Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54997 |
|---|---|
| ensemblid | ENSG00000088992.18 |
| hgncid | 26065 |
| symbol | TESC |
| name | tescalcin |
| refseq_nuc | NM_017899.4 |
| refseq_prot | NP_060369.3 |
| ensembl_nuc | ENST00000335209.12 |
| ensembl_prot | ENSP00000334785.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 117038923 |
| end | 117099416 |
| strand | - |
| ver | v1.2 |
| region | chr12:117038923-117099416 |
| region5000 | chr12:117033923-117104416 |
| regionname0 | TESC_chr12_117038923_117099416 |
| regionname5000 | TESC_chr12_117033923_117104416 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 214 | 310 | 98 | 50 | 116 | 11 | 33 | 82 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0002 | 0/0 | 214 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0003 | 0/0 | 214 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 645 | 307 | 96 | 50 | 115 | 11 | 33 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| c0002 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| c0003 | 0/0 | 645 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| c0004 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| c0005 | 0/0 | 645 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 345 | 236 | 55 | 37 | 106 | 7 | 29 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0002 | 0/0 | 345 | 32 | 15 | 9 | 1 | 3 | 4 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0003 | 0/0 | 344 | 27 | 22 | 2 | 3 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0004 | 0/0 | 343 | 6 | 5 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0005 | 0/0 | 344 | 4 | 0 | 1 | 3 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0006 | 0/0 | 345 | 2 | 0 | 0 | 0 | 2 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0007 | 0/0 | 345 | 2 | 1 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0008 | 0/0 | 345 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0009 | 0/0 | 345 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| t0010 | 0/0 | 345 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 645 | 307 | 96 | 50 | 115 | 11 | 33 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0002 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0004 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0002c0005 | 0/0 | 645 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0003c0003 | 0/0 | 645 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 989 | 231 | 53 | 37 | 105 | 6 | 28 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0002 | 0/0 | 989 | 32 | 15 | 9 | 1 | 3 | 4 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0003 | 0/0 | 988 | 27 | 22 | 2 | 3 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0004 | 0/0 | 987 | 6 | 5 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0005 | 0/0 | 988 | 4 | 0 | 1 | 3 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0006 | 0/0 | 989 | 2 | 0 | 0 | 0 | 2 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0007 | 0/0 | 989 | 2 | 1 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0008 | 0/0 | 989 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0009 | 0/0 | 989 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0001t0010 | 0/0 | 989 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0002t0001 | 0/0 | 989 | 2 | 2 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0001c0004t0001 | 0/0 | 989 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0002c0005t0001 | 0/0 | 989 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| a0003c0003t0001 | 0/0 | 989 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | copy fasta | chr12 | 117033923 | 117104416 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0001t0010g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0002c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0193 | EUR | GBR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0259 | EUR | FIN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0137 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0196 | EUR | IBS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0155 | EUR | IBS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0194 | EUR | IBS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02056 | hp1 | a0001 | c0001 | t0009 | g0254 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02083 | hp1 | a0001 | c0001 | t0010 | g0297 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CDX | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02602 | hp1 | a0002 | c0005 | t0001 | g0244 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0299 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | GWD | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0013 | SAS | STU | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0280 | EAS | CHB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | YRI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | LWK | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | LWK | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | LWK | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | YRI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ASW | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | TSI | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | GIH | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | ACB | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | MSL | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | USA | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | USA | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0298 | EAS | JPT | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0133 | REF | REF | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0156 | REF | REF | TESC_chr12_117033923_117104416 | TESC | chr12 | 117033923 | 117104416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:117041966
|
G | C | 1 | a0003 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.548C>G | p.Thr183Ser | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/8 | 682/989 | 548/645 | 183/214 | chr12 | 117041966 | ||
| chr12:117075334
|
G | A | 1 | a0002 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.65C>T | p.Ser22Leu | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/8 | 199/989 | 65/645 | 22/214 | chr12 | 117075334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:117046631
|
G | A | 1 | a0001c0002 | 2 | HG03453.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.447C>T | p.Ile149Ile | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/8 | 581/989 | 447/645 | 149/214 | chr12 | 117046631 | ||
| chr12:117049071
|
G | A | 1 | a0001c0004 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.297C>T | p.Asp99Asp | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/8 | 431/989 | 297/645 | 99/214 | chr12 | 117049071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:117038936
|
CT | C | 2 | a0001c0001t0003a0001c0001t0005 | 31 | HG00735.hp2 HG00741.hp1 HG01256.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*196delA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 8/8 | 196 | chr12 | 117038936 | |||||
| chr12:117038936
|
CTT | C | 1 | a0001c0001t0004 | 6 | HG01106.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*195_*196delAA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 8/8 | 195 | chr12 | 117038936 | |||||
| chr12:117039078
|
C | T | 1 | a0001c0001t0006 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*55G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 8/8 | 55 | chr12 | 117039078 | |||||
| chr12:117039088
|
C | T | 1 | a0001c0001t0009 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 8/8 | 45 | chr12 | 117039088 | |||||
| chr12:117039091
|
C | A | 2 | a0001c0001t0002a0001c0001t0005 | 36 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*42G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 8/8 | 42 | chr12 | 117039091 | |||||
| chr12:117099300
|
C | T | 1 | a0001c0001t0008 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/8 | 18 | chr12 | 117099300 | |||||
| chr12:117099352
|
G | A | 1 | a0001c0001t0010 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/8 | 70 | chr12 | 117099352 | |||||
| chr12:117099383
|
G | A | 1 | a0001c0001t0007 | 2 | HG03209.hp2 NA18955.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-101C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/8 | chr12 | 117099383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:117039221
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 9 | HG00544.hp1 HG01099.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.568-11G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039221 | ||||||
| chr12:117039277
|
G | A | 5 | a0001c0001t0002g0187a0001c0001t0002g0189a0001c0001t0002g0193others(2): Show | 5 | HG00140.hp2 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-67C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039277 | ||||||
| chr12:117039299
|
C | T | 64 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0020others(61): Show | 64 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.568-89G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039299 | ||||||
| chr12:117039328
|
A | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-118T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039328 | ||||||
| chr12:117039412
|
A | T | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.568-202T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039412 | ||||||
| chr12:117039568
|
T | TTCCATGA others(14): Show |
30 | a0001c0001t0003g0017a0001c0001t0003g0019a0001c0001t0003g0021others(27): Show | 30 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.568-359_568-358ins others(21): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039568 | ||||||
| chr12:117039617
|
C | T | 29 | a0001c0001t0003g0019a0001c0001t0003g0021a0001c0001t0003g0028others(26): Show | 29 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.568-407G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039617 | ||||||
| chr12:117039627
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.568-417A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039627 | ||||||
| chr12:117039637
|
G | A | 28 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0075others(25): Show | 28 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.568-427C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039637 | ||||||
| chr12:117039662
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0010g0297 | 3 | HG02083.hp1 NA18953.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.568-452G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039662 | ||||||
| chr12:117039676
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.568-466G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039676 | ||||||
| chr12:117039677
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.568-467C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039677 | ||||||
| chr12:117039722
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.568-512A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039722 | ||||||
| chr12:117039728
|
C | T | 35 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0020others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.568-518G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039728 | ||||||
| chr12:117039779
|
A | T | 28 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0075others(25): Show | 28 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.568-569T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039779 | ||||||
| chr12:117039901
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.568-691G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039901 | ||||||
| chr12:117039982
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.568-772C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039982 | ||||||
| chr12:117039993
|
C | T | 61 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0060others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.568-783G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117039993 | ||||||
| chr12:117040002
|
G | A | 46 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0045others(43): Show | 46 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.568-792C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040002 | ||||||
| chr12:117040011
|
G | A | 33 | a0001c0001t0001g0126a0001c0001t0002g0016a0001c0001t0002g0018others(30): Show | 33 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.568-801C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040011 | ||||||
| chr12:117040146
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.568-936G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040146 | ||||||
| chr12:117040271
|
G | A | 27 | a0001c0001t0003g0017a0001c0001t0003g0019a0001c0001t0003g0021others(24): Show | 27 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.568-1061C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040271 | ||||||
| chr12:117040431
|
C | A | 34 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0020others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.568-1221G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040431 | ||||||
| chr12:117040445
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568-1235C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040445 | ||||||
| chr12:117040473
|
G | C | 16 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0085others(13): Show | 16 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.568-1263C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040473 | ||||||
| chr12:117040589
|
G | A | 29 | a0001c0001t0003g0017a0001c0001t0003g0019a0001c0001t0003g0021others(26): Show | 29 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.567+1358C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040589 | ||||||
| chr12:117040668
|
G | C | 2 | a0001c0002t0001g0076a0001c0002t0001g0077 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.567+1279C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040668 | ||||||
| chr12:117040707
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.567+1240G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040707 | ||||||
| chr12:117040777
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(86): Show | 95 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.567+1170G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040777 | ||||||
| chr12:117040781
|
C | G | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.567+1166G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040781 | ||||||
| chr12:117040914
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(23): Show | 26 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.567+1033G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040914 | ||||||
| chr12:117040962
|
TTCC | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(132): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.567+982_567+984del others(3): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117040962 | ||||||
| chr12:117041014
|
G | A | 14 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0025others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.567+933C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041014 | ||||||
| chr12:117041020
|
C | CGGGGAGG others(7): Show |
4 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0245others(1): Show | 6 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.567+913_567+926dup others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041020 | ||||||
| chr12:117041160
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0051others(9): Show | 15 | HG00741.hp1 HG01074.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.567+787C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041160 | ||||||
| chr12:117041174
|
G | A | 137 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(134): Show | 140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.567+773C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041174 | ||||||
| chr12:117041192
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.567+755C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041192 | ||||||
| chr12:117041196
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.567+751C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041196 | ||||||
| chr12:117041214
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(164): Show | 173 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.567+733A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041214 | ||||||
| chr12:117041237
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.567+710G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041237 | ||||||
| chr12:117041243
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567+704G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041243 | ||||||
| chr12:117041247
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.567+700C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041247 | ||||||
| chr12:117041380
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.567+567A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041380 | ||||||
| chr12:117041384
|
GTACAGTG others(6): Show |
G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064 | 3 | HG02615.hp2 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.567+550_567+562del others(13): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041384 | ||||||
| chr12:117041388
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.567+559T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041388 | ||||||
| chr12:117041419
|
A | AC | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064 | 3 | HG02615.hp2 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.567+527dupG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041419 | ||||||
| chr12:117041457
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.567+490G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041457 | ||||||
| chr12:117041477
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.567+470G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041477 | ||||||
| chr12:117041623
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.567+324C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041623 | ||||||
| chr12:117041624
|
C | T | 2 | a0001c0001t0003g0070a0001c0001t0003g0104 | 2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.567+323G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041624 | ||||||
| chr12:117041859
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.567+88C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 7/7 | chr12 | 117041859 | ||||||
| chr12:117042029
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.520-35G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042029 | ||||||
| chr12:117042051
|
G | A | 10 | a0001c0001t0001g0074a0001c0001t0001g0222a0001c0001t0001g0225others(7): Show | 10 | HG02572.hp1 HG03491.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-57C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042051 | ||||||
| chr12:117042130
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.520-136T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042130 | ||||||
| chr12:117042205
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(41): Show | 50 | HG00423.hp1 HG01074.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.520-211A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042205 | ||||||
| chr12:117042324
|
A | C | 2 | a0001c0001t0001g0039a0001c0001t0003g0046 | 2 | NA19055.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.520-330T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042324 | ||||||
| chr12:117042419
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(134): Show | 143 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.520-425G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042419 | ||||||
| chr12:117042458
|
C | T | 29 | a0001c0001t0001g0238a0001c0001t0003g0017a0001c0001t0003g0019others(26): Show | 29 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.520-464G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042458 | ||||||
| chr12:117042572
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-578C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042572 | ||||||
| chr12:117042574
|
AG | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(138): Show | 147 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.520-581delC | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042574 | ||||||
| chr12:117042651
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0283 | 5 | HG01891.hp2 HG02055.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-657C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042651 | ||||||
| chr12:117042720
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0116 | 3 | HG01257.hp2 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.520-726C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042720 | ||||||
| chr12:117042751
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0271 | 2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.520-757G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042751 | ||||||
| chr12:117042773
|
G | T | 1 | a0001c0001t0003g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-779C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042773 | ||||||
| chr12:117042831
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.520-837C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042831 | ||||||
| chr12:117042881
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.520-887G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042881 | ||||||
| chr12:117042889
|
C | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0060others(7): Show | 10 | HG01884.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-895G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042889 | ||||||
| chr12:117042896
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(167): Show | 176 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.520-902C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042896 | ||||||
| chr12:117042945
|
T | C | 15 | a0001c0001t0001g0045a0001c0001t0001g0085a0001c0001t0001g0117others(12): Show | 15 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-951A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117042945 | ||||||
| chr12:117043044
|
C | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0260 | 2 | NA18971.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.520-1050G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043044 | ||||||
| chr12:117043175
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0085 | 2 | NA18947.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.520-1181T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043175 | ||||||
| chr12:117043404
|
C | T | 17 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0085others(14): Show | 17 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.520-1410G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043404 | ||||||
