Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 299 | 66 | 57 | 133 | 11 | 30 | 104 | RGN_chrX_47073443_47098313 | RGN | MSSIK others(294): Show |
chrX | 47073443 | 47098313 |
| a0002 | 0/0 | 299 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RGN_chrX_47073443_47098313 | RGN | MSSIK others(294): Show |
chrX | 47073443 | 47098313 |
| a0003 | 0/0 | 299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | MSSIK others(294): Show |
chrX | 47073443 | 47098313 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 897 | 296 | 66 | 57 | 130 | 11 | 30 | RGN_chrX_47073443_47098313 | RGN | ATGTC others(892): Show |
chrX | 47073443 | 47098313 | ||
| a0001c0004 | 0/0 | 897 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | ATGTC others(892): Show |
chrX | 47073443 | 47098313 | ||
| a0001c0005 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | ATGTC others(892): Show |
chrX | 47073443 | 47098313 | ||
| a0002c0002 | 0/0 | 897 | 3 | 0 | 0 | 3 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | ATGTC others(892): Show |
chrX | 47073443 | 47098313 | ||
| a0003c0003 | 0/0 | 897 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | ATGTC others(892): Show |
chrX | 47073443 | 47098313 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2168 | 206 | 48 | 34 | 88 | 8 | 26 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0002 | 0/0 | 2168 | 52 | 0 | 15 | 34 | 2 | 1 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0003 | 0/0 | 2168 | 9 | 7 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0004 | 0/0 | 2168 | 7 | 0 | 3 | 0 | 1 | 3 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0005 | 0/0 | 2169 | 5 | 5 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2164): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0006 | 0/0 | 2168 | 5 | 0 | 0 | 5 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0007 | 0/0 | 2168 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0008 | 0/0 | 2168 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0009 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0010 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0012 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0013 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0014 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0015 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0016 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0001t0017 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0004t0001 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0004t0011 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0001c0005t0001 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0002c0002t0001 | 0/0 | 2168 | 3 | 0 | 0 | 3 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| a0003c0003t0001 | 0/0 | 2168 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | AGACC others(2163): Show |
chrX | 47073443 | 47098313 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0016 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0055 | 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 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0167 | 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 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0174 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0115 | 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 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0007g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0010g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0012g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0013g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0015g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0016g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0001t0017g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0004t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0003c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| a0003c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0058 | EUR | GBR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | FIN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0066 | 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 | g0118 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0229 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0280 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0278 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0155 | 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 | g0233 | 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 | g0171 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | IBS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0224 | EUR | IBS | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02129 | hp1 | a0001 | c0001 | t0016 | g0085 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0092 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0231 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0244 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0090 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0253 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0087 | 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 | t0001 | g0047 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0109 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0263 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0091 | 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 | g0249 | SAS | BEB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18947 | hp1 | a0001 | c0005 | t0001 | g0173 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18956 | hp2 | a0001 | c0001 | t0013 | g0239 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18975 | hp1 | a0001 | c0004 | t0011 | g0040 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0104 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19056 | hp1 | a0001 | c0001 | t0017 | g0079 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0097 | 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 | g0207 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ASW | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0187 | 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 | g0129 | EUR | TSI | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0194 | SAS | GIH | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | CLM | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0055 | 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 | g0191 | AFR | USA | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0238 | REF | REF | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0162 | REF | REF | RGN_chrX_47073443_47098313 | RGN | chrX | 47073443 | 47098313 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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: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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:47084425 | A | C | 1 | a0001c0004 | 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 | a0001c0005 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX: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:47078529 | C | T | 1 | a0001c0001t0017 | 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:47078607 | C | T | 3 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0017 |
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: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:47080420 | C | A | 1 | a0001c0001t0016 | 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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0014 others(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:47080544 | C | T | 1 | a0001c0001t0013 | 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 | a0001c0001t0014 | 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: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:47080892 | T | C | 1 | a0001c0001t0009 | 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 | a0001c0001t0010 | 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 | a0001c0004t0011 | 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 | a0001c0004t0011 | 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:47081141 | G | A | 1 | a0001c0001t0012 | 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 | a0001c0001t0008 a0001c0001t0015 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:47078743 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-636+34C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47078743 | |||||||
