Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 53344 |
|---|---|
| ensemblid | ENSG00000204116.12 |
| hgncid | 1934 |
| symbol | CHIC1 |
| name | cysteine rich hydrophobic domain 1 |
| refseq_nuc | NM_001039840.4 |
| refseq_prot | NP_001034929.2 |
| ensembl_nuc | ENST00000373502.10 |
| ensembl_prot | ENSP00000362601.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 73563197 |
| end | 73687111 |
| strand | + |
| ver | v1.2 |
| region | chrX:73563197-73687111 |
| region5000 | chrX:73558197-73692111 |
| regionname0 | CHIC1_chrX_73563197_73687111 |
| regionname5000 | CHIC1_chrX_73558197_73692111 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 224 | 208 | 64 | 43 | 68 | 9 | 22 | 51 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 675 | 208 | 64 | 43 | 68 | 9 | 22 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6195 | 123 | 10 | 27 | 62 | 6 | 18 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0002 | 0/0 | 6195 | 29 | 15 | 9 | 0 | 3 | 2 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0003 | 0/0 | 6197 | 16 | 15 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0004 | 0/0 | 6195 | 9 | 8 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0005 | 0/0 | 6195 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0006 | 0/0 | 6195 | 3 | 3 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0007 | 0/0 | 6195 | 3 | 0 | 3 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0008 | 0/0 | 6195 | 3 | 3 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0009 | 0/0 | 6195 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0010 | 1/0 | 6195 | 2 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0011 | 0/0 | 6195 | 2 | 1 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0012 | 0/1 | 6195 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0013 | 0/0 | 6195 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0014 | 0/0 | 6195 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0015 | 0/0 | 6195 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0016 | 0/0 | 6195 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0017 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0018 | 0/0 | 6195 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0019 | 0/0 | 6195 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0020 | 0/0 | 6195 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0021 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0022 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| t0023 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 675 | 208 | 64 | 43 | 68 | 9 | 22 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6869 | 123 | 10 | 27 | 62 | 6 | 18 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0002 | 0/0 | 6869 | 29 | 15 | 9 | 0 | 3 | 2 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0003 | 0/0 | 6871 | 16 | 15 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0004 | 0/0 | 6869 | 9 | 8 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0005 | 0/0 | 6869 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0006 | 0/0 | 6869 | 3 | 3 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0007 | 0/0 | 6869 | 3 | 0 | 3 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0008 | 0/0 | 6869 | 3 | 3 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0009 | 0/0 | 6869 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0010 | 1/0 | 6869 | 2 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0011 | 0/0 | 6869 | 2 | 1 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0012 | 0/1 | 6869 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0013 | 0/0 | 6869 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0014 | 0/0 | 6869 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0015 | 0/0 | 6869 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0016 | 0/0 | 6869 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0017 | 0/0 | 6869 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0018 | 0/0 | 6869 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0019 | 0/0 | 6869 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0020 | 0/0 | 6869 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0021 | 0/0 | 6871 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0022 | 0/0 | 6871 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| a0001c0001t0023 | 0/0 | 6869 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | copy fasta | chrX | 73558197 | 73692111 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0010g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0012g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0013g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0014g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0015g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0018g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0019g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0021g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0022g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| a0001c0001t0023g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | FIN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01074 | hp1 | a0001 | c0001 | t0018 | g0038 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0201 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0055 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | IBS | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | IBS | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0072 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0100 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03017 | hp1 | a0001 | c0001 | t0019 | g0040 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0173 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | ESN | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0031 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | YRI | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0114 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18986 | hp1 | a0001 | c0001 | t0015 | g0165 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18989 | hp1 | a0001 | c0001 | t0020 | g0159 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18995 | hp1 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0099 | AFR | LWK | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19056 | hp1 | a0001 | c0001 | t0016 | g0156 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19079 | hp1 | a0001 | c0001 | t0013 | g0150 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0066 | AFR | YRI | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ASW | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | ASW | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | USA | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | USA | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | USA | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| NA20300 | hp2 | a0001 | c0001 | t0017 | g0046 | AFR | USA | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0052 | REF | REF | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0051 | REF | REF | CHIC1_chrX_73558197_73692111 | CHIC1 | chrX | 73558197 | 73692111 |
| 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 |
|---|
| 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 |
|---|
| 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:73681076
|
A | C | 1 | a0001c0001t0023 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 71 | chrX | 73681076 | |||||
| chrX:73681904
|
C | T | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(5): Show | 57 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*899C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 899 | chrX | 73681904 | |||||
| chrX:73682143
|
C | A | 1 | a0001c0001t0006 | 3 | HG02280.hp2 HG03195.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1138C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 1138 | chrX | 73682143 | |||||
| chrX:73682895
|
C | G | 1 | a0001c0001t0020 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1890C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 1890 | chrX | 73682895 | |||||
| chrX:73683088
|
G | A | 1 | a0001c0001t0012 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2083G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 2083 | chrX | 73683088 | |||||
| chrX:73683397
|
G | A | 1 | a0001c0001t0013 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2392G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 2392 | chrX | 73683397 | |||||
| chrX:73683530
|
G | T | 1 | a0001c0001t0005 | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2525G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 2525 | chrX | 73683530 | |||||
| chrX:73683752
|
T | G | 1 | a0001c0001t0014 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2747T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 2747 | chrX | 73683752 | |||||
| chrX:73684186
|
A | G | 1 | a0001c0001t0006 | 3 | HG02280.hp2 HG03195.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3181A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3181 | chrX | 73684186 | |||||
| chrX:73684322
|
A | T | 1 | a0001c0001t0005 | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3317A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3317 | chrX | 73684322 | |||||
| chrX:73684422
|
A | G | 1 | a0001c0001t0011 | 2 | HG01109.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3417A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3417 | chrX | 73684422 | |||||
| chrX:73684612
|
A | G | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(3): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3607A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3607 | chrX | 73684612 | |||||
| chrX:73684749
|
G | A | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(11): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3744G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3744 | chrX | 73684749 | |||||
| chrX:73684821
|
A | T | 1 | a0001c0001t0019 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3816A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3816 | chrX | 73684821 | |||||
| chrX:73684889
|
C | A | 1 | a0001c0001t0021 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3884C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3884 | chrX | 73684889 | |||||
| chrX:73684889
|
C | G | 1 | a0001c0001t0018 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3884C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 3884 | chrX | 73684889 | |||||
| chrX:73685213
|
C | CAT | 3 | a0001c0001t0003a0001c0001t0021a0001c0001t0022 | 18 | HG00735.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4208_*4209insAT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 4209 | chrX | 73685213 | |||||
| chrX:73685324
|
T | C | 1 | a0001c0001t0015 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4319T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 4319 | chrX | 73685324 | |||||
| chrX:73685474
|
C | T | 1 | a0001c0001t0017 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4469C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 4469 | chrX | 73685474 | |||||
| chrX:73685814
|
T | C | 1 | a0001c0001t0022 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4809T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 4809 | chrX | 73685814 | |||||
| chrX:73686152
|
G | A | 1 | a0001c0001t0004 | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5147G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 5147 | chrX | 73686152 | |||||
| chrX:73686242
|
A | C | 1 | a0001c0001t0016 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5237A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 5237 | chrX | 73686242 | |||||
| chrX:73686249
|
G | C | 1 | a0001c0001t0009 | 2 | NA18944.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5244G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 5244 | chrX | 73686249 | |||||
| chrX:73686615
|
T | C | 1 | a0001c0001t0007 | 3 | HG00639.hp1 HG01169.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5610T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 6/6 | 5610 | chrX | 73686615 |
| 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:73564178
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.296+598G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73564178 | ||||||
| chrX:73564508
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009 | 3 | HG00735.hp1 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.296+928G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73564508 | ||||||
| chrX:73564791
|
G | GT | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(113): Show | 117 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(114): Show |
intron_variant | MODIFIER | c.296+1234dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73564791 | |||||
| chrX:73564791
|
G | GTT | 26 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(23): Show | 26 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.296+1233_296+1234d others(4): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73564791 | |||||
| chrX:73564791
|
G | GTTT | 1 | a0001c0001t0002g0202 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.296+1232_296+1234d others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73564791 | |||||
| chrX:73564791
|
GT | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.296+1234delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73564791 | |||||
| chrX:73564827
|
C | CA | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.296+1248dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73564827 | |||||
| chrX:73565794
|
G | C | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.296+2214G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73565794 | ||||||
| chrX:73565958
|
C | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.296+2378C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73565958 | ||||||
| chrX:73566734
|
T | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.296+3154T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73566734 | ||||||
| chrX:73567199
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.296+3619C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73567199 | ||||||
| chrX:73567324
|
C | G | 2 | a0001c0001t0011g0173a0001c0001t0011g0201 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.296+3744C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73567324 | ||||||
| chrX:73567340
|
C | A | 5 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.296+3760C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73567340 | ||||||
| chrX:73567473
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.296+3893A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73567473 | ||||||
| chrX:73567801
|
G | GT | 3 | a0001c0001t0001g0062a0001c0001t0003g0076a0001c0001t0003g0077 | 3 | HG02647.hp1 HG02723.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.296+4232dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73567801 | |||||
| chrX:73568655
|
T | C | 6 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(3): Show | 6 | HG00738.hp1 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.296+5075T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73568655 | ||||||
| chrX:73569516
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.296+5936G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73569516 | ||||||
| chrX:73569626
|
A | T | 2 | a0001c0001t0002g0172a0001c0001t0002g0200 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.296+6046A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73569626 | ||||||
| chrX:73569874
|
A | G | 21 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 21 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.296+6294A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73569874 | ||||||
| chrX:73570506
|
G | A | 1 | a0001c0001t0004g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.297-6901G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73570506 | ||||||
| chrX:73571094
|
A | AAG | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.297-6309_297-6308d others(4): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73571094 | |||||
| chrX:73571206
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.297-6201G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73571206 | ||||||
| chrX:73571377
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.297-6030C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73571377 | ||||||
| chrX:73571558
|
G | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.297-5849G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73571558 | ||||||
| chrX:73571886
|
G | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.297-5521G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73571886 | ||||||
| chrX:73571950
|
G | GT | 1 | a0001c0001t0001g0198 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.297-5447dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73571950 | |||||
| chrX:73571995
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01081.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.297-5412C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73571995 | ||||||
| chrX:73572070
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.297-5337A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73572070 | ||||||
| chrX:73572614
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.297-4793C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73572614 | ||||||
| chrX:73572668
|
G | C | 1 | a0001c0001t0007g0021 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.297-4739G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73572668 | ||||||
| chrX:73573686
|
G | A | 5 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.297-3721G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73573686 | ||||||
| chrX:73574287
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297-3120G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73574287 | ||||||
| chrX:73574486
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.297-2921C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73574486 | ||||||
| chrX:73574487
|
G | A | 1 | a0001c0001t0003g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.297-2920G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73574487 | ||||||
| chrX:73574710
|
G | T | 1 | a0001c0001t0006g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.297-2697G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73574710 | ||||||
| chrX:73574897
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.297-2510A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73574897 | ||||||
| chrX:73575045
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.297-2362A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73575045 | ||||||
| chrX:73575350
|
G | A | 1 | a0001c0001t0004g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.297-2057G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73575350 | ||||||
| chrX:73575471
|
T | C | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.297-1936T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73575471 | ||||||
| chrX:73575667
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.297-1740G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73575667 | ||||||
| chrX:73575691
|
T | TGTGA | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.297-1696_297-1693d others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73575691 | |||||
| chrX:73575893
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.297-1514T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73575893 | ||||||
| chrX:73576086
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.297-1321A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73576086 | ||||||
| chrX:73576267
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.297-1140C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73576267 | ||||||
| chrX:73576415
|
AACATT | A | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.297-988_297-984del others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 73576415 | |||||
| chrX:73576859
|
G | A | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.297-548G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73576859 | ||||||
| chrX:73577077
|
T | C | 3 | a0001c0001t0002g0095a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | HG00323.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.297-330T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73577077 | ||||||
| chrX:73577224
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.297-183T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73577224 | ||||||
| chrX:73577274
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.297-133A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73577274 | ||||||
| chrX:73577343
|
T | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(17): Show | 20 | HG00642.hp1 HG01192.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.297-64T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73577343 | ||||||
| chrX:73577344
|
A | T | 6 | a0001c0001t0001g0056a0001c0001t0008g0096a0001c0001t0008g0097others(3): Show | 6 | HG02886.hp1 HG02970.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.297-63A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 1/5 | chrX | 73577344 | ||||||
| chrX:73577527