| chr12:117043455
|
A | ATTTGT | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(137): Show | 146 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.520-1466_520-1462d others(7): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043455 | ||||||
| chr12:117043690
|
T | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 41 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.520-1696A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043690 | ||||||
| chr12:117043810
|
G | T | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.520-1816C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043810 | ||||||
| chr12:117043844
|
C | T | 1 | a0001c0001t0005g0137 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.520-1850G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043844 | ||||||
| chr12:117043984
|
A | C | 2 | a0001c0001t0001g0133a0003c0003t0001g0155 | 2 | HG01516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.520-1990T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117043984 | ||||||
| chr12:117044103
|
A | C | 1 | a0001c0001t0002g0016 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.520-2109T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044103 | ||||||
| chr12:117044214
|
T | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-2220A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044214 | ||||||
| chr12:117044250
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-2256G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044250 | ||||||
| chr12:117044293
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.519+2266T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044293 | ||||||
| chr12:117044339
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.519+2220G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044339 | ||||||
| chr12:117044365
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.519+2194C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044365 | ||||||
| chr12:117044379
|
G | A | 1 | a0001c0001t0001g0001 | 3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.519+2180C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044379 | ||||||
| chr12:117044460
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+2099T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044460 | ||||||
| chr12:117044472
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+2087A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044472 | ||||||
| chr12:117044496
|
T | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+2063A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044496 | ||||||
| chr12:117044511
|
C | G | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519+2048G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044511 | ||||||
| chr12:117044519
|
T | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+2040A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044519 | ||||||
| chr12:117044564
|
A | C | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.519+1995T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044564 | ||||||
| chr12:117044619
|
C | A | 5 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+1940G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044619 | ||||||
| chr12:117044627
|
A | C | 16 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0085others(13): Show | 16 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.519+1932T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044627 | ||||||
| chr12:117044672
|
T | G | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519+1887A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044672 | ||||||
| chr12:117044681
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(166): Show | 175 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.519+1878A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044681 | ||||||
| chr12:117044696
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0283 | 5 | HG01891.hp2 HG02055.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+1863C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044696 | ||||||
| chr12:117044714
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+1845A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044714 | ||||||
| chr12:117044754
|
G | T | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519+1805C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044754 | ||||||
| chr12:117044758
|
G | A | 30 | a0001c0001t0001g0238a0001c0001t0003g0017a0001c0001t0003g0019others(27): Show | 30 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.519+1801C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044758 | ||||||
| chr12:117044790
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0160 | 2 | NA18944.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.519+1769C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044790 | ||||||
| chr12:117044846
|
G | A | 30 | a0001c0001t0001g0238a0001c0001t0003g0017a0001c0001t0003g0019others(27): Show | 30 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.519+1713C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044846 | ||||||
| chr12:117044847
|
A | C | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519+1712T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044847 | ||||||
| chr12:117044887
|
A | T | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519+1672T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044887 | ||||||
| chr12:117044914
|
AAG | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(131): Show | 140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.519+1643_519+1644d others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044914 | ||||||
| chr12:117044994
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+1565A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044994 | ||||||
| chr12:117044997
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.519+1562G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117044997 | ||||||
| chr12:117045035
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+1524A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045035 | ||||||
| chr12:117045062
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.519+1497G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045062 | ||||||
| chr12:117045130
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.519+1429T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045130 | ||||||
| chr12:117045252
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+1307C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045252 | ||||||
| chr12:117045276
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG02622.hp1 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519+1283G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045276 | ||||||
| chr12:117045324
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0241 | 2 | NA18954.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.519+1235G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045324 | ||||||
| chr12:117045596
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.519+963C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045596 | ||||||
| chr12:117045620
|
C | T | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+939G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045620 | ||||||
| chr12:117045642
|
G | A | 3 | a0001c0001t0001g0078a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG02109.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.519+917C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045642 | ||||||
| chr12:117045647
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0246others(1): Show | 6 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+912G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045647 | ||||||
| chr12:117045678
|
C | G | 1 | a0001c0001t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.519+881G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117045678 | ||||||
| chr12:117046038
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+521T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046038 | ||||||
| chr12:117046104
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.519+455A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046104 | ||||||
| chr12:117046112
|
A | G | 3 | a0001c0001t0001g0078a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG02109.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.519+447T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046112 | ||||||
| chr12:117046114
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+445G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046114 | ||||||
| chr12:117046139
|
C | T | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+420G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046139 | ||||||
| chr12:117046161
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0042 | 2 | NA18944.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.519+398C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046161 | ||||||
| chr12:117046182
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.519+377C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046182 | ||||||
| chr12:117046257
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(155): Show | 164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.519+302C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046257 | ||||||
| chr12:117046274
|
C | T | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+285G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046274 | ||||||
| chr12:117046305
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+254C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046305 | ||||||
| chr12:117046457
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.519+102A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046457 | ||||||
| chr12:117046529
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.519+30C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046529 | ||||||
| chr12:117046530
|
C | T | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.519+29G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046530 | ||||||
| chr12:117046531
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+28C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046531 | ||||||
| chr12:117046536
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.519+23C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 6/7 | chr12 | 117046536 | ||||||
| chr12:117046868
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.350-30C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117046868 | ||||||
| chr12:117046977
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350-139C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117046977 | ||||||
| chr12:117046993
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.350-155A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117046993 | ||||||
| chr12:117047077
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.350-239A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047077 | ||||||
| chr12:117047113
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-275G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047113 | ||||||
| chr12:117047178
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-340C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047178 | ||||||
| chr12:117047201
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-363C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047201 | ||||||
| chr12:117047217
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350-379A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047217 | ||||||
| chr12:117047283
|
T | A | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.350-445A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047283 | ||||||
| chr12:117047321
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.350-483C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047321 | ||||||
| chr12:117047408
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.350-570C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047408 | ||||||
| chr12:117047414
|
A | AT | 92 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(89): Show | 92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.350-577dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047414 | ||||||
| chr12:117047414
|
A | ATT | 7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0051others(4): Show | 10 | HG01074.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-578_350-577dup others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047414 | ||||||
| chr12:117047449
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.350-611A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047449 | ||||||
| chr12:117047478
|
G | A | 1 | a0001c0001t0005g0279 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.350-640C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047478 | ||||||
| chr12:117047552
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.350-714C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047552 | ||||||
| chr12:117047560
|
G | C | 1 | a0001c0001t0003g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.350-722C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047560 | ||||||
| chr12:117047714
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0051others(2): Show | 8 | HG01074.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-876C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047714 | ||||||
| chr12:117047718
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.350-880A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047718 | ||||||
| chr12:117047727
|
A | G | 41 | a0001c0001t0001g0191a0001c0001t0001g0273a0001c0001t0002g0016others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.350-889T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047727 | ||||||
| chr12:117047747
|
A | G | 2 | a0001c0001t0002g0259a0001c0001t0002g0271 | 2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.350-909T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047747 | ||||||
| chr12:117047781
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-943C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047781 | ||||||
| chr12:117047912
|
T | C | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.350-1074A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047912 | ||||||
| chr12:117047946
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.349+1073G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047946 | ||||||
| chr12:117047970
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18971.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.349+1049C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047970 | ||||||
| chr12:117047982
|
T | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.349+1037A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117047982 | ||||||
| chr12:117048028
|
AC | A | 4 | a0001c0001t0002g0187a0001c0001t0002g0189a0001c0001t0002g0193others(1): Show | 4 | HG00140.hp2 HG01361.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+990delG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048028 | ||||||
| chr12:117048052
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.349+967G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048052 | ||||||
| chr12:117048230
|
T | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.349+789A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048230 | ||||||
| chr12:117048244
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0002t0001g0076others(1): Show | 4 | HG02109.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+775C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048244 | ||||||
| chr12:117048393
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0214 | 2 | NA18951.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.349+626C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048393 | ||||||
| chr12:117048416
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.349+603C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048416 | ||||||
| chr12:117048581
|
G | A | 2 | a0001c0001t0006g0194a0001c0001t0006g0196 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.349+438C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048581 | ||||||
| chr12:117048584
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0037others(15): Show | 20 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.349+435C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048584 | ||||||
| chr12:117048666
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.349+353C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048666 | ||||||
| chr12:117048673
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(128): Show | 137 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.349+346G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048673 | ||||||
| chr12:117048723
|
C | T | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+296G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048723 | ||||||
| chr12:117048769
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.349+250G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048769 | ||||||
| chr12:117048837
|
T | A | 68 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 71 | HG00423.hp1 HG00544.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.349+182A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 4/7 | chr12 | 117048837 | ||||||
| chr12:117049202
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.210-44C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049202 | ||||||
| chr12:117049202
|
G | C | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.210-44C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049202 | ||||||
| chr12:117049536
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.210-378G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049536 | ||||||
| chr12:117049626
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(163): Show | 172 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.210-468A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049626 | ||||||
| chr12:117049627
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(161): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.210-469C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049627 | ||||||
| chr12:117049674
|
GC | G | 65 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(62): Show | 68 | HG00423.hp1 HG00544.hp2 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.210-517delG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049674 | ||||||
| chr12:117049700
|
A | C | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-542T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049700 | ||||||
| chr12:117049745
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(161): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.210-587C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049745 | ||||||
| chr12:117049820
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.210-662C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049820 | ||||||
| chr12:117049831
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.210-673C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049831 | ||||||
| chr12:117049903
|
G | GA | 12 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0127others(9): Show | 12 | HG01109.hp1 HG01978.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.210-746dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049903 | ||||||
| chr12:117049903
|
GA | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(132): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.210-746delT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049903 | ||||||
| chr12:117049903
|
GAA | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 7 | HG02886.hp1 HG02896.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.210-747_210-746del others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049903 | ||||||
| chr12:117049903
|
GAAA | G | 19 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.210-748_210-746del others(3): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049903 | ||||||
| chr12:117049903
|
GAAAAAAA | G | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-752_210-746del others(7): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117049903 | ||||||
| chr12:117050032
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(161): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.210-874T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050032 | ||||||
| chr12:117050059
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.210-901A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050059 | ||||||
| chr12:117050139
|
C | CA | 6 | a0001c0001t0001g0144a0001c0001t0003g0028a0001c0001t0003g0286others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-982dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050139 | ||||||
| chr12:117050431
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.210-1273G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050431 | ||||||
| chr12:117050456
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.210-1298A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050456 | ||||||
| chr12:117050648
|
G | A | 3 | a0001c0001t0001g0078a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG02109.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.210-1490C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050648 | ||||||
| chr12:117050670
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.210-1512G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050670 | ||||||
| chr12:117050951
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.210-1793C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117050951 | ||||||
| chr12:117051016
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.210-1858T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051016 | ||||||
| chr12:117051068
|
T | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.210-1910A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051068 | ||||||
| chr12:117051442
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.210-2284G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051442 | ||||||
| chr12:117051594
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.210-2436G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051594 | ||||||
| chr12:117051737
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0125a0001c0001t0001g0170others(2): Show | 5 | HG00609.hp1 NA19003.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2579C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051737 | ||||||
| chr12:117051737
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210-2579C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051737 | ||||||