| chrX:47078844 | G | T | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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:47078941 | G | GC | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0282 others(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:47078948 | A | C | 1 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0240 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0277 a0001c0001t0001g0279 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0038 others(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:47078986 | G | T | 1 | a0001c0001t0001g0276 | 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 | 58 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0081 others(55): 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:47079231 | A | C | 4 | a0001c0001t0001g0279 a0001c0001t0001g0281 a0001c0001t0007g0278 others(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:47079356 | G | GT | 24 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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:47079358 | T | G | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
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 | a0001c0001t0001g0038 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-636+651T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079360 | |||||||
| chrX:47079364 | TTTTG | T | 156 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): 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 | a0001c0001t0001g0055 a0001c0001t0001g0086 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0230 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0154 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0246 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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:47079417 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-636+708T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079417 | |||||||
| chrX:47079438 | G | GT | 13 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0233 others(10): 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 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-636+729G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079438 | |||||||
| chrX:47079439 | T | G | 1 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-635-780T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079537 | |||||||
| chrX:47079642 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0273 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-635-645C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079672 | |||||||
| chrX:47079823 | T | C | 1 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-635-416A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079901 | |||||||
| chrX:47079926 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): 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:47079950 | C | T | 1 | a0001c0001t0009g0231 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-635-367C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47079950 | |||||||
| chrX:47080089 | C | A | 1 | a0001c0004t0011g0040 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-228C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47080089 | |||||||
| chrX:47080213 | C | A | 1 | a0001c0004t0011g0040 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-635-104C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 1/7 | chrX | 47080213 | |||||||
| chrX:47080975 | G | A | 2 | a0001c0001t0003g0102 a0001c0001t0014g0104 |
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 | a0001c0001t0002g0057 | 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 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15-36C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 2/7 | chrX | 47081094 | |||||||
| chrX:47081334 | AGCCAGCT others(18): Show |
A | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
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:47081355 | G | A | 1 | a0001c0001t0008g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+48G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081355 | |||||||
| chrX:47081362 | C | G | 1 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.163+177T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081484 | |||||||
| chrX:47081522 | T | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | TG | T | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(79): Show |
84 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.163+226delG | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 47081522 | ||||||
| chrX:47081523 | G | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): 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 | 71 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(68): 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0038 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163+226G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081533 | |||||||
| chrX:47081616 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0271 a0001c0001t0001g0272 |
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:47081689 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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:47081770 | C | A | 1 | a0001c0004t0011g0040 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163+463C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081770 | |||||||
| chrX:47081826 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
15 | HG00323.hp1 HG00741.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.163+519C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47081826 | |||||||
| chrX:47082011 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.163+704T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082011 | |||||||
| chrX:47082059 | G | A | 196 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.163+752G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082059 | |||||||
| chrX:47082135 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.163+828C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082135 | |||||||
| chrX:47082303 | C | CT | 34 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0049 others(31): Show |
35 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(32): 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 | CTT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | 69 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0016 others(66): 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 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0030 others(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 | CT | C | 20 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(17): 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:47082361 | A | G | 97 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0028 others(94): 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:47082456 | A | G | 5 | a0001c0001t0001g0096 a0001c0001t0001g0270 a0001c0001t0003g0012 others(2): 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 | a0001c0001t0010g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.163+1158C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082465 | |||||||
| chrX:47082514 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1207T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47082514 | |||||||
| chrX:47082604 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0232 |
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:47082783 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0009 |
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:47083099 | T | A | 1 | a0001c0004t0011g0040 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-1319T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083099 | |||||||
| chrX:47083100 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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:47083136 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-1282T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083136 | |||||||
| chrX:47083254 | G | A | 2 | a0001c0001t0005g0125 a0001c0001t0005g0253 |
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:47083328 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0002g0064 |
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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0132 a0001c0001t0001g0202 others(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:47083472 | G | C | 157 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(154): 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:47083557 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0025 others(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:47083621 | G | A | 1 | a0001c0001t0005g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164-797G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083621 | |||||||
| chrX:47083776 | G | A | 1 | a0001c0001t0005g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164-642G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083776 | |||||||
| chrX:47083914 | AAC | A | 16 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 others(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:47083916 | C | CA | 3 | a0001c0001t0001g0034 a0001c0001t0003g0234 a0001c0001t0003g0288 |
