Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9104 |
|---|---|
| ensemblid | ENSG00000130988.13 |
| hgncid | 9989 |
| symbol | RGN |
| name | regucalcin |
| refseq_nuc | NM_152869.4 |
| refseq_prot | NP_690608.1 |
| ensembl_nuc | ENST00000397180.6 |
| ensembl_prot | ENSP00000380365.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 47078443 |
| end | 47093313 |
| strand | + |
| ver | v1.2 |
| region | chrX:47078443-47093313 |
| region5000 | chrX:47073443-47098313 |
| regionname0 | RGN_chrX_47078443_47093313 |
| regionname5000 | RGN_chrX_47073443_47098313 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 299 | 291 | 63 | 56 | 129 | 11 | 30 | 101 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0002 | 0/0 | 299 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0003 | 0/0 | 299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0004 | 0/0 | 94 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0005 | 0/0 | 94 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0006 | 0/0 | 208 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0007 | 0/0 | 139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0008 | 0/0 | 299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0009 | 0/0 | 94 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0010 | 0/0 | 83 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0011 | 0/0 | 31 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 900 | 289 | 63 | 56 | 127 | 11 | 30 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0002 | 0/0 | 900 | 3 | 0 | 0 | 3 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0003 | 0/0 | 900 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0004 | 0/0 | 898 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0005 | 0/0 | 901 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0006 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0007 | 0/0 | 901 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0008 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0009 | 0/0 | 901 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0010 | 0/0 | 901 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0011 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0012 | 0/0 | 901 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| c0013 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1269 | 206 | 48 | 33 | 90 | 8 | 25 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0002 | 0/0 | 1269 | 52 | 0 | 15 | 34 | 2 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0003 | 0/0 | 1269 | 9 | 7 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0004 | 0/0 | 1269 | 7 | 0 | 3 | 0 | 1 | 3 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0005 | 0/0 | 1270 | 5 | 5 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0006 | 0/0 | 1269 | 5 | 0 | 0 | 5 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0007 | 0/0 | 1269 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0008 | 0/0 | 1269 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0009 | 0/0 | 1270 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0010 | 0/0 | 1268 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0011 | 0/0 | 1273 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0012 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0013 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0014 | 0/0 | 1268 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0015 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0016 | 0/0 | 1270 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0017 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0018 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0019 | 0/0 | 1277 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0020 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0021 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0022 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0023 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| t0024 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 900 | 289 | 63 | 56 | 127 | 11 | 30 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0008 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0011 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0002c0002 | 0/0 | 900 | 3 | 0 | 0 | 3 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0003c0003 | 0/0 | 900 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0004c0005 | 0/0 | 901 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0005c0010 | 0/0 | 901 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0006c0007 | 0/0 | 901 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0007c0009 | 0/0 | 901 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0008c0006 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0009c0012 | 0/0 | 901 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0010c0013 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0011c0004 | 0/0 | 898 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2168 | 194 | 44 | 32 | 83 | 8 | 25 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0002 | 0/0 | 2168 | 52 | 0 | 15 | 34 | 2 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0003 | 0/0 | 2168 | 9 | 7 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0004 | 0/0 | 2168 | 7 | 0 | 3 | 0 | 1 | 3 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0005 | 0/0 | 2169 | 5 | 5 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0006 | 0/0 | 2168 | 5 | 0 | 0 | 5 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0007 | 0/0 | 2168 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0008 | 0/0 | 2168 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0009 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0010 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0012 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0013 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0014 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0015 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0016 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0017 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0018 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0020 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0021 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0022 | 0/0 | 2170 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0001t0024 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0008t0001 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0001c0011t0001 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0002c0002t0001 | 0/0 | 2168 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0002c0002t0023 | 0/0 | 2170 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0003c0003t0001 | 0/0 | 2168 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0004c0005t0001 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0005c0010t0001 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0006c0007t0001 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0007c0009t0001 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0008c0006t0001 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0009c0012t0011 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0010c0013t0019 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| a0011c0004t0001 | 0/0 | 2166 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | copy fasta | chrX | 47073443 | 47098313 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0007g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0009g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0013g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0016g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0017g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0018g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0020g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0021g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0022g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0024g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0008t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0011t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0002c0002t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0003c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0003c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0004c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0005c0010t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0006c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0007c0009t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0008c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0009c0012t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0010c0013t0019g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0011c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00673 | hp1 | a0004 | c0005 | t0001 | g0004 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00738 | hp1 | a0001 | c0001 | t0018 | g0240 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0290 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0288 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01168 | hp2 | a0001 | c0001 | t0020 | g0181 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | IBS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0231 | EUR | IBS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01952 | hp1 | a0005 | c0010 | t0001 | g0049 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02129 | hp1 | a0001 | c0001 | t0021 | g0093 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0112 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0257 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0283 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0036 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0106 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0239 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0275 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0143 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18947 | hp1 | a0001 | c0008 | t0001 | g0167 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18951 | hp1 | a0006 | c0007 | t0001 | g0129 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18956 | hp2 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0220 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18975 | hp1 | a0009 | c0012 | t0011 | g0037 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18978 | hp1 | a0001 | c0001 | t0016 | g0301 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18994 | hp1 | a0001 | c0011 | t0001 | g0226 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18999 | hp2 | a0011 | c0004 | t0001 | g0183 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19030 | hp2 | a0010 | c0013 | t0019 | g0287 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0182 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19056 | hp1 | a0001 | c0001 | t0024 | g0079 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19081 | hp1 | a0002 | c0002 | t0023 | g0005 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19084 | hp2 | a0001 | c0001 | t0022 | g0007 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19240 | hp2 | a0007 | c0009 | t0001 | g0051 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ASW | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | GIH | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02109 | hp2 | a0008 | c0006 | t0001 | g0227 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0201 | AFR | USA | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0233 | REF | REF | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0158 | REF | REF | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| 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:47081174
|
G | GC | 1 | a0010 | 1 | NA19030.hp2 | frameshift_variant | HIGH | c.32dupC | p.Glu12fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 935/2168 | 33/900 | 11/299 | INFO_REALIGN_3_PRIME | chrX | 47081174 | |
| chrX:47081174
|
GC | G | 1 | a0011 | 1 | NA18999.hp2 | frameshift_variant | HIGH | c.32delC | p.Pro11fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 934/2168 | 32/900 | 11/299 | INFO_REALIGN_3_PRIME | chrX | 47081174 | |
| chrX:47081187
|
C | CG | 1 | a0010 | 1 | NA19030.hp2 | frameshift_variant | HIGH | c.45dupG | p.Cys16fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 948/2168 | 46/900 | 16/299 | INFO_REALIGN_3_PRIME | chrX | 47081187 | |
| chrX:47081212
|
A | AGGAAG | 1 | a0010 | 1 | NA19030.hp2 | frameshift_variant | HIGH | c.69_73dupGGAAG | p.Val25fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 976/2168 | 74/900 | 25/299 | INFO_REALIGN_3_PRIME | chrX | 47081212 | |
| chrX:47081259
|
G | GT | 1 | a0009 | 1 | NA18975.hp1 | frameshift_variant | HIGH | c.118dupT | p.Cys40fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 1021/2168 | 119/900 | 40/299 | INFO_REALIGN_3_PRIME | chrX | 47081259 | |
| chrX:47081295
|
C | CGAG | 1 | a0010 | 1 | NA19030.hp2 | disruptive_inframe_insertion | MODERATE | c.152_154dupGAG | p.Arg51_Val52insGly | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 1057/2168 | 155/900 | 52/299 | INFO_REALIGN_3_PRIME | chrX | 47081295 | |
| chrX:47084421
|
C | T | 1 | a0002 | 3 | NA18962.hp1 NA18973.hp2 NA19081.hp1 |
missense_variant | MODERATE | c.167C>T | p.Ala56Val | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1069/2168 | 167/900 | 56/299 | chrX | 47084421 | ||
| chrX:47084430
|
G | GC | 1 | a0004 | 1 | HG00673.hp1 | frameshift_variant | HIGH | c.177dupC | p.Ser60fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1080/2168 | 178/900 | 60/299 | INFO_REALIGN_3_PRIME | chrX | 47084430 | |
| chrX:47084525
|
G | GC | 1 | a0005 | 1 | HG01952.hp1 | frameshift_variant | HIGH | c.273dupC | p.Thr92fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1176/2168 | 274/900 | 92/299 | INFO_REALIGN_3_PRIME | chrX | 47084525 | |
| chrX:47084555
|
C | T | 1 | a0003 | 2 | HG02572.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.301C>T | p.Arg101Cys | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1203/2168 | 301/900 | 101/299 | chrX | 47084555 | ||
| chrX:47084578
|
T | TC | 1 | a0008 | 1 | HG02109.hp2 | frameshift_variant | HIGH | c.327dupC | p.Ala110fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1230/2168 | 328/900 | 110/299 | INFO_REALIGN_3_PRIME | chrX | 47084578 | |
| chrX:47084588
|
AG | A | 1 | a0008 | 1 | HG02109.hp2 | frameshift_variant | HIGH | c.336delG | p.Arg112fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1238/2168 | 336/900 | 112/299 | INFO_REALIGN_3_PRIME | chrX | 47084588 | |
| chrX:47089840
|
C | CT | 1 | a0007 | 1 | NA19240.hp2 | frameshift_variant | HIGH | c.414dupT | p.Pro139fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/8 | 1317/2168 | 415/900 | 139/299 | INFO_REALIGN_3_PRIME | chrX | 47089840 | |
| chrX:47089971
|
A | AC | 1 | a0006 | 1 | NA18951.hp1 | frameshift_variant | HIGH | c.544dupC | p.Leu182fs | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/8 | 1447/2168 | 545/900 | 182/299 | INFO_REALIGN_3_PRIME | chrX | 47089971 |
| 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:47084425
|
A | C | 2 | a0001c0011a0009c0012 | 2 | NA18975.hp1 NA18994.hp1 |
synonymous_variant | LOW | c.171A>C | p.Pro57Pro | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/8 | 1073/2168 | 171/900 | 57/299 | chrX | 47084425 | ||
| chrX:47089867
|
C | T | 1 | a0001c0008 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.438C>T | p.Tyr146Tyr | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/8 | 1340/2168 | 438/900 | 146/299 | chrX | 47089867 |
| 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:47078474
|
A | G | 1 | a0001c0001t0006 | 5 | NA18945.hp1 NA18957.hp1 NA18971.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-871A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2671 | chrX | 47078474 | |||||
| chrX:47078526
|
G | GC | 1 | a0002c0002t0023 | 1 | NA19081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-816dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2615 | INFO_REALIGN_3_PRIME | chrX | 47078526 | ||||
| chrX:47078529
|
C | T | 1 | a0001c0001t0024 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-816C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2616 | chrX | 47078529 | |||||
| chrX:47078541
|
C | CG | 2 | a0001c0001t0022a0002c0002t0023 | 2 | NA19081.hp1 NA19084.hp2 |
5_prime_UTR_variant | MODIFIER | c.-801dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2600 | INFO_REALIGN_3_PRIME | chrX | 47078541 | ||||
| chrX:47078570
|
G | GC | 1 | a0001c0001t0009 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-772dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2571 | INFO_REALIGN_3_PRIME | chrX | 47078570 | ||||
| chrX:47078607
|
C | T | 3 | a0001c0001t0002a0001c0001t0021a0001c0001t0024 | 54 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-738C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2538 | chrX | 47078607 | |||||
| chrX:47078619
|
T | TC | 1 | a0001c0001t0022 | 1 | NA19084.hp2 | 5_prime_UTR_variant | MODIFIER | c.-723dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2522 | INFO_REALIGN_3_PRIME | chrX | 47078619 | ||||
| chrX:47078619
|
TC | T | 1 | a0001c0001t0010 | 1 | NA18956.hp2 | 5_prime_UTR_variant | MODIFIER | c.-723delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/8 | 2523 | INFO_REALIGN_3_PRIME | chrX | 47078619 | ||||
| chrX:47080336
|
TC | T | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-613delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 806 | INFO_REALIGN_3_PRIME | chrX | 47080336 | ||||
| chrX:47080354
|
G | C | 1 | a0001c0001t0005 | 5 | HG02809.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-598G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 791 | chrX | 47080354 | |||||
| chrX:47080365
|
TA | T | 1 | a0001c0001t0020 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-584delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 777 | INFO_REALIGN_3_PRIME | chrX | 47080365 | ||||
| chrX:47080396
|
T | TG | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-554dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 746 | INFO_REALIGN_3_PRIME | chrX | 47080396 | ||||
| chrX:47080401
|
T | TC | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-550dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 742 | INFO_REALIGN_3_PRIME | chrX | 47080401 | ||||
| chrX:47080403
|
T | TA | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-547dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 739 | INFO_REALIGN_3_PRIME | chrX | 47080403 | ||||
| chrX:47080420
|
C | A | 1 | a0001c0001t0021 | 1 | HG02129.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-532C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | chrX | 47080420 | ||||||
| chrX:47080461
|
C | G | 4 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(1): Show | 16 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-491C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 684 | chrX | 47080461 | |||||
| chrX:47080474
|
G | GC | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-476dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 668 | INFO_REALIGN_3_PRIME | chrX | 47080474 | ||||
| chrX:47080496
|
C | CT | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-452dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 644 | INFO_REALIGN_3_PRIME | chrX | 47080496 | ||||
| chrX:47080525
|
T | TG | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-425dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 617 | INFO_REALIGN_3_PRIME | chrX | 47080525 | ||||
| chrX:47080540
|
A | AGG | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-411_-410insGG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 603 | INFO_REALIGN_3_PRIME | chrX | 47080540 | ||||
| chrX:47080544
|
C | T | 1 | a0001c0001t0010 | 1 | NA18956.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-408C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | chrX | 47080544 | ||||||
| chrX:47080581
|
T | TA | 1 | a0001c0001t0005 | 5 | HG02809.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-366dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 558 | INFO_REALIGN_3_PRIME | chrX | 47080581 | ||||
| chrX:47080618
|
G | A | 1 | a0001c0001t0017 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-334G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 527 | chrX | 47080618 | |||||
| chrX:47080668
|
GC | G | 1 | a0001c0001t0020 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-281delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 474 | INFO_REALIGN_3_PRIME | chrX | 47080668 | ||||
| chrX:47080692
|
A | AG | 1 | a0001c0001t0020 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-256dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 448 | INFO_REALIGN_3_PRIME | chrX | 47080692 | ||||
| chrX:47080718
|
T | TG | 1 | a0001c0001t0016 | 1 | NA18978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-229dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 421 | INFO_REALIGN_3_PRIME | chrX | 47080718 | ||||
| chrX:47080734
|
G | A | 1 | a0001c0001t0005 | 5 | HG02809.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-218G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 411 | chrX | 47080734 | |||||
| chrX:47080797
|
G | GC | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-152dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 344 | INFO_REALIGN_3_PRIME | chrX | 47080797 | ||||
| chrX:47080801
|
A | AG | 1 | a0001c0001t0020 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-148dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 340 | INFO_REALIGN_3_PRIME | chrX | 47080801 | ||||