| chr12:117051753
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.210-2595T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051753 | ||||||
| chr12:117051813
|
C | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(21): Show | 24 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.210-2655G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051813 | ||||||
| chr12:117051825
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-2667C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117051825 | ||||||
| chr12:117052355
|
C | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0051others(2): Show | 8 | HG01074.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-3197G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052355 | ||||||
| chr12:117052425
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.210-3267A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052425 | ||||||
| chr12:117052480
|
C | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02056.hp2 HG02132.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-3322G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052480 | ||||||
| chr12:117052541
|
T | C | 24 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(21): Show | 24 | HG00544.hp2 HG00741.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.210-3383A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052541 | ||||||
| chr12:117052683
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0246others(1): Show | 6 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-3525C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052683 | ||||||
| chr12:117052705
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.210-3547T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052705 | ||||||
| chr12:117052804
|
C | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.210-3646G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052804 | ||||||
| chr12:117052858
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.210-3700G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052858 | ||||||
| chr12:117052949
|
TCTC | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 112 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.210-3794_210-3792d others(5): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117052949 | ||||||
| chr12:117053029
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209+3777G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053029 | ||||||
| chr12:117053031
|
C | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 45 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.209+3775G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053031 | ||||||
| chr12:117053060
|
T | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0246others(1): Show | 6 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.209+3746A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053060 | ||||||
| chr12:117053076
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.209+3730C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053076 | ||||||
| chr12:117053158
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.209+3648G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053158 | ||||||
| chr12:117053158
|
C | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(20): Show | 23 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.209+3648G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053158 | ||||||
| chr12:117053377
|
G | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0131 | 2 | NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.209+3429C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053377 | ||||||
| chr12:117053396
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.209+3410A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053396 | ||||||
| chr12:117053516
|
G | A | 7 | a0001c0001t0002g0023a0001c0001t0002g0089a0001c0001t0003g0028others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.209+3290C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053516 | ||||||
| chr12:117053579
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.209+3227C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053579 | ||||||
| chr12:117053694
|
T | C | 24 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(21): Show | 24 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.209+3112A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053694 | ||||||
| chr12:117053731
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): Show | 137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.209+3075G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053731 | ||||||
| chr12:117053732
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.209+3074A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053732 | ||||||
| chr12:117053739
|
C | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 9 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.209+3067G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053739 | ||||||
| chr12:117053743
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.209+3063G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053743 | ||||||
| chr12:117053749
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209+3057G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053749 | ||||||
| chr12:117053808
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0245others(2): Show | 7 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.209+2998A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053808 | ||||||
| chr12:117053887
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+2919C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053887 | ||||||
| chr12:117053898
|
T | C | 41 | a0001c0001t0001g0191a0001c0001t0001g0273a0001c0001t0002g0016others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.209+2908A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053898 | ||||||
| chr12:117053917
|
C | T | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.209+2889G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053917 | ||||||
| chr12:117053977
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.209+2829C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117053977 | ||||||
| chr12:117054019
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(130): Show | 138 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.209+2787T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054019 | ||||||
| chr12:117054119
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 112 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.209+2687C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054119 | ||||||
| chr12:117054209
|
G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(21): Show | 24 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.209+2597C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054209 | ||||||
| chr12:117054234
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+2572G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054234 | ||||||
| chr12:117054280
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.209+2526T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054280 | ||||||
| chr12:117054285
|
C | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(38): Show | 42 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.209+2521G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054285 | ||||||
| chr12:117054304
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 112 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.209+2502G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054304 | ||||||
| chr12:117054378
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+2428G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054378 | ||||||
| chr12:117054401
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209+2405C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054401 | ||||||
| chr12:117054442
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.209+2364C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054442 | ||||||
| chr12:117054451
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(130): Show | 138 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.209+2355C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054451 | ||||||
| chr12:117054585
|
G | A | 5 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+2221C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054585 | ||||||
| chr12:117054649
|
C | A | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.209+2157G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054649 | ||||||
| chr12:117054676
|
G | C | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.209+2130C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054676 | ||||||
| chr12:117054677
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.209+2129G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054677 | ||||||
| chr12:117054687
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+2119A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054687 | ||||||
| chr12:117054720
|
G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(30): Show | 34 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.209+2086C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054720 | ||||||
| chr12:117054769
|
C | T | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.209+2037G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054769 | ||||||
| chr12:117054799
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(167): Show | 176 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.209+2007T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054799 | ||||||
| chr12:117054856
|
C | T | 7 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(4): Show | 7 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.209+1950G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054856 | ||||||
| chr12:117054886
|
G | C | 59 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0273others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.209+1920C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054886 | ||||||
| chr12:117054896
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0230 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.209+1910G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117054896 | ||||||
| chr12:117055059
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0029others(120): Show | 126 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.209+1747T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055059 | ||||||
| chr12:117055102
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0212 | 2 | HG00423.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.209+1704G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055102 | ||||||
| chr12:117055178
|
G | A | 1 | a0001c0001t0004g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.209+1628C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055178 | ||||||
| chr12:117055198
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.209+1608C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055198 | ||||||
| chr12:117055266
|
C | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.209+1540G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055266 | ||||||
| chr12:117055318
|
T | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0089 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.209+1488A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055318 | ||||||
| chr12:117055430
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0085others(12): Show | 15 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.209+1376C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055430 | ||||||
| chr12:117055647
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+1159A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055647 | ||||||
| chr12:117055648
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+1158G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055648 | ||||||
| chr12:117055665
|
C | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.209+1141G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055665 | ||||||
| chr12:117055684
|
G | A | 35 | a0001c0001t0001g0273a0001c0001t0002g0016a0001c0001t0002g0018others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.209+1122C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055684 | ||||||
| chr12:117055754
|
G | C | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.209+1052C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055754 | ||||||
| chr12:117055912
|
CTT | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0060others(13): Show | 17 | HG00741.hp1 HG01074.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.209+892_209+893del others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055912 | ||||||
| chr12:117055912
|
CTTT | C | 14 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0085others(11): Show | 14 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+891_209+893del others(3): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117055912 | ||||||
| chr12:117056019
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.209+787G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056019 | ||||||
| chr12:117056258
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0214 | 2 | NA18951.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.209+548A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056258 | ||||||
| chr12:117056323
|
C | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 44 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.209+483G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056323 | ||||||
| chr12:117056337
|
G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(21): Show | 24 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.209+469C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056337 | ||||||
| chr12:117056380
|
C | CTTCCTCA others(61): Show |
31 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(28): Show | 32 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+425_209+426ins others(68): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056380 | ||||||
| chr12:117056448
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209+358T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056448 | ||||||
| chr12:117056449
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.209+357G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056449 | ||||||
| chr12:117056458
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.209+348G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056458 | ||||||
| chr12:117056459
|
G | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG01891.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+347C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056459 | ||||||
| chr12:117056485
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.209+321T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056485 | ||||||
| chr12:117056487
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0079others(3): Show | 8 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.209+319G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056487 | ||||||
| chr12:117056488
|
G | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 69 | HG00423.hp1 HG00544.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.209+318C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056488 | ||||||
| chr12:117056696
|
C | G | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.209+110G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056696 | ||||||
| chr12:117056738
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.209+68T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056738 | ||||||
| chr12:117056747
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.209+59C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056747 | ||||||
| chr12:117056782
|
G | C | 59 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0273others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.209+24C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 3/7 | chr12 | 117056782 | ||||||
| chr12:117056899
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129-13T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117056899 | ||||||
| chr12:117056903
|
A | C | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.129-17T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117056903 | ||||||
| chr12:117056971
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.129-85C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117056971 | ||||||
| chr12:117057036
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.129-150C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057036 | ||||||
| chr12:117057122
|
G | T | 24 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(21): Show | 24 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.129-236C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057122 | ||||||
| chr12:117057125
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.129-239T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057125 | ||||||
| chr12:117057394
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0215 | 2 | HG01243.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.129-508G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057394 | ||||||
| chr12:117057395
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-509C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057395 | ||||||
| chr12:117057613
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.129-727G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057613 | ||||||
| chr12:117057623
|
C | T | 3 | a0001c0001t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.129-737G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057623 | ||||||
| chr12:117057804
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.129-918G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057804 | ||||||
| chr12:117057809
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129-923T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117057809 | ||||||
| chr12:117058054
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.129-1168A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058054 | ||||||
| chr12:117058070
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0131 | 2 | NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.129-1184T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058070 | ||||||
| chr12:117058237
|
G | A | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.129-1351C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058237 | ||||||
| chr12:117058354
|
G | A | 3 | a0001c0001t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.129-1468C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058354 | ||||||
| chr12:117058385
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.129-1499A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058385 | ||||||
| chr12:117058565
|
T | TA | 21 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0039others(18): Show | 21 | HG02258.hp2 HG02280.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.129-1680dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058565 | ||||||
| chr12:117058565
|
T | TAA | 25 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0038others(22): Show | 27 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.129-1681_129-1680d others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058565 | ||||||
| chr12:117058565
|
T | TAAA | 62 | a0001c0001t0001g0191a0001c0001t0001g0209a0001c0001t0001g0238others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.129-1682_129-1680d others(5): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058565 | ||||||
| chr12:117058669
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.129-1783C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058669 | ||||||
| chr12:117058689
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-1803C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058689 | ||||||
| chr12:117058702
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.129-1816G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058702 | ||||||
| chr12:117058745
|
T | TA | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(135): Show | 144 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.129-1860dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058745 | ||||||
| chr12:117058745
|
T | TAA | 11 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0078others(8): Show | 11 | HG00741.hp1 HG02109.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.129-1861_129-1860d others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058745 | ||||||
| chr12:117058745
|
TA | T | 31 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0060others(28): Show | 31 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.129-1860delT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058745 | ||||||
| chr12:117058763
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.129-1877C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058763 | ||||||
| chr12:117058929
|
C | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(132): Show | 141 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.129-2043G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117058929 | ||||||
| chr12:117059174
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.129-2288T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059174 | ||||||
| chr12:117059259
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.129-2373G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059259 | ||||||
| chr12:117059261
|
C | A | 59 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0273others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.129-2375G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059261 | ||||||
| chr12:117059336
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.129-2450C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059336 | ||||||
| chr12:117059364
|
G | T | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0002t0001g0076others(1): Show | 4 | HG02109.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-2478C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059364 | ||||||
| chr12:117059717
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129-2831G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059717 | ||||||
| chr12:117059742
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.129-2856C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059742 | ||||||
| chr12:117059749
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(160): Show | 168 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.129-2863G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059749 | ||||||
| chr12:117059784
