
|
A | ATAG | 3 | a0001c0001t0001g0099a0001c0001t0005g0033a0001c0001t0005g0034 | 3 | HG02615.hp1 HG02976.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.55+2844_55+2845ins others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037099 | ||||||
| chrX:66037100
|
TA | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2843delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037100 | ||||||
| chrX:66037109
|
A | AAT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2833_55+2834dup others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037109 | ||||||
| chrX:66037110
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2834T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037110 | ||||||
| chrX:66037111
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2833A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037111 | ||||||
| chrX:66037113
|
T | TA | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2830dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037113 | ||||||
| chrX:66037113
|
TA | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2830delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037113 | ||||||
| chrX:66037118
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2826A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037118 | ||||||
| chrX:66037119
|
A | ATAAT | 4 | a0001c0001t0001g0099a0001c0001t0002g0022a0001c0001t0005g0033others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2824_55+2825ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037119 | ||||||
| chrX:66037119
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2825T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037119 | ||||||
| chrX:66037121
|
A | AATATATA others(716): Show |
1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(723): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(753): Show |
1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(760): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(682): Show |
1 | a0001c0001t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(689): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(695): Show |
1 | a0001c0001t0002g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(702): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(797): Show |
1 | a0007c0007t0001g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(804): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(653): Show |
2 | a0001c0001t0002g0023a0001c0001t0002g0025 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(660): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
1 | a0001c0001t0002g0027 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(650): Show |
1 | a0001c0001t0002g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(657): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0035others(4): Show | 11 | HG01884.hp1 HG02257.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(718): Show |
1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(725): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(786): Show |
1 | a0001c0001t0001g0062 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(793): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(781): Show |
1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(788): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(752): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG00735.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(759): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
1 | a0001c0001t0001g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
2 | a0003c0005t0001g0053a0003c0005t0001g0054 | 2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG03492.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(685): Show |
1 | a0001c0001t0001g0057 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(692): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(687): Show |
1 | a0001c0004t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(694): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(684): Show |
5 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG01496.hp2 HG01978.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(651): Show |
1 | a0001c0001t0002g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(658): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(585): Show |
1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(592): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(582): Show |
1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(589): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(608): Show |
1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(615): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(584): Show |
1 | a0001c0001t0001g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(612): Show |
1 | a0001c0001t0001g0100 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(619): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(554): Show |
5 | a0001c0001t0001g0016a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG00438.hp1 HG00438.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(561): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(672): Show |
1 | a0002c0002t0001g0018 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(679): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(688): Show |
2 | a0002c0002t0001g0147a0002c0002t0001g0148 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(695): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(729): Show |
2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(736): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(669): Show |
1 | a0001c0001t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(676): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(584): Show |
1 | a0001c0001t0001g0163 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(616): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0131others(1): Show | 6 | NA18957.hp2 NA18960.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(623): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(620): Show |
1 | a0001c0001t0003g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(627): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(629): Show |
1 | a0001c0001t0001g0090 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(636): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(584): Show |
1 | a0001c0001t0001g0133 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(581): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0138 | 3 | NA18971.hp1 NA18986.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(588): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(615): Show |
1 | a0001c0001t0001g0168 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(622): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(584): Show |
71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(618): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG01361.hp1 HG02074.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(625): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(621): Show |
1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(628): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(609): Show |
1 | a0001c0001t0001g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(616): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(581): Show |
3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG02155.hp2 NA18945.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(588): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(614): Show |
1 | a0001c0001t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(621): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(582): Show |
2 | a0001c0001t0001g0092a0001c0001t0007g0091 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(589): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(582): Show |
1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(589): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(614): Show |