|
T | G | 2 | a0001c0001t0003g0076a0001c0001t0003g0077 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.351+66T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73577527 | ||||||
| chrX:73578067
|
A | G | 1 | a0001c0001t0007g0055 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.351+606A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73578067 | ||||||
| chrX:73578779
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.351+1318G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73578779 | ||||||
| chrX:73578884
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.351+1423G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73578884 | ||||||
| chrX:73578885
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.351+1424T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73578885 | ||||||
| chrX:73579720
|
A | T | 1 | a0001c0001t0003g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.351+2259A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73579720 | ||||||
| chrX:73579730
|
C | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2269C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73579730 | ||||||
| chrX:73579877
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.351+2416C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73579877 | ||||||
| chrX:73579882
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.351+2421T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73579882 | ||||||
| chrX:73579990
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.351+2529A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73579990 | ||||||
| chrX:73580289
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2828G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73580289 | ||||||
| chrX:73580395
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | NA18747.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2934G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73580395 | ||||||
| chrX:73580726
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.351+3265T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73580726 | ||||||
| chrX:73580728
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.351+3267A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73580728 | ||||||
| chrX:73580743
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.351+3282A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73580743 | ||||||
| chrX:73581232
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.352-3185C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73581232 | ||||||
| chrX:73581959
|
T | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-2458T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73581959 | ||||||
| chrX:73582064
|
AT | A | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.352-2343delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 73582064 | |||||
| chrX:73582342
|
T | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.352-2075T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73582342 | ||||||
| chrX:73582374
|
C | T | 32 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(29): Show | 32 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.352-2043C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73582374 | ||||||
| chrX:73582420
|
TAAGA | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.352-1996_352-1993d others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73582420 | ||||||
| chrX:73582469
|
C | CT | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.352-1938dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 73582469 | |||||
| chrX:73582497
|
C | T | 1 | a0001c0001t0011g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.352-1920C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73582497 | ||||||
| chrX:73582890
|
T | C | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0202 | 3 | HG01243.hp1 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.352-1527T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73582890 | ||||||
| chrX:73583179
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.352-1238G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73583179 | ||||||
| chrX:73583418
|
C | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-999C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73583418 | ||||||
| chrX:73583740
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.352-677C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73583740 | ||||||
| chrX:73583873
|
A | C | 1 | a0001c0001t0003g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352-544A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73583873 | ||||||
| chrX:73583969
|
A | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.352-448A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73583969 | ||||||
| chrX:73584061
|
T | C | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-356T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73584061 | ||||||
| chrX:73584163
|
A | G | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0184 | 3 | HG02055.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.352-254A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | chrX | 73584163 | ||||||
| chrX:73584246
|
ATTG | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.352-166_352-164del others(3): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 73584246 | |||||
| chrX:73584985
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+413T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73584985 | ||||||
| chrX:73585494
|
G | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(135): Show | 139 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.507+922G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73585494 | ||||||
| chrX:73585755
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.507+1183G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73585755 | ||||||
| chrX:73585999
|
A | G | 2 | a0001c0001t0006g0003a0001c0001t0006g0059 | 3 | HG02280.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.507+1427A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73585999 | ||||||
| chrX:73586147
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.507+1575G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586147 | ||||||
| chrX:73586156
|
G | A | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+1584G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586156 | ||||||
| chrX:73586324
|
C | T | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0084others(1): Show | 4 | HG02451.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+1752C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586324 | ||||||
| chrX:73586542
|
T | G | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+1970T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586542 | ||||||
| chrX:73586596
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.507+2024A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586596 | ||||||
| chrX:73586788
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.507+2216G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586788 | ||||||
| chrX:73586859
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+2287G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73586859 | ||||||
| chrX:73587271
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.507+2699G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73587271 | ||||||
| chrX:73587360
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+2788G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73587360 | ||||||
| chrX:73587865
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.507+3293G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73587865 | ||||||
| chrX:73588034
|
C | T | 1 | a0001c0001t0015g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.507+3462C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73588034 | ||||||
| chrX:73588371
|
G | T | 1 | a0001c0001t0007g0021 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.507+3799G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73588371 | ||||||
| chrX:73588412
|
C | T | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+3840C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73588412 | ||||||
| chrX:73588461
|
C | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0186 | 3 | HG02080.hp1 NA18965.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.507+3889C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73588461 | ||||||
| chrX:73588775
|
T | G | 1 | a0001c0001t0011g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.507+4203T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73588775 | ||||||
| chrX:73589517
|
G | A | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.507+4945G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73589517 | ||||||
| chrX:73589539
|
ATGT | A | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.507+4975_507+4977d others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73589539 | |||||
| chrX:73589725
|
A | G | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+5153A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73589725 | ||||||
| chrX:73589928
|
T | C | 1 | a0001c0001t0015g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.507+5356T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73589928 | ||||||
| chrX:73590107
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+5535A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73590107 | ||||||
| chrX:73590450
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01081.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.507+5878C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73590450 | ||||||
| chrX:73590552
|
A | G | 3 | a0001c0001t0006g0003a0001c0001t0006g0059a0001c0001t0010g0100 | 4 | HG02280.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+5980A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73590552 | ||||||
| chrX:73591189
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.507+6617G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73591189 | ||||||
| chrX:73591954
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.507+7382C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73591954 | ||||||
| chrX:73592067
|
GT | G | 5 | a0001c0001t0001g0029a0001c0001t0005g0010a0001c0001t0005g0011others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+7505delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73592067 | |||||
| chrX:73592129
|
A | G | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.507+7557A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592129 | ||||||
| chrX:73592210
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.507+7638C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592210 | ||||||
| chrX:73592268
|
T | G | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+7696T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592268 | ||||||
| chrX:73592355
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.507+7783G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592355 | ||||||
| chrX:73592586
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+8014G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592586 | ||||||
| chrX:73592634
|
A | G | 5 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+8062A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592634 | ||||||
| chrX:73592679
|
G | T | 57 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(54): Show | 57 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.507+8107G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73592679 | ||||||
| chrX:73592908
|
A | AT | 1 | a0001c0001t0001g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.507+8345dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73592908 | |||||
| chrX:73593572
|
A | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.507+9000A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73593572 | ||||||
| chrX:73593681
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+9109T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73593681 | ||||||
| chrX:73594084
|
AG | A | 1 | a0001c0001t0003g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.507+9516delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594084 | |||||
| chrX:73594088
|
G | GT | 1 | a0001c0001t0010g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.507+9524dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594088 | |||||
| chrX:73594088
|
G | T | 16 | a0001c0001t0003g0063a0001c0001t0003g0065a0001c0001t0003g0067others(13): Show | 16 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.507+9516G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73594088 | ||||||
| chrX:73594142
|
C | CTTTGT | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(34): Show | 38 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.507+9612_507+9616d others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594142 | |||||
| chrX:73594142
|
C | CTTTGTTT others(3): Show |
62 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0102others(59): Show | 62 | HG00673.hp1 HG01258.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.507+9607_507+9616d others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594142 | |||||
| chrX:73594142
|
CTTTGT | C | 17 | a0001c0001t0002g0078a0001c0001t0002g0103a0001c0001t0002g0172others(14): Show | 17 | HG01109.hp1 HG01123.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+9612_507+9616d others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594142 | |||||
| chrX:73594253
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | NA18948.hp1 NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.507+9681G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73594253 | ||||||
| chrX:73594328
|
GC | G | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.507+9759delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594328 | |||||
| chrX:73594842
|
G | GA | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.507+10273dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594842 | |||||
| chrX:73594919
|
AT | A | 1 | a0001c0001t0002g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.507+10350delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594919 | |||||
| chrX:73594935
|
A | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(154): Show | 159 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.507+10363A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73594935 | ||||||
| chrX:73594969
|
AAATATCA others(1): Show |
A | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+10399_507+1040 others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73594969 | |||||
| chrX:73595180
|
C | CT | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+10615dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595180 | |||||
| chrX:73595325
|
A | AC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+10758dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595325 | |||||
| chrX:73595371
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.507+10799T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73595371 | ||||||
| chrX:73595371
|
T | TG | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+10800dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595371 | |||||
| chrX:73595434
|
T | TG | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+10863dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595434 | |||||
| chrX:73595453
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.507+10881T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73595453 | ||||||
| chrX:73595552
|
A | AC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+10980_507+1098 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73595552 | ||||||
| chrX:73595564
|
C | CA | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+10993dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595564 | |||||
| chrX:73595628
|
TA | T | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+11059delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595628 | |||||
| chrX:73595740
|
G | GA | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+11170dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73595740 | |||||
| chrX:73595843
|
C | G | 1 | a0001c0001t0014g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.507+11271C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73595843 | ||||||
| chrX:73595884
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.507+11312G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73595884 | ||||||
| chrX:73595993
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.507+11421A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73595993 | ||||||
| chrX:73596077
|
T | TG | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+11506dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596077 | |||||
| chrX:73596371
|
T | TG | 1 | a0001c0001t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.507+11802dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596371 | |||||
| chrX:73596425
|
T | A | 6 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(3): Show | 6 | HG00738.hp1 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+11853T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73596425 | ||||||
| chrX:73596479
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+11911dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596479 | |||||
| chrX:73596600
|
A | AG | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12030dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596600 | |||||
| chrX:73596725
|
A | AC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12154dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596725 | |||||
| chrX:73596754
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.507+12182C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73596754 | ||||||
| chrX:73596789
|
AT | A | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12220delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596789 | |||||
| chrX:73596918
|
T | TA | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12350dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73596918 | |||||
| chrX:73597029
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.507+12457G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597029 | ||||||
| chrX:73597065
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.507+12493A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597065 | ||||||
| chrX:73597139
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+12567C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597139 | ||||||
| chrX:73597226
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12657dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597226 | |||||
| chrX:73597253
|
C | CT | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12685dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597253 | |||||
| chrX:73597320
|
A | AT | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12752dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597320 | |||||
| chrX:73597342
|
T | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+12770T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597342 | ||||||
| chrX:73597444
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+12873dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597444 | |||||
| chrX:73597530
|
A | G | 5 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+12958A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597530 | ||||||
| chrX:73597592
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+13020C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597592 | ||||||
| chrX:73597594
|
C | CAT | 1 | a0001c0001t0003g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.507+13032_507+1303 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597594 | |||||
| chrX:73597604
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.507+13032T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597604 | ||||||
| chrX:73597604
|
T | TAC | 1 | a0001c0001t0001g0129 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.507+13048_507+1304 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597604 | |||||
| chrX:73597606
|
C | T | 19 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(16): Show | 19 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.507+13034C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597606 | ||||||
| chrX:73597620
|
C | CAT | 4 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0181others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+13062_507+1306 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597620 | |||||
| chrX:73597634
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.507+13062T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597634 | ||||||
| chrX:73597747
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13176dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597747 | |||||
| chrX:73597771
|
G | GC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13205dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597771 | |||||
| chrX:73597843
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13274dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597843 | |||||
| chrX:73597857
|