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 45 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.129-2898C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117059784 | ||||||
| chr12:117060075
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.129-3189C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060075 | ||||||
| chr12:117060131
|
G | A | 5 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-3245C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060131 | ||||||
| chr12:117060342
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129-3456G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060342 | ||||||
| chr12:117060345
|
G | A | 30 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.129-3459C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060345 | ||||||
| chr12:117060626
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.129-3740T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060626 | ||||||
| chr12:117060639
|
G | A | 14 | a0001c0001t0001g0273a0001c0001t0002g0016a0001c0001t0002g0018others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.129-3753C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060639 | ||||||
| chr12:117060838
|
G | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-3952C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060838 | ||||||
| chr12:117060881
|
C | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(21): Show | 24 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.129-3995G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060881 | ||||||
| chr12:117060959
|
G | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(23): Show | 26 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.129-4073C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117060959 | ||||||
| chr12:117061020
|
C | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(155): Show | 163 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.129-4134G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061020 | ||||||
| chr12:117061055
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.129-4169G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061055 | ||||||
| chr12:117061131
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-4245C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061131 | ||||||
| chr12:117061193
|
C | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(163): Show | 172 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.129-4307G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061193 | ||||||
| chr12:117061211
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.129-4325G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061211 | ||||||
| chr12:117061239
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(162): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.129-4353C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061239 | ||||||
| chr12:117061335
|
C | T | 2 | a0001c0001t0001g0133a0003c0003t0001g0155 | 2 | HG01516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.129-4449G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061335 | ||||||
| chr12:117061364
|
CCCTTCCC others(6): Show |
C | 30 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.129-4491_129-4479d others(15): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061364 | ||||||
| chr12:117061417
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.129-4531C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061417 | ||||||
| chr12:117061650
|
G | GCT | 8 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0075others(5): Show | 10 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-4766_129-4765d others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061650 | ||||||
| chr12:117061781
|
C | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 45 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.129-4895G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117061781 | ||||||
| chr12:117062137
|
T | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(24): Show | 28 | HG00544.hp2 HG01074.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.129-5251A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062137 | ||||||
| chr12:117062173
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.129-5287A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062173 | ||||||
| chr12:117062405
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129-5519T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062405 | ||||||
| chr12:117062463
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.129-5577G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062463 | ||||||
| chr12:117062464
|
T | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0031others(55): Show | 59 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.129-5578A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062464 | ||||||
| chr12:117062615
|
GTGGT | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0045others(31): Show | 35 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.129-5733_129-5730d others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062615 | ||||||
| chr12:117062637
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.129-5751C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062637 | ||||||
| chr12:117062682
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0031others(46): Show | 50 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.129-5796G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062682 | ||||||
| chr12:117062683
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0031others(48): Show | 52 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.129-5797T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062683 | ||||||
| chr12:117062754
|
C | T | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-5868G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062754 | ||||||
| chr12:117062755
|
G | A | 25 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0060others(22): Show | 25 | HG00544.hp2 HG02080.hp2 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.129-5869C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062755 | ||||||
| chr12:117062884
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0003g0070a0001c0002t0001g0076others(1): Show | 4 | HG03453.hp1 HG03471.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-5998C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062884 | ||||||
| chr12:117062905
|
A | G | 8 | a0001c0001t0001g0203a0001c0001t0001g0283a0001c0001t0003g0017others(5): Show | 8 | HG00741.hp1 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-6019T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062905 | ||||||
| chr12:117062975
|
C | T | 9 | a0001c0001t0003g0019a0001c0001t0003g0021a0001c0001t0003g0068others(6): Show | 9 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-6089G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117062975 | ||||||
| chr12:117063066
|
T | C | 7 | a0001c0001t0001g0295a0001c0001t0003g0017a0001c0001t0003g0056others(4): Show | 7 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-6180A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063066 | ||||||
| chr12:117063292
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-6406G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063292 | ||||||
| chr12:117063313
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.129-6427C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063313 | ||||||
| chr12:117063345
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0185a0001c0001t0001g0186 | 4 | HG01123.hp1 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-6459G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063345 | ||||||
| chr12:117063359
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0295a0001c0001t0003g0017others(5): Show | 9 | HG00741.hp1 HG01074.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-6473T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063359 | ||||||
| chr12:117063449
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.129-6563A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063449 | ||||||
| chr12:117063508
|
C | T | 2 | a0001c0001t0002g0189a0001c0001t0002g0234 | 2 | HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.129-6622G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063508 | ||||||
| chr12:117063896
|
C | T | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-7010G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063896 | ||||||
| chr12:117063983
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(165): Show | 174 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.129-7097T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117063983 | ||||||
| chr12:117064140
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-7254G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064140 | ||||||
| chr12:117064165
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129-7279G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064165 | ||||||
| chr12:117064171
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.129-7285G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064171 | ||||||
| chr12:117064215
|
C | T | 3 | a0001c0001t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.129-7329G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064215 | ||||||
| chr12:117064265
|
A | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0295a0001c0001t0003g0017others(5): Show | 9 | HG00741.hp1 HG01074.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-7379T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064265 | ||||||
| chr12:117064303
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0085others(12): Show | 15 | HG00544.hp2 HG02080.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.129-7417C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064303 | ||||||
| chr12:117064305
|
G | C | 1 | a0001c0001t0008g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.129-7419C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064305 | ||||||
| chr12:117064337
|
A | T | 1 | a0001c0001t0004g0192 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.129-7451T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064337 | ||||||
| chr12:117064532
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129-7646G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064532 | ||||||
| chr12:117064537
|
C | T | 7 | a0001c0001t0001g0295a0001c0001t0003g0017a0001c0001t0003g0056others(4): Show | 7 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-7651G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064537 | ||||||
| chr12:117064542
|
C | G | 1 | a0001c0001t0003g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129-7656G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064542 | ||||||
| chr12:117064696
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129-7810C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064696 | ||||||
| chr12:117064710
|
C | T | 4 | a0001c0001t0002g0018a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG01891.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-7824G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064710 | ||||||
| chr12:117064961
|
TAAG | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0246others(1): Show | 6 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-8078_129-8076d others(5): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117064961 | ||||||
| chr12:117065295
|
G | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0114others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.129-8409C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065295 | ||||||
| chr12:117065296
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129-8410C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065296 | ||||||
| chr12:117065388
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.129-8502C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065388 | ||||||
| chr12:117065447
|
A | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0002t0001g0076others(1): Show | 4 | HG02109.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-8561T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065447 | ||||||
| chr12:117065554
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.129-8668A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065554 | ||||||
| chr12:117065669
|
C | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(175): Show | 184 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.129-8783G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065669 | ||||||
| chr12:117065746
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-8860C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117065746 | ||||||
| chr12:117066018
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(165): Show | 173 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.129-9132G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066018 | ||||||
| chr12:117066200
|
C | CT | 18 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0075others(15): Show | 18 | HG00544.hp1 HG01106.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.128+9070dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTT | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 19 | HG01074.hp1 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.128+9067_128+9070d others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTT | 14 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0073others(11): Show | 14 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.128+9066_128+9070d others(7): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTT | 11 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0041others(8): Show | 11 | HG02027.hp2 HG02074.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.128+9065_128+9070d others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT | 24 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(21): Show | 26 | HG00408.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.128+9064_128+9070d others(9): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0060others(15): Show | 18 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.128+9063_128+9070d others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0045a0001c0001t0001g0142a0001c0001t0001g0149others(10): Show | 13 | HG00544.hp2 HG02523.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.128+9062_128+9070d others(11): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(3): Show |
12 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0222others(9): Show | 12 | HG02109.hp1 HG02602.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.128+9061_128+9070d others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(4): Show |
16 | a0001c0001t0001g0082a0001c0001t0001g0191a0001c0001t0001g0226others(13): Show | 16 | HG00323.hp2 HG01256.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.128+9060_128+9070d others(13): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(5): Show |
18 | a0001c0001t0001g0201a0001c0001t0002g0027a0001c0001t0002g0044others(15): Show | 18 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.128+9059_128+9070d others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(6): Show |
12 | a0001c0001t0001g0114a0001c0001t0001g0273a0001c0001t0002g0018others(9): Show | 12 | HG00140.hp2 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.128+9058_128+9070d others(15): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(7): Show |
4 | a0001c0001t0002g0197a0001c0001t0002g0234a0001c0001t0002g0292others(1): Show | 4 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+9057_128+9070d others(16): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.128+9056_128+9070d others(17): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066200
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0189 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128+9055_128+9070d others(18): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066200 | ||||||
| chr12:117066226
|
G | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.128+9045C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066226 | ||||||
| chr12:117066246
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.128+9025C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066246 | ||||||
| chr12:117066373
|
A | AT | 156 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 161 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.128+8897dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066373 | ||||||
| chr12:117066504
|
T | C | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 45 | HG00408.hp1 HG00423.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.128+8767A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066504 | ||||||
| chr12:117066624
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+8647G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066624 | ||||||
| chr12:117066982
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.128+8289C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066982 | ||||||
| chr12:117066999
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.128+8272T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117066999 | ||||||
| chr12:117067013
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0002g0044a0001c0001t0002g0200 | 3 | HG02647.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128+8258C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067013 | ||||||
| chr12:117067293
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.128+7978C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067293 | ||||||
| chr12:117067329
|
C | CTGAGGCA others(11): Show |
1 | a0001c0001t0001g0010 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.128+7924_128+7941d others(20): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067329 | ||||||
| chr12:117067392
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.128+7879C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067392 | ||||||
| chr12:117067409
|
T | A | 3 | a0001c0001t0001g0183a0001c0001t0002g0047a0001c0001t0002g0052 | 3 | HG01358.hp1 HG02155.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.128+7862A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067409 | ||||||
| chr12:117067496
|
C | T | 69 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0191others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.128+7775G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067496 | ||||||
| chr12:117067572
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+7699G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067572 | ||||||
| chr12:117067790
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128+7481C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067790 | ||||||
| chr12:117067819
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0007g0299 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.128+7452A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067819 | ||||||
| chr12:117067988
|
C | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 38 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+7283G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117067988 | ||||||
| chr12:117068218
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128+7053C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068218 | ||||||
| chr12:117068221
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128+7050T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068221 | ||||||
| chr12:117068222
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128+7049C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068222 | ||||||
| chr12:117068224
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128+7047C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068224 | ||||||
| chr12:117068225
|
C | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128+7046G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068225 | ||||||
| chr12:117068295
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0004g0032a0001c0001t0004g0067others(4): Show | 7 | HG01106.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+6976G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068295 | ||||||
| chr12:117068301
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0056a0001c0001t0003g0057others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+6970C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068301 | ||||||
| chr12:117068366
|
C | G | 15 | a0001c0001t0001g0273a0001c0001t0002g0016a0001c0001t0002g0018others(12): Show | 15 | HG00323.hp2 HG00642.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.128+6905G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068366 | ||||||
| chr12:117068601
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.128+6670G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068601 | ||||||
| chr12:117068827
|
C | T | 8 | a0001c0001t0001g0114a0001c0001t0002g0187a0001c0001t0002g0189others(5): Show | 8 | HG00140.hp2 HG01261.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+6444G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117068827 | ||||||
| chr12:117069063
|
TG | T | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.128+6207delC | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069063 | ||||||
| chr12:117069098
|
C | CT | 69 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0191others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.128+6172dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069098 | ||||||
| chr12:117069098
|
CT | C | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.128+6172delA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069098 | ||||||
| chr12:117069134
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.128+6137C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069134 | ||||||
| chr12:117069191
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.128+6080G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069191 | ||||||
| chr12:117069204
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.128+6067C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069204 | ||||||
| chr12:117069272
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.128+5999G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069272 | ||||||
| chr12:117069318
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.128+5953G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069318 | ||||||
| chr12:117069364
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0295a0001c0002t0001g0076others(1): Show | 4 | HG02572.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+5907C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069364 | ||||||
| chr12:117069395
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.128+5876G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069395 | ||||||
| chr12:117069440