1 | a0001c0001t0003g0141 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(621): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(648): Show |
2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | NA18999.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(655): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(584): Show |
1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(759): Show |
1 | a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(766): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(620): Show |
1 | a0005c0010t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(627): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATATA others(604): Show |
1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(611): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | AATATTAT others(715): Show |
1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(722): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037121
|
A | T | 7 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2823T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | ||||||
| chrX:66037123
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2821A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037123 | ||||||
| chrX:66037124
|
AT | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2819delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037124 | ||||||
| chrX:66037125
|
T | TATAATAT others(503): Show |
1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2818_55+2819ins others(510): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | ||||||
| chrX:66037125
|
T | TATATAAT others(549): Show |
1 | a0001c0001t0001g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.55+2818_55+2819ins others(556): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | ||||||
| chrX:66037125
|
T | TATATAAT others(482): Show |
1 | a0001c0001t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+2818_55+2819ins others(489): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | ||||||
| chrX:66037125
|
T | TATATAAT others(549): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0081others(1): Show | 5 | HG03834.hp1 HG04228.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2818_55+2819ins others(556): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | ||||||
| chrX:66037126
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2818A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037126 | ||||||
| chrX:66037128
|
T | TA | 2 | a0001c0001t0001g0150a0001c0001t0001g0169 | 2 | NA18906.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.55+2815dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037128 | ||||||
| chrX:66037129
|
A | AG | 5 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0081others(2): Show | 6 | HG01074.hp1 HG03834.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2814_55+2815ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037129 | ||||||
| chrX:66037131
|
A | ACATT | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2812_55+2813ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037131 | ||||||
| chrX:66037131
|
A | G | 4 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2813T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037131 | ||||||
| chrX:66037131
|
A | T | 3 | a0001c0001t0001g0043a0001c0001t0002g0027a0001c0001t0002g0028 | 3 | HG01516.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.55+2813T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037131 | ||||||
| chrX:66037134
|
A | ATATATAA others(118): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2809_55+2810ins others(125): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037134 | ||||||
| chrX:66037135
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2809T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037135 | ||||||
| chrX:66037136
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2808A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037136 | ||||||
| chrX:66037136
|
T | TA | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2807dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037136 | ||||||
| chrX:66037137
|
A | ATAATGTA others(68): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2806_55+2807ins others(75): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037137 | ||||||
| chrX:66037138
|
TA | T | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.55+2805delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037138 | ||||||
| chrX:66037139
|
A | C | 3 | a0001c0001t0001g0044a0001c0001t0002g0024a0001c0001t0002g0026 | 3 | HG02922.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2805T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037139 | ||||||
| chrX:66037152
|
A | T | 7 | a0001c0001t0001g0043a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2792T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037152 | ||||||
| chrX:66037157
|
T | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2787A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037157 | ||||||
| chrX:66037159
|
T | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG00621.hp1 HG01361.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2785A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037159 | ||||||
| chrX:66037162
|
T | TATA | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2779_55+2781dup others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037162 | ||||||
| chrX:66037163
|
A | ATAG | 2 | a0001c0001t0001g0150a0001c0001t0001g0169 | 2 | NA18906.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.55+2780_55+2781ins others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037163 | ||||||
| chrX:66037165
|
A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0025 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2779T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037165 | ||||||
| chrX:66037165
|
AATAAT | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2774_55+2778del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037165 | ||||||
| chrX:66037167
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2777A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037167 | ||||||
| chrX:66037169
|
AT | A | 1 | a0001c0001t0003g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55+2774delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037169 | ||||||
| chrX:66037173
|
A | C | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 3 | HG01884.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2771T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037173 | ||||||
| chrX:66037174
|
A | ATG | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2769_55+2770ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037174 | ||||||
| chrX:66037178
|
A | ATATTATA others(2): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2765_55+2766ins others(9): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037178 | ||||||
| chrX:66037179
|
A | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2765T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037179 | ||||||
| chrX:66037180
|
T | TATATAAT others(20): Show |
1 | a0001c0001t0001g0081 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.55+2763_55+2764ins others(27): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037180 | ||||||
| chrX:66037180
|
T | TTA | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2763_55+2764ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037180 | ||||||
| chrX:66037186
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0025 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2758T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037186 | ||||||
| chrX:66037187
|
T | TAATA | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2756_55+2757ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037187 | ||||||
| chrX:66037190
|
A | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2754T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037190 | ||||||
| chrX:66037193
|
A | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0019others(56): Show | 66 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.55+2751T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037193 | ||||||
| chrX:66037199
|
A | AGT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2744_55+2745ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037199 | ||||||
| chrX:66037199
|
A | ATTAT | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2744_55+2745ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037199 | ||||||
| chrX:66037199
|
A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0025 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2745T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037199 | ||||||
| chrX:66037201
|
T | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2743A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037201 | ||||||
| chrX:66037201
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2742dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037201 | ||||||
| chrX:66037202
|
A | AT | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2741_55+2742ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037202 | ||||||
| chrX:66037204
|
TA | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2739delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037204 | ||||||
| chrX:66037206
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2737dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037206 | ||||||
| chrX:66037207
|
A | C | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 3 | HG01884.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2737T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037207 | ||||||
| chrX:66037207
|
A | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2737T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037207 | ||||||
| chrX:66037213
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2731T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037213 | ||||||
| chrX:66037214
|
T | TAATA | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2729_55+2730ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037214 | ||||||
| chrX:66037216
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.55+2728A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037216 | ||||||
| chrX:66037217
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2727T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037217 | ||||||
| chrX:66037218
|
T | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2726A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037218 | ||||||
| chrX:66037218
|
TAA | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2724_55+2725del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037218 | ||||||
| chrX:66037219
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2725T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037219 | ||||||
| chrX:66037220
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2724T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037220 | ||||||
| chrX:66037227
|
T | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0140others(5): Show | 9 | HG00733.hp1 HG01074.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+2717A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037227 | ||||||
| chrX:66037232
|
TA | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2711delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037232 | ||||||
| chrX:66037235
|
TAATA | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2705_55+2708del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037235 | ||||||
| chrX:66037237
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2707T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037237 | ||||||
| chrX:66037241
|
A | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2703T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037241 | ||||||
| chrX:66037244
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.55+2700T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037244 | ||||||
| chrX:66037246
|
A | ATATAATA others(137): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2697_55+2698ins others(144): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037246 | ||||||
| chrX:66037248
|
T | TA | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2695dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037248 | ||||||
| chrX:66037250
|
T | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0038others(12): Show | 17 | HG00733.hp2 HG01168.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.55+2694A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037250 | ||||||
| chrX:66037251
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2693T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037251 | ||||||
| chrX:66037253
|
A | ATTATATT others(124): Show |
1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2690_55+2691ins others(131): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037253 | ||||||
| chrX:66037261
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+2683A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037261 | ||||||
| chrX:66037261
|
TTA | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2681_55+2682del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037261 | ||||||
| chrX:66037264
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2680A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037264 | ||||||
| chrX:66037264
|
TATA | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.55+2677_55+2679del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037264 | ||||||
| chrX:66037267
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.55+2677T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037267 | ||||||
| chrX:66037267
|
AATAAT | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0161 | 2 | HG01192.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.55+2672_55+2676del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037267 | ||||||
| chrX:66037269
|
TA | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2674delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037269 | ||||||
| chrX:66037272
|
T | TAATATAA others(43): Show |
1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+2671_55+2672ins others(50): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037272 | ||||||
| chrX:66037272
|
T | TATAATAT others(22): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 7 | HG01081.hp2 HG01256.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+2643_55+2671dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037272 | ||||||
| chrX:66037273
|
A | AATATAAC others(14): Show |
2 | a0001c0001t0001g0068a0001c0008t0001g0162 | 2 | HG00738.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2670_55+2671ins others(21): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037273 | ||||||
| chrX:66037273
|
A | AATATAAT others(44): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2670_55+2671ins others(51): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037273 | ||||||
| chrX:66037275
|
A | C | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+2669T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037275 | ||||||
| chrX:66037285
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2659T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037285 | ||||||
| chrX:66037286
|
TA | T | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2657delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037286 | ||||||
| chrX:66037288
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.55+2656T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037288 | ||||||
| chrX:66037290
|
A | AT | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.55+2653dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037290 | ||||||
| chrX:66037291
|