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:47083920 | A | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0052 others(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:47083921 | C | A | 46 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 others(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:47083925 | C | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(275): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.164-493C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083925 | |||||||
| chrX:47083926 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.164-492A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47083926 | |||||||
| chrX:47084052 | C | T | 1 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-344T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084074 | |||||||
| chrX:47084094 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.164-324C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084094 | |||||||
| chrX:47084139 | G | T | 188 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(185): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.164-279G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 3/7 | chrX | 47084139 | |||||||
| chrX:47084391 | T | A | 1 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0243 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.346+125G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084725 | |||||||
| chrX:47084756 | A | C | 187 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(184): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.346+156A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084756 | |||||||
| chrX:47084880 | A | C | 1 | a0001c0001t0003g0289 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.346+280A>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084880 | |||||||
| chrX:47084984 | T | A | 1 | a0003c0003t0001g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+384T>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47084984 | |||||||
| chrX:47085067 | CA | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0080 others(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:47085218 | G | A | 184 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(181): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): 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:47085377 | G | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0101 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.346+790G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085390 | |||||||
| chrX:47085641 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0053 others(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:47085898 | C | G | 214 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(211): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.346+1298C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47085898 | |||||||
| chrX:47086035 | A | G | 1 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0201 a0001c0001t0001g0215 a0001c0001t0001g0269 |
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:47086168 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.346+1568T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086168 | |||||||
| chrX:47086366 | T | A | 2 | a0002c0002t0001g0026 a0002c0002t0001g0036 |
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:47086410 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1810A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086410 | |||||||
| chrX:47086573 | G | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0217 a0001c0001t0001g0260 others(2): Show |
5 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(2): 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 | a0001c0001t0001g0170 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.346+2041C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086641 | |||||||
| chrX:47086734 | G | GGA | 24 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0039 others(21): 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 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0165 a0001c0001t0001g0182 others(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 | a0001c0001t0002g0097 | 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 | a0001c0001t0001g0044 a0001c0001t0002g0070 a0001c0001t0002g0088 others(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 | a0001c0001t0017g0079 | 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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0049 others(19): 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 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0043 others(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 | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(12): Show |
15 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(12): 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 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0290 a0001c0001t0008g0090 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0047 others(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 | 16 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0095 others(13): 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 | a0001c0001t0001g0086 a0001c0001t0005g0125 a0001c0001t0005g0253 |
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 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0264 others(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 | a0001c0001t0003g0235 | 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:47086783 | GA | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0228 a0001c0001t0001g0284 others(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 | AGAGAGAG others(2): Show |
3 | a0001c0001t0001g0176 a0001c0001t0001g0210 a0001c0001t0001g0271 |
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 | a0001c0001t0002g0071 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0008g0090 a0001c0001t0008g0092 |
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:47086933 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.346+2333G>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47086933 | |||||||
| chrX:47087005 | C | G | 187 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(184): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.346+2405C>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087005 | |||||||
| chrX:47087081 | G | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): 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 | a0001c0001t0002g0093 | 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:47087345 | A | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0183 a0001c0001t0002g0060 |
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:47087495 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.347-2281T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087495 | |||||||
| chrX:47087567 | T | C | 193 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(190): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.347-2209T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087567 | |||||||
| chrX:47087602 | T | A | 1 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0052 others(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:47087946 | A | G | 174 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(171): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.347-1830A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47087946 | |||||||
| chrX:47088070 | G | GCTATGCA others(28): Show |
1 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0136 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.347-1696T>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088080 | |||||||
| 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 | a0001c0001t0001g0152 | 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 | 185 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(182): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.347-1016C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47088760 | |||||||
| chrX:47088890 | C | T | 1 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0264 others(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:47088945 | AAAG | A | 17 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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:47088947 | AG | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0197 a0001c0001t0001g0281 |
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 | 156 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(153): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): 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 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 others(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:47089178 | G | GAGCAAGT others(1124): Show |
1 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0287 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0054 a0001c0001t0001g0119 a0001c0001t0001g0168 others(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 |
125 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0016 others(122): 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 | a0001c0001t0005g0251 | 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0272 | 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 |