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.128+5831A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069440 | ||||||
| chr12:117069481
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.128+5790G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069481 | ||||||
| chr12:117069529
|
C | T | 25 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0086others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.128+5742G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069529 | ||||||
| chr12:117069530
|
GC | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 38 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+5740delG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069530 | ||||||
| chr12:117069534
|
G | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 38 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+5737C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069534 | ||||||
| chr12:117069637
|
T | TC | 4 | a0001c0001t0001g0142a0001c0001t0001g0221a0001c0001t0001g0223others(1): Show | 4 | HG02630.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+5633dupG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117069637 | ||||||
| chr12:117070080
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+5191T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070080 | ||||||
| chr12:117070126
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.128+5145A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070126 | ||||||
| chr12:117070209
|
G | A | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.128+5062C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070209 | ||||||
| chr12:117070507
|
G | A | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.128+4764C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070507 | ||||||
| chr12:117070519
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.128+4752G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070519 | ||||||
| chr12:117070532
|
C | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(74): Show | 81 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.128+4739G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070532 | ||||||
| chr12:117070533
|
C | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0002g0089others(1): Show | 5 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+4738G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070533 | ||||||
| chr12:117070538
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.128+4733C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070538 | ||||||
| chr12:117070687
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0223a0001c0001t0001g0228 | 3 | HG01884.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.128+4584A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070687 | ||||||
| chr12:117070783
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.128+4488G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070783 | ||||||
| chr12:117070975
|
T | TA | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0051others(8): Show | 13 | HG01074.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.128+4295dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070975 | ||||||
| chr12:117070975
|
TA | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 152 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.128+4295delT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117070975 | ||||||
| chr12:117071025
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.128+4246G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071025 | ||||||
| chr12:117071103
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0002g0200 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.128+4168G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071103 | ||||||
| chr12:117071104
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 161 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.128+4167T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071104 | ||||||
| chr12:117071164
|
C | T | 26 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 29 | HG00423.hp1 HG00609.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.128+4107G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071164 | ||||||
| chr12:117071195
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054 | 3 | HG01192.hp1 HG01358.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.128+4076G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071195 | ||||||
| chr12:117071325
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 176 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.128+3946T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071325 | ||||||
| chr12:117071379
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.128+3892C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071379 | ||||||
| chr12:117071441
|
C | CT | 36 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 40 | HG00423.hp1 HG00609.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.128+3829dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071441 | ||||||
| chr12:117071546
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0295others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+3725T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071546 | ||||||
| chr12:117071793
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0125 | 2 | NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.128+3478C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117071793 | ||||||
| chr12:117072040
|
C | T | 6 | a0001c0001t0003g0068a0001c0001t0003g0104a0001c0001t0003g0261others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+3231G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072040 | ||||||
| chr12:117072091
|
C | T | 30 | a0001c0001t0001g0086a0001c0001t0001g0203a0001c0001t0001g0258others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.128+3180G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072091 | ||||||
| chr12:117072254
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128+3017C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072254 | ||||||
| chr12:117072295
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.128+2976G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072295 | ||||||
| chr12:117072305
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0002g0200 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.128+2966G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072305 | ||||||
| chr12:117072476
|
C | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0290 | 2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.128+2795G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072476 | ||||||
| chr12:117072525
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.128+2746C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072525 | ||||||
| chr12:117072547
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.128+2724G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072547 | ||||||
| chr12:117072743
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.128+2528G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072743 | ||||||
| chr12:117072747
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.128+2524G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072747 | ||||||
| chr12:117072917
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.128+2354T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117072917 | ||||||
| chr12:117073024
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.128+2247G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073024 | ||||||
| chr12:117073058
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.128+2213T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073058 | ||||||
| chr12:117073070
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 6 | HG00408.hp2 HG00558.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+2201A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073070 | ||||||
| chr12:117073131
|
A | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 163 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.128+2140T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073131 | ||||||
| chr12:117073265
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 160 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.128+2006C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073265 | ||||||
| chr12:117073301
|
C | A | 5 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0025others(2): Show | 5 | HG01891.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+1970G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073301 | ||||||
| chr12:117073332
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.128+1939C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073332 | ||||||
| chr12:117073413
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.128+1858C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073413 | ||||||
| chr12:117073657
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.128+1614T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073657 | ||||||
| chr12:117073757
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.128+1514G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073757 | ||||||
| chr12:117073761
|
C | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+1510G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073761 | ||||||
| chr12:117073799
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.128+1472T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073799 | ||||||
| chr12:117073862
|
T | C | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.128+1409A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073862 | ||||||
| chr12:117073913
|
C | CA | 68 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 71 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.128+1357dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073913 | ||||||
| chr12:117073954
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.128+1317G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117073954 | ||||||
| chr12:117074005
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.128+1266G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074005 | ||||||
| chr12:117074092
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078 | 5 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+1179C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074092 | ||||||
| chr12:117074094
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.128+1177C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074094 | ||||||
| chr12:117074162
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.128+1109G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074162 | ||||||
| chr12:117074168
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.128+1103G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074168 | ||||||
| chr12:117074169
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.128+1102C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074169 | ||||||
| chr12:117074641
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.128+630G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074641 | ||||||
| chr12:117074722
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128+549C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074722 | ||||||
| chr12:117074963
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.128+308C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074963 | ||||||
| chr12:117074998
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.128+273A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117074998 | ||||||
| chr12:117075184
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.128+87C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117075184 | ||||||
| chr12:117075209
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.128+62G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 2/7 | chr12 | 117075209 | ||||||
| chr12:117075524
|
C | T | 5 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0025others(2): Show | 5 | HG01891.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-184G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075524 | ||||||
| chr12:117075590
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-250G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075590 | ||||||
| chr12:117075628
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.59-288G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075628 | ||||||
| chr12:117075682
|
G | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0021 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-342C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075682 | ||||||
| chr12:117075719
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.59-379G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075719 | ||||||
| chr12:117075726
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.59-386C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075726 | ||||||
| chr12:117075798
|
G | C | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-458C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075798 | ||||||
| chr12:117075836
|
C | CGT | 3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-498_59-497dupAC | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075836 | ||||||
| chr12:117075843
|
G | GTGTGTAT others(13): Show |
1 | a0001c0001t0001g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.59-523_59-504dupTA others(18): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075843 | ||||||
| chr12:117075847
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(2): Show | 7 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-507C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075847 | ||||||
| chr12:117075847
|
G | GTGTA | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-508_59-507insTA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075847 | ||||||
| chr12:117075847
|
G | GTGTATAT others(27): Show |
1 | a0001c0001t0002g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.59-508_59-507insTA others(32): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075847 | ||||||
| chr12:117075847
|
GTA | G | 29 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0098others(26): Show | 30 | HG00323.hp2 HG01106.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-509_59-508delTA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075847 | ||||||
| chr12:117075847
|
GTATA | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0168a0001c0001t0001g0242others(1): Show | 4 | HG00558.hp2 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-511_59-508delTA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075847 | ||||||
| chr12:117075849
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0222others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-510_59-509insCA others(16): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075849 | ||||||
| chr12:117075849
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0033others(73): Show | 77 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.59-509T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075849 | ||||||
| chr12:117075851
|
A | ATATATAT others(9): Show |
20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 23 | HG00423.hp1 HG00609.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-512_59-511insCA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075851 | ||||||
| chr12:117075851
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0223a0001c0001t0001g0228 | 3 | HG01975.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.59-512_59-511insCA others(16): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075851 | ||||||
| chr12:117075851
|
A | G | 3 | a0001c0001t0001g0245a0001c0001t0002g0047a0001c0001t0002g0293 | 3 | HG01243.hp2 HG02155.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.59-511T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075851 | ||||||
| chr12:117075851
|
ATATATAT others(113): Show |
A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-631_59-512del | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075851 | ||||||
| chr12:117075853
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-514_59-513insCA others(32): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075853 | ||||||
| chr12:117075853
|
A | ATATATAT others(9): Show |
5 | a0001c0001t0001g0206a0001c0001t0001g0221a0001c0001t0001g0230others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-514_59-513insCA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075853 | ||||||
| chr12:117075853
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0003g0080 | 2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.59-513T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075853 | ||||||
| chr12:117075864
|
TATATATG others(114): Show |
T | 2 | a0001c0001t0001g0201a0001c0001t0001g0283 | 2 | HG02055.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.59-645_59-525del | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075864 | ||||||
| chr12:117075865
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0003g0017a0001c0001t0003g0070 | 3 | HG00741.hp1 HG03471.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.59-525T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075865 | ||||||
| chr12:117075865
|
ATATATGT others(45): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.59-577_59-526delCA others(50): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075865 | ||||||
| chr12:117075867
|
A | G | 13 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0001g0188others(10): Show | 13 | HG00741.hp1 HG01192.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-527T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075867 | ||||||
| chr12:117075867
|
ATATG | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0153a0001c0001t0002g0016 | 3 | HG03490.hp1 HG03491.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.59-531_59-528delCA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075867 | ||||||
| chr12:117075868
|
TATGTGTG others(110): Show |
T | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-645_59-529del | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075868 | ||||||
| chr12:117075869
|
A | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.59-529T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075869 | ||||||
| chr12:117075871
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 32 | HG00423.hp1 HG00609.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.59-531C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075871 | ||||||
| chr12:117075873
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0003g0055a0001c0001t0005g0281 | 3 | HG02615.hp1 HG03471.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.59-533C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075873
|
GTGTATA | G | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(8): Show | 11 | HG00621.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-539_59-534delTA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075873
|
GTGTATAT others(1): Show |
G | 22 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0094others(19): Show | 22 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-541_59-534delTA others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075873
|
GTGTATAT others(3): Show |
G | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(33): Show | 39 | HG00438.hp1 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-543_59-534delTA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075873
|
GTGTATAT others(5): Show |
G | 13 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(10): Show | 15 | HG00408.hp2 HG01074.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-545_59-534delTA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075873
|
GTGTATAT others(7): Show |
G | 6 | a0001c0001t0001g0030a0001c0001t0001g0081a0001c0001t0001g0122others(3): Show | 6 | HG01256.hp1 HG01515.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-547_59-534delTA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075873
|
GTGTATAT others(9): Show |
G | 2 | a0001c0001t0001g0121a0001c0001t0001g0172 | 2 | HG00140.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.59-549_59-534delTA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075873 | ||||||
| chr12:117075875
|
G | A | 61 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(58): Show | 61 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.59-535C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075875 | ||||||
| chr12:117075875
|
GTATA | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG00544.hp2 HG02257.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-539_59-536delTA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075875 | ||||||
| chr12:117075875
|
GTATATA | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0102a0001c0001t0001g0111 | 3 | HG01433.hp1 HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.59-541_59-536delTA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075875 | ||||||
| chr12:117075875
|
GTATATAT others(1): Show |
G | 10 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0128others(7): Show | 10 | HG00438.hp2 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-543_59-536delTA others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075875 | ||||||
| chr12:117075875
|
GTATATAT others(3): Show |
G | 6 | a0001c0001t0001g0097a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG00558.hp2 HG02965.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-545_59-536delTA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075875 | ||||||
| chr12:117075875
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.59-547_59-536delTA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075875 | ||||||
| chr12:117075877
|
A | G | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(18): Show | 23 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-537T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075877 | ||||||
| chr12:117075879
|
A | G | 4 | a0001c0001t0001g0188a0001c0001t0003g0017a0001c0001t0003g0070others(1): Show | 4 | HG00741.hp1 HG01884.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-539T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075879 | ||||||
| chr12:117075883
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0049 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.59-544_59-543insCA others(24): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075883 | ||||||
| chr12:117075883
|
A | G | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.59-543T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075883 | ||||||
| chr12:117075885
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0041a0001c0001t0002g0052 | 2 | HG01358.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.59-546_59-545insCA others(26): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075885 | ||||||