T | TA | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2652dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037291 | ||||||
| chrX:66037295
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2649A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037295 | ||||||
| chrX:66037296
|
T | TAATA | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2647_55+2648ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037296 | ||||||
| chrX:66037300
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2644A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037300 | ||||||
| chrX:66037300
|
T | TTATAA | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2643_55+2644ins others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037300 | ||||||
| chrX:66037301
|
A | AATAAT | 41 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(38): Show | 47 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.55+2638_55+2642dup others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | ||||||
| chrX:66037301
|
A | AATAATAT others(27): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG00280.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.55+2609_55+2642dup others(34): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | ||||||
| chrX:66037301
|
A | AGTAATAA others(1): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2642_55+2643ins others(8): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | ||||||
| chrX:66037301
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0002g0022 | 2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.55+2643T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | ||||||
| chrX:66037309
|
AAT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0149a0002c0002t0001g0018others(2): Show | 7 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2633_55+2634del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037309 | ||||||
| chrX:66037311
|
T | TA | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2632dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037311 | ||||||
| chrX:66037314
|
A | AATATG | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2629_55+2630ins others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037314 | ||||||
| chrX:66037316
|
A | ATAATAAT others(221): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2627_55+2628ins others(228): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037316 | ||||||
| chrX:66037316
|
A | ATTATATA others(2): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2627_55+2628ins others(9): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037316 | ||||||
| chrX:66037319
|
AT | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2624delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037319 | ||||||
| chrX:66037324
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0149 | 3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2620A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037324 | ||||||
| chrX:66037330
|
A | ATT | 2 | a0001c0001t0001g0019a0001c0001t0001g0149 | 3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2613_55+2614ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037330 | ||||||
| chrX:66037330
|
AATAAT | A | 1 | a0001c0001t0001g0020 | 2 | NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.55+2609_55+2613del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037330 | ||||||
| chrX:66037332
|
TA | T | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2611delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037332 | ||||||
| chrX:66037334
|
A | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0149 | 3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2610T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037334 | ||||||
| chrX:66037335
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0149 | 3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2609A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | ||||||
| chrX:66037335
|
T | TATAATAT others(22): Show |
1 | a0001c0001t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+2580_55+2608dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | ||||||
| chrX:66037335
|
T | TATAATAT others(85): Show |
1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.55+2608_55+2609ins others(92): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | ||||||
| chrX:66037335
|
T | TATAATAT others(46): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.55+2608_55+2609ins others(53): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | ||||||
| chrX:66037335
|
T | TATAATAT others(263): Show |
2 | a0001c0001t0001g0068a0001c0008t0001g0162 | 2 | HG00738.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2608_55+2609ins others(270): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | ||||||
| chrX:66037335
|
T | TATAATAT others(288): Show |
1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+2608_55+2609ins others(295): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | ||||||
| chrX:66037351
|
A | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2593T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037351 | ||||||
| chrX:66037362
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0075 | 3 | NA18946.hp2 NA18973.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.55+2582T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037362 | ||||||
| chrX:66037371
|
TA | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2572delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037371 | ||||||
| chrX:66037377
|
AAT | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2565_55+2566del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037377 | ||||||
| chrX:66037383
|
TA | T | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55+2560delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037383 | ||||||
| chrX:66037385
|
A | T | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2559T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037385 | ||||||
| chrX:66037391
|
A | AT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2552dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037391 | ||||||
| chrX:66037396
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(47): Show | 56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.55+2548C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037396 | ||||||
| chrX:66037405
|
T | TAATA | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2538_55+2539ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037405 | ||||||
| chrX:66037410
|
AT | A | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2533delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037410 | ||||||
| chrX:66037413
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2530dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037413 | ||||||
| chrX:66037423
|
C | CATATAAT others(21): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02071.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.55+2493_55+2520dup others(28): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037423 | ||||||
| chrX:66037423
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2521G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037423 | ||||||
| chrX:66037434
|
A | AT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2509dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037434 | ||||||
| chrX:66037442
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2501dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037442 | ||||||
| chrX:66037443
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2501T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037443 | ||||||
| chrX:66037448
|
A | AT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2495_55+2496ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037448 | ||||||
| chrX:66037451
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2493A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037451 | ||||||
| chrX:66037455