29 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(26): Show |
30 | HG00140.hp1 HG02109.hp1 HG02109.hp2 others(27): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0132 | 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:47089342 | T | A | 1 | a0001c0001t0001g0153 | 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 | a0001c0001t0012g0263 | 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:47089390 | A | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0193 others(4): 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:47089400 | A | AATATATT others(1090): Show |
1 | a0001c0001t0001g0275 | 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 |
1 | a0001c0001t0002g0003 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0172 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0003g0289 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
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 | a0001c0001t0001g0219 | 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 | a0001c0001t0008g0092 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0154 | 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 | a0002c0002t0001g0026 a0002c0002t0001g0036 a0002c0002t0001g0124 |
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 | a0001c0001t0001g0128 | 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 | a0001c0001t0014g0104 | 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 | a0001c0001t0008g0090 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0201 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0262 |
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 |
2 | a0001c0001t0001g0156 a0001c0001t0002g0004 |
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 | a0001c0001t0002g0057 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0091 | 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 |
11 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0039 others(8): 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 |
1 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0226 a0001c0001t0002g0084 |
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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0228 |
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 | a0001c0005t0001g0173 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0159 |
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 |
5 | a0001c0001t0001g0096 a0001c0001t0001g0106 a0001c0001t0001g0189 others(2): 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 | a0001c0001t0003g0235 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0016g0085 | 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 | a0001c0001t0015g0229 | 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 |
1 | a0001c0001t0002g0009 | 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 | a0001c0001t0005g0253 | 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 | a0001c0001t0005g0125 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0002g0242 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0285 |
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 |
2 | a0001c0001t0001g0008 a0001c0001t0001g0133 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0002g0094 | 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 | a0001c0001t0012g0263 | 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 | 7 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0193 others(4): 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 | a0001c0001t0002g0069 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0002g0006 | 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 | a0001c0001t0002g0089 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0272 | 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(1631): Show |
1 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0165 a0001c0001t0002g0062 a0001c0001t0017g0079 |
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 | a0001c0001t0002g0070 | 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 | a0001c0001t0002g0071 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0002g0100 | 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 | a0001c0001t0006g0205 | 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0004g0224 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0004g0115 a0001c0001t0004g0194 a0001c0001t0004g0223 |
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 | a0001c0001t0001g0176 | 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 | a0001c0001t0004g0017 | 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 | a0001c0001t0002g0065 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0002g0073 a0001c0001t0002g0099 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0002g0064 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0225 |
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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0117 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0220 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0032 |
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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0210 a0001c0001t0001g0276 |
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 | a0001c0004t0001g0213 a0001c0004t0011g0040 |
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 | a0001c0001t0006g0265 | 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 | a0001c0001t0001g0183 a0001c0001t0002g0060 |
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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0207 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0136 | 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 | a0001c0001t0006g0222 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0167 a0001c0001t0002g0077 |
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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0002g0078 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0013g0239 | 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 | a0001c0001t0006g0268 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0003g0234 | 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 | a0001c0001t0005g0250 | 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 | a0001c0001t0003g0288 | 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 | a0003c0003t0001g0244 | 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 | a0003c0003t0001g0191 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0264 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0227 | 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 | a0001c0001t0010g0109 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0218 |
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 | a0001c0001t0005g0252 a0001c0001t0009g0231 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0005g0251 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0002g0056 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0168 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0007g0278 a0001c0001t0007g0280 |
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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0034 | 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:47089407 | A | AT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0193 others(4): 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 | 183 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(180): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.347-369A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089407 | |||||||
| chrX:47089410 | C | A | 191 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(188): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.347-366C>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089410 | |||||||
| chrX:47089515 | ACATATTA others(8): Show |
A | 1 | a0001c0001t0001g0232 | 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 | a0001c0001t0002g0073 a0001c0001t0002g0099 |
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:47089530 | T | A | 1 | a0001c0001t0001g0095 | 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 | a0001c0001t0010g0109 | 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 | 189 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(186): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): 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 | a0001c0001t0001g0095 a0001c0001t0001g0232 a0001c0001t0010g0109 |
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:47089552 | C | T | 192 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(189): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.347-224C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089552 | |||||||
| chrX:47089579 | T | TA | 156 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): 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 | TTA | 2 | a0001c0001t0001g0120 a0001c0001t0002g0009 |