| chrX:47080808
|
T | TG | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-143dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 335 | INFO_REALIGN_3_PRIME | chrX | 47080808 | ||||
| chrX:47080873
|
G | GC | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79_-78insC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 271 | chrX | 47080873 | |||||
| chrX:47080891
|
C | CT | 1 | a0010c0013t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 247 | INFO_REALIGN_3_PRIME | chrX | 47080891 | ||||
| chrX:47080892
|
T | C | 1 | a0001c0001t0012 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 253 | chrX | 47080892 | |||||
| chrX:47080898
|
G | A | 1 | a0001c0001t0013 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 247 | chrX | 47080898 | |||||
| chrX:47080902
|
T | C | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 243 | chrX | 47080902 | |||||
| chrX:47080903
|
C | T | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 242 | chrX | 47080903 | |||||
| chrX:47080903
|
CT | C | 1 | a0001c0001t0014 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 237 | INFO_REALIGN_3_PRIME | chrX | 47080903 | ||||
| chrX:47080923
|
G | GA | 1 | a0009c0012t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/8 | 218 | INFO_REALIGN_3_PRIME | chrX | 47080923 | ||||
| chrX:47081141
|
G | A | 1 | a0001c0001t0015 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/8 | 4 | chrX | 47081141 | |||||
| chrX:47092999
|
C | T | 1 | a0001c0001t0004 | 7 | HG01123.hp2 HG01346.hp1 HG01361.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*52C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 8/8 | 52 | chrX | 47092999 | |||||
| chrX:47093154
|
G | A | 1 | a0001c0001t0007 | 2 | HG00741.hp2 HG01070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*207G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 8/8 | 207 | chrX | 47093154 | |||||
| chrX:47093192
|
C | G | 1 | a0001c0001t0007 | 2 | HG00741.hp2 HG01070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*245C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 8/8 | 245 | chrX | 47093192 | |||||
| chrX:47093218
|
C | T | 2 | a0001c0001t0008a0001c0001t0018 | 3 | HG00738.hp1 HG02257.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*271C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 8/8 | 271 | chrX | 47093218 |
| 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:47078710
|
G | GT | 1 | a0001c0001t0016g0301 | 1 | NA18978.hp1 | splice_region_variant&intron_variant | LOW | c.-636+2dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078710 | |||||
| chrX:47078712
|
A | AC | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | splice_region_variant&intron_variant | LOW | c.-636+7dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078712 | |||||
| chrX:47078739
|
G | GC | 1 | a0002c0002t0023g0005 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-636+34dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078739 | |||||
| chrX:47078743
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-636+34C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078743 | ||||||
| chrX:47078745
|
T | TC | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-636+40dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078745 | |||||
| chrX:47078768
|
A | AC | 1 | a0001c0001t0022g0007 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-636+63dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078768 | |||||
| chrX:47078818
|
T | TC | 1 | a0001c0001t0001g0008 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-636+113dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078818 | |||||
| chrX:47078844
|
G | T | 2 | a0001c0001t0003g0298a0001c0001t0003g0299 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-636+135G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078844 | ||||||
| chrX:47078846
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00558.hp1 HG01081.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-636+137G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078846 | ||||||
| chrX:47078849
|
TG | T | 1 | a0001c0001t0016g0301 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-636+144delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078849 | |||||
| chrX:47078941
|
G | GC | 8 | a0001c0001t0001g0006a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG01515.hp1 HG01981.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-636+238dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078941 | |||||
| chrX:47078941
|
GC | G | 1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-636+238delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078941 | |||||
| chrX:47078947
|
C | CCA | 1 | a0001c0001t0001g0292 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-636+238_-636+239i others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078947 | ||||||
| chrX:47078948
|
A | AC | 3 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0004g0032 | 3 | HG01123.hp2 NA18989.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-636+244dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078948 | |||||
| chrX:47078948
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-636+239A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078948 | ||||||
| chrX:47078955
|
C | CT | 43 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0033others(40): Show | 43 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-636+266dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078955 | |||||
| chrX:47078955
|
C | CTT | 6 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0003g0299others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-636+265_-636+266d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078955 | |||||
| chrX:47078955
|
CT | C | 21 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0038others(18): Show | 21 | HG00323.hp1 HG00673.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.-636+266delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078955 | |||||
| chrX:47078975
|
T | TC | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-636+268dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47078975 | |||||
| chrX:47078986
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-636+277G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078986 | ||||||
| chrX:47079040
|
ACCT | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0081others(60): Show | 65 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-636+340_-636+342d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079040 | |||||
| chrX:47079085
|
T | TA | 1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-636+377dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079085 | |||||
| chrX:47079231
|
A | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0007g0288others(1): Show | 4 | HG00741.hp2 HG01070.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-636+522A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079231 | ||||||
| chrX:47079344
|
G | GT | 1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-636+642dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079344 | |||||
| chrX:47079348
|
TTTTG | T | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-636+647_-636+650d others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079348 | |||||
| chrX:47079349
|
TTTG | T | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-636+643_-636+645d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079349 | |||||
| chrX:47079356
|
G | GT | 24 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(21): Show | 24 | HG00558.hp1 HG01081.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-636+658dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079356 | |||||
| chrX:47079356
|
G | GTT | 1 | a0001c0001t0001g0028 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-636+657_-636+658d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079356 | |||||
| chrX:47079356
|
GT | G | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-636+658delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079356 | |||||
| chrX:47079356
|
GTTT | G | 5 | a0001c0001t0005g0106a0001c0001t0005g0258a0001c0001t0005g0259others(2): Show | 5 | HG02809.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-636+656_-636+658d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079356 | |||||
| chrX:47079356
|
GTTTT | G | 5 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(2): Show | 5 | HG00280.hp1 HG00733.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-636+655_-636+658d others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079356 | |||||
| chrX:47079358
|
T | G | 2 | a0001c0001t0003g0298a0001c0001t0003g0299 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-636+649T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079358 | ||||||
| chrX:47079360
|
T | G | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-636+651T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079360 | ||||||
| chrX:47079363
|
TTTTTG | T | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-636+665_-636+669d others(7): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079363 | |||||
| chrX:47079364
|
T | TG | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-636+655_-636+656i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079364 | ||||||
| chrX:47079364
|
TTTTG | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0038others(160): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-636+659_-636+662d others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079364 | |||||
| chrX:47079365
|
TTTG | T | 7 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0107others(4): Show | 7 | HG02486.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-636+659_-636+661d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079365 | |||||
| chrX:47079366
|
TTG | T | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0289others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-636+659_-636+660d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079366 | |||||
| chrX:47079368
|
G | T | 2 | a0001c0001t0001g0251a0004c0005t0001g0004 | 2 | HG00673.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-636+659G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079368 | ||||||
| chrX:47079368
|
GT | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-636+663delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079368 | |||||
| chrX:47079369
|
T | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0262a0001c0001t0001g0289others(5): Show | 8 | HG00741.hp2 HG01070.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-636+660T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079369 | ||||||
| chrX:47079374
|
T | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(23): Show | 26 | HG00558.hp1 HG01081.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-636+665T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079374 | ||||||
| chrX:47079389
|
GT | G | 1 | a0001c0001t0014g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-636+683delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079389 | |||||
| chrX:47079415
|
TG | T | 1 | a0001c0001t0001g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-636+707delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079415 | ||||||
| chrX:47079417
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-636+708T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079417 | ||||||
| chrX:47079421
|
G | GT | 1 | a0001c0001t0001g0248 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-636+719dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079421 | |||||
| chrX:47079438
|
G | GT | 14 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0180others(11): Show | 14 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-636+739dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079438 | |||||
| chrX:47079438
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-636+729G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079438 | ||||||
| chrX:47079438
|
GT | G | 2 | a0001c0001t0014g0036a0001c0001t0020g0181 | 2 | HG01168.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-636+739delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079438 | |||||
| chrX:47079439
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-636+730T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079439 | ||||||
| chrX:47079523
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-635-794C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079523 | ||||||
| chrX:47079537
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-635-780T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079537 | ||||||
| chrX:47079597
|
A | AT | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-635-713dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079597 | |||||
| chrX:47079642
|
A | G | 2 | a0001c0001t0001g0256a0007c0009t0001g0051 | 2 | HG01255.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-635-675A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079642 | ||||||
| chrX:47079672
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-635-645C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079672 | ||||||
| chrX:47079715
|
G | GC | 1 | a0001c0001t0016g0301 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-635-600dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079715 | |||||
| chrX:47079784
|
A | AT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-528dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079784 | |||||
| chrX:47079784
|
AT | A | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-635-528delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079784 | |||||
| chrX:47079823
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-635-494T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079823 | ||||||
| chrX:47079901
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-635-416A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079901 | ||||||
| chrX:47079923
|
GC | G | 1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-635-391delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079923 | |||||
| chrX:47079926
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(84): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-635-391C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079926 | ||||||
| chrX:47079938
|
C | CA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-378dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079938 | |||||
| chrX:47079945
|
A | AT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-371dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079945 | |||||
| chrX:47079950
|
C | T | 1 | a0001c0001t0012g0112 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-635-367C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079950 | ||||||
| chrX:47079973
|
T | TC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-342dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47079973 | |||||
| chrX:47080027
|
G | GC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-289dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080027 | |||||
| chrX:47080059
|
G | GT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-254dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080059 | |||||
| chrX:47080089
|
C | A | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-228C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47080089 | ||||||
| chrX:47080092
|
A | AC | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-224dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080092 | |||||
| chrX:47080097
|
A | AG | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-219dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080097 | |||||
| chrX:47080213
|
C | A | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-104C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47080213 | ||||||
| chrX:47080223
|
A | AG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-635-91dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080223 | |||||
| chrX:47080277
|
TC | T | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-37delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080277 | |||||
| chrX:47080287
|
GA | G | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-29delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47080287 | ||||||
| chrX:47080292
|
T | TTATC | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-635-23_-635-20dup others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 47080292 | |||||
| chrX:47080960
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-16+26dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 47080960 | |||||
| chrX:47080975
|
G | A | 2 | a0001c0001t0003g0105a0001c0001t0017g0182 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-16+39G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/7 | chrX | 47080975 | ||||||
| chrX:47081012
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-16+76T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/7 | chrX | 47081012 | ||||||
| chrX:47081094
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15-36C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/7 | chrX | 47081094 | ||||||
| chrX:47081305
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | splice_donor_variant&intron_variant | HIGH | c.163+1dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081305 | |||||
| chrX:47081305
|
TG | T | 1 | a0011c0004t0001g0183 | 1 | NA18999.hp2 | splice_donor_variant&intron_variant | HIGH | c.163+1delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081305 | |||||
| chrX:47081320
|
GC | G | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+14delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081320 | ||||||
| chrX:47081334
|
AGCCAGCT others(18): Show |
A | 2 | a0001c0001t0003g0298a0001c0001t0003g0299 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.163+29_163+53delCC others(23): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081334 | |||||
| chrX:47081337
|
C | CA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+31dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081337 | |||||
| chrX:47081348
|
TC | T | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+44delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081348 | |||||
| chrX:47081352
|
AG | A | 1 | a0011c0004t0001g0183 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.163+49delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081352 | |||||
| chrX:47081355
|
G | A | 1 | a0001c0001t0008g0059 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+48G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081355 | ||||||
| chrX:47081357
|
A | AG | 1 | a0001c0001t0001g0270 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.163+54dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081357 | |||||
| chrX:47081361
|
G | GGGC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+54_163+55insGG others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081361 | ||||||
| chrX:47081362
|
C | G | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+55C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081362 | ||||||
| chrX:47081484
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.163+177T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081484 | ||||||
| chrX:47081508
|
TC | T | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163+203delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081508 | |||||
| chrX:47081513
|
G | GT | 4 | a0001c0001t0001g0014a0001c0001t0001g0115a0001c0001t0001g0179others(1): Show | 4 | HG01928.hp1 HG02257.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+215dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081513 | |||||
| chrX:47081513
|
G | GTT | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.163+214_163+215dup others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081513 | |||||
| chrX:47081521
|
T | TG | 1 | a0001c0001t0001g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.163+214_163+215ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081521 | ||||||
| chrX:47081522
|
T | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(2): Show | 5 | HG02717.hp1 HG03516.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+215T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081522 | ||||||
| chrX:47081522
|
T | TG | 12 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0050others(9): Show | 12 | HG00140.hp1 HG00621.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+226dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081522 | |||||
| chrX:47081522
|
T | TTG | 1 | a0001c0001t0001g0013 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.163+215_163+216ins others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081522 | ||||||
| chrX:47081522
|
T | TTGG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+215_163+216ins others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081522 | ||||||
| chrX:47081522
|
TG | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0039others(81): Show | 85 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.163+226delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081522 | |||||
| chrX:47081522
|
TGG | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0003g0105 | 3 | HG02056.hp1 NA18906.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.163+225_163+226del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081522 | |||||
| chrX:47081523
|
G | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(85): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.163+216G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081523 | ||||||
| chrX:47081524
|
G | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(74): Show | 79 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.163+217G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081524 | ||||||
| chrX:47081525
|
G | T | 1 | a0001c0001t0003g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163+218G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081525 | ||||||
| chrX:47081532
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG03654.hp1 HG04204.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+225G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081532 | ||||||
| chrX:47081533
|
G | T | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163+226G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081533 | ||||||
| chrX:47081535
|
GT | G | 1 | a0001c0001t0001g0031 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.163+233delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081535 | |||||
| chrX:47081537
|
TTTTG | T | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.163+234_163+237del others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081537 | |||||
| chrX:47081546
|
T | TTTTA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+242_163+243ins others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081546 | |||||
| chrX:47081616
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0284a0001c0001t0009g0283 | 3 | HG01074.hp1 HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.163+309C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081616 | ||||||
| chrX:47081670
|
T | TC | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+366dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081670 | |||||
| chrX:47081689
|
C | T | 7 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG01952.hp1 HG03654.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+382C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081689 | ||||||
| chrX:47081721
|
AT | A | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163+420delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081721 | |||||
| chrX:47081727
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+421dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081727 | |||||
| chrX:47081770
|
C | A | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+463C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081770 | ||||||
| chrX:47081803
|
T | TC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+499dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081803 | |||||
| chrX:47081814
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+510dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081814 | |||||
| chrX:47081826
|
C | T | 16 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(13): Show | 16 | HG00323.hp1 HG00741.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+519C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081826 | ||||||
| chrX:47081855
|
G | GT | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+552dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081855 | |||||
| chrX:47081870
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+567dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081870 | |||||
| chrX:47081912
|
AC | A | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+607delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081912 | |||||
| chrX:47081979
|
CA | C | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163+676delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081979 | |||||
| chrX:47081989
|
C | CAA | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+686_163+687dup others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081989 | |||||
| chrX:47082003
|
TC | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+697delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082003 | ||||||
| chrX:47082011
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.163+704T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082011 | ||||||
| chrX:47082019
|
G | GA | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+716dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082019 | |||||
| chrX:47082053
|
A | AG | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+748dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082053 | |||||
| chrX:47082059
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.163+752G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082059 | ||||||
| chrX:47082087
|
C | CA | 1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.163+781dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082087 | |||||
| chrX:47082135
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.163+828C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082135 | ||||||
| chrX:47082205
|
G | GA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+901dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082205 | |||||
| chrX:47082238
|
G | GA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+937dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082238 | |||||
| chrX:47082299
|
TC | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+993delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082299 | ||||||
| chrX:47082303
|
C | CT | 35 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0033others(32): Show | 36 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.163+1021dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
C | CTCTTTT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+997_163+998ins others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
C | CTT | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 14 | HG01081.hp2 HG01243.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.163+1020_163+1021d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
C | CTTT | 70 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(67): Show | 70 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.163+1019_163+1021d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
C | CTTTT | 31 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+1018_163+1021d others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
C | CTTTTT | 1 | a0001c0001t0004g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.163+1017_163+1021d others(7): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
CT | C | 21 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(18): Show | 21 | HG00099.hp1 HG01070.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.163+1021delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082303
|
CTT | C | 1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.163+1020_163+1021d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082303 | |||||
| chrX:47082333
|
C | CA | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+1028dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082333 | |||||
| chrX:47082361
|
A | G | 102 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0023others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.163+1054A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082361 | ||||||
| chrX:47082362
|
G | GT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1056dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082362 | |||||
| chrX:47082456
|
A | G | 6 | a0001c0001t0001g0100a0001c0001t0001g0282a0001c0001t0003g0241others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+1149A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082456 | ||||||
| chrX:47082465
|
C | T | 1 | a0001c0001t0013g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.163+1158C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082465 | ||||||
| chrX:47082487
|
A | AT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+1186dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082487 | |||||
| chrX:47082498
|
A | AG | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163+1192dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082498 | |||||
| chrX:47082514
|
T | A | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1207T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082514 | ||||||
| chrX:47082569
|
TC | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+1265delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082569 | |||||
| chrX:47082604
|
C | G | 2 | a0001c0001t0001g0247a0008c0006t0001g0227 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.163+1297C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082604 | ||||||
| chrX:47082658
|
AC | A | 2 | a0001c0001t0020g0181a0005c0010t0001g0049 | 2 | HG01168.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.163+1354delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082658 | |||||
| chrX:47082674
|
G | GT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+1368dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082674 | |||||
| chrX:47082707
|
T | TG | 1 | a0001c0011t0001g0226 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.163+1404dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082707 | |||||
| chrX:47082713
|
T | TG | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+1410dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082713 | |||||
| chrX:47082717
|
G | GGT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1410_163+1411i others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082717 | ||||||
| chrX:47082751
|
A | AC | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+1445dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082751 | |||||
| chrX:47082779
|
G | GC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1475dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082779 | |||||
| chrX:47082779
|
GC | G | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.163+1475delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082779 | |||||
| chrX:47082783
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0002g0173others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+1476G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082783 | ||||||
| chrX:47082783
|
G | GC | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163+1481dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082783 | |||||
| chrX:47082799
|
G | GC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1497dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082799 | |||||
| chrX:47082799
|
GC | G | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163+1497delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082799 | |||||
| chrX:47082804
|
C | CA | 1 | a0001c0011t0001g0226 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.163+1499dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082804 | |||||
| chrX:47082911
|
TG | T | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-1504delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082911 | |||||
| chrX:47082938
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1479dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082938 | |||||
| chrX:47082949
|
CT | C | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.164-1466delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082949 | |||||
| chrX:47082976
|
TC | T | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.164-1439delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082976 | |||||
| chrX:47082995
|
A | AGG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1420_164-1419d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47082995 | |||||
| chrX:47083017
|
CA | C | 2 | a0001c0001t0020g0181a0010c0013t0019g0287 | 2 | HG01168.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-1397delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083017 | |||||
| chrX:47083080
|
T | TA | 3 | a0001c0001t0001g0210a0001c0001t0001g0228a0009c0012t0011g0037 | 3 | HG02683.hp2 HG04228.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.164-1331dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083080 | |||||
| chrX:47083095
|
AAT | A | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-1322_164-1321d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083095 | ||||||
| chrX:47083099
|
T | A | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-1319T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083099 | ||||||
| chrX:47083099
|
TA | T | 1 | a0001c0011t0001g0226 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.164-1310delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083099 | |||||
| chrX:47083100
|
A | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0205a0001c0001t0005g0106others(3): Show | 6 | HG01243.hp1 HG01952.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1318A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083100 | ||||||
| chrX:47083113
|
T | TC | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-1304dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083113 | |||||
| chrX:47083115
|
TTG | T | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.164-1302_164-1301d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083115 | ||||||
| chrX:47083118
|
GC | G | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164-1298delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083118 | |||||
| chrX:47083120
|
C | CG | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-1295dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083120 | |||||
| chrX:47083136
|
T | G | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-1282T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083136 | ||||||
| chrX:47083144
|
A | AT | 1 | a0001c0001t0001g0270 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.164-1273dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083144 | |||||
| chrX:47083153
|
C | CT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1261dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083153 | |||||
| chrX:47083162
|
G | GA | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-1256_164-1255i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083162 | ||||||
| chrX:47083189
|
C | CA | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-1228dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083189 | |||||
| chrX:47083221
|
G | GA | 1 | a0001c0001t0016g0301 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.164-1194dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083221 | |||||
| chrX:47083227
|
G | GT | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164-1190dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083227 | |||||
| chrX:47083228
|
T | TG | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-1189dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083228 | |||||
| chrX:47083232
|
T | TC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1185dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083232 | |||||
| chrX:47083245
|
CA | C | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.164-1168delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083245 | |||||
| chrX:47083254
|
G | A | 2 | a0001c0001t0005g0106a0001c0001t0005g0261 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.164-1164G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083254 | ||||||
| chrX:47083262
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1154dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083262 | |||||
| chrX:47083280
|
T | TC | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164-1135dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083280 | |||||
| chrX:47083291
|
AG | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-1124delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083291 | |||||
| chrX:47083295
|
A | AG | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-1121dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083295 | |||||
| chrX:47083301
|
A | AG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1115dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083301 | |||||
| chrX:47083328
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0002g0052 | 2 | HG00733.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.164-1090G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083328 | ||||||
| chrX:47083331
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.164-1087G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083331 | ||||||
| chrX:47083398
|
C | CA | 8 | a0001c0001t0001g0128a0001c0001t0001g0211a0001c0001t0002g0058others(5): Show | 8 | HG00738.hp1 HG02083.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-1007dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083398 | |||||
| chrX:47083398
|
CA | C | 5 | a0001c0001t0001g0109a0001c0001t0002g0063a0001c0001t0003g0243others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-1007delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083398 | |||||
| chrX:47083458
|
TA | T | 1 | a0001c0001t0020g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.164-955delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083458 | |||||
| chrX:47083466
|
TA | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-948delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083466 | |||||
| chrX:47083472
|
G | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(155): Show | 160 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.164-946G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083472 | ||||||
| chrX:47083528
|
GT | G | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-887delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083528 | |||||
| chrX:47083535
|
A | AT | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-877dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083535 | |||||
| chrX:47083557
|
A | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(13): Show | 16 | HG00558.hp1 HG00609.hp1 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-861A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083557 | ||||||
| chrX:47083567
|
CT | C | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164-850delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083567 | ||||||
| chrX:47083621
|
G | A | 1 | a0001c0001t0005g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164-797G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083621 | ||||||
| chrX:47083624
|
TC | T | 1 | a0001c0011t0001g0226 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.164-792delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083624 | |||||
| chrX:47083704
|
A | AG | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-713dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083704 | |||||
| chrX:47083709
|
G | GA | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.164-706dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083709 | |||||
| chrX:47083719
|
TG | T | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-697delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083719 | |||||
| chrX:47083754
|
TA | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-663delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083754 | ||||||
| chrX:47083760
|
T | TA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-653dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083760 | |||||
| chrX:47083776
|
G | A | 1 | a0001c0001t0005g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164-642G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083776 | ||||||
| chrX:47083777
|
TG | T | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-639delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083777 | |||||
| chrX:47083793
|
T | TC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-622dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083793 | |||||
| chrX:47083893
|
CA | C | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-523delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083893 | |||||
| chrX:47083910
|
C | CA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-508_164-507ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083910 | ||||||
| chrX:47083912
|
CA | C | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.164-503delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083912 | |||||
| chrX:47083914
|
AAC | A | 16 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG00741.hp2 HG01070.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-502_164-501del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083914 | |||||
| chrX:47083915
|
AC | A | 1 | a0001c0001t0001g0292 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164-502delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083915 | ||||||
| chrX:47083916
|
C | CA | 3 | a0001c0001t0003g0241a0001c0001t0003g0298a0001c0001t0016g0301 | 3 | HG02559.hp1 HG03098.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.164-498dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083916 | |||||
| chrX:47083919
|
A | AC | 2 | a0001c0001t0001g0197a0001c0001t0001g0300 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.164-499_164-498ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083919 | ||||||
| chrX:47083920
|
A | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0050others(3): Show | 7 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-498A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083920 | ||||||
| chrX:47083920
|
AC | A | 1 | a0001c0001t0001g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.164-497delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083920 | ||||||
| chrX:47083921
|
C | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(43): Show | 47 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.164-497C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083921 | ||||||
| chrX:47083921
|
C | CA | 16 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0048others(13): Show | 16 | HG00438.hp2 HG01928.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-494dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083921 | |||||
| chrX:47083924
|
A | C | 17 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0001g0081others(14): Show | 17 | HG00741.hp2 HG01070.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.164-494A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083924 | ||||||
| chrX:47083924
|
AC | A | 2 | a0001c0001t0024g0079a0001c0011t0001g0226 | 2 | NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.164-493delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083924 | ||||||
| chrX:47083925
|
C | A | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(286): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.164-493C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083925 | ||||||
| chrX:47083925
|
C | CA | 5 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0175others(2): Show | 5 | HG02056.hp1 HG02523.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-482dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47083925 | |||||
| chrX:47083926
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.164-492A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083926 | ||||||
| chrX:47084000
|
G | GT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-415dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084000 | |||||
| chrX:47084003
|
T | TG | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-414dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084003 | |||||
| chrX:47084040
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-374dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084040 | |||||
| chrX:47084052
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.164-366C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084052 | ||||||
| chrX:47084073
|
G | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-345G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084073 | ||||||
| chrX:47084074
|
T | G | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-344T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084074 | ||||||
| chrX:47084075
|
G | GC | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164-339dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084075 | |||||
| chrX:47084082
|
G | GA | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-335dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084082 | |||||
| chrX:47084087
|
G | GA | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-328dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084087 | |||||
| chrX:47084094
|
C | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-324C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084094 | ||||||
| chrX:47084130
|
T | TG | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-286dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084130 | |||||
| chrX:47084139
|
G | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.164-279G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084139 | ||||||
| chrX:47084141
|
CT | C | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-274delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084141 | |||||
| chrX:47084153
|
T | TG | 1 | a0009c0012t0011g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-264dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084153 | |||||
| chrX:47084164
|
C | CA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-252dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084164 | |||||
| chrX:47084189
|
TG | T | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-226delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084189 | |||||
| chrX:47084192
|
G | GT | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.164-219dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084192 | |||||
| chrX:47084203
|
A | AT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-212dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084203 | |||||
| chrX:47084203
|
AT | A | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-212delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084203 | |||||
| chrX:47084234
|
CA | C | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-180delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084234 | |||||
| chrX:47084268
|
T | TA | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-149dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084268 | |||||
| chrX:47084314
|
G | GA | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.164-103dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084314 | |||||
| chrX:47084319
|
C | CG | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-99_164-98insG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084319 | ||||||
| chrX:47084389
|
G | GT | 1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164-23dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47084389 | |||||
| chrX:47084391
|
T | A | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-27T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084391 | ||||||
| chrX:47084725
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.346+125G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084725 | ||||||
| chrX:47084740
|
GC | G | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+143delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084740 | |||||
| chrX:47084756
|
A | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(186): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.346+156A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084756 | ||||||
| chrX:47084778
|
A | AC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+181dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084778 | |||||
| chrX:47084784
|
T | TC | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+185dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084784 | |||||
| chrX:47084811
|
TG | T | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+214delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084811 | |||||
| chrX:47084851
|
AG | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+253delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084851 | |||||
| chrX:47084880
|
A | C | 1 | a0001c0001t0003g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.346+280A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084880 | ||||||
| chrX:47084884
|
G | GT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+287dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084884 | |||||
| chrX:47084955
|
G | GA | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+361dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084955 | |||||
| chrX:47084955
|
GA | G | 2 | a0001c0001t0001g0035a0010c0013t0019g0287 | 2 | NA19030.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.346+361delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47084955 | |||||
| chrX:47084984
|
T | A | 1 | a0003c0003t0001g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+384T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084984 | ||||||
| chrX:47085028
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+431dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085028 | |||||
| chrX:47085067
|
C | CA | 1 | a0001c0001t0002g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.346+477dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085067 | |||||
| chrX:47085067
|
CA | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0080others(11): Show | 14 | HG00741.hp2 HG01070.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.346+477delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085067 | |||||
| chrX:47085138
|
AT | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+542delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085138 | |||||
| chrX:47085218
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.346+618G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085218 | ||||||
| chrX:47085245
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+645G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085245 | ||||||
| chrX:47085253
|
T | TC | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+654dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085253 | |||||
| chrX:47085276
|
TG | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+679delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085276 | |||||
| chrX:47085370
|
AT | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+772delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085370 | |||||
| chrX:47085376
|
C | CG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+779dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085376 | |||||
| chrX:47085377
|
G | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0001g0081others(4): Show | 7 | HG02809.hp2 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+777G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085377 | ||||||
| chrX:47085390
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.346+790G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085390 | ||||||
| chrX:47085516
|
C | CA | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+927dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085516 | |||||
| chrX:47085580
|
A | AC | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+981dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085580 | |||||
| chrX:47085641
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0080others(11): Show | 15 | HG00741.hp2 HG01070.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+1041A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085641 | ||||||
| chrX:47085654
|
T | TA | 16 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 17 | HG00408.hp1 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+1064dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085654 | |||||
| chrX:47085654
|
T | TAA | 3 | a0001c0001t0001g0205a0001c0001t0005g0259a0003c0003t0001g0201 | 3 | HG02809.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.346+1063_346+1064d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085654 | |||||
| chrX:47085654
|
TA | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0197 | 2 | HG03688.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.346+1064delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085654 | |||||
| chrX:47085723
|
T | TC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1125dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085723 | |||||
| chrX:47085758
|
A | AG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1160dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085758 | |||||
| chrX:47085779
|
G | GC | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1181dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085779 | |||||
| chrX:47085894
|
G | GT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1296dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085894 | |||||
| chrX:47085898
|
C | G | 217 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.346+1298C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085898 | ||||||
| chrX:47085917
|
G | GT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+1320dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47085917 | |||||
| chrX:47086035
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.346+1435A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086035 | ||||||
| chrX:47086038
|
G | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0222a0001c0001t0001g0281 | 3 | HG00642.hp1 HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.346+1438G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086038 | ||||||
| chrX:47086068
|
CT | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0160 | 2 | HG02083.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.346+1474delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086068 | |||||
| chrX:47086086
|
AT | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1490delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086086 | |||||
| chrX:47086096
|
C | CT | 2 | a0001c0001t0001g0300a0008c0006t0001g0227 | 2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.346+1503dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086096 | |||||
| chrX:47086108
|
G | GT | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+1514dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086108 | |||||
| chrX:47086142
|
GC | G | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1544delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086142 | |||||
| chrX:47086145
|
A | AG | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+1547dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086145 | |||||
| chrX:47086161
|
C | CA | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+1561_346+1562i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086161 | ||||||
| chrX:47086168
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.346+1568T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086168 | ||||||
| chrX:47086173
|
AG | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1576delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086173 | |||||
| chrX:47086185
|
AT | A | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1588delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086185 | |||||
| chrX:47086203
|
G | GT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1606dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086203 | |||||
| chrX:47086305
|
G | GA | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+1705_346+1706i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086305 | ||||||
| chrX:47086315
|
G | GT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1717dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086315 | |||||
| chrX:47086340
|
AG | A | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+1742delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086340 | |||||
| chrX:47086343
|
C | CA | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+1743_346+1744i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086343 | ||||||
| chrX:47086366
|
T | A | 2 | a0002c0002t0001g0021a0002c0002t0023g0005 | 2 | NA18962.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.346+1766T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086366 | ||||||
| chrX:47086371
|
A | AT | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+1776dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086371 | |||||
| chrX:47086383
|
AT | A | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+1786delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086383 | |||||
| chrX:47086399
|
T | TGG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1803_346+1804d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086399 | |||||
| chrX:47086410
|
A | T | 1 | a0008c0006t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1810A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086410 | ||||||
| chrX:47086436
|
A | AC | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.346+1839dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086436 | |||||
| chrX:47086505
|
TG | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+1908delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086505 | |||||
| chrX:47086526
|
G | GA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+1927dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086526 | |||||
| chrX:47086573
|
G | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0210a0001c0001t0001g0233others(3): Show | 6 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+1973G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086573 | ||||||
| chrX:47086641
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.346+2041C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086641 | ||||||
| chrX:47086672
|
A | AG | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+2073dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086672 | |||||
| chrX:47086732
|
CAGGAGAG others(2): Show |
C | 1 | a0001c0001t0003g0298 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.346+2135_346+2143d others(11): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086732 | |||||
| chrX:47086734
|
G | GGA | 25 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0033others(22): Show | 25 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.346+2183_346+2184d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGA | 30 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(27): Show | 30 | HG00558.hp2 HG01123.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.346+2181_346+2184d others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGA | 32 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.346+2179_346+2184d others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGAG others(1): Show |
17 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0141others(14): Show | 17 | HG00544.hp1 HG01346.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.346+2177_346+2184d others(10): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGAG others(3): Show |
10 | a0001c0001t0001g0031a0001c0001t0001g0144a0001c0001t0001g0195others(7): Show | 10 | HG02155.hp1 HG02165.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+2175_346+2184d others(12): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGAG others(5): Show |
4 | a0001c0001t0001g0121a0001c0001t0001g0145a0001c0001t0001g0163others(1): Show | 4 | HG02074.hp1 NA18950.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+2173_346+2184d others(14): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGAG others(7): Show |
1 | a0001c0001t0002g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.346+2171_346+2184d others(16): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGAG others(9): Show |
4 | a0001c0001t0001g0041a0001c0001t0002g0078a0001c0001t0002g0095others(1): Show | 4 | HG03654.hp1 NA18949.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+2169_346+2184d others(18): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
G | GGAGAGAG others(11): Show |
1 | a0001c0001t0024g0079 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.346+2167_346+2184d others(20): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGA | G | 23 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 24 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.346+2183_346+2184d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGA | G | 23 | a0001c0001t0001g0040a0001c0001t0001g0147a0001c0001t0001g0148others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.346+2181_346+2184d others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGA | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(13): Show | 16 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+2179_346+2184d others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(1): Show |
G | 9 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0043others(6): Show | 10 | HG02027.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.346+2177_346+2184d others(10): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(3): Show |
G | 11 | a0001c0001t0001g0012a0001c0001t0001g0124a0001c0001t0001g0146others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+2175_346+2184d others(12): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(5): Show |
G | 3 | a0001c0001t0001g0228a0001c0001t0001g0300a0001c0001t0008g0097 | 3 | HG02145.hp1 HG02615.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.346+2173_346+2184d others(14): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(7): Show |
G | 13 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0046others(10): Show | 14 | HG00741.hp2 HG01070.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.346+2171_346+2184d others(16): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(9): Show |
G | 17 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0100others(14): Show | 17 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+2169_346+2184d others(18): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(11): Show |
G | 3 | a0001c0001t0001g0104a0001c0001t0005g0106a0001c0001t0005g0261 | 3 | HG02922.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.346+2167_346+2184d others(20): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(13): Show |
G | 6 | a0001c0001t0001g0235a0001c0001t0001g0256a0001c0001t0001g0276others(3): Show | 6 | HG01255.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+2165_346+2184d others(22): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086734
|
GGAGAGAG others(15): Show |
G | 1 | a0001c0001t0003g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.346+2163_346+2184d others(24): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086734 | |||||
| chrX:47086777
|
GAGAGAGA others(1): Show |
G | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.346+2185_346+2192d others(10): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086777 | |||||
| chrX:47086779
|
GAGAGAA | G | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.346+2185_346+2190d others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086779 | |||||
| chrX:47086780
|
A | AGAGAGAG others(1): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.346+2184_346+2185i others(10): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086780 | |||||