| chr12:117075885
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0010g0297 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.59-546_59-545insCA others(26): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075885 | ||||||
| chr12:117075885
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0050 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.59-546_59-545insCA others(22): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075885 | ||||||
| chr12:117075885
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.59-546_59-545insCA others(60): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075885 | ||||||
| chr12:117075885
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.59-546_59-545insCA others(26): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075885 | ||||||
| chr12:117075885
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0007g0299 | 2 | HG03209.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.59-545T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075885 | ||||||
| chr12:117075887
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0005g0040 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.59-548_59-547insCA others(24): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0001g0048 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-548_59-547insCA others(60): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0002g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59-548_59-547insCA others(26): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-548_59-547insCA others(30): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0036 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.59-548_59-547insCA others(22): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0003g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59-548_59-547insCA others(28): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0033a0001c0001t0004g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59-548_59-547insCA others(24): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59-548_59-547insCA others(24): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075887
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0007g0299 | 2 | HG03209.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.59-547T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075887 | ||||||
| chr12:117075889
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0190 | 2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.59-550_59-549insCA others(22): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075889 | ||||||
| chr12:117075889
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0042 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.59-550_59-549insCA others(20): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075889 | ||||||
| chr12:117075889
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0003g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.59-550_59-549insCA others(28): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075889 | ||||||
| chr12:117075889
|
A | ATATGTGT others(7): Show |
1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-550_59-549insCA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075889 | ||||||
| chr12:117075889
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0007g0299 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.59-549T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075889 | ||||||
| chr12:117075891
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-552_59-551insCA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075891 | ||||||
| chr12:117075891
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-551T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075891 | ||||||
| chr12:117075893
|
A | ATGTG | 17 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(14): Show | 17 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-554_59-553insCA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075893 | ||||||
| chr12:117075893
|
A | ATGTGTG | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0185others(11): Show | 16 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-554_59-553insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075893 | ||||||
| chr12:117075893
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0188a0001c0001t0001g0204others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-553T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075893 | ||||||
| chr12:117075895
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0038 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.59-556_59-555insCA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075895 | ||||||
| chr12:117075895
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.59-556_59-555insCA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075895 | ||||||
| chr12:117075895
|
A | ATGTG | 3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-556_59-555insCA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075895 | ||||||
| chr12:117075895
|
A | ATGTGTG | 3 | a0001c0001t0001g0075a0001c0001t0001g0207a0001c0002t0001g0076 | 3 | HG01975.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.59-556_59-555insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075895 | ||||||
| chr12:117075895
|
A | G | 18 | a0001c0001t0001g0170a0001c0001t0001g0188a0001c0001t0001g0204others(15): Show | 18 | HG00609.hp1 HG00741.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-555T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075895 | ||||||
| chr12:117075897
|
A | G | 8 | a0001c0001t0001g0188a0001c0001t0001g0204a0001c0001t0001g0205others(5): Show | 8 | HG00741.hp1 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-557T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075897 | ||||||
| chr12:117075899
|
A | ATATGTGT others(5): Show |
1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.59-560_59-559insCA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075899 | ||||||
| chr12:117075899
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0188a0001c0001t0001g0226others(1): Show | 4 | HG00741.hp1 HG02145.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-559T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075899 | ||||||
| chr12:117075899
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.59-575_59-560delCA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075899 | ||||||
| chr12:117075901
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0188others(3): Show | 6 | HG00741.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-561T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075901 | ||||||
| chr12:117075901
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0243 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-575_59-562delCA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075901 | ||||||
| chr12:117075903
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0188a0001c0001t0003g0017 | 3 | HG00741.hp1 HG02145.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.59-563T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075903 | ||||||
| chr12:117075903
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0107a0001c0001t0002g0089 | 2 | HG03139.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.59-575_59-564delCA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075903 | ||||||
| chr12:117075904
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-564A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075904 | ||||||
| chr12:117075905
|
A | ATGTATG | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-566_59-565insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075905 | ||||||
| chr12:117075905
|
A | G | 7 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0051others(4): Show | 7 | HG01175.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-565T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075905 | ||||||
| chr12:117075905
|
ATATATAT others(3): Show |
A | 9 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0099others(6): Show | 10 | HG01257.hp2 HG01258.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-575_59-566delCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075905 | ||||||
| chr12:117075907
|
A | ATG | 3 | a0001c0001t0002g0020a0001c0001t0002g0096a0001c0001t0002g0290 | 3 | HG02486.hp2 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.59-568_59-567insCA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075907 | ||||||
| chr12:117075907
|
A | ATGTATG | 3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-568_59-567insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075907 | ||||||
| chr12:117075907
|
A | ATGTG | 4 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG03453.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-568_59-567insCA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075907 | ||||||
| chr12:117075907
|
A | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0191a0001c0001t0001g0294others(3): Show | 6 | HG01175.hp2 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-567T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075907 | ||||||
| chr12:117075909
|
A | ATG | 6 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG01516.hp1 HG01517.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-570_59-569insCA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075909 | ||||||
| chr12:117075909
|
A | ATGTG | 4 | a0001c0001t0001g0085a0001c0001t0002g0189a0001c0001t0002g0193others(1): Show | 4 | HG00140.hp2 HG01106.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-570_59-569insCA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075909 | ||||||
| chr12:117075909
|
A | ATGTGTG | 7 | a0001c0001t0001g0045a0001c0001t0001g0249a0001c0001t0001g0250others(4): Show | 7 | HG02056.hp1 HG02056.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-570_59-569insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075909 | ||||||
| chr12:117075909
|
A | ATGTGTGT others(25): Show |
1 | a0001c0001t0003g0046 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.59-570_59-569insCA others(30): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075909 | ||||||
| chr12:117075909
|
A | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0074a0001c0001t0001g0191others(15): Show | 18 | HG01175.hp2 HG01192.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-569T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075909 | ||||||
| chr12:117075911
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.59-572_59-571insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075911 | ||||||
| chr12:117075911
|
A | G | 46 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0045others(43): Show | 46 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.59-571T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075911 | ||||||
| chr12:117075913
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.59-574_59-573insCA others(28): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0267 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.59-574_59-573insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATATATGT others(1): Show |
3 | a0001c0001t0001g0266a0001c0001t0001g0277a0001c0001t0005g0281 | 3 | NA18975.hp2 NA18995.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.59-574_59-573insCA others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.59-574_59-573insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATATATGT others(7): Show |
1 | a0001c0001t0002g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59-574_59-573insCA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATATGTG | 3 | a0001c0001t0001g0086a0001c0001t0001g0282a0001c0004t0001g0280 | 3 | NA18747.hp2 NA18949.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.59-574_59-573insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATATGTGT others(3): Show |
1 | a0001c0001t0003g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59-574_59-573insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATGTGTG | 11 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(8): Show | 11 | HG01358.hp1 HG01891.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-579_59-574dupCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATGTGTGT others(33): Show |
1 | a0001c0001t0002g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.59-574_59-573insCA others(38): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0038a0001c0001t0001g0114a0001c0001t0004g0219 | 3 | HG00408.hp1 HG01975.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.59-581_59-574dupCA others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0198a0001c0001t0001g0248a0001c0001t0001g0251 | 3 | NA18970.hp2 NA18972.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.59-583_59-574dupCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075913
|
A | G | 88 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(85): Show | 91 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.59-573T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075913 | ||||||
| chr12:117075915
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(17): Show | 21 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-575C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075915 | ||||||
| chr12:117075917
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-577C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075917 | ||||||
| chr12:117075919
|
G | A | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-579C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075919 | ||||||
| chr12:117075921
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(17): Show | 21 | HG00609.hp1 HG00741.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-581C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075921 | ||||||
| chr12:117075923
|
G | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(43): Show | 49 | HG00423.hp1 HG00609.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.59-583C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTATA | 10 | a0001c0001t0001g0075a0001c0001t0001g0204a0001c0001t0001g0205others(7): Show | 10 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-587_59-584dupTA others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0003g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-584_59-583insTG others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0003g0068a0001c0001t0003g0104 | 2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.59-584_59-583insTA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTGTATAT others(7): Show |
1 | a0001c0001t0005g0279 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-584_59-583insTA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTGTGTAT others(5): Show |
1 | a0001c0001t0003g0269 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.59-584_59-583insTA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTGTGTAT others(9): Show |
2 | a0001c0001t0001g0265a0001c0001t0001g0278 | 2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.59-584_59-583insTA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
G | GTGTGTAT others(49): Show |
1 | a0001c0001t0003g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-584_59-583insTA others(54): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0001g0203a0001c0001t0001g0258 | 2 | HG03831.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.59-597_59-584delTA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075923
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0016 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.59-599_59-584delTA others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075923 | ||||||
| chr12:117075924
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0003g0017 | 2 | HG00741.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.59-584A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075924 | ||||||
| chr12:117075925
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(36): Show | 40 | HG00558.hp1 HG00609.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.59-585T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075925 | ||||||
| chr12:117075928
|
T | TACATATA others(9): Show |
1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-589_59-588insGT others(14): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075928 | ||||||
| chr12:117075929
|
A | ATATGTAT others(27): Show |
1 | a0001c0001t0001g0108 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59-590_59-589insCA others(32): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075929 | ||||||
| chr12:117075937
|
A | ATATATAT others(7): Show |
5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0275others(2): Show | 5 | HG03942.hp2 NA18952.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-598_59-597insCA others(12): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075937 | ||||||
| chr12:117075937
|
A | ATATATAT others(41): Show |
1 | a0001c0001t0003g0264 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.59-598_59-597insCA others(46): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075937 | ||||||
| chr12:117075937
|
A | ATATATAT others(5): Show |
7 | a0001c0001t0001g0086a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00642.hp2 HG02451.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-598_59-597insCA others(10): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075937 | ||||||
| chr12:117075937
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0260a0001c0001t0001g0268a0001c0001t0001g0270others(2): Show | 5 | HG00323.hp2 HG02015.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-598_59-597insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075937 | ||||||
| chr12:117075937
|
A | ATATATAT others(75): Show |
1 | a0001c0001t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.59-598_59-597insCA others(80): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075937 | ||||||
| chr12:117075937
|
A | G | 30 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(27): Show | 30 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.59-597T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075937 | ||||||
| chr12:117075939
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0258 | 2 | HG03831.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.59-599T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075939 | ||||||
| chr12:117075943
|
A | G | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.59-603T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075943 | ||||||
| chr12:117075945
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-605T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075945 | ||||||
| chr12:117075950
|
C | CAT | 59 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.59-612_59-611dupAT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075950 | ||||||
| chr12:117075950
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 19 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.59-610G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075950 | ||||||
| chr12:117075951
|
A | ATGTATG | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-612_59-611insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075951 | ||||||
| chr12:117075952
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-612A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075952 | ||||||
| chr12:117075955
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.59-616_59-615insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075955 | ||||||
| chr12:117075955
|
A | ATGTATG | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-616_59-615insCA others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075955 | ||||||
| chr12:117075955
|
A | ATGTATGT others(3): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-616_59-615insCA others(8): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075955 | ||||||
| chr12:117075955
|
A | ATGTGTAT others(103): Show |
1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.59-616_59-615insCA others(108): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075955 | ||||||
| chr12:117075955
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-615T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075955 | ||||||
| chr12:117075969
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-629T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075969 | ||||||
| chr12:117075973
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0081others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-633T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075973 | ||||||
| chr12:117075983
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.59-643T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075983 | ||||||
| chr12:117075985
|
A | AT | 53 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 57 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.59-646dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075985 | ||||||
| chr12:117075985
|
A | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0035others(91): Show | 95 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.59-645T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075985 | ||||||
| chr12:117075986
|
T | TA | 5 | a0001c0001t0001g0170a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | HG00609.hp1 HG01109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-647_59-646insT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075986 | ||||||
| chr12:117075987
|
T | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0168 | 2 | HG00621.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.59-647A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117075987 | ||||||
| chr12:117076108
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.59-768G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076108 | ||||||
| chr12:117076190
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0003g0017a0001c0001t0003g0070 | 3 | HG00741.hp1 HG03471.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.59-850T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076190 | ||||||
| chr12:117076520
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.59-1180A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076520 | ||||||
| chr12:117076534
|
T | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-1194A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076534 | ||||||
| chr12:117076553
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(2): Show | 7 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-1213G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076553 | ||||||
| chr12:117076593
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | NA18945.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.59-1253C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076593 | ||||||
| chr12:117076600