G | A | 1 | a0001c0001t0009g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.507+13285G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597857 | ||||||
| chrX:73597930
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13361dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73597930 | |||||
| chrX:73597970
|
A | G | 2 | a0001c0001t0002g0179a0001c0001t0002g0202 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.507+13398A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597970 | ||||||
| chrX:73597975
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+13403A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73597975 | ||||||
| chrX:73598016
|
A | ACTT | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13444_507+1344 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598016 | ||||||
| chrX:73598017
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13445T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598017 | ||||||
| chrX:73598105
|
G | GA | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13535dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598105 | |||||
| chrX:73598231
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13661dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598231 | |||||
| chrX:73598259
|
T | C | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+13687T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598259 | ||||||
| chrX:73598275
|
A | AC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13705dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598275 | |||||
| chrX:73598290
|
A | T | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.507+13718A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598290 | ||||||
| chrX:73598308
|
T | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+13736T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598308 | ||||||
| chrX:73598329
|
C | CT | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(128): Show | 132 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.507+13768dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598329 | |||||
| chrX:73598329
|
CT | C | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.507+13768delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598329 | |||||
| chrX:73598338
|
T | TA | 18 | a0001c0001t0001g0131a0001c0001t0003g0063a0001c0001t0003g0064others(15): Show | 18 | HG01258.hp1 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.507+13766_507+1376 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598338 | ||||||
| chrX:73598420
|
C | T | 11 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(8): Show | 11 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+13848C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598420 | ||||||
| chrX:73598457
|
A | G | 2 | a0001c0001t0010g0100a0001c0001t0023g0099 | 2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+13885A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598457 | ||||||
| chrX:73598460
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13891dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598460 | |||||
| chrX:73598475
|
T | TC | 1 | a0001c0001t0002g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+13909dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598475 | |||||
| chrX:73598482
|
T | TC | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0196others(1): Show | 4 | HG00621.hp1 HG02145.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+13916dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598482 | |||||
| chrX:73598494
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.507+13922A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598494 | ||||||
| chrX:73598501
|
T | TC | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+13933dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598501 | |||||
| chrX:73598600
|
C | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+14028C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598600 | ||||||
| chrX:73598693
|
G | A | 7 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(4): Show | 7 | HG00735.hp2 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+14121G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598693 | ||||||
| chrX:73598781
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.507+14209G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598781 | ||||||
| chrX:73598795
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.507+14223T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598795 | ||||||
| chrX:73598880
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+14308A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73598880 | ||||||
| chrX:73598967
|
AT | A | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+14398delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73598967 | |||||
| chrX:73599088
|
A | G | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+14516A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599088 | ||||||
| chrX:73599107
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 53 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.507+14535T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599107 | ||||||
| chrX:73599115
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.507+14543C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599115 | ||||||
| chrX:73599146
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.507+14574G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599146 | ||||||
| chrX:73599197
|
A | AT | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+14625_507+1462 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599197 | ||||||
| chrX:73599200
|
CTGTTTGA others(12681): Show |
C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+14680_507+2736 others(4): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73599200 | |||||
| chrX:73599203
|
T | TTTGAGTT others(2): Show |
1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+14635_507+1464 others(13): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73599203 | |||||
| chrX:73599208
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.507+14636G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599208 | ||||||
| chrX:73599283
|
A | G | 3 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200 | 3 | HG01884.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.507+14711A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599283 | ||||||
| chrX:73599413
|
A | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(132): Show | 136 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.507+14841A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599413 | ||||||
| chrX:73599479
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0186 | 3 | HG02080.hp1 NA18965.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.507+14907G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599479 | ||||||
| chrX:73599498
|
T | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+14926T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599498 | ||||||
| chrX:73599526
|
G | C | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+14954G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599526 | ||||||
| chrX:73599565
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0184 | 3 | HG02055.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.507+14993C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599565 | ||||||
| chrX:73599668
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.507+15096C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599668 | ||||||
| chrX:73599775
|
C | T | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+15203C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599775 | ||||||
| chrX:73599801
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+15229G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599801 | ||||||
| chrX:73599892
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.507+15320G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599892 | ||||||
| chrX:73599952
|
T | A | 20 | a0001c0001t0001g0029a0001c0001t0001g0115a0001c0001t0001g0132others(17): Show | 20 | HG02083.hp1 HG02135.hp1 NA18944.hp1 others(17): Show |
intron_variant | MODIFIER | c.507+15380T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599952 | ||||||
| chrX:73599956
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.507+15384T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599956 | ||||||
| chrX:73599990
|
T | G | 41 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(38): Show | 41 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.507+15418T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73599990 | ||||||
| chrX:73600037
|
G | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+15465G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600037 | ||||||
| chrX:73600043
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.507+15471C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600043 | ||||||
| chrX:73600142
|
T | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.507+15570T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600142 | ||||||
| chrX:73600172
|
T | C | 2 | a0001c0001t0011g0173a0001c0001t0011g0201 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.507+15600T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600172 | ||||||
| chrX:73600173
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.507+15601A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600173 | ||||||
| chrX:73600351
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.507+15779C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600351 | ||||||
| chrX:73600650
|
A | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+16078A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600650 | ||||||
| chrX:73600718
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.507+16146C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600718 | ||||||
| chrX:73600764
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.507+16192A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600764 | ||||||
| chrX:73600949
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+16377A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73600949 | ||||||
| chrX:73600993
|
TCAA | T | 1 | a0001c0001t0001g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.507+16428_507+1643 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73600993 | |||||
| chrX:73601607
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.507+17035A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73601607 | ||||||
| chrX:73601625
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.507+17053A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73601625 | ||||||
| chrX:73601703
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.507+17131C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73601703 | ||||||
| chrX:73601707
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.507+17135A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73601707 | ||||||
| chrX:73601758
|
T | G | 1 | a0001c0001t0005g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.507+17186T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73601758 | ||||||
| chrX:73602010
|
A | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+17438A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73602010 | ||||||
| chrX:73602756
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.507+18184A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73602756 | ||||||
| chrX:73603064
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.507+18492C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73603064 | ||||||
| chrX:73603378
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.507+18806A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73603378 | ||||||
| chrX:73603579
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.507+19007G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73603579 | ||||||
| chrX:73603712
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.507+19140G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73603712 | ||||||
| chrX:73603734
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.507+19162C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73603734 | ||||||
| chrX:73604079
|
G | A | 2 | a0001c0001t0009g0114a0001c0001t0009g0130 | 2 | NA18944.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.507+19507G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73604079 | ||||||
| chrX:73604129
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.507+19557G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73604129 | ||||||
| chrX:73604425
|
G | A | 4 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(1): Show | 4 | HG02970.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+19853G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73604425 | ||||||
| chrX:73604525
|
AT | A | 4 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(1): Show | 4 | HG02970.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+19955delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73604525 | |||||
| chrX:73605019
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.507+20447T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73605019 | ||||||
| chrX:73605021
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.507+20449G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73605021 | ||||||
| chrX:73605187
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.507+20615A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73605187 | ||||||
| chrX:73605383
|
T | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+20811T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73605383 | ||||||
| chrX:73605862
|
A | G | 36 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(33): Show | 36 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.507+21290A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73605862 | ||||||
| chrX:73606343
|
A | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+21771A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73606343 | ||||||
| chrX:73606446
|
G | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+21874G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73606446 | ||||||
| chrX:73606548
|
TG | T | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.507+21981delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73606548 | |||||
| chrX:73606556
|
A | G | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+21984A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73606556 | ||||||
| chrX:73606563
|
A | G | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+21991A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73606563 | ||||||
| chrX:73606916
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.507+22344G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73606916 | ||||||
| chrX:73607018
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(82): Show | 86 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.507+22446G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73607018 | ||||||
| chrX:73607105
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.507+22533T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73607105 | ||||||
| chrX:73607129
|
T | C | 1 | a0001c0001t0012g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.507+22557T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73607129 | ||||||
| chrX:73607132
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(82): Show | 86 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.507+22560A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73607132 | ||||||
| chrX:73607530
|
G | GA | 2 | a0001c0001t0001g0024a0001c0001t0005g0011 | 2 | HG00642.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.507+22967dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73607530 | |||||
| chrX:73608174
|
A | G | 41 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(38): Show | 41 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.507+23602A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73608174 | ||||||
| chrX:73608380
|
TA | T | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+23809delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73608380 | ||||||
| chrX:73608414
|
A | AT | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+23850dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73608414 | |||||
| chrX:73608470
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG02818.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.507+23898C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73608470 | ||||||
| chrX:73608983
|
A | G | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+24411A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73608983 | ||||||
| chrX:73609063
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.507+24491G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73609063 | ||||||
| chrX:73609144
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.507+24572G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73609144 | ||||||
| chrX:73609155
|
T | TA | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.507+24599dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73609155 | |||||
| chrX:73609155
|
TA | T | 51 | a0001c0001t0001g0049a0001c0001t0001g0136a0001c0001t0002g0078others(48): Show | 51 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.507+24599delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73609155 | |||||
| chrX:73609190
|
A | T | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(137): Show | 142 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.507+24618A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73609190 | ||||||
| chrX:73609534
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.507+24962G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73609534 | ||||||
| chrX:73609697
|
A | G | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+25125A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73609697 | ||||||
| chrX:73609964
|
C | G | 11 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(8): Show | 11 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+25392C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73609964 | ||||||
| chrX:73610509
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.507+25937G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73610509 | ||||||
| chrX:73610795
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG00735.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.507+26223G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73610795 | ||||||
| chrX:73610885
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.507+26313G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73610885 | ||||||
| chrX:73610943
|
G | GT | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01081.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.507+26381dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73610943 | |||||
| chrX:73611590
|
G | A | 9 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+27018G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73611590 | ||||||
| chrX:73611791
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.507+27219T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73611791 | ||||||
| chrX:73611900
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.507+27328A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73611900 | ||||||
| chrX:73611944
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+27372C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73611944 | ||||||
| chrX:73612190
|
T | C | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+27618T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73612190 | ||||||
| chrX:73612466
|
T | C | 21 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 21 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+27894T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73612466 | ||||||
| chrX:73612605
|
T | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.507+28033T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73612605 | ||||||
| chrX:73612844
|
A | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+28272A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73612844 | ||||||
| chrX:73613062
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.507+28490A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613062 | ||||||
| chrX:73613249
|
C | A | 1 | a0001c0001t0002g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.507+28677C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613249 | ||||||
| chrX:73613391
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.507+28819G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613391 | ||||||
| chrX:73613536
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.507+28964C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613536 | ||||||
| chrX:73613536
|
C | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+28964C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613536 | ||||||
| chrX:73613612
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+29040T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613612 | ||||||
| chrX:73613738