| chrX:47086781
|
GAGA | G | 1 | a0001c0001t0001g0281 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.346+2183_346+2185d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086781 | |||||
| chrX:47086783
|
GA | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0236a0001c0001t0001g0295others(1): Show | 4 | HG01074.hp1 HG01361.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+2186delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086783 | |||||
| chrX:47086784
|
A | AG | 2 | a0001c0001t0001g0137a0001c0001t0002g0070 | 2 | NA19074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.346+2184_346+2185i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086784 | ||||||
| chrX:47086784
|
A | AGAG | 2 | a0001c0001t0002g0054a0001c0001t0015g0275 | 2 | HG01192.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.346+2184_346+2185i others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086784 | ||||||
| chrX:47086784
|
A | AGAGAGAG | 1 | a0001c0001t0002g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.346+2184_346+2185i others(9): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086784 | ||||||
| chrX:47086784
|
A | AGAGAGAG others(2): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0219a0001c0001t0009g0283 | 3 | HG01106.hp1 HG02738.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.346+2184_346+2185i others(11): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086784 | ||||||
| chrX:47086784
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0002g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.346+2184_346+2185i others(13): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086784 | ||||||
| chrX:47086785
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.346+2185A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086785 | ||||||
| chrX:47086800
|
C | A | 2 | a0001c0001t0008g0059a0001c0001t0008g0097 | 2 | HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.346+2200C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086800 | ||||||
| chrX:47086855
|
TA | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+2256delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086855 | ||||||
| chrX:47086880
|
T | TG | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+2282dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086880 | |||||
| chrX:47086914
|
A | AG | 2 | a0001c0001t0001g0128a0010c0013t0019g0287 | 2 | HG02083.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.346+2317dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086914 | |||||
| chrX:47086916
|
G | GT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+2316_346+2317i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086916 | ||||||
| chrX:47086933
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.346+2333G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086933 | ||||||
| chrX:47086934
|
TG | T | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.346+2337delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47086934 | |||||
| chrX:47087005
|
C | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(186): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.346+2405C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087005 | ||||||
| chrX:47087006
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346+2408dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087006 | |||||
| chrX:47087008
|
G | GTC | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346+2409_346+2410d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087008 | |||||
| chrX:47087081
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(185): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.346+2481G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087081 | ||||||
| chrX:47087135
|
T | TTAGATAC others(19): Show |
1 | a0001c0001t0002g0098 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.346+2537_346+2562d others(28): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087135 | |||||
| chrX:47087252
|
T | TC | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-2524_347-2523i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087252 | ||||||
| chrX:47087322
|
TC | T | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.347-2451delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087322 | |||||
| chrX:47087345
|
A | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0177a0001c0001t0002g0061 | 3 | NA18953.hp1 NA19000.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.347-2431A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087345 | ||||||
| chrX:47087361
|
C | CG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-2412dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087361 | |||||
| chrX:47087367
|
AG | A | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-2407delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087367 | |||||
| chrX:47087392
|
C | CT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-2383dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087392 | |||||
| chrX:47087495
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.347-2281T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087495 | ||||||
| chrX:47087510
|
T | TC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-2265dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087510 | |||||
| chrX:47087564
|
G | GC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-2210dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087564 | |||||
| chrX:47087567
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.347-2209T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087567 | ||||||
| chrX:47087591
|
G | GC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-2184dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087591 | |||||
| chrX:47087602
|
T | A | 1 | a0001c0001t0001g0294 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.347-2174T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087602 | ||||||
| chrX:47087604
|
C | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0050others(5): Show | 9 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.347-2172C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087604 | ||||||
| chrX:47087607
|
A | AT | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-2164dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087607 | |||||
| chrX:47087705
|
CAGG | C | 1 | a0001c0001t0001g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.347-2068_347-2066d others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087705 | |||||
| chrX:47087732
|
C | CA | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-2043dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087732 | |||||
| chrX:47087792
|
TA | T | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1982delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087792 | |||||
| chrX:47087802
|
CT | C | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1972delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087802 | |||||
| chrX:47087930
|
TTA | T | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1841_347-1840d others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47087930 | |||||
| chrX:47087946
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(173): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.347-1830A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087946 | ||||||
| chrX:47088005
|
C | CT | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-1770dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088005 | |||||
| chrX:47088025
|
CA | C | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-1750delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088025 | ||||||
| chrX:47088043
|
G | GC | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1733_347-1732i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088043 | ||||||
| chrX:47088070
|
G | GCTATGCA others(28): Show |
1 | a0001c0001t0001g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.347-1704_347-1670d others(37): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088070 | |||||
| chrX:47088080
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.347-1696T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088080 | ||||||
| chrX:47088147
|
C | CT | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1629_347-1628i others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088147 | ||||||
| chrX:47088148
|
A | AG | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-1626dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088148 | |||||
| chrX:47088150
|
GC | G | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.347-1623delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088150 | |||||
| chrX:47088155
|
G | GA | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-1616dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088155 | |||||
| chrX:47088163
|
T | TG | 1 | a0010c0013t0019g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1609dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088163 | |||||
| chrX:47088179
|
T | TC | 1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.347-1596dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088179 | |||||
| chrX:47088265
|
A | AG | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-1510dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088265 | |||||
| chrX:47088291
|
AC | A | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-1483delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088291 | |||||
| chrX:47088371
|
AG | A | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-1402delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088371 | |||||
| chrX:47088387
|
T | TA | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-1386dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088387 | |||||
| chrX:47088420
|
AG | A | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-1353delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088420 | |||||
| chrX:47088590
|
TG | T | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.347-1182delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088590 | |||||
| chrX:47088597
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.347-1179G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088597 | ||||||
| chrX:47088698
|
G | C | 1 | a0001c0001t0001g0147 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.347-1078G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088698 | ||||||
| chrX:47088760
|
C | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.347-1016C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088760 | ||||||
| chrX:47088789
|
GC | G | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-985delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088789 | |||||
| chrX:47088800
|
TG | T | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-974delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088800 | |||||
| chrX:47088816
|
T | TC | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-957dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088816 | |||||
| chrX:47088870
|
G | GC | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-905dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088870 | |||||
| chrX:47088890
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.347-886C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088890 | ||||||
| chrX:47088891
|
G | A | 5 | a0001c0001t0001g0235a0001c0001t0001g0256a0001c0001t0001g0276others(2): Show | 5 | HG01255.hp1 HG02647.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-885G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088891 | ||||||
| chrX:47088908
|
T | TG | 1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.347-865dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088908 | |||||
| chrX:47088931
|
C | CA | 2 | a0001c0001t0001g0297a0001c0001t0002g0055 | 2 | HG01981.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.347-829dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088931 | |||||
| chrX:47088931
|
CA | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0126a0001c0001t0001g0225others(2): Show | 5 | HG01515.hp1 HG02293.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-829delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088931 | |||||
| chrX:47088931
|
CAA | C | 1 | a0001c0001t0001g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.347-830_347-829del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088931 | |||||
| chrX:47088931
|
CAAA | C | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.347-831_347-829del others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088931 | |||||
| chrX:47088943
|
AAAAAG | A | 2 | a0001c0001t0005g0259a0003c0003t0001g0201 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.347-830_347-826del others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088943 | |||||
| chrX:47088945
|
AAAG | A | 17 | a0001c0001t0001g0031a0001c0001t0001g0117a0001c0001t0001g0118others(14): Show | 17 | HG00621.hp1 HG00741.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.347-811_347-809del others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088945 | |||||
| chrX:47088946
|
AAG | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0081 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.347-828_347-827del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088946 | |||||
| chrX:47088946
|
AAGAAG | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0213others(2): Show | 5 | HG01952.hp1 HG02965.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-828_347-824del others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088946 | |||||
| chrX:47088947
|
AG | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0205a0001c0001t0001g0291 | 3 | HG02809.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.347-828delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088947 | ||||||
| chrX:47088947
|
AGAAG | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(155): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.347-828_347-825del others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088947 | ||||||
| chrX:47088951
|
G | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0080others(19): Show | 22 | HG00621.hp1 HG00741.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.347-825G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088951 | ||||||
| chrX:47088968
|
T | TAGA | 1 | a0001c0001t0001g0236 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.347-799_347-797dup others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47088968 | |||||
| chrX:47089012
|
TG | T | 1 | a0001c0001t0005g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.347-762delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089012 | |||||
| chrX:47089030
|
AC | A | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-742delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089030 | |||||
| chrX:47089045
|
A | AG | 1 | a0001c0001t0002g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.347-729dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089045 | |||||
| chrX:47089078
|
A | AG | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-697dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089078 | |||||
| chrX:47089099
|
A | AG | 1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.347-675dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089099 | |||||
| chrX:47089117
|
T | TG | 2 | a0001c0001t0001g0262a0005c0010t0001g0049 | 2 | HG01952.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.347-654dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089117 | |||||
| chrX:47089178
|
G | GAGCAAGT others(1124): Show |
1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1131): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1120): Show |
1 | a0001c0001t0001g0160 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.347-598_347-597ins others(1127): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1121): Show |
2 | a0001c0001t0001g0292a0007c0009t0001g0051 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-598_347-597ins others(1128): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1121): Show |
14 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0146others(11): Show | 14 | HG00408.hp1 HG00621.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.347-598_347-597ins others(1128): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1122): Show |
1 | a0001c0001t0001g0296 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.347-598_347-597ins others(1129): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1120): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0198 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.347-598_347-597ins others(1127): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1120): Show |
4 | a0001c0001t0001g0164a0001c0001t0001g0178a0001c0001t0001g0189others(1): Show | 4 | HG00609.hp1 NA18951.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-598_347-597ins others(1127): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1120): Show |
126 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.347-598_347-597ins others(1127): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1119): Show |
1 | a0001c0001t0005g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.347-598_347-597ins others(1126): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1122): Show |
1 | a0001c0001t0003g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1129): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1119): Show |
1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1126): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1119): Show |
1 | a0001c0001t0001g0284 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1126): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1119): Show |
30 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0046others(27): Show | 31 | HG00140.hp1 HG02109.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.347-598_347-597ins others(1126): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1116): Show |
1 | a0006c0007t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1123): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1118): Show |
6 | a0001c0001t0001g0235a0001c0001t0001g0256a0001c0001t0001g0276others(3): Show | 6 | HG01255.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-598_347-597ins others(1125): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1119): Show |
1 | a0001c0001t0001g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1126): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089178
|
G | GAGCAAGT others(1125): Show |
1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-598_347-597ins others(1132): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089178 | ||||||
| chrX:47089266
|
G | GT | 1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-507dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089266 | |||||
| chrX:47089306
|
G | GT | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.347-466dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089306 | |||||
| chrX:47089342
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.347-434T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089342 | ||||||
| chrX:47089351
|
T | TTAATTTG others(36): Show |
1 | a0001c0001t0015g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.347-425_347-424ins others(43): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089351 | ||||||
| chrX:47089359
|
T | TA | 1 | a0001c0001t0015g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.347-416dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089359 | |||||
| chrX:47089377
|
AT | A | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.347-397delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089377 | |||||
| chrX:47089390
|
A | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0140others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-386A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089390 | ||||||
| chrX:47089396
|
A | AAAT | 1 | a0001c0001t0001g0289 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-380_347-379ins others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089396 | ||||||
| chrX:47089400
|
A | AATATATT others(1090): Show |
1 | a0001c0001t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1097): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1125): Show |
2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | NA18956.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1132): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1227): Show |
1 | a0001c0001t0001g0211 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1234): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1194): Show |
1 | a0001c0001t0002g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1201): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1303): Show |
1 | a0001c0001t0001g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1310): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1196): Show |
1 | a0001c0001t0001g0238 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1203): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1196): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0175a0001c0001t0001g0195others(1): Show | 4 | HG02523.hp2 HG03654.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-370_347-369ins others(1203): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1231): Show |