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG01123.hp2 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1260G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076600 | ||||||
| chr12:117076645
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-1305G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076645 | ||||||
| chr12:117076735
|
C | T | 30 | a0001c0001t0001g0086a0001c0001t0001g0203a0001c0001t0001g0258others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-1395G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076735 | ||||||
| chr12:117076901
|
T | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0033others(17): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-1561A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117076901 | ||||||
| chr12:117077025
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59-1685G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077025 | ||||||
| chr12:117077101
|
T | C | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 37 | HG00423.hp1 HG00609.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.59-1761A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077101 | ||||||
| chr12:117077160
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.59-1820G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077160 | ||||||
| chr12:117077165
|
C | G | 2 | a0001c0001t0001g0075a0001c0002t0001g0076 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.59-1825G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077165 | ||||||
| chr12:117077431
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-2091T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077431 | ||||||
| chr12:117077439
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.59-2099G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077439 | ||||||
| chr12:117077550
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0245others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2210T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077550 | ||||||
| chr12:117077764
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 171 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.59-2424G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077764 | ||||||
| chr12:117077878
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.59-2538G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077878 | ||||||
| chr12:117077883
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-2543T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077883 | ||||||
| chr12:117077886
|
C | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(13): Show | 17 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-2546G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077886 | ||||||
| chr12:117077919
|
A | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-2579T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077919 | ||||||
| chr12:117077999
|
C | G | 2 | a0001c0001t0001g0188a0001c0001t0003g0017 | 2 | HG00741.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.59-2659G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117077999 | ||||||
| chr12:117078008
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-2668C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078008 | ||||||
| chr12:117078067
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.59-2727G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078067 | ||||||
| chr12:117078082
|
T | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 21 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-2742A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078082 | ||||||
| chr12:117078089
|
C | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0033others(57): Show | 63 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.59-2749G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078089 | ||||||
| chr12:117078189
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.59-2849G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078189 | ||||||
| chr12:117078260
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.59-2920T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078260 | ||||||
| chr12:117078381
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0295others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3041C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078381 | ||||||
| chr12:117078420
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078 | 5 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3080G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078420 | ||||||
| chr12:117078440
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-3100A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078440 | ||||||
| chr12:117078449
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.59-3109C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078449 | ||||||
| chr12:117078487
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0085 | 2 | NA18947.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.59-3147A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078487 | ||||||
| chr12:117078493
|
A | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3153T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078493 | ||||||
| chr12:117078515
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.59-3175G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078515 | ||||||
| chr12:117078557
|
G | GA | 11 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(8): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3218dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078557 | ||||||
| chr12:117078557
|
GA | G | 59 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.59-3218delT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078557 | ||||||
| chr12:117078607
|
T | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3267A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078607 | ||||||
| chr12:117078899
|
G | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0081others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3559C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117078899 | ||||||
| chr12:117079008
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-3668A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079008 | ||||||
| chr12:117079117
|
G | C | 30 | a0001c0001t0001g0045a0001c0001t0001g0085a0001c0001t0001g0114others(27): Show | 30 | HG00140.hp2 HG01106.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-3777C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079117 | ||||||
| chr12:117079182
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 12 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3842A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079182 | ||||||
| chr12:117079214
|
A | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0295others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3874T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079214 | ||||||
| chr12:117079220
|
A | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0043others(21): Show | 27 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.59-3880T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079220 | ||||||
| chr12:117079561
|
C | CA | 69 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0036others(66): Show | 70 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.59-4222dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079561 | ||||||
| chr12:117079732
|
G | C | 30 | a0001c0001t0001g0086a0001c0001t0001g0203a0001c0001t0001g0258others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-4392C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079732 | ||||||
| chr12:117079892
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG01074.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.59-4552A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117079892 | ||||||
| chr12:117080109
|
G | C | 21 | a0001c0001t0001g0086a0001c0001t0001g0260a0001c0001t0001g0265others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-4769C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080109 | ||||||
| chr12:117080225
|
C | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0033others(18): Show | 24 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-4885G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080225 | ||||||
| chr12:117080230
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.59-4890C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080230 | ||||||
| chr12:117080412
|
G | A | 1 | a0001c0001t0003g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-5072C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080412 | ||||||
| chr12:117080515
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.59-5175A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080515 | ||||||
| chr12:117080623
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-5283C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080623 | ||||||
| chr12:117080731
|
C | T | 5 | a0001c0001t0002g0284a0001c0001t0003g0285a0001c0001t0003g0286others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5391G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080731 | ||||||
| chr12:117080760
|
C | T | 5 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5420G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080760 | ||||||
| chr12:117080794
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 18 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-5454C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080794 | ||||||
| chr12:117080841
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078 | 5 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5501G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080841 | ||||||
| chr12:117080981
|
C | A | 8 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0081others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-5641G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117080981 | ||||||
| chr12:117081101
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(13): Show | 17 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-5761T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081101 | ||||||
| chr12:117081116
|
G | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01257.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.59-5776C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081116 | ||||||
| chr12:117081318
|
T | A | 1 | a0001c0001t0003g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-5978A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081318 | ||||||
| chr12:117081450
|
A | C | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-6110T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081450 | ||||||
| chr12:117081560
|
G | A | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.59-6220C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081560 | ||||||
| chr12:117081734
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.59-6394A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081734 | ||||||
| chr12:117081812
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-6472C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081812 | ||||||
| chr12:117081823
|
G | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0060others(8): Show | 12 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-6483C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117081823 | ||||||
| chr12:117082060
|
C | CA | 57 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 62 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.59-6721dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082060 | ||||||
| chr12:117082060
|
C | CAA | 11 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-6722_59-6721dup others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082060 | ||||||
| chr12:117082060
|
C | CAAAA | 13 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 14 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-6724_59-6721dup others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082060 | ||||||
| chr12:117082061
|
A | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 7 | HG00544.hp1 HG01099.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-6721T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082061 | ||||||
| chr12:117082091
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-6751C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082091 | ||||||
| chr12:117082091
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 16 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-6751C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082091 | ||||||
| chr12:117082163
|
T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(13): Show | 17 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-6823A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082163 | ||||||
| chr12:117082405
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0060others(8): Show | 12 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-7065C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082405 | ||||||
| chr12:117082479
|
G | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 16 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-7139C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082479 | ||||||
| chr12:117082501
|
T | TA | 10 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0043others(7): Show | 11 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-7162dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082501 | ||||||
| chr12:117082501
|
TA | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 19 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-7162delT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082501 | ||||||
| chr12:117082557
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(1): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-7217A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082557 | ||||||
| chr12:117082720
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.59-7380C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082720 | ||||||
| chr12:117082861
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(4): Show | 9 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-7521C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117082861 | ||||||
| chr12:117083089
|
AT | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-7750delA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083089 | ||||||
| chr12:117083139
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-7799T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083139 | ||||||
| chr12:117083148
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0233others(2): Show | 7 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-7808G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083148 | ||||||
| chr12:117083279
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(4): Show | 9 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-7939C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083279 | ||||||
| chr12:117083350
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-8010T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083350 | ||||||
| chr12:117083375
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-8035T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083375 | ||||||
| chr12:117083453
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 5 | HG01123.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-8113C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083453 | ||||||
| chr12:117083492
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0188a0001c0001t0002g0016others(2): Show | 5 | HG00741.hp1 HG02074.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-8152G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083492 | ||||||
| chr12:117083563
|
A | T | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 37 | HG00423.hp1 HG00609.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.59-8223T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083563 | ||||||
| chr12:117083671
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0277 | 3 | NA18952.hp1 NA18995.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.59-8331G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083671 | ||||||
| chr12:117083895
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(13): Show | 17 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-8555T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083895 | ||||||
| chr12:117083917
|
G | C | 28 | a0001c0001t0001g0203a0001c0001t0001g0258a0001c0001t0001g0260others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-8577C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083917 | ||||||
| chr12:117083949
|
C | G | 6 | a0001c0001t0003g0068a0001c0001t0003g0104a0001c0001t0003g0261others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-8609G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083949 | ||||||
| chr12:117083964
|
C | T | 5 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-8624G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117083964 | ||||||
| chr12:117084093
|
C | CA | 10 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0103others(7): Show | 10 | HG00741.hp2 HG01168.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-8754dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084093 | ||||||
| chr12:117084093
|
CA | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0024others(104): Show | 110 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.59-8754delT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084093 | ||||||
| chr12:117084130
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-8790C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084130 | ||||||
| chr12:117084152
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-8812T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084152 | ||||||
| chr12:117084195
|
T | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078 | 5 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-8855A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084195 | ||||||
| chr12:117084252
|
A | G | 1 | a0001c0001t0003g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59-8912T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084252 | ||||||
| chr12:117084449
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.59-9109C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084449 | ||||||
| chr12:117084486
|
C | A | 3 | a0001c0001t0001g0188a0001c0001t0002g0016a0001c0001t0003g0017 | 3 | HG00741.hp1 HG03490.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.59-9146G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084486 | ||||||
| chr12:117084496
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.59-9156C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084496 | ||||||
| chr12:117084755
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.59-9415C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084755 | ||||||
| chr12:117084813
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.59-9473C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084813 | ||||||
| chr12:117084884
|
G | A | 1 | a0001c0001t0007g0298 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.59-9544C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084884 | ||||||
| chr12:117084970
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.59-9630T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117084970 | ||||||
| chr12:117085014
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.59-9674G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085014 | ||||||
| chr12:117085015
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-9675C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085015 | ||||||
| chr12:117085112
|
G | A | 63 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.59-9772C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085112 | ||||||
| chr12:117085122
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-9782C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085122 | ||||||
| chr12:117085280
|
T | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0033others(58): Show | 64 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.59-9940A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085280 | ||||||
| chr12:117085585
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-10245C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085585 | ||||||
| chr12:117085811
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.59-10471C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085811 | ||||||
| chr12:117085829
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 12 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-10489G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085829 | ||||||
| chr12:117085913
|
A | C | 1 | a0001c0001t0002g0189 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.59-10573T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117085913 | ||||||
| chr12:117086068
|
A | G | 28 | a0001c0001t0001g0203a0001c0001t0001g0258a0001c0001t0001g0260others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-10728T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086068 | ||||||
| chr12:117086196
|
C | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0021 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-10856G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086196 | ||||||
| chr12:117086268
|
A | ATT | 12 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 13 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-10930_59-10929d others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086268 | ||||||
| chr12:117086268
|
AT | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 39 | HG00423.hp1 HG00609.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-10929delA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086268 | ||||||
| chr12:117086460
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 168 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.59-11120C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086460 | ||||||
| chr12:117086558
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-11218C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086558 | ||||||
| chr12:117086824
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.59-11484G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086824 | ||||||
| chr12:117086879
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.59-11539C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086879 | ||||||
| chr12:117086970
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.59-11630G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117086970 | ||||||
| chr12:117087037
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.59-11697G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087037 | ||||||