|
TA | T | 1 | a0008c0006t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.55+2488delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037455 | ||||||
| chrX:66037462
|
AT | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2481delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037462 | ||||||
| chrX:66037475
|
TA | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2468delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037475 | ||||||
| chrX:66037485
|
A | ATAT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2458_55+2459ins others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037485 | ||||||
| chrX:66037488
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2456G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037488 | ||||||
| chrX:66037489
|
A | ATATATAT others(117): Show |
1 | a0001c0001t0001g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.55+2454_55+2455ins others(124): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037489 | ||||||
| chrX:66037496
|
A | AT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2447_55+2448ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037496 | ||||||
| chrX:66037504
|
T | TAATACAA others(7): Show |
1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2439_55+2440ins others(14): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037504 | ||||||
| chrX:66037507
|
TATA | T | 4 | a0001c0001t0001g0041a0001c0001t0004g0011a0001c0001t0005g0033others(1): Show | 5 | HG01433.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2434_55+2436del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037507 | ||||||
| chrX:66037511
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2433T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037511 | ||||||
| chrX:66037512
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2432A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037512 | ||||||
| chrX:66037520
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2424A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037520 | ||||||
| chrX:66037534
|
C | CT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2409_55+2410ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037534 | ||||||
| chrX:66037538
|
ATATAT | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0003g0154others(1): Show | 4 | HG00621.hp1 HG00738.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2401_55+2405del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037538 | ||||||
| chrX:66037541
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.55+2403A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037541 | ||||||
| chrX:66037552
|
AT | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2391delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037552 | ||||||
| chrX:66037557
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2387T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037557 | ||||||
| chrX:66037559
|
AT | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2384delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037559 | ||||||
| chrX:66037570
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2374A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037570 | ||||||
| chrX:66037571
|
AT | A | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2372delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037571 | ||||||
| chrX:66037573
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2371A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037573 | ||||||
| chrX:66037575
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2369A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037575 | ||||||
| chrX:66037576
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2368T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037576 | ||||||
| chrX:66037577
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2367A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037577 | ||||||
| chrX:66037578
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2366A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037578 | ||||||
| chrX:66037580
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2364A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037580 | ||||||
| chrX:66037581
|
A | AC | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2362_55+2363ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037581 | ||||||
| chrX:66037581
|
AT | A | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2362delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037581 | ||||||
| chrX:66037582
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2362A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037582 | ||||||
| chrX:66037583
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2361A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037583 | ||||||
| chrX:66037585
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2359G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037585 | ||||||
| chrX:66037593
|
A | AT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2350dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037593 | ||||||
| chrX:66037605
|
A | AT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2338_55+2339ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037605 | ||||||
| chrX:66037632
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2311dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037632 | ||||||
| chrX:66037643
|
T | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0008t0001g0162 | 3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2301A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037643 | ||||||
| chrX:66037647
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2296dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037647 | ||||||
| chrX:66037671
|
A | AT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2272dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037671 | ||||||
| chrX:66037740
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2203dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037740 | ||||||
| chrX:66037757
|
C | CGTATATA others(16): Show |
4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2164_55+2186dup others(23): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037757 | ||||||
| chrX:66037757
|
C | CGTATATA others(39): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(29): Show | 37 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.55+2141_55+2186dup others(46): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037757 | ||||||
| chrX:66037757
|
C | CGTATATA others(62): Show |
4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01255.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2186_55+2187ins others(69): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037757 | ||||||
| chrX:66037789
|
A | AC | 1 | a0001c0001t0001g0171 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.55+2154dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037789 | ||||||
| chrX:66037805
|
T | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2139A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037805 | ||||||
| chrX:66037808
|
A | ATATACTT others(40): Show |
1 | a0001c0001t0002g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+2135_55+2136ins others(47): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037808 | ||||||
| chrX:66037813
|
C | CTTATTGC others(5): Show |
1 | a0001c0001t0002g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+2130_55+2131ins others(12): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037813 | ||||||
| chrX:66037818
|
T | TATATACA others(3): Show |
1 | a0001c0001t0002g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+2125_55+2126ins others(10): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037818 | ||||||
| chrX:66037836
|
T | TG | 1 | a0001c0001t0002g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+2107dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037836 | ||||||