1 | a0001c0001t0001g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1238): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1336): Show |
1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1343): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1122): Show |
1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1129): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1084): Show |
1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1091): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1249): Show |
1 | a0001c0001t0001g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1256): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1006): Show |
1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1013): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1198): Show |
1 | a0001c0001t0001g0224 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1205): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(916): Show |
1 | a0001c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(923): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(946): Show |
1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(953): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(941): Show |
1 | a0001c0001t0003g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(948): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1283): Show |
1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1290): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1013): Show |
1 | a0001c0001t0001g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1020): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1048): Show |
1 | a0001c0001t0001g0023 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1055): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1013): Show |
1 | a0001c0001t0001g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1020): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1020): Show |
2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1027): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1166): Show |
1 | a0001c0001t0001g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1173): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(811): Show |
1 | a0001c0001t0008g0059 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(818): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1056): Show |
1 | a0001c0001t0001g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1063): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1056): Show |
1 | a0001c0001t0001g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1063): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1091): Show |
3 | a0002c0002t0001g0021a0002c0002t0001g0194a0002c0002t0023g0005 | 3 | NA18962.hp1 NA18973.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1098): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1126): Show |
1 | a0001c0001t0001g0125 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1133): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(903): Show |
1 | a0001c0001t0017g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(910): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(803): Show |
1 | a0001c0001t0008g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(810): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1140): Show |
1 | a0001c0001t0001g0149 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1147): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1087): Show |
4 | a0001c0001t0001g0152a0001c0001t0001g0294a0001c0001t0001g0295others(1): Show | 4 | HG01928.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-370_347-369ins others(1094): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1118): Show |
1 | a0001c0001t0002g0083 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1125): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1261): Show |
1 | a0001c0001t0001g0222 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1268): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1261): Show |
2 | a0001c0001t0001g0209a0001c0001t0001g0281 | 2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1268): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1108): Show |
1 | a0001c0001t0002g0082 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1115): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1150): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0269 | 2 | NA18944.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1157): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1087): Show |
3 | a0001c0001t0001g0153a0001c0001t0002g0086a0001c0001t0002g0089 | 3 | HG01975.hp1 HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1094): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1192): Show |
1 | a0001c0001t0002g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1199): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1122): Show |
2 | a0001c0001t0001g0166a0001c0001t0001g0293 | 2 | HG01515.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1129): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1148): Show |
1 | a0001c0001t0002g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1155): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1087): Show |
15 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0038others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.347-370_347-369ins others(1094): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1135): Show |
2 | a0001c0001t0002g0087a0001c0001t0002g0090 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1142): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1082): Show |
1 | a0001c0001t0001g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1089): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1115): Show |
1 | a0001c0001t0001g0009 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1122): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1052): Show |
1 | a0001c0001t0001g0002 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1059): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1087): Show |
1 | a0001c0001t0001g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1094): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1017): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0232a0001c0001t0002g0054 | 3 | HG01192.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1024): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1122): Show |
1 | a0001c0001t0001g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1129): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1087): Show |
1 | a0001c0001t0001g0151 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1094): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1048): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0236 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1055): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1154): Show |
1 | a0001c0008t0001g0167 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1161): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1049): Show |
1 | a0001c0001t0001g0191 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1056): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(976): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(983): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(976): Show |
6 | a0001c0001t0001g0100a0001c0001t0001g0199a0001c0001t0001g0249others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-370_347-369ins others(983): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1078): Show |
1 | a0001c0001t0003g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1085): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1124): Show |
1 | a0001c0001t0001g0147 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1131): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1081): Show |
1 | a0001c0001t0021g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1088): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1161): Show |
1 | a0001c0001t0018g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1168): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1221): Show |
2 | a0001c0001t0002g0173a0001c0001t0002g0174 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1228): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1181): Show |
1 | a0001c0001t0005g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1188): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1212): Show |
1 | a0001c0001t0005g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1219): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1081): Show |
1 | a0001c0001t0001g0196 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1088): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | AATATATT others(1083): Show |
1 | a0001c0001t0001g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1090): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089400 | |||||
| chrX:47089400
|
A | ATATATAT others(1059): Show |
1 | a0001c0001t0002g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.347-376_347-375ins others(1066): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089400 | ||||||
| chrX:47089400
|
A | ATTAATGT others(1487): Show |
1 | a0001c0001t0001g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.347-376_347-375ins others(1494): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089400 | ||||||
| chrX:47089400
|
A | ATTATATA others(999): Show |
1 | a0001c0001t0001g0289 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-376_347-375ins others(1006): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089400 | ||||||
| chrX:47089401
|
A | AAATTATA others(1516): Show |
1 | a0001c0001t0002g0063 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.347-375_347-374ins others(1523): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089401 | ||||||
| chrX:47089401
|
A | AAATTATA others(1472): Show |
2 | a0001c0001t0001g0251a0001c0001t0001g0296 | 2 | HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.347-375_347-374ins others(1479): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089401 | ||||||
| chrX:47089401
|
A | AAATTATA others(1498): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0140 | 3 | HG00639.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.347-375_347-374ins others(1505): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089401 | ||||||
| chrX:47089401
|
A | AAATTATA others(1694): Show |
1 | a0001c0001t0001g0297 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.347-375_347-374ins others(1701): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089401 | ||||||
| chrX:47089401
|
A | AAATTATA others(1579): Show |
1 | a0001c0001t0002g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.347-375_347-374ins others(1586): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089401 | ||||||
| chrX:47089402
|
T | TTAATGTT others(1397): Show |
1 | a0001c0001t0015g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.347-374_347-373ins others(1404): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089402 | ||||||
| chrX:47089404
|
T | C | 8 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0140others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-372T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089404 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1437): Show |
1 | a0001c0001t0002g0071 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1444): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1442): Show |
1 | a0001c0001t0001g0133 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1449): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1440): Show |
1 | a0001c0001t0001g0119 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1447): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1442): Show |
1 | a0001c0001t0002g0001 | 2 | NA18941.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1449): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1389): Show |
1 | a0001c0001t0002g0096 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1396): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1514): Show |
1 | a0001c0001t0001g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1521): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1485): Show |
1 | a0001c0001t0001g0284 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1492): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1594): Show |
1 | a0001c0001t0001g0233 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1601): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1631): Show |
1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1638): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1553): Show |
1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1560): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1488): Show |
1 | a0001c0001t0001g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1495): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1437): Show |
1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1444): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1218): Show |
1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1225): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1489): Show |
1 | a0001c0001t0001g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1496): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1492): Show |
1 | a0001c0001t0003g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1499): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1527): Show |
3 | a0001c0001t0001g0163a0001c0001t0002g0065a0001c0001t0024g0079 | 3 | NA18960.hp1 NA19007.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1534): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1553): Show |
1 | a0001c0001t0002g0078 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1560): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1529): Show |
1 | a0001c0001t0002g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1536): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1555): Show |
1 | a0001c0001t0002g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1562): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1529): Show |
1 | a0001c0001t0002g0103 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1536): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1496): Show |
1 | a0001c0001t0006g0220 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1503): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1505): Show |
1 | a0001c0001t0002g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1512): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1560): Show |
1 | a0006c0007t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1567): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1495): Show |
1 | a0001c0001t0004g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1502): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1500): Show |
1 | a0001c0001t0004g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1507): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1386): Show |
1 | a0001c0001t0001g0172 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1393): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1464): Show |
3 | a0001c0001t0004g0032a0001c0001t0004g0202a0001c0001t0004g0230 | 3 | HG01123.hp2 HG01361.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1471): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1492): Show |
1 | a0001c0001t0001g0169 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1499): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1516): Show |
1 | a0001c0001t0004g0143 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1523): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1542): Show |
1 | a0001c0001t0004g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1549): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1383): Show |
1 | a0001c0001t0002g0066 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1390): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1513): Show |
1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1520): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1413): Show |
1 | a0011c0004t0001g0183 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1420): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1437): Show |
1 | a0001c0001t0001g0031 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1444): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1463): Show |
2 | a0001c0001t0002g0072a0001c0001t0002g0102 | 2 | NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1470): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1465): Show |
1 | a0001c0001t0001g0013 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1472): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1410): Show |
2 | a0001c0001t0001g0048a0001c0001t0001g0159 | 2 | NA18970.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1417): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1522): Show |
1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1529): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1520): Show |
1 | a0001c0001t0001g0187 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1527): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1466): Show |
1 | a0001c0001t0002g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1473): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0234 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1416): Show |
1 | a0001c0001t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1423): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1494): Show |
1 | a0001c0001t0001g0045 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1501): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1439): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0176 | 2 | NA18995.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1446): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1442): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0136a0001c0001t0001g0186others(1): Show | 4 | NA18963.hp2 NA19011.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-370_347-369ins others(1449): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1442): Show |
1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1449): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1466): Show |
1 | a0001c0001t0001g0273 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1473): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1465): Show |
1 | a0001c0001t0002g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1472): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1466): Show |
1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1473): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
2 | a0001c0001t0001g0206a0001c0001t0020g0181 | 2 | HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1494): Show |
1 | a0001c0001t0001g0117 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1501): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1520): Show |
1 | a0001c0001t0002g0060 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1527): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1538): Show |
1 | a0001c0001t0001g0279 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1545): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1385): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0027 | 2 | HG02735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1392): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1437): Show |
1 | a0001c0001t0001g0268 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1444): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1465): Show |
1 | a0001c0001t0001g0216 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1472): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1461): Show |
1 | a0001c0001t0001g0144 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1468): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1463): Show |
1 | a0001c0001t0001g0214 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1470): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1465): Show |
2 | a0001c0001t0001g0219a0001c0001t0001g0286 | 2 | NA18968.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1472): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1453): Show |
2 | a0001c0011t0001g0226a0009c0012t0011g0037 | 2 | NA18975.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1460): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1435): Show |
1 | a0001c0001t0006g0277 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1442): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1463): Show |
2 | a0001c0001t0001g0177a0001c0001t0002g0061 | 2 | NA18953.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1470): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1489): Show |
1 | a0004c0005t0001g0004 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1496): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1491): Show |
2 | a0001c0001t0001g0215a0001c0001t0001g0217 | 2 | NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1498): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1513): Show |
1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1520): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1432): Show |
1 | a0001c0001t0001g0138 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1439): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1409): Show |
1 | a0001c0001t0001g0020 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1416): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1372): Show |