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+29166A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613738 | ||||||
| chrX:73613956
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+29384T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73613956 | ||||||
| chrX:73614029
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.507+29457T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614029 | ||||||
| chrX:73614036
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+29464G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614036 | ||||||
| chrX:73614160
|
A | AT | 1 | a0001c0001t0002g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+29597dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73614160 | |||||
| chrX:73614269
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.507+29697A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614269 | ||||||
| chrX:73614282
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.507+29710G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614282 | ||||||
| chrX:73614454
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.507+29882G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614454 | ||||||
| chrX:73614689
|
A | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+30117A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614689 | ||||||
| chrX:73614773
|
T | C | 1 | a0001c0001t0007g0021 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.507+30201T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614773 | ||||||
| chrX:73614872
|
T | A | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.507+30300T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73614872 | ||||||
| chrX:73615271
|
G | T | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.507+30699G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73615271 | ||||||
| chrX:73615393
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.507+30821G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73615393 | ||||||
| chrX:73615598
|
T | A | 32 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(29): Show | 32 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.507+31026T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73615598 | ||||||
| chrX:73615786
|
T | TG | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.507+31219dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73615786 | |||||
| chrX:73615876
|
C | T | 1 | a0001c0001t0008g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.507+31304C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73615876 | ||||||
| chrX:73615960
|
G | C | 5 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0018others(2): Show | 5 | HG00738.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+31388G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73615960 | ||||||
| chrX:73615973
|
A | G | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+31401A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73615973 | ||||||
| chrX:73615996
|
TG | T | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+31427delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73615996 | |||||
| chrX:73616082
|
T | TC | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.507+31516dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73616082 | |||||
| chrX:73616161
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+31589G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73616161 | ||||||
| chrX:73616243
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507+31671A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73616243 | ||||||
| chrX:73616439
|
T | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+31867T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73616439 | ||||||
| chrX:73616654
|
G | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(154): Show | 159 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.507+32082G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73616654 | ||||||
| chrX:73616828
|
A | AT | 1 | a0001c0001t0001g0141 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.507+32262dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73616828 | |||||
| chrX:73616936
|
C | T | 8 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | NA18945.hp1 NA18953.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.507+32364C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73616936 | ||||||
| chrX:73617124
|
G | T | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+32552G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73617124 | ||||||
| chrX:73617366
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.507+32794G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73617366 | ||||||
| chrX:73617720
|
TG | T | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+33153delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73617720 | |||||
| chrX:73617895
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.507+33323C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73617895 | ||||||
| chrX:73617930
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.507+33358C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73617930 | ||||||
| chrX:73618039
|
ATTAT | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+33470_507+3347 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73618039 | |||||
| chrX:73618124
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0189 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.507+33552C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618124 | ||||||
| chrX:73618150
|
C | A | 1 | a0001c0001t0014g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.507+33578C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618150 | ||||||
| chrX:73618217
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.507+33645G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618217 | ||||||
| chrX:73618256
|
GC | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+33686delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73618256 | |||||
| chrX:73618347
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.507+33775T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618347 | ||||||
| chrX:73618349
|
T | TC | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+33779dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73618349 | |||||
| chrX:73618456
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+33884C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618456 | ||||||
| chrX:73618543
|
A | AG | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+33974dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73618543 | |||||
| chrX:73618563
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.507+33991G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618563 | ||||||
| chrX:73618831
|
A | AT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+34263dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73618831 | |||||
| chrX:73618914
|
C | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+34342C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73618914 | ||||||
| chrX:73619020
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.507+34448C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73619020 | ||||||
| chrX:73619161
|
C | CG | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+34593dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73619161 | |||||
| chrX:73619192
|
A | G | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.507+34620A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73619192 | ||||||
| chrX:73619463
|
TC | T | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+34894delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73619463 | |||||
| chrX:73619487
|
TC | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+34917delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73619487 | |||||
| chrX:73619783
|
G | GT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+35212dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73619783 | |||||
| chrX:73619870
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+35298C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73619870 | ||||||
| chrX:73619951
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+35379T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73619951 | ||||||
| chrX:73619981
|
GT | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+35412delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73619981 | |||||
| chrX:73620006
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+35434T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73620006 | ||||||
| chrX:73620088
|
C | CT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+35516_507+3551 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73620088 | ||||||
| chrX:73620551
|
GT | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+35984delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73620551 | |||||
| chrX:73620623
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+36051C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73620623 | ||||||
| chrX:73620624
|
T | TA | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+36055dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73620624 | |||||
| chrX:73620751
|
G | T | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.507+36179G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73620751 | ||||||
| chrX:73620886
|
T | C | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.507+36314T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73620886 | ||||||
| chrX:73620918
|
G | A | 4 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(1): Show | 4 | HG02970.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+36346G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73620918 | ||||||
| chrX:73620963
|
T | TC | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+36395dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73620963 | |||||
| chrX:73621138
|
C | CA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+36566_507+3656 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621138 | ||||||
| chrX:73621197
|
C | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+36625C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621197 | ||||||
| chrX:73621306
|
CA | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+36736delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73621306 | |||||
| chrX:73621340
|
G | GT | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+36773dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73621340 | |||||
| chrX:73621360
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.507+36788C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621360 | ||||||
| chrX:73621639
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.507+37067A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621639 | ||||||
| chrX:73621742
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.507+37170A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621742 | ||||||
| chrX:73621790
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0146 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.507+37218G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621790 | ||||||
| chrX:73621843
|
A | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+37271A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73621843 | ||||||
| chrX:73622048
|
A | T | 3 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083 | 3 | HG02615.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.507+37476A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73622048 | ||||||
| chrX:73622157
|
C | CT | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.507+37592dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622157 | |||||
| chrX:73622157
|
CT | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+37592delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622157 | |||||
| chrX:73622235
|
C | CTG | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+37664_507+3766 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622235 | |||||
| chrX:73622346
|
CTA | C | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+37776_507+3777 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622346 | |||||
| chrX:73622384
|
T | TC | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+37813dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622384 | |||||
| chrX:73622443
|
G | GT | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+37874dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622443 | |||||
| chrX:73622616
|
G | T | 1 | a0001c0001t0020g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.507+38044G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73622616 | ||||||
| chrX:73622693
|
C | A | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+38121C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73622693 | ||||||
| chrX:73622729
|
CT | C | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+38162delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622729 | |||||
| chrX:73622859
|
T | TG | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+38288dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73622859 | |||||
| chrX:73622990
|
C | T | 1 | a0001c0001t0004g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.507+38418C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73622990 | ||||||
| chrX:73623051
|
A | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+38479A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73623051 | ||||||
| chrX:73623066
|
G | GT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+38496dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73623066 | |||||
| chrX:73623509
|
G | GT | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.507+38947dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73623509 | |||||
| chrX:73623509
|
GT | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+38947delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73623509 | |||||
| chrX:73623732
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.507+39160T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73623732 | ||||||
| chrX:73623757
|
TA | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39189delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73623757 | |||||
| chrX:73623773
|
T | TC | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39204dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73623773 | |||||
| chrX:73623858
|
G | T | 152 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(149): Show | 153 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.507+39286G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73623858 | ||||||
| chrX:73623920
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+39348A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73623920 | ||||||
| chrX:73623973
|
CT | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39404delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73623973 | |||||
| chrX:73624032
|
TC | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39465delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624032 | |||||
| chrX:73624053
|
AT | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39486delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624053 | |||||
| chrX:73624081
|
A | G | 1 | a0001c0001t0004g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.507+39509A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624081 | ||||||
| chrX:73624136
|
GA | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39567delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624136 | |||||
| chrX:73624400
|
TA | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39831delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624400 | |||||
| chrX:73624455
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.507+39883A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624455 | ||||||
| chrX:73624457
|
AT | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39888delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624457 | |||||
| chrX:73624517
|
G | A | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0202 | 3 | HG01243.hp1 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.507+39945G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624517 | ||||||
| chrX:73624563
|
C | CT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+39991_507+3999 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624563 | ||||||
| chrX:73624618
|
AT | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+40047delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624618 | ||||||
| chrX:73624659
|
A | AC | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+40089dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624659 | |||||
| chrX:73624661
|
CA | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+40091delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624661 | |||||
| chrX:73624757
|
A | AC | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+40187dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624757 | |||||
| chrX:73624787
|
GC | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+40218delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624787 | |||||
| chrX:73624864
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+40292A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624864 | ||||||
| chrX:73624887
|
A | AT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+40317dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73624887 | |||||
| chrX:73624946
|
ATT | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+40375_507+4037 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73624946 | ||||||
| chrX:73625108
|
AT | A | 3 | a0001c0001t0002g0095a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | HG00323.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.507+40547delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73625108 | |||||
| chrX:73625531
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.507+40959A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73625531 | ||||||
| chrX:73625564
|
AG | A | 1 | a0001c0001t0001g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.507+40995delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73625564 | |||||
| chrX:73625675
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+41103A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73625675 | ||||||
| chrX:73625922
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.507+41350T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73625922 | ||||||
| chrX:73625984
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.507+41412G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73625984 | ||||||
| chrX:73626016
|
C | T | 1 | a0001c0001t0004g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.507+41444C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73626016 | ||||||
| chrX:73626294
|
C | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.507+41722C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73626294 | ||||||
| chrX:73626376
|
T | C | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.507+41804T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73626376 | ||||||
| chrX:73627065
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+42493G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73627065 | ||||||
| chrX:73627117
|
CTTCT | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+42552_507+4255 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627117 | |||||
| chrX:73627137
|
C | CA | 29 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(26): Show | 29 | HG00323.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.507+42586dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627137
|
C | CAA | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00735.hp2 HG01123.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+42585_507+4258 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627137
|
C | CAAA | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0202 | 3 | HG01167.hp1 HG01169.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.507+42584_507+4258 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627137
|
CA | C | 6 | a0001c0001t0001g0129a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01975.hp1 HG01975.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+42586delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627137
|
CAA | C | 1 | a0001c0001t0003g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.507+42585_507+4258 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627137
|
CAAA | C | 16 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(13): Show | 16 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.507+42584_507+4258 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627137
|
CAAAA | C | 1 | a0001c0001t0001g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.507+42583_507+4258 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73627137 | |||||
| chrX:73627485
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.507+42913T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73627485 | ||||||
| chrX:73627517
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.507+42945A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73627517 | ||||||