| chrX:66037852
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.55+2092T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037852 | ||||||
| chrX:66037886
|
GA | G | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2057delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037886 | ||||||
| chrX:66037889
|
G | GA | 1 | a0001c0001t0001g0171 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.55+2054dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037889 | ||||||
| chrX:66037956
|
T | TC | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1987dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037956 | ||||||
| chrX:66037998
|
A | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1946T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037998 | ||||||
| chrX:66038092
|
A | AT | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1851dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038092 | ||||||
| chrX:66038100
|
GA | G | 2 | a0001c0001t0001g0069a0001c0001t0002g0023 | 2 | HG01884.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.55+1843delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038100 | ||||||
| chrX:66038112
|
A | AG | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+1831_55+1832ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038112 | ||||||
| chrX:66038119
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1824dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038119 | ||||||
| chrX:66038144
|
T | TA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1799dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038144 | ||||||
| chrX:66038147
|
A | AT | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+1796dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038147 | ||||||
| chrX:66038174
|
G | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.55+1770C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038174 | ||||||
| chrX:66038174
|
G | GC | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1769dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038174 | ||||||
| chrX:66038202
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.55+1742A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038202 | ||||||
| chrX:66038204
|
TG | T | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1739delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038204 | ||||||
| chrX:66038214
|
A | AG | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1729dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038214 | ||||||
| chrX:66038373
|
G | C | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1571C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038373 | ||||||
| chrX:66038391
|
TC | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+1552delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038391 | ||||||
| chrX:66038426
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55+1518C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038426 | ||||||
| chrX:66038442
|
TG | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+1501delC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038442 | ||||||
| chrX:66038475
|
T | TC | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.55+1468dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038475 | ||||||
| chrX:66038479
|
TCTCA | T | 3 | a0001c0001t0002g0023a0001c0001t0002g0025a0001c0001t0002g0026 | 3 | HG01884.hp2 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.55+1461_55+1464del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038479 | ||||||
| chrX:66038481
|
T | A | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1463A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | ||||||
| chrX:66038481
|
T | TCA | 5 | a0001c0001t0001g0032a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG00438.hp1 HG02135.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1461_55+1462dup others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | ||||||
| chrX:66038481
|
TCA | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0021others(41): Show | 50 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.55+1461_55+1462del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | ||||||
| chrX:66038481
|
TCACA | T | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+1459_55+1462del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | ||||||
| chrX:66038482
|
C | CA | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1461dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038482 | ||||||
| chrX:66038485
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+1459T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038485 | ||||||
| chrX:66038528
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.55+1416G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038528 | ||||||
| chrX:66038534
|
CA | C | 1 | a0008c0006t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.55+1409delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038534 | ||||||
| chrX:66038609
|
A | AG | 1 | a0001c0001t0002g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+1334dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038609 | ||||||
| chrX:66038685
|
G | GT | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.55+1258dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038685 | ||||||
| chrX:66038728
|
T | TG | 1 | a0001c0001t0001g0168 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.55+1215dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038728 | ||||||
| chrX:66038835
|
CAG | C | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+1107_55+1108del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038835 | ||||||
| chrX:66038847
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.55+1097G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038847 | ||||||
| chrX:66038847
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.55+1097G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038847 | ||||||
| chrX:66038993
|
G | GA | 1 | a0001c0001t0002g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+950dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038993 | ||||||
| chrX:66039040
|
C | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+904G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039040 | ||||||
| chrX:66039049
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.55+895T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039049 | ||||||
| chrX:66039153
|
C | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+791G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039153 | ||||||
| chrX:66039188
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55+756G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039188 | ||||||
| chrX:66039251
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.55+693C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039251 | ||||||
| chrX:66039328
|
GT | G | 1 | a0001c0001t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.55+615delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039328 | ||||||
| chrX:66039541
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.55+403G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039541 | ||||||
| chrX:66039648
|
G | A | 6 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(3): Show | 6 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+296C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039648 | ||||||
| chrX:66039720
|
GA | G | 1 | a0008c0006t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.55+223delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039720 | ||||||
| chrX:66039925
|
G | GC | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+18dupG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039925 | ||||||
| chrX:66039925
|
GC | G | 1 | a0008c0006t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.55+18delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039925 |