1 | a0001c0001t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1379): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1491): Show |
1 | a0001c0001t0001g0116 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1498): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1417): Show |
1 | a0001c0001t0001g0218 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1424): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1412): Show |
1 | a0001c0001t0001g0015 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1419): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1466): Show |
1 | a0001c0001t0002g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1473): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1502): Show |
1 | a0001c0001t0001g0203 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1509): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1458): Show |
1 | a0001c0001t0001g0145 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1465): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1554): Show |
1 | a0001c0001t0001g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1561): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1466): Show |
1 | a0001c0001t0002g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1473): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1547): Show |
1 | a0001c0001t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1554): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1517): Show |
1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1524): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1270): Show |
1 | a0001c0001t0001g0127 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1277): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1295): Show |
1 | a0001c0001t0001g0122 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1302): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1531): Show |
1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1538): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1517): Show |
1 | a0001c0001t0002g0064 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1524): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1543): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0192 | 2 | NA18942.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1550): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
1 | a0001c0001t0001g0248 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1271): Show |
1 | a0001c0001t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1278): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1416): Show |
1 | a0001c0001t0002g0098 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1423): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1442): Show |
1 | a0001c0001t0002g0075 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1449): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1466): Show |
1 | a0001c0001t0001g0008 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1473): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0266 | 2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1503): Show |
1 | a0001c0001t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1510): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1473): Show |
1 | a0001c0001t0006g0229 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1480): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1513): Show |
1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1520): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1268): Show |
1 | a0001c0001t0002g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1275): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1532): Show |
1 | a0001c0001t0001g0272 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1539): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1502): Show |
1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1509): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1505): Show |
2 | a0001c0001t0001g0267a0001c0001t0009g0283 | 2 | HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1512): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1488): Show |
1 | a0001c0001t0001g0263 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1495): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1437): Show |
1 | a0001c0001t0002g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1444): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1270): Show |
1 | a0001c0001t0001g0212 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1277): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1611): Show |
1 | a0001c0001t0001g0264 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1618): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1386): Show |
1 | a0001c0001t0001g0160 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1393): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1388): Show |
2 | a0001c0001t0001g0161a0001c0001t0002g0070 | 2 | NA18950.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1395): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1494): Show |
1 | a0001c0001t0001g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1501): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1441): Show |
1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1448): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1364): Show |
1 | a0001c0001t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1371): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1445): Show |
1 | a0001c0001t0002g0095 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1452): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1468): Show |
1 | a0001c0001t0002g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1475): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1442): Show |
1 | a0001c0001t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1449): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1520): Show |
1 | a0001c0001t0010g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1527): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1474): Show |
1 | a0001c0001t0006g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1481): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1463): Show |
1 | a0001c0001t0001g0131 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1470): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1610): Show |
1 | a0001c0001t0001g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1617): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1562): Show |
1 | a0001c0001t0001g0300 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1569): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1532): Show |
1 | a0001c0001t0003g0241 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1539): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1588): Show |
1 | a0001c0001t0005g0258 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1595): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1564): Show |
1 | a0001c0001t0003g0298 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1571): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1526): Show |
1 | a0003c0003t0001g0257 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1533): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1385): Show |
1 | a0003c0003t0001g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1392): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1396): Show |
1 | a0001c0001t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1403): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1541): Show |
1 | a0001c0001t0001g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1548): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1467): Show |
1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1474): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1531): Show |
1 | a0001c0001t0001g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1538): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1495): Show |
1 | a0001c0001t0001g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1502): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1460): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0276a0010c0013t0019g0287 | 3 | HG01255.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1467): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1517): Show |
1 | a0001c0001t0001g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1524): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1522): Show |
1 | a0001c0001t0013g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1529): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1584): Show |
1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1591): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1610): Show |
1 | a0001c0001t0001g0207 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1617): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1636): Show |
1 | a0001c0001t0014g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1643): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1607): Show |
1 | a0001c0001t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1614): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1739): Show |
1 | a0001c0001t0001g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1746): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1647): Show |
2 | a0001c0001t0001g0003a0008c0006t0001g0227 | 3 | HG02109.hp1 HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1654): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1647): Show |
2 | a0001c0001t0005g0260a0001c0001t0012g0112 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1654): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1642): Show |
1 | a0001c0001t0001g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1649): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1367): Show |
1 | a0001c0001t0005g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1374): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1492): Show |
1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1499): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1383): Show |
1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1390): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1502): Show |
1 | a0001c0001t0001g0292 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1509): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1461): Show |
1 | a0001c0001t0001g0198 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1468): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1503): Show |
1 | a0001c0001t0001g0178 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1510): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1558): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0146 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1565): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1604): Show |
1 | a0001c0001t0001g0039 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1611): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1578): Show |
1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1585): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1469): Show |
1 | a0001c0001t0002g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1476): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1544): Show |
1 | a0001c0001t0001g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1551): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1578): Show |
1 | a0001c0001t0001g0028 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1585): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1552): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0164 | 2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1559): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1599): Show |
1 | a0001c0001t0001g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1606): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1651): Show |
1 | a0001c0001t0022g0007 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1658): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1599): Show |
1 | a0001c0001t0001g0012 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.347-370_347-369ins others(1606): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1574): Show |
1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1581): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1512): Show |
2 | a0001c0001t0007g0288a0001c0001t0007g0290 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.347-370_347-369ins others(1519): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1511): Show |
1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1518): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
T | TTAATGTT others(1539): Show |
1 | a0001c0001t0016g0301 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.347-370_347-369ins others(1546): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089406 | ||||||
| chrX:47089406
|
TA | T | 1 | a0001c0001t0015g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.347-368delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089406 | |||||
| chrX:47089407
|
A | AT | 8 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0140others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-369_347-368ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089407 | ||||||
| chrX:47089407
|
A | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.347-369A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089407 | ||||||
| chrX:47089407
|
AATC | A | 1 | a0001c0001t0001g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.347-366_347-364del others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089407 | |||||
| chrX:47089410
|
C | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(190): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.347-366C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089410 | ||||||
| chrX:47089486
|
AT | A | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-289delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089486 | ||||||
| chrX:47089510
|
T | TA | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-265dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089510 | |||||
| chrX:47089515
|
ACATATTA others(8): Show |
A | 1 | a0001c0001t0001g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.347-255_347-241del others(15): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089515 | |||||
| chrX:47089526
|
A | G | 2 | a0001c0001t0002g0072a0001c0001t0002g0102 | 2 | NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.347-250A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089526 | ||||||
| chrX:47089528
|
AC | A | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-247delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089528 | ||||||
| chrX:47089530
|
T | A | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-246T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089530 | ||||||
| chrX:47089530
|
T | TTATATAT others(37): Show |
1 | a0001c0001t0013g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.347-246_347-245ins others(44): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089530 | ||||||
| chrX:47089530
|
TCA | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.347-245_347-244del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089530 | ||||||
| chrX:47089532
|
A | T | 3 | a0001c0001t0001g0247a0001c0001t0013g0239a0007c0009t0001g0051 | 3 | HG02486.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-244A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089532 | ||||||
| chrX:47089549
|
A | AT | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-226dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089549 | |||||
| chrX:47089552
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(191): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.347-224C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089552 | ||||||
| chrX:47089579
|
T | TA | 158 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.347-197_347-196ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089579 | ||||||
| chrX:47089579
|
T | TATA | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.347-197_347-196ins others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089579 | ||||||
| chrX:47089579
|
T | TTA | 3 | a0001c0001t0001g0190a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG00099.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.347-178_347-177dup others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089579 | |||||
| chrX:47089579
|
TTA | T | 2 | a0001c0001t0001g0110a0001c0001t0017g0182 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.347-178_347-177del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089579 | |||||
| chrX:47089579
|
TTATA | T | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.347-180_347-177del others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089579 | |||||
| chrX:47089583
|
A | ACATAT | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.347-193_347-192ins others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089583 | ||||||
| chrX:47089585
|
A | ACATAT | 156 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(153): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.347-191_347-190ins others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089585 | ||||||
| chrX:47089586
|
T | C | 2 | a0006c0007t0001g0129a0007c0009t0001g0051 | 2 | NA18951.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-190T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089586 | ||||||
| chrX:47089589
|
A | AT | 1 | a0006c0007t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.347-186dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089589 | |||||
| chrX:47089590
|
TA | T | 1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-185delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089590 | ||||||
| chrX:47089591
|
A | ACTT | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.347-185_347-184ins others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089591 | ||||||
| chrX:47089593
|
A | AC | 146 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.347-183_347-182ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089593 | ||||||
| chrX:47089593
|
A | ACTT | 10 | a0001c0001t0001g0119a0001c0001t0001g0133a0001c0001t0001g0256others(7): Show | 10 | HG00140.hp1 HG00621.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-183_347-182ins others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089593 | ||||||
| chrX:47089595
|
A | T | 146 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.347-181A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089595 | ||||||
| chrX:47089596
|
T | TAC | 1 | a0001c0001t0002g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.347-179_347-178ins others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089596 | |||||
| chrX:47089597
|
A | ACTT | 1 | a0006c0007t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.347-179_347-178ins others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089597 | ||||||
| chrX:47089598
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0002g0055 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.347-178T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089598 | ||||||
| chrX:47089598
|
T | TAC | 10 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0041others(7): Show | 10 | HG02132.hp1 HG02165.hp2 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-144_347-143dup others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
T | TACAC | 1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.347-146_347-143dup others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
T | TATAC | 1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.347-177_347-176ins others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
TAC | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00323.hp2 HG01081.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-144_347-143del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
TACAC | T | 12 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0104others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-146_347-143del others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
TACACAC | T | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.347-148_347-143del others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0013g0239a0001c0001t0016g0301 | 2 | HG03486.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.347-156_347-143del others(14): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089598
|
TACACACA others(9): Show |
T | 33 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 34 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.347-158_347-143del others(16): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089598 | |||||
| chrX:47089600
|
C | CTTTATAT others(3): Show |
1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-176_347-175ins others(10): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089600 | ||||||
| chrX:47089600
|
C | T | 162 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.347-176C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089600 | ||||||
| chrX:47089602
|
C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.347-174C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089602 | ||||||
| chrX:47089604
|
C | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.347-172C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089604 | ||||||
| chrX:47089606
|
C | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.347-170C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089606 | ||||||
| chrX:47089608
|
C | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(156): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.347-168C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089608 | ||||||
| chrX:47089610
|
C | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(156): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.347-166C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089610 | ||||||
| chrX:47089612
|
C | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(156): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.347-164C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089612 | ||||||
| chrX:47089614
|
C | T | 154 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.347-162C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089614 | ||||||
| chrX:47089616
|
C | T | 2 | a0001c0001t0001g0273a0006c0007t0001g0129 | 2 | NA18951.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.347-160C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089616 | ||||||
| chrX:47089630
|
CACAT | C | 1 | a0001c0001t0001g0196 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.347-144_347-141del others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089630 | |||||
| chrX:47089632
|
C | CAT | 4 | a0001c0001t0001g0147a0001c0001t0001g0285a0001c0001t0002g0084others(1): Show | 4 | HG00558.hp2 NA18747.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-133_347-132dup others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089632 | |||||
| chrX:47089634
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.347-142T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089634 | ||||||
| chrX:47089639
|
AT | A | 1 | a0006c0007t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.347-136delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089639 | ||||||
| chrX:47089698
|
TC | T | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-75delC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 47089698 | |||||
| chrX:47090004
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(191): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.562+13C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090004 | ||||||
| chrX:47090050
|
CTAG | C | 1 | a0002c0002t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.562+62_562+64delGT others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090050 | |||||
| chrX:47090176
|
T | TC | 1 | a0001c0001t0002g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.562+187dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090176 | |||||
| chrX:47090226
|
TG | T | 1 | a0001c0001t0002g0095 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.562+239delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090226 | |||||
| chrX:47090244
|
A | AT | 1 | a0006c0007t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.562+254dupT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090244 | |||||
| chrX:47090277
|
CT | C | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.562+290delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090277 | |||||
| chrX:47090325
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.562+334C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090325 | ||||||
| chrX:47090486
|
C | CA | 2 | a0001c0001t0001g0232a0001c0001t0002g0255 | 2 | HG01928.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.562+506dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090486 | |||||
| chrX:47090486
|
CA | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0267a0001c0001t0002g0095 | 3 | HG01433.hp1 NA18949.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.562+506delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090486 | |||||
| chrX:47090566
|
G | GA | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.562+577dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090566 | |||||
| chrX:47090667
|
G | GA | 1 | a0001c0001t0002g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.562+682dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090667 | |||||
| chrX:47090731
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.562+740T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090731 | ||||||
| chrX:47090811
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.562+820C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090811 | ||||||
| chrX:47090812
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.562+821G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090812 | ||||||
| chrX:47090859
|
C | CA | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.563-809dupA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090859 | |||||
| chrX:47090867
|
AAAGAAAG others(16): Show |
A | 1 | a0001c0001t0001g0166 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.563-792_563-770del others(23): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090867 | |||||
| chrX:47090884
|
A | AG | 1 | a0001c0001t0001g0013 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.563-794_563-793ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090884 | ||||||
| chrX:47090890
|
G | GAAGA | 3 | a0001c0001t0001g0208a0001c0001t0001g0250a0001c0001t0001g0262 | 3 | HG01891.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.563-770_563-767dup others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090890 | |||||
| chrX:47090900
|
AGAAAGAA others(8): Show |
A | 2 | a0001c0001t0005g0106a0001c0001t0005g0261 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.563-766_563-752del others(15): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090900 | |||||
| chrX:47090906
|
AAAG | A | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.563-765_563-763del others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090906 | |||||
| chrX:47090908
|
AGAAGAAG | A | 1 | a0001c0001t0001g0196 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.563-766_563-760del others(7): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090908 | |||||
| chrX:47090909
|
G | GAAGAAAG others(52): Show |
1 | a0007c0009t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.563-764_563-763ins others(59): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090909 | |||||
| chrX:47090909
|
G | GAAGAAAG others(56): Show |
2 | a0001c0001t0007g0288a0001c0001t0007g0290 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.563-764_563-763ins others(63): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090909 | |||||
| chrX:47090909
|
G | GAAGAAAG others(40): Show |
4 | a0001c0001t0001g0256a0001c0001t0001g0276a0001c0001t0013g0239others(1): Show | 4 | HG01255.hp1 HG03486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-764_563-763ins others(47): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090909 | |||||
| chrX:47090909
|
G | GAAGAAAG others(44): Show |
1 | a0001c0001t0001g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.563-764_563-763ins others(51): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090909 | |||||
| chrX:47090909
|
GAAGAAGG others(1): Show |
G | 1 | a0001c0001t0002g0091 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.563-763_563-756del others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090909 | |||||
| chrX:47090911
|
A | AG | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.563-766dupG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090911 | |||||
| chrX:47090911
|
A | AGAAAGAA others(49): Show |
1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.563-764_563-763ins others(56): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090911 | |||||
| chrX:47090911
|
A | AGAAAGAA others(64): Show |
1 | a0001c0001t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.563-764_563-763ins others(71): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090911 | |||||
| chrX:47090911
|
A | AGAAAGAA others(60): Show |
1 | a0003c0003t0001g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.563-764_563-763ins others(67): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090911 | |||||
| chrX:47090912
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01081.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.563-766G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090912 | ||||||
| chrX:47090912
|
GAAGGAAA others(2): Show |
G | 1 | a0001c0001t0002g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.563-762_563-754del others(9): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090912 | |||||
| chrX:47090913
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01081.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.563-765A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090913 | ||||||
| chrX:47090915
|
G | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.563-763G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090915 | ||||||
| chrX:47090915
|
G | GAA | 1 | a0001c0001t0001g0166 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.563-763_563-762ins others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090915 | ||||||
| chrX:47090915
|
G | GGAAA | 11 | a0001c0001t0001g0022a0001c0001t0001g0111a0001c0001t0001g0165others(8): Show | 11 | HG00099.hp2 HG00323.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.563-696_563-693dup others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090915
|
G | GGAAAGAA others(1): Show |
4 | a0001c0001t0001g0153a0001c0001t0001g0222a0001c0001t0001g0238others(1): Show | 4 | HG00642.hp1 HG01516.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-700_563-693dup others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090915
|
G | GGAAAGAA others(5): Show |
1 | a0001c0001t0001g0033 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.563-704_563-693dup others(12): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090915
|
GGA | G | 1 | a0001c0001t0001g0009 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.563-762_563-761del others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090915 | ||||||
| chrX:47090915
|
GGAAA | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0107a0001c0001t0001g0114others(14): Show | 17 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.563-696_563-693del others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090915
|
GGAAAGAA others(1): Show |
G | 14 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0044others(11): Show | 15 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.563-700_563-693del others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090915
|
GGAAAGAA others(5): Show |
G | 11 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0104others(8): Show | 11 | HG02015.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.563-704_563-693del others(12): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090915
|
GGAAAGAA others(9): Show |
G | 6 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0232others(3): Show | 6 | HG01192.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-708_563-693del others(16): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090915 | |||||
| chrX:47090916
|
GAAAGA | G | 1 | a0001c0001t0001g0224 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.563-759_563-755del others(5): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090916 | |||||
| chrX:47090917
|
A | AAAG | 173 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(170): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.563-758_563-756dup others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090917 | |||||
| chrX:47090919
|
A | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(5): Show | 8 | HG00741.hp2 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.563-759A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090919 | ||||||
| chrX:47090920
|
GA | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0094a0001c0001t0001g0131others(1): Show | 4 | HG01099.hp1 HG03130.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-755delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090920 | |||||
| chrX:47090921
|
A | AAG | 1 | a0001c0001t0002g0098 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.563-756_563-755ins others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090921 | |||||
| chrX:47090927
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0196a0001c0001t0002g0255 | 3 | HG01099.hp1 HG01928.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.563-751A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090927 | ||||||
| chrX:47090928
|
GA | G | 2 | a0001c0001t0005g0106a0001c0001t0005g0261 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.563-747delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090928 | |||||
| chrX:47090931
|
A | AGAAGAAA others(1): Show |
1 | a0001c0001t0001g0166 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.563-744_563-743ins others(8): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090931 | |||||
| chrX:47090935
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0081others(5): Show | 8 | HG02258.hp1 HG02886.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.563-743A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090935 | ||||||
| chrX:47090939
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.563-739A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090939 | ||||||
| chrX:47090943
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(165): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.563-735A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090943 | ||||||
| chrX:47090944
|
G | GAA | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.563-732_563-731dup others(2): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090944 | |||||
| chrX:47090944
|
G | GAAAGAAA others(15): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0176 | 2 | NA18995.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.563-724_563-723ins others(22): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090944 | |||||
| chrX:47090944
|
GAAAGAAA others(6): Show |
G | 7 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0185others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.563-731_563-719del others(13): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090944 | |||||
| chrX:47090947
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0131others(9): Show | 12 | HG01255.hp1 HG02647.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.563-731A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090947 | ||||||
| chrX:47090949
|
A | AG | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.563-729_563-728ins others(1): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090949 | ||||||
| chrX:47090951
|
A | G | 5 | a0001c0001t0001g0235a0001c0001t0001g0256a0001c0001t0001g0276others(2): Show | 5 | HG01255.hp1 HG02647.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-727A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090951 | ||||||
| chrX:47090956
|
G | GGAAA | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.563-722_563-721ins others(4): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090956 | ||||||
| chrX:47090956
|
GA | G | 1 | a0001c0001t0002g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.563-719delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090956 | |||||
| chrX:47090957
|
A | AAAGAAAG others(30): Show |
1 | a0001c0001t0001g0028 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.563-712_563-711ins others(37): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090957 | |||||
| chrX:47090957
|
A | AAAGAAAG others(34): Show |
1 | a0001c0001t0004g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.563-712_563-711ins others(41): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090957 | |||||
| chrX:47090957
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.563-721A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090957 | ||||||
| chrX:47090960
|
GA | G | 6 | a0001c0001t0001g0080a0001c0001t0001g0205a0001c0001t0007g0288others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-715delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090960 | |||||
| chrX:47090961
|
A | AAAG | 8 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0176others(5): Show | 8 | HG01255.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.563-714_563-712dup others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAAGAAAG others(48): Show |
1 | a0001c0001t0005g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.563-704_563-703ins others(55): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAAGAAAG others(30): Show |
1 | a0001c0001t0001g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.563-708_563-707ins others(37): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAAGAAAG others(34): Show |
1 | a0001c0001t0003g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.563-708_563-707ins others(41): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAAGAAAG others(44): Show |
1 | a0001c0001t0001g0292 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.563-708_563-707ins others(51): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAAGAAGG others(26): Show |
15 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0029others(12): Show | 15 | HG00558.hp1 HG00609.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.563-712_563-711ins others(33): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAAGAAGG others(30): Show |
37 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0046others(34): Show | 38 | HG00140.hp1 HG00639.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.563-712_563-711ins others(37): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAGGAAGG others(22): Show |
1 | a0001c0001t0002g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.563-716_563-715ins others(29): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAGGAAGG others(26): Show |
114 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(111): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.563-716_563-715ins others(33): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAGGAAGG others(27): Show |
1 | a0005c0010t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.563-716_563-715ins others(34): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAGGAAGG others(60): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0081 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.563-716_563-715ins others(67): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090961
|
A | AAGGAAGG others(63): Show |
1 | a0001c0001t0001g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.563-716_563-715ins others(70): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090961 | |||||
| chrX:47090964
|
G | GAAAGAA | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.563-712_563-707dup others(6): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090964 | |||||
| chrX:47090965
|
A | AAGGAAGG others(26): Show |
1 | a0001c0001t0001g0131 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.563-712_563-711ins others(33): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47090965 | |||||
| chrX:47091133
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.563-545C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47091133 | ||||||
| chrX:47091138
|
A | AC | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.563-534dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47091138 | |||||
| chrX:47091145
|
T | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01081.hp1 HG01243.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-533T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47091145 | ||||||
| chrX:47091337
|
G | A | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.563-341G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47091337 | ||||||
| chrX:47091405
|
CA | C | 1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.563-268delA | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47091405 | |||||
| chrX:47091447
|
CT | C | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.563-225delT | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 47091447 | |||||
| chrX:47091605
|
G | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.563-73G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47091605 | ||||||
| chrX:47092033
|
A | AC | 1 | a0001c0001t0016g0301 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.695-27dupC | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 47092033 | |||||
| chrX:47092336
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG03195.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.849+121C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092336 | ||||||
| chrX:47092448
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.849+233T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092448 | ||||||
| chrX:47092652
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850-245G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092652 | ||||||
| chrX:47092674
|
GTTT | G | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-221_850-219del others(3): Show |
RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 47092674 | |||||
| chrX:47092718
|
T | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.850-179T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092718 | ||||||
| chrX:47092761
|
G | T | 1 | a0001c0001t0002g0075 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.850-136G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092761 | ||||||
| chrX:47092820
|
A | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.850-77A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092820 |