| chrX:73627857
|
A | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+43285A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73627857 | ||||||
| chrX:73628295
|
G | A | 28 | a0001c0001t0001g0190a0001c0001t0002g0078a0001c0001t0002g0079others(25): Show | 28 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.507+43723G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73628295 | ||||||
| chrX:73628297
|
G | A | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+43725G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73628297 | ||||||
| chrX:73628465
|
ACTGGAAT others(13): Show |
A | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.507+43898_507+4391 others(24): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73628465 | |||||
| chrX:73628567
|
G | T | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.507+43995G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73628567 | ||||||
| chrX:73628632
|
G | A | 27 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(24): Show | 27 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.507+44060G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73628632 | ||||||
| chrX:73628861
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+44289G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73628861 | ||||||
| chrX:73629697
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+45125A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73629697 | ||||||
| chrX:73630074
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+45502A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73630074 | ||||||
| chrX:73630712
|
G | GTCCT | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+46142_507+4614 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73630712 | |||||
| chrX:73630817
|
T | G | 7 | a0001c0001t0001g0190a0001c0001t0002g0078a0001c0001t0002g0178others(4): Show | 7 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+46245T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73630817 | ||||||
| chrX:73630929
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+46357T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73630929 | ||||||
| chrX:73631084
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.507+46512A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73631084 | ||||||
| chrX:73631425
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.507+46853G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73631425 | ||||||
| chrX:73631428
|
A | C | 1 | a0001c0001t0014g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.507+46856A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73631428 | ||||||
| chrX:73631627
|
CA | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+47068delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73631627 | |||||
| chrX:73632030
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.508-47296C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632030 | ||||||
| chrX:73632198
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-47128T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632198 | ||||||
| chrX:73632312
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508-47014G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632312 | ||||||
| chrX:73632550
|
A | AT | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.508-46768dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73632550 | |||||
| chrX:73632561
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.508-46765A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632561 | ||||||
| chrX:73632720
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.508-46606G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632720 | ||||||
| chrX:73632763
|
C | CT | 16 | a0001c0001t0001g0047a0001c0001t0001g0120a0001c0001t0001g0134others(13): Show | 16 | HG01243.hp1 HG02145.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.508-46540dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73632763 | |||||
| chrX:73632763
|
CT | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0058 | 2 | HG01943.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.508-46540delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73632763 | |||||
| chrX:73632792
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.508-46534G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632792 | ||||||
| chrX:73632844
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-46482C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632844 | ||||||
| chrX:73632856
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.508-46470C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632856 | ||||||
| chrX:73632944
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.508-46382A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632944 | ||||||
| chrX:73632958
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-46368T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632958 | ||||||
| chrX:73632970
|
G | A | 1 | a0001c0001t0004g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.508-46356G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632970 | ||||||
| chrX:73632985
|
G | T | 1 | a0001c0001t0017g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.508-46341G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73632985 | ||||||
| chrX:73633058
|
C | T | 10 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(7): Show | 10 | HG02451.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-46268C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633058 | ||||||
| chrX:73633075
|
T | TA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-46250dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73633075 | |||||
| chrX:73633228
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0189 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.508-46098C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633228 | ||||||
| chrX:73633239
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0171 | 2 | NA18988.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.508-46087C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633239 | ||||||
| chrX:73633288
|
G | T | 2 | a0001c0001t0011g0173a0001c0001t0011g0201 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.508-46038G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633288 | ||||||
| chrX:73633320
|
T | G | 1 | a0001c0001t0012g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.508-46006T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633320 | ||||||
| chrX:73633371
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-45955A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633371 | ||||||
| chrX:73633416
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-45910T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633416 | ||||||
| chrX:73633434
|
G | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.508-45892G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633434 | ||||||
| chrX:73633618
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.508-45708A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73633618 | ||||||
| chrX:73634033
|
CTA | C | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.508-45291_508-4529 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73634033 | |||||
| chrX:73634188
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508-45138A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634188 | ||||||
| chrX:73634208
|
C | G | 19 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(16): Show | 19 | HG00673.hp1 HG01258.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.508-45118C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634208 | ||||||
| chrX:73634295
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0050others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-45031G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634295 | ||||||
| chrX:73634455
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-44871C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634455 | ||||||
| chrX:73634523
|
AG | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-44799delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73634523 | |||||
| chrX:73634566
|
T | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.508-44760T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634566 | ||||||
| chrX:73634710
|
TC | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-44612delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73634710 | |||||
| chrX:73634805
|
C | CA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-44517dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73634805 | |||||
| chrX:73634916
|
C | G | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.508-44410C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634916 | ||||||
| chrX:73634996
|
G | C | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-44330G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73634996 | ||||||
| chrX:73635100
|
CT | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-44223delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73635100 | |||||
| chrX:73635253
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.508-44073C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635253 | ||||||
| chrX:73635435
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.508-43891G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635435 | ||||||
| chrX:73635470
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-43856T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635470 | ||||||
| chrX:73635499
|
T | G | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-43827T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635499 | ||||||
| chrX:73635516
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.508-43810T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635516 | ||||||
| chrX:73635581
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-43745C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635581 | ||||||
| chrX:73635943
|
T | C | 2 | a0001c0001t0011g0173a0001c0001t0011g0201 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.508-43383T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73635943 | ||||||
| chrX:73636028
|
G | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-43298G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73636028 | ||||||
| chrX:73636300
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.508-43026G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73636300 | ||||||
| chrX:73636372
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-42954A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73636372 | ||||||
| chrX:73636856
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(198): Show | 206 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.508-42470C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73636856 | ||||||
| chrX:73637049
|
GT | G | 1 | a0001c0001t0023g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-42276delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73637049 | ||||||
| chrX:73637128
|
G | A | 4 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(1): Show | 4 | HG02970.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-42198G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73637128 | ||||||
| chrX:73637205
|
T | TC | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-42120dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73637205 | |||||
| chrX:73637295
|
G | GT | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-42016dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73637295 | |||||
| chrX:73637668
|
A | G | 9 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-41658A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73637668 | ||||||
| chrX:73637726
|
CT | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-41593delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73637726 | |||||
| chrX:73637960
|
G | GA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-41360dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73637960 | |||||
| chrX:73637975
|
G | A | 1 | a0001c0001t0009g0130 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.508-41351G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73637975 | ||||||
| chrX:73638344
|
A | G | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-40982A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73638344 | ||||||
| chrX:73638353
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-40973A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73638353 | ||||||
| chrX:73638401
|
G | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-40925G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73638401 | ||||||
| chrX:73638527
|
T | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-40799T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73638527 | ||||||
| chrX:73638528
|
TA | T | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.508-40788delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73638528 | |||||
| chrX:73638553
|
G | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-40773G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73638553 | ||||||
| chrX:73638926
|
T | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-40400T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73638926 | ||||||
| chrX:73639090
|
A | AG | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-40234dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73639090 | |||||
| chrX:73639190
|
A | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-40136A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73639190 | ||||||
| chrX:73639474
|
C | T | 1 | a0001c0001t0012g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.508-39852C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73639474 | ||||||
| chrX:73639528
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.508-39798A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73639528 | ||||||
| chrX:73639721
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.508-39605A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73639721 | ||||||
| chrX:73639843
|
C | T | 1 | a0001c0001t0004g0028 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.508-39483C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73639843 | ||||||
| chrX:73640098
|
C | T | 1 | a0001c0001t0011g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508-39228C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73640098 | ||||||
| chrX:73640115
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-39211T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73640115 | ||||||
| chrX:73640264
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-39062G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73640264 | ||||||
| chrX:73640569
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.508-38757C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73640569 | ||||||
| chrX:73640803
|
A | AT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-38520dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73640803 | |||||
| chrX:73640838
|
TC | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-38486delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73640838 | |||||
| chrX:73640988
|
AT | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-38335delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73640988 | |||||
| chrX:73641359
|
A | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-37967A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641359 | ||||||
| chrX:73641482
|
G | A | 21 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 21 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.508-37844G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641482 | ||||||
| chrX:73641507
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.508-37819C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641507 | ||||||
| chrX:73641517
|
A | T | 1 | a0001c0001t0001g0155 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.508-37809A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641517 | ||||||
| chrX:73641538
|
T | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090 | 3 | HG01261.hp1 HG01361.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.508-37788T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641538 | ||||||
| chrX:73641561
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-37765T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641561 | ||||||
| chrX:73641647
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.508-37679C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641647 | ||||||
| chrX:73641662
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-37664T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641662 | ||||||
| chrX:73641666
|
C | CCT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-37659_508-3765 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73641666 | |||||
| chrX:73641669
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-37657T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641669 | ||||||
| chrX:73641678
|
A | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-37648A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641678 | ||||||
| chrX:73641739
|
G | T | 2 | a0001c0001t0003g0076a0001c0001t0003g0077 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.508-37587G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641739 | ||||||
| chrX:73641791
|
G | A | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-37535G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73641791 | ||||||
| chrX:73642030
|
AC | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-37293delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73642030 | |||||
| chrX:73642113
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-37213G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642113 | ||||||
| chrX:73642130
|
C | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-37196C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642130 | ||||||
| chrX:73642387
|
T | G | 1 | a0001c0001t0013g0150 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.508-36939T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642387 | ||||||
| chrX:73642413
|
A | G | 66 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0102others(63): Show | 66 | HG00673.hp1 HG01258.hp1 HG01975.hp2 others(63): Show |
intron_variant | MODIFIER | c.508-36913A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642413 | ||||||
| chrX:73642470
|
G | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-36856G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642470 | ||||||
| chrX:73642681
|
T | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-36645T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642681 | ||||||
| chrX:73642733
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0060others(2): Show | 6 | HG01081.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-36593A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642733 | ||||||
| chrX:73642737
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.508-36589A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642737 | ||||||
| chrX:73642824
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(41): Show | 47 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.508-36502C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642824 | ||||||
| chrX:73642839
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(83): Show | 87 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.508-36487G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642839 | ||||||
| chrX:73642841
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508-36485T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642841 | ||||||
| chrX:73642842
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508-36484G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642842 | ||||||
| chrX:73642918
|
C | G | 2 | a0001c0001t0006g0003a0001c0001t0006g0059 | 3 | HG02280.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.508-36408C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642918 | ||||||
| chrX:73642997
|
G | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-36329G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73642997 | ||||||
| chrX:73643011
|
GT | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-36313delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73643011 | |||||
| chrX:73643071
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-36255A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643071 | ||||||
| chrX:73643083
|
C | CA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-36242dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73643083 | |||||
| chrX:73643131
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.508-36195T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643131 | ||||||
| chrX:73643150
|
AT | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-36174delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73643150 | |||||
| chrX:73643225
|
G | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0105others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-36101G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643225 | ||||||