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:47089585 | A | ACATAT | 154 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(151): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): 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 | a0001c0001t0001g0095 a0001c0001t0001g0134 |
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:47089593 | A | AC | 144 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(141): Show |
146 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(143): 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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0245 others(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 | 144 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(141): Show |
146 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.347-181A>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089595 | |||||||
| chrX:47089598 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0002g0091 |
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 | 9 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0044 others(6): 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 | TAC | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0096 others(8): 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 | TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0034 a0001c0001t0010g0109 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0095 | 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 | 160 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.347-176C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089600 | |||||||
| chrX:47089602 | C | T | 166 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(163): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.347-174C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089602 | |||||||
| chrX:47089604 | C | T | 158 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(155): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.347-172C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089604 | |||||||
| chrX:47089606 | C | T | 158 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(155): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.347-170C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089606 | |||||||
| chrX:47089608 | C | T | 157 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.347-168C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089608 | |||||||
| chrX:47089610 | C | T | 157 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.347-166C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089610 | |||||||
| chrX:47089612 | C | T | 157 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.347-164C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089612 | |||||||
| chrX:47089614 | C | T | 152 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0001g0134 a0001c0001t0001g0248 |
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:47089632 | C | CAT | 3 | a0001c0001t0001g0152 a0001c0001t0001g0275 a0001c0001t0002g0003 |
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 | a0001c0001t0001g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.347-142T>C | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 4/7 | chrX | 47089634 | |||||||
| chrX:47090004 | C | T | 192 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(189): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.562+13C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090004 | |||||||
| chrX:47090325 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.562+334C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090325 | |||||||
| chrX:47090731 | T | C | 1 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0002g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.562+821G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090812 | |||||||
| chrX:47090867 | AAAGAAAG others(16): Show |
A | 1 | a0001c0001t0001g0170 | 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:47090890 | G | GAAGA | 3 | a0001c0001t0001g0200 a0001c0001t0001g0230 a0001c0001t0001g0246 |
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 | a0001c0001t0005g0125 a0001c0001t0005g0253 |
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:47090909 | G | GAAGAAAG others(52): Show |
1 | a0001c0001t0001g0095 | 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 | a0001c0001t0007g0278 a0001c0001t0007g0280 |
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 | a0001c0001t0001g0245 a0001c0001t0001g0264 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0227 | 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: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 | a0001c0001t0001g0197 | 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 | a0003c0003t0001g0191 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 |
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:47090913 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | 188 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(185): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.563-763G>A | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090915 | |||||||
| chrX:47090915 | G | GGAAA | 10 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0159 others(7): 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 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0274 | 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 | GGAAA | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0101 others(13): 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 | 13 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(10): 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 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0152 a0001c0001t0001g0226 others(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:47090917 | A | AAAG | 171 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(168): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): 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 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0149 others(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:47090927 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0186 a0001c0001t0002g0243 |
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:47090935 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0015 | 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 | 166 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(163): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.563-735A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47090943 | |||||||
| chrX:47090944 | G | GAAAGAAA others(15): Show |
2 | a0001c0001t0001g0177 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0153 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0144 others(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:47090951 | A | G | 5 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0264 others(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:47090957 | A | AAAGAAAG others(30): Show |
1 | a0001c0001t0001g0014 | 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 | a0001c0001t0004g0194 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0177 a0001c0001t0001g0181 others(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 | a0001c0001t0005g0251 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(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 |
36 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0047 others(33): Show |
37 | HG00140.hp1 HG00639.hp1 HG01106.hp1 others(34): 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 | a0001c0001t0002g0056 | 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 |
113 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(110): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0281 | 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:47090965 | A | AAGGAAGG others(26): Show |
1 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0273 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.563-545C>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47091133 | |||||||
| chrX:47091145 | T | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
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:47091605 | G | T | 189 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(186): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.563-73G>T | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 5/7 | chrX | 47091605 | |||||||
| chrX:47092336 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
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:47092718 | T | A | 189 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(186): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): 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 | a0001c0001t0002g0076 | 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 | 189 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(186): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.850-77A>G | RGN | ENSG00000130988.13 | transcript | ENST00000397180.6 | protein_coding | 7/7 | chrX | 47092820 |