| chrX:73643256
|
TC | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-36067delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73643256 | |||||
| chrX:73643271
|
C | A | 32 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(29): Show | 32 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-36055C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643271 | ||||||
| chrX:73643340
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.508-35986C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643340 | ||||||
| chrX:73643343
|
G | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-35983G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643343 | ||||||
| chrX:73643380
|
T | C | 1 | a0001c0001t0019g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.508-35946T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643380 | ||||||
| chrX:73643453
|
T | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-35873T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643453 | ||||||
| chrX:73643601
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.508-35725G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643601 | ||||||
| chrX:73643885
|
G | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-35441G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643885 | ||||||
| chrX:73643914
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.508-35412G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73643914 | ||||||
| chrX:73644163
|
C | G | 2 | a0001c0001t0002g0172a0001c0001t0002g0200 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.508-35163C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644163 | ||||||
| chrX:73644268
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.508-35058G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644268 | ||||||
| chrX:73644332
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.508-34994G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644332 | ||||||
| chrX:73644342
|
T | A | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0184 | 3 | HG02055.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.508-34984T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644342 | ||||||
| chrX:73644360
|
G | A | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508-34966G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644360 | ||||||
| chrX:73644482
|
A | G | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-34844A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644482 | ||||||
| chrX:73644668
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.508-34658G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644668 | ||||||
| chrX:73644875
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.508-34451C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644875 | ||||||
| chrX:73644883
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.508-34443T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644883 | ||||||
| chrX:73644959
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-34367C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644959 | ||||||
| chrX:73644970
|
A | AC | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.508-34353dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73644970 | |||||
| chrX:73644991
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0144a0001c0001t0001g0163 | 3 | NA19060.hp1 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508-34335G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73644991 | ||||||
| chrX:73645085
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-34241A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73645085 | ||||||
| chrX:73645100
|
C | T | 1 | a0001c0001t0011g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508-34226C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73645100 | ||||||
| chrX:73645105
|
A | G | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.508-34221A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73645105 | ||||||
| chrX:73645357
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.508-33969G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73645357 | ||||||
| chrX:73645757
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508-33569A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73645757 | ||||||
| chrX:73646183
|
AC | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-33141delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73646183 | |||||
| chrX:73646223
|
A | G | 1 | a0001c0001t0004g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.508-33103A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73646223 | ||||||
| chrX:73646286
|
G | GT | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-33036dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73646286 | |||||
| chrX:73646375
|
T | C | 9 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-32951T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73646375 | ||||||
| chrX:73646509
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.508-32817G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73646509 | ||||||
| chrX:73646559
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-32767G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73646559 | ||||||
| chrX:73646871
|
AC | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-32452delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73646871 | |||||
| chrX:73646915
|
T | C | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508-32411T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73646915 | ||||||
| chrX:73647116
|
TG | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-32206delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73647116 | |||||
| chrX:73647222
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.508-32104A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647222 | ||||||
| chrX:73647424
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.508-31902G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647424 | ||||||
| chrX:73647638
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.508-31688C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647638 | ||||||
| chrX:73647655
|
G | GC | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-31669dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73647655 | |||||
| chrX:73647719
|
G | A | 1 | a0001c0001t0003g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508-31607G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647719 | ||||||
| chrX:73647776
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.508-31550C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647776 | ||||||
| chrX:73647811
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-31515C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647811 | ||||||
| chrX:73647812
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-31514T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647812 | ||||||
| chrX:73647846
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.508-31480C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647846 | ||||||
| chrX:73647970
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.508-31356C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73647970 | ||||||
| chrX:73648203
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508-31123C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73648203 | ||||||
| chrX:73648211
|
C | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0186 | 3 | HG02080.hp1 NA18965.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.508-31115C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73648211 | ||||||
| chrX:73648226
|
TAAAC | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(82): Show | 86 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.508-31095_508-3109 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73648226 | |||||
| chrX:73648254
|
TCAACAAC others(2): Show |
T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-31059_508-3105 others(13): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73648254 | |||||
| chrX:73648334
|
T | C | 66 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(63): Show | 66 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.508-30992T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73648334 | ||||||
| chrX:73648397
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-30929G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73648397 | ||||||
| chrX:73648433
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG00735.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.508-30893A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73648433 | ||||||
| chrX:73648714
|
T | C | 1 | a0001c0001t0004g0028 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.508-30612T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73648714 | ||||||
| chrX:73649023
|
GA | G | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-30301delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73649023 | |||||
| chrX:73649132
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-30194C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73649132 | ||||||
| chrX:73649214
|
AG | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.508-30110delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73649214 | |||||
| chrX:73649294
|
G | A | 4 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(1): Show | 4 | HG02970.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-30032G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73649294 | ||||||
| chrX:73649364
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508-29962G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73649364 | ||||||
| chrX:73649497
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.508-29829A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73649497 | ||||||
| chrX:73649713
|
A | G | 1 | a0001c0001t0023g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-29613A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73649713 | ||||||
| chrX:73650333
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.508-28993T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73650333 | ||||||
| chrX:73650442
|
TAAGG | T | 3 | a0001c0001t0002g0095a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | HG00323.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.508-28880_508-2887 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73650442 | |||||
| chrX:73650639
|
G | A | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508-28687G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73650639 | ||||||
| chrX:73650677
|
G | A | 21 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 21 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-28649G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73650677 | ||||||
| chrX:73650701
|
C | CA | 16 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(13): Show | 16 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.508-28607dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73650701 | |||||
| chrX:73650701
|
C | CAA | 1 | a0001c0001t0003g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.508-28608_508-2860 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73650701 | |||||
| chrX:73650701
|
CA | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.508-28607delA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73650701 | |||||
| chrX:73650701
|
CAA | C | 7 | a0001c0001t0001g0137a0001c0001t0002g0078a0001c0001t0002g0178others(4): Show | 7 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-28608_508-2860 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73650701 | |||||
| chrX:73650764
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.508-28562A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73650764 | ||||||
| chrX:73650992
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-28334G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73650992 | ||||||
| chrX:73651234
|
A | G | 2 | a0001c0001t0011g0173a0001c0001t0011g0201 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.508-28092A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651234 | ||||||
| chrX:73651326
|
G | A | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-28000G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651326 | ||||||
| chrX:73651352
|
C | CA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-27972dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73651352 | |||||
| chrX:73651459
|
C | T | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-27867C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651459 | ||||||
| chrX:73651460
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.508-27866G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651460 | ||||||
| chrX:73651488
|
T | A | 6 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(3): Show | 6 | HG00738.hp1 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-27838T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651488 | ||||||
| chrX:73651725
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.508-27601A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651725 | ||||||
| chrX:73651806
|
G | A | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-27520G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651806 | ||||||
| chrX:73651969
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0198 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.508-27357C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73651969 | ||||||
| chrX:73652115
|
A | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0189 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.508-27211A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73652115 | ||||||
| chrX:73652566
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.508-26760A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73652566 | ||||||
| chrX:73653046
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.508-26280C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73653046 | ||||||
| chrX:73653257
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.508-26069C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73653257 | ||||||
| chrX:73653475
|
A | G | 1 | a0001c0001t0021g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.508-25851A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73653475 | ||||||
| chrX:73653781
|
CTT | C | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.508-25543_508-2554 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73653781 | |||||
| chrX:73653898
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.508-25428T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73653898 | ||||||
| chrX:73654356
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.508-24970C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73654356 | ||||||
| chrX:73654419
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-24907A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73654419 | ||||||
| chrX:73654634
|
A | G | 3 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0181 | 3 | HG01123.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.508-24692A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73654634 | ||||||
| chrX:73655385
|
G | GTA | 1 | a0001c0001t0001g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.508-23933_508-2393 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655385 | |||||
| chrX:73655403
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.508-23923A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655403 | ||||||
| chrX:73655428
|
G | GTGTGTAT others(23): Show |
8 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(5): Show | 8 | HG00323.hp1 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-23883_508-2385 others(34): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655428 | |||||
| chrX:73655430
|
G | GTGTATAT others(21): Show |
5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-23892_508-2386 others(32): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655430 | |||||
| chrX:73655432
|
G | GTATATAT others(25): Show |
1 | a0001c0001t0010g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.508-23811_508-2378 others(36): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655432 | |||||
| chrX:73655432
|
GTATATAT others(25): Show |
G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.508-23811_508-2378 others(36): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655432 | |||||
| chrX:73655432
|
GTATATAT others(57): Show |
G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-23843_508-2378 others(68): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655432 | |||||
| chrX:73655458
|
TTG | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.508-23864_508-2386 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655458 | |||||
| chrX:73655462
|
G | A | 15 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.508-23864G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655462 | ||||||
| chrX:73655462
|
GTA | G | 14 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(11): Show | 14 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-23853_508-2385 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655462 | |||||
| chrX:73655462
|
GTATATAT others(27): Show |
G | 14 | a0001c0001t0001g0030a0001c0001t0001g0116a0001c0001t0001g0117others(11): Show | 14 | HG00323.hp2 HG00609.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-23853_508-2382 others(38): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655462 | |||||
| chrX:73655483
|
C | CACAATAT others(25): Show |
9 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-23812_508-2381 others(36): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655483 | |||||
| chrX:73655483
|
C | T | 7 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(4): Show | 7 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-23843C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655483 | ||||||
| chrX:73655483
|
CACAATAT others(57): Show |
C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0060others(2): Show | 6 | HG01081.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-23823_508-2376 others(68): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655483 | |||||
| chrX:73655492
|
G | GTATATAT others(55): Show |
1 | a0001c0001t0003g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-23833_508-2383 others(66): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655492 | |||||
| chrX:73655494
|
G | A | 14 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(11): Show | 14 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.508-23832G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655494 | ||||||
| chrX:73655494
|
GTATATAT others(27): Show |
G | 1 | a0001c0001t0004g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.508-23821_508-2378 others(38): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655494 | |||||
| chrX:73655496
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-23830A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655496 | ||||||
| chrX:73655515
|
C | CACAATAT others(25): Show |
2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.508-23791_508-2376 others(36): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655515 | |||||
| chrX:73655515
|
C | CACAATAT others(57): Show |
1 | a0001c0001t0002g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.508-23760_508-2375 others(68): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655515 | |||||
| chrX:73655515
|
C | CACAATAT others(25): Show |
1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-23793_508-2379 others(36): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655515 | |||||
| chrX:73655515
|
C | T | 20 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-23811C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655515 | ||||||
| chrX:73655526
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-23800G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655526 | ||||||
| chrX:73655526
|
G | GTATATAT others(23): Show |
13 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(10): Show | 13 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.508-23790_508-2378 others(34): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655526 | |||||
| chrX:73655526
|
G | GTATATAT others(55): Show |
2 | a0001c0001t0003g0073a0001c0001t0003g0177 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.508-23790_508-2378 others(66): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655526 | |||||
| chrX:73655526
|
G | GTATATAT others(53): Show |
1 | a0001c0001t0003g0074 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.508-23790_508-2378 others(64): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655526 | |||||
| chrX:73655534
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-23792A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655534 | ||||||
| chrX:73655537
|
T | CACATATA others(25): Show |
1 | a0001c0001t0002g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.508-23790_508-2378 others(36): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655537 | ||||||
| chrX:73655545
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.508-23781T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655545 | ||||||
| chrX:73655547
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-23779T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655547 | ||||||
| chrX:73655580
|
T | TA | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-23745dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655580 | |||||
| chrX:73655607
|
A | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-23719A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655607 | ||||||
| chrX:73655630
|
ATAGTGT | A | 1 | a0001c0001t0001g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-23695_508-2369 others(10): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655630 | ||||||
| chrX:73655631
|
T | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-23695T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655631 | ||||||
| chrX:73655632
|
A | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-23694A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655632 | ||||||
| chrX:73655643
|
GTGTGTGT others(1): Show |
G | 1 | a0001c0001t0001g0174 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.508-23681_508-2367 others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655643 | |||||
| chrX:73655645
|
GTGTGTAT others(1): Show |
G | 81 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0060others(78): Show | 81 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.508-23679_508-2367 others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655645 | |||||
| chrX:73655647
|
GTGTATA | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG00735.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-23677_508-2367 others(10): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655647 | |||||
| chrX:73655647
|
GTGTATAT others(1): Show |
G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG02818.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.508-23677_508-2367 others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655647 | |||||
| chrX:73655649
|
G | GTA | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508-23656_508-2365 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655649 | |||||
| chrX:73655649
|
GTA | G | 1 | a0001c0001t0004g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.508-23656_508-2365 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655649 | |||||
| chrX:73655649
|
GTATA | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(73): Show | 80 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.508-23658_508-2365 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655649 | |||||
| chrX:73655649
|
GTATATA | G | 11 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(8): Show | 11 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.508-23660_508-2365 others(10): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655649 | |||||
| chrX:73655649
|
GTATATAT others(1): Show |
G | 16 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(13): Show | 16 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.508-23662_508-2365 others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73655649 | |||||
| chrX:73655655
|
A | G | 26 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(23): Show | 26 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.508-23671A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655655 | ||||||
| chrX:73655657
|
A | G | 5 | a0001c0001t0003g0177a0001c0001t0005g0010a0001c0001t0005g0011others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-23669A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655657 | ||||||
| chrX:73655890
|
C | G | 32 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(29): Show | 32 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-23436C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73655890 | ||||||
| chrX:73656020
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-23306C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656020 | ||||||
| chrX:73656033
|
A | AG | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(198): Show | 206 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.508-23293_508-2329 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656033 | ||||||
| chrX:73656361
|
G | A | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-22965G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656361 | ||||||
| chrX:73656477
|
A | G | 1 | a0001c0001t0012g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.508-22849A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656477 | ||||||
| chrX:73656522
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.508-22804C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656522 | ||||||
| chrX:73656717
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.508-22609T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656717 | ||||||
| chrX:73656742
|
T | C | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-22584T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656742 | ||||||
| chrX:73656995
|
C | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-22331C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73656995 | ||||||
| chrX:73657061
|
A | AT | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.508-22249dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73657061 | |||||
| chrX:73657061
|
A | ATT | 2 | a0001c0001t0001g0007a0001c0001t0002g0184 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.508-22250_508-2224 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73657061 | |||||
| chrX:73657061
|
AT | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0160a0001c0001t0001g0194others(1): Show | 4 | HG03516.hp2 NA18977.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-22249delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73657061 | |||||
| chrX:73657070
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.508-22256T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657070 | ||||||
| chrX:73657093
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.508-22233T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657093 | ||||||
| chrX:73657099
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.508-22227G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657099 | ||||||
| chrX:73657122
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.508-22204C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657122 | ||||||
| chrX:73657201
|
A | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-22125A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657201 | ||||||
| chrX:73657249
|
A | G | 2 | a0001c0001t0008g0096a0001c0001t0008g0097 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.508-22077A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657249 | ||||||
| chrX:73657305
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.508-22021C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657305 | ||||||
| chrX:73657308
|
C | T | 1 | a0001c0001t0021g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.508-22018C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657308 | ||||||
| chrX:73657350
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.508-21976C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657350 | ||||||
| chrX:73657358
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.508-21968C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657358 | ||||||
| chrX:73657504
|
A | T | 11 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(8): Show | 11 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-21822A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657504 | ||||||
| chrX:73657505
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508-21821C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657505 | ||||||
| chrX:73657758
|
A | G | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-21568A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73657758 | ||||||
| chrX:73658148
|
G | T | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508-21178G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73658148 | ||||||
| chrX:73658248
|
G | GT | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(74): Show | 80 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.508-21047dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
G | GTT | 45 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(42): Show | 46 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.508-21048_508-2104 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
G | GTTT | 31 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0044others(28): Show | 32 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-21049_508-2104 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
G | GTTTT | 13 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0107others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.508-21050_508-2104 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
G | GTTTTT | 2 | a0001c0001t0001g0024a0001c0001t0001g0120 | 2 | HG00642.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.508-21051_508-2104 others(9): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
GT | G | 3 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0023g0099 | 3 | HG02922.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-21047delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
GTT | G | 1 | a0001c0001t0005g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.508-21048_508-2104 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
GTTT | G | 3 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012 | 3 | HG02809.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.508-21049_508-2104 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658248
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0174 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.508-21061_508-2104 others(19): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73658248 | |||||
| chrX:73658278
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0011g0173 | 2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.508-21048T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73658278 | ||||||
| chrX:73658278
|
T | TC | 3 | a0001c0001t0002g0172a0001c0001t0002g0200a0001c0001t0011g0201 | 3 | HG01109.hp1 HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.508-21048_508-2104 others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73658278 | ||||||
| chrX:73658373
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-20953G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73658373 | ||||||
| chrX:73658475
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.508-20851A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73658475 | ||||||
| chrX:73658491
|
T | A | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-20835T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73658491 | ||||||
| chrX:73659361
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508-19965T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73659361 | ||||||
| chrX:73659370
|
C | CT | 9 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-19933dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73659370 | |||||
| chrX:73659370
|
C | CTT | 7 | a0001c0001t0003g0065a0001c0001t0003g0070a0001c0001t0003g0071others(4): Show | 7 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-19934_508-1993 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73659370 | |||||
| chrX:73659370
|
C | CTTT | 12 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0067others(9): Show | 12 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-19935_508-1993 others(7): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73659370 | |||||
| chrX:73659370
|
CT | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.508-19933delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73659370 | |||||
| chrX:73659370
|
CTT | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0154others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.508-19934_508-1993 others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73659370 | |||||
| chrX:73659527
|
TTGAC | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-19796_508-1979 others(8): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73659527 | |||||
| chrX:73659618
|
A | G | 4 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(1): Show | 4 | HG02970.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-19708A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73659618 | ||||||
| chrX:73659777
|
T | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-19549T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73659777 | ||||||
| chrX:73660157
|
A | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-19169A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660157 | ||||||
| chrX:73660300
|
C | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-19026C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660300 | ||||||
| chrX:73660502
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0118 | 2 | HG00323.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.508-18824C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660502 | ||||||
| chrX:73660588
|
C | A | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.508-18738C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660588 | ||||||
| chrX:73660643
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508-18683C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660643 | ||||||
| chrX:73660707
|
A | AC | 1 | a0001c0001t0001g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.508-18617dupC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73660707 | |||||
| chrX:73660906
|
T | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-18420T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660906 | ||||||
| chrX:73660946
|
C | T | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-18380C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73660946 | ||||||
| chrX:73661065
|
TG | T | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.508-18256delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73661065 | |||||
| chrX:73661801
|
A | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-17525A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73661801 | ||||||
| chrX:73661829
|
C | A | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-17497C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73661829 | ||||||
| chrX:73661868
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.508-17458G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73661868 | ||||||
| chrX:73662042
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.508-17284A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662042 | ||||||
| chrX:73662051
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.508-17275A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662051 | ||||||
| chrX:73662063
|
TAAATAAA others(3): Show |
T | 1 | a0001c0001t0001g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.508-17252_508-1724 others(14): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73662063 | |||||
| chrX:73662084
|
T | C | 1 | a0001c0001t0004g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-17242T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662084 | ||||||
| chrX:73662336
|
G | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-16990G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662336 | ||||||
| chrX:73662585
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.508-16741A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662585 | ||||||
| chrX:73662768
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.508-16558T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662768 | ||||||
| chrX:73662806
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.508-16520G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662806 | ||||||
| chrX:73662931
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02129.hp1 NA18747.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-16395C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73662931 | ||||||
| chrX:73663051
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0059 | 3 | HG02280.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.508-16275G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73663051 | ||||||
| chrX:73663622
|
C | T | 1 | a0001c0001t0014g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.508-15704C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73663622 | ||||||
| chrX:73664023
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0146 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.508-15303C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73664023 | ||||||
| chrX:73664302
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(196): Show | 203 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.508-15024C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73664302 | ||||||
| chrX:73664418
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.508-14908T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73664418 | ||||||
| chrX:73664701
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-14625C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73664701 | ||||||
| chrX:73665765
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508-13561G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73665765 | ||||||
| chrX:73665954
|
C | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-13372C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73665954 | ||||||
| chrX:73666004
|
G | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-13322G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666004 | ||||||
| chrX:73666092
|
G | T | 1 | a0001c0001t0001g0033 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.508-13234G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666092 | ||||||
| chrX:73666219
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-13107A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666219 | ||||||
| chrX:73666464
|
T | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-12862T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666464 | ||||||
| chrX:73666572
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.508-12754T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666572 | ||||||
| chrX:73666605
|
A | T | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0202 | 3 | HG01243.hp1 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.508-12721A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666605 | ||||||
| chrX:73666905
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(82): Show | 86 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.508-12421C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73666905 | ||||||
| chrX:73667372
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-11952delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73667372 | |||||
| chrX:73667464
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-11862G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73667464 | ||||||
| chrX:73667732
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.508-11594A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73667732 | ||||||
| chrX:73667842
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-11480delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73667842 | |||||
| chrX:73668084
|
T | C | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-11242T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668084 | ||||||
| chrX:73668304
|
A | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-11022A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668304 | ||||||
| chrX:73668398
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508-10928C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668398 | ||||||
| chrX:73668573
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.508-10753T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668573 | ||||||
| chrX:73668837
|
A | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-10489A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668837 | ||||||
| chrX:73668941
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508-10385G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668941 | ||||||
| chrX:73668979
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.508-10347G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73668979 | ||||||
| chrX:73669294
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0144a0001c0001t0001g0163 | 3 | NA19060.hp1 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508-10032G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73669294 | ||||||
| chrX:73669513
|
A | G | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-9813A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73669513 | ||||||
| chrX:73669609
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.508-9717G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73669609 | ||||||
| chrX:73669645
|
G | T | 6 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0073others(3): Show | 6 | HG02280.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-9681G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73669645 | ||||||
| chrX:73669666
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.508-9660C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73669666 | ||||||
| chrX:73669943
|
T | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-9383T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73669943 | ||||||
| chrX:73670015
|
C | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-9311C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73670015 | ||||||
| chrX:73670201
|
GC | G | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-9121delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73670201 | |||||
| chrX:73670477
|
AT | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-8842delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73670477 | |||||
| chrX:73670594
|
A | ATTCT | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-8730_508-8727d others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73670594 | |||||
| chrX:73670616
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.508-8710C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73670616 | ||||||
| chrX:73670648
|
G | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 6 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-8678G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73670648 | ||||||
| chrX:73670668
|
ACTT | A | 1 | a0001c0001t0020g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.508-8654_508-8652d others(5): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73670668 | |||||
| chrX:73670671
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.508-8655T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73670671 | ||||||
| chrX:73670687
|
G | C | 1 | a0001c0001t0004g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.508-8639G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73670687 | ||||||
| chrX:73671033
|
T | C | 9 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-8293T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671033 | ||||||
| chrX:73671057
|
GT | G | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-8263delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73671057 | |||||
| chrX:73671122
|
C | T | 57 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(54): Show | 57 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.508-8204C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671122 | ||||||
| chrX:73671271
|
C | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-8055C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671271 | ||||||
| chrX:73671375
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.508-7951T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671375 | ||||||
| chrX:73671444
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-7882A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671444 | ||||||
| chrX:73671550
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.508-7776A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671550 | ||||||
| chrX:73671674
|
C | G | 1 | a0001c0001t0010g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.508-7652C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671674 | ||||||
| chrX:73671721
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508-7605C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671721 | ||||||
| chrX:73671760
|
CT | C | 1 | a0001c0001t0001g0142 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.508-7556delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73671760 | |||||
| chrX:73671772
|
AT | A | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-7550delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73671772 | |||||
| chrX:73671856
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-7470G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671856 | ||||||
| chrX:73671886
|
C | T | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-7440C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671886 | ||||||
| chrX:73671918
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.508-7408C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671918 | ||||||
| chrX:73671945
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.508-7381G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671945 | ||||||
| chrX:73671954
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-7372G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73671954 | ||||||
| chrX:73672011
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508-7315C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672011 | ||||||
| chrX:73672091
|
C | CATGAACT others(482): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7173_508-7172i others(491): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73672091 | |||||
| chrX:73672166
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7160T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672166 | ||||||
| chrX:73672167
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7159G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672167 | ||||||
| chrX:73672175
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7151A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672175 | ||||||
| chrX:73672218
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7108A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672218 | ||||||
| chrX:73672220
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7106T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672220 | ||||||
| chrX:73672265
|
A | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7061A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672265 | ||||||
| chrX:73672268
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7058C>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672268 | ||||||
| chrX:73672279
|
T | C | 2 | a0001c0001t0004g0016a0001c0001t0004g0020 | 2 | HG00738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.508-7047T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672279 | ||||||
| chrX:73672294
|
A | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA18961.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.508-7032A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672294 | ||||||
| chrX:73672595
|
C | T | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508-6731C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672595 | ||||||
| chrX:73672646
|
A | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.508-6680A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672646 | ||||||
| chrX:73672793
|
G | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6533G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672793 | ||||||
| chrX:73672862
|
T | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6464T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672862 | ||||||
| chrX:73672864
|
C | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6462C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672864 | ||||||
| chrX:73672868
|
A | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6458A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672868 | ||||||
| chrX:73672873
|
T | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6453T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672873 | ||||||
| chrX:73672881
|
G | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6445G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672881 | ||||||
| chrX:73672887
|
C | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6439C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672887 | ||||||
| chrX:73672906
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6420A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672906 | ||||||
| chrX:73672908
|
G | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6418G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672908 | ||||||
| chrX:73672927
|
T | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6399T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672927 | ||||||
| chrX:73672949
|
G | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6377G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672949 | ||||||
| chrX:73672959
|
C | G | 5 | a0001c0001t0003g0070a0001c0001t0005g0010a0001c0001t0005g0011others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-6367C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672959 | ||||||
| chrX:73672982
|
A | C | 15 | a0001c0001t0001g0030a0001c0001t0001g0116a0001c0001t0001g0117others(12): Show | 15 | HG00323.hp2 HG00609.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.508-6344A>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672982 | ||||||
| chrX:73672985
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.508-6341G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73672985 | ||||||
| chrX:73672989
|
GC | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6335delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73672989 | |||||
| chrX:73673021
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6305A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73673021 | ||||||
| chrX:73673487
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0060others(2): Show | 6 | HG01081.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-5839G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73673487 | ||||||
| chrX:73673610
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-5716T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73673610 | ||||||
| chrX:73673960
|
G | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0118 | 2 | HG00323.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.508-5366G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73673960 | ||||||
| chrX:73673983
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.508-5343C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73673983 | ||||||
| chrX:73674100
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.508-5226G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73674100 | ||||||
| chrX:73674162
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.508-5164T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73674162 | ||||||
| chrX:73674263
|
A | G | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-5063A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73674263 | ||||||
| chrX:73674445
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-4879delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73674445 | |||||
| chrX:73674710
|
AG | A | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.508-4613delG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73674710 | |||||
| chrX:73674728
|
A | G | 9 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-4598A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73674728 | ||||||
| chrX:73674762
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508-4564C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73674762 | ||||||
| chrX:73674812
|
TTTAA | T | 66 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0102others(63): Show | 66 | HG00673.hp1 HG01258.hp1 HG01975.hp2 others(63): Show |
intron_variant | MODIFIER | c.508-4511_508-4508d others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73674812 | |||||
| chrX:73675053
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.508-4273G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675053 | ||||||
| chrX:73675220
|
G | GT | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.508-4106_508-4105i others(3): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675220 | ||||||
| chrX:73675330
|
G | A | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-3996G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675330 | ||||||
| chrX:73675348
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.508-3978A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675348 | ||||||
| chrX:73675368
|
A | G | 21 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 21 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-3958A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675368 | ||||||
| chrX:73675380
|
G | A | 1 | a0001c0001t0009g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.508-3946G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675380 | ||||||
| chrX:73675530
|
T | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0146 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.508-3796T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675530 | ||||||
| chrX:73675771
|
G | A | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-3555G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675771 | ||||||
| chrX:73675871
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.508-3455G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675871 | ||||||
| chrX:73675900
|
A | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.508-3426A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73675900 | ||||||
| chrX:73676155
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.508-3171G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676155 | ||||||
| chrX:73676377
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.508-2949C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676377 | ||||||
| chrX:73676451
|
G | A | 53 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-2875G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676451 | ||||||
| chrX:73676633
|
C | G | 1 | a0001c0001t0003g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-2693C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676633 | ||||||
| chrX:73676700
|
G | C | 1 | a0001c0001t0004g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.508-2626G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676700 | ||||||
| chrX:73676710
|
T | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-2616T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676710 | ||||||
| chrX:73676807
|
TC | T | 2 | a0001c0001t0003g0067a0001c0001t0003g0075 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.508-2518delC | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676807 | ||||||
| chrX:73676808
|
CTGATTTT others(4): Show |
C | 15 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.508-2517_508-2507d others(13): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676808 | ||||||
| chrX:73676811
|
ATTTTTAC others(3): Show |
A | 2 | a0001c0001t0003g0067a0001c0001t0003g0075 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.508-2512_508-2503d others(12): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73676811 | |||||
| chrX:73676821
|
T | A | 15 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.508-2505T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676821 | ||||||
| chrX:73676822
|
T | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-2504T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676822 | ||||||
| chrX:73676838
|
C | G | 1 | a0001c0001t0003g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508-2488C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676838 | ||||||
| chrX:73676865
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.508-2461A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676865 | ||||||
| chrX:73676883
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.508-2443A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676883 | ||||||
| chrX:73676922
|
CT | C | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.508-2401delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73676922 | |||||
| chrX:73676940
|
T | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.508-2386T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73676940 | ||||||
| chrX:73677147
|
G | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-2179G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677147 | ||||||
| chrX:73677505
|
T | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.508-1821T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677505 | ||||||
| chrX:73677714
|
C | T | 6 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0073others(3): Show | 6 | HG02280.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-1612C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677714 | ||||||
| chrX:73677737
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0186 | 3 | HG02080.hp1 NA18965.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.508-1589C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677737 | ||||||
| chrX:73677785
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.508-1541G>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677785 | ||||||
| chrX:73677785
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.508-1541G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677785 | ||||||
| chrX:73677824
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.508-1502C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677824 | ||||||
| chrX:73677990
|
T | TG | 28 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0149others(25): Show | 28 | HG00642.hp1 HG00735.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.508-1335dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73677990 | |||||
| chrX:73677991
|
GT | G | 5 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0180others(2): Show | 5 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-1319delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 73677991 | |||||
| chrX:73677992
|
T | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.508-1334T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677992 | ||||||
| chrX:73677993
|
T | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0012others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1333T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677993 | ||||||
| chrX:73677993
|
T | G | 5 | a0001c0001t0002g0078a0001c0001t0002g0178a0001c0001t0002g0180others(2): Show | 5 | HG01123.hp2 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-1333T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73677993 | ||||||
| chrX:73678027
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0189 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.508-1299C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678027 | ||||||
| chrX:73678030
|
C | G | 1 | a0001c0001t0008g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508-1296C>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678030 | ||||||
| chrX:73678035
|
A | G | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-1291A>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678035 | ||||||
| chrX:73678263
|
TTTGG | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508-1062_508-1059d others(6): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678263 | ||||||
| chrX:73678275
|
G | T | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-1051G>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678275 | ||||||
| chrX:73678285
|
G | C | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-1041G>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678285 | ||||||
| chrX:73678343
|
T | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0172a0001c0001t0002g0200others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-983T>A | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678343 | ||||||
| chrX:73678495
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(82): Show | 86 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.508-831C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678495 | ||||||
| chrX:73678994
|
A | T | 1 | a0001c0001t0014g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.508-332A>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 3/5 | chrX | 73678994 | ||||||
| chrX:73679530
|
T | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0116a0001c0001t0001g0117others(11): Show | 14 | HG00323.hp2 HG00609.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-124T>C | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 4/5 | chrX | 73679530 | ||||||
| chrX:73679570
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.565-84T>G | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 4/5 | chrX | 73679570 | ||||||
| chrX:73680098
|
C | CT | 6 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0116others(3): Show | 6 | HG01884.hp2 HG02602.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+401dupT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chrX | 73680098 | |||||
| chrX:73680098
|
CT | C | 18 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0199others(15): Show | 18 | HG00735.hp2 HG01123.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.624+401delT | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chrX | 73680098 | |||||
| chrX:73680098
|
CTT | C | 2 | a0001c0001t0011g0173a0001c0001t0011g0201 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.624+400_624+401del others(2): Show |
CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chrX | 73680098 | |||||
| chrX:73680370
|
T | TA | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.625-584dupA | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chrX | 73680370 | |||||
| chrX:73680516
|
C | T | 17 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.625-439C>T | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 5/5 | chrX | 73680516 | ||||||
| chrX:73680641
|
T | TG | 1 | a0001c0001t0001g0192 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.625-309dupG | CHIC1 | ENSG00000204116.12 | transcript | ENST00000373502.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chrX | 73680641 |