| chr12:117087118
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-11778G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087118 | ||||||
| chr12:117087264
|
C | A | 51 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.59-11924G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087264 | ||||||
| chr12:117087296
|
A | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 7 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+11929T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087296 | ||||||
| chr12:117087419
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58+11806C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087419 | ||||||
| chr12:117087430
|
G | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0035others(58): Show | 62 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.58+11795C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087430 | ||||||
| chr12:117087448
|
C | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(159): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.58+11777G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087448 | ||||||
| chr12:117087478
|
C | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0003g0056others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+11747G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087478 | ||||||
| chr12:117087757
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+11468G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087757 | ||||||
| chr12:117087762
|
G | A | 1 | a0001c0001t0003g0264 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.58+11463C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087762 | ||||||
| chr12:117087829
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.58+11396G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087829 | ||||||
| chr12:117087984
|
G | T | 59 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0036others(56): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.58+11241C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117087984 | ||||||
| chr12:117088145
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58+11080C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088145 | ||||||
| chr12:117088172
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+11053A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088172 | ||||||
| chr12:117088275
|
G | A | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG00735.hp1 HG01123.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+10950C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088275 | ||||||
| chr12:117088371
|
T | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0003g0080 | 3 | HG01884.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+10854A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088371 | ||||||
| chr12:117088464
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 174 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.58+10761C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088464 | ||||||
| chr12:117088502
|
A | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(6): Show | 9 | HG00741.hp1 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+10723T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088502 | ||||||
| chr12:117088680
|
C | CA | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(67): Show | 75 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.58+10544dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088680 | ||||||
| chr12:117088680
|
C | CAA | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0060others(19): Show | 25 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.58+10543_58+10544d others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088680 | ||||||
| chr12:117088680
|
C | CAAA | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0188others(6): Show | 9 | HG00741.hp1 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+10542_58+10544d others(5): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088680 | ||||||
| chr12:117088680
|
C | CAAAA | 55 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(52): Show | 55 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.58+10541_58+10544d others(6): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088680 | ||||||
| chr12:117088680
|
C | CAAAAA | 7 | a0001c0001t0001g0252a0001c0001t0001g0294a0001c0001t0002g0018others(4): Show | 7 | HG01891.hp1 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+10540_58+10544d others(7): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088680 | ||||||
| chr12:117088697
|
T | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+10528A>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088697 | ||||||
| chr12:117088821
|
G | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 12 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+10404C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088821 | ||||||
| chr12:117088873
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 173 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.58+10352T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088873 | ||||||
| chr12:117088985
|
G | A | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0003g0056others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+10240C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117088985 | ||||||
| chr12:117089131
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.58+10094C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089131 | ||||||
| chr12:117089184
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(84): Show | 90 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.58+10041G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089184 | ||||||
| chr12:117089276
|
C | A | 14 | a0001c0001t0001g0045a0001c0001t0001g0085a0001c0001t0001g0198others(11): Show | 14 | HG02056.hp1 HG02056.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.58+9949G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089276 | ||||||
| chr12:117089372
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(84): Show | 90 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.58+9853C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089372 | ||||||
| chr12:117089509
|
T | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 41 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+9716A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089509 | ||||||
| chr12:117089784
|
T | C | 61 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0036others(58): Show | 61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.58+9441A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089784 | ||||||
| chr12:117089825
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58+9400A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117089825 | ||||||
| chr12:117090070
|
T | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0203others(22): Show | 26 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.58+9155A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090070 | ||||||
| chr12:117090201
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.58+9024T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090201 | ||||||
| chr12:117090258
|
G | C | 3 | a0001c0001t0001g0188a0001c0001t0002g0016a0001c0001t0003g0017 | 3 | HG00741.hp1 HG03490.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.58+8967C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090258 | ||||||
| chr12:117090259
|
G | A | 61 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0036others(58): Show | 61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.58+8966C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090259 | ||||||
| chr12:117090346
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+8879C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090346 | ||||||
| chr12:117090656
|
C | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(84): Show | 90 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.58+8569G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090656 | ||||||
| chr12:117090769
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+8456C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090769 | ||||||
| chr12:117090933
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 163 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.58+8292T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090933 | ||||||
| chr12:117090948
|
G | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 13 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+8277C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117090948 | ||||||
| chr12:117091177
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0203others(27): Show | 31 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+8048C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091177 | ||||||
| chr12:117091195
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+8030G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091195 | ||||||
| chr12:117091227
|
C | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 41 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+7998G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091227 | ||||||
| chr12:117091250
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.58+7975G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091250 | ||||||
| chr12:117091347
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58+7878T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091347 | ||||||
| chr12:117091373
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0085a0001c0001t0001g0253others(1): Show | 4 | HG02056.hp1 NA18947.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+7852A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091373 | ||||||
| chr12:117091520
|
A | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+7705T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091520 | ||||||
| chr12:117091527
|
G | A | 3 | a0001c0001t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58+7698C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091527 | ||||||
| chr12:117091563
|
G | A | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0003g0056others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+7662C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091563 | ||||||
| chr12:117091616
|
A | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 7 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+7609T>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091616 | ||||||
| chr12:117091652
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0004g0032 | 3 | HG02145.hp1 HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.58+7573T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091652 | ||||||
| chr12:117091703
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.58+7522G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091703 | ||||||
| chr12:117091906
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.58+7319A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117091906 | ||||||
| chr12:117092023
|
C | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | NA18964.hp1 NA18981.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+7202G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092023 | ||||||
| chr12:117092084
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 175 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.58+7141T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092084 | ||||||
| chr12:117092251
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.58+6974C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092251 | ||||||
| chr12:117092283
|
C | T | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.58+6942G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092283 | ||||||
| chr12:117092333
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0203others(27): Show | 31 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+6892C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092333 | ||||||
| chr12:117092338
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(78): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.58+6887A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092338 | ||||||
| chr12:117092412
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+6813A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092412 | ||||||
| chr12:117092441
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0073a0001c0001t0001g0113others(3): Show | 7 | HG02027.hp1 NA18944.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+6784C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092441 | ||||||
| chr12:117092514
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+6711C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092514 | ||||||
| chr12:117092540
|
T | TG | 10 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0107others(7): Show | 11 | HG00438.hp2 HG01074.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+6684dupC | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092540 | ||||||
| chr12:117092598
|
C | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+6627G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092598 | ||||||
| chr12:117092631
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0233others(2): Show | 7 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+6594G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092631 | ||||||
| chr12:117092884
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.58+6341G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117092884 | ||||||
| chr12:117093067
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.58+6158C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093067 | ||||||
| chr12:117093069
|
C | T | 6 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(3): Show | 6 | HG00423.hp1 HG02074.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+6156G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093069 | ||||||
| chr12:117093085
|
G | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0004g0032 | 3 | HG02145.hp1 HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.58+6140C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093085 | ||||||
| chr12:117093126
|
C | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0003g0056others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+6099G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093126 | ||||||
| chr12:117093197
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+6028G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093197 | ||||||
| chr12:117093254
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58+5971G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093254 | ||||||
| chr12:117093290
|
T | C | 4 | a0001c0001t0001g0282a0001c0001t0005g0279a0001c0001t0005g0281others(1): Show | 4 | NA18747.hp2 NA18949.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5935A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093290 | ||||||
| chr12:117093314
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(85): Show | 91 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.58+5911A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093314 | ||||||
| chr12:117093345
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0035others(71): Show | 76 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.58+5880C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093345 | ||||||
| chr12:117093430
|
TC | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG00544.hp1 HG01099.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+5794delG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093430 | ||||||
| chr12:117093447
|
G | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0003g0056others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+5778C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093447 | ||||||
| chr12:117093781
|
A | AT | 14 | a0001c0001t0001g0051a0001c0001t0001g0081a0001c0001t0001g0090others(11): Show | 14 | HG00735.hp1 HG01358.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.58+5443dupA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093781 | ||||||
| chr12:117093781
|
A | ATT | 7 | a0001c0001t0001g0079a0001c0001t0003g0056a0001c0001t0003g0057others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+5442_58+5443dup others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093781 | ||||||
| chr12:117093781
|
AT | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 49 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.58+5443delA | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093781 | ||||||
| chr12:117093938
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(1): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+5287G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117093938 | ||||||
| chr12:117094025
|
C | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 174 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.58+5200G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094025 | ||||||
| chr12:117094032
|
T | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 174 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.58+5193A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094032 | ||||||
| chr12:117094047
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58+5178G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094047 | ||||||
| chr12:117094070
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 174 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.58+5155A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094070 | ||||||
| chr12:117094125
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.58+5100G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094125 | ||||||
| chr12:117094224
|
A | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0184others(28): Show | 32 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.58+5001T>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094224 | ||||||
| chr12:117094272
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0003g0105 | 3 | HG01433.hp2 NA18969.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58+4953G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094272 | ||||||
| chr12:117094293
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(95): Show | 101 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.58+4932T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094293 | ||||||
| chr12:117094361
|
C | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0184others(28): Show | 32 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.58+4864G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094361 | ||||||
| chr12:117094401
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58+4824G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094401 | ||||||
| chr12:117094412
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0098others(5): Show | 8 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+4813G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094412 | ||||||
| chr12:117094442
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(1): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+4783A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094442 | ||||||
| chr12:117094469
|
T | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0204others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+4756A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094469 | ||||||
| chr12:117094510
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+4715G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094510 | ||||||
| chr12:117094656
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.58+4569C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094656 | ||||||
| chr12:117094670
|
G | C | 3 | a0001c0001t0001g0206a0001c0001t0001g0230a0001c0001t0004g0231 | 3 | HG01168.hp1 HG01169.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.58+4555C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094670 | ||||||
| chr12:117094873
|
G | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 41 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+4352C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094873 | ||||||
| chr12:117094910
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58+4315G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117094910 | ||||||
| chr12:117095016
|
C | CA | 39 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(36): Show | 39 | HG00423.hp1 HG01109.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.58+4208dupT | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095016 | ||||||
| chr12:117095016
|
C | CAA | 39 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 43 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+4207_58+4208dup others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095016 | ||||||
| chr12:117095016
|
CAA | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(82): Show | 88 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.58+4207_58+4208del others(2): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095016 | ||||||
| chr12:117095237
|
GCTAA | G | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 42 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.58+3984_58+3987del others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095237 | ||||||
| chr12:117095409
|
C | G | 71 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.58+3816G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095409 | ||||||
| chr12:117095431
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 83 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.58+3794G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095431 | ||||||
| chr12:117095451
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 4 | HG01243.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3774G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095451 | ||||||
| chr12:117095495
|
A | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG01123.hp2 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3730T>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095495 | ||||||
| chr12:117095764
|
T | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0204others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+3461A>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095764 | ||||||
| chr12:117095971
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 73 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+3254C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095971 | ||||||
| chr12:117095988
|
CCTCT | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 42 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.58+3233_58+3236del others(4): Show |
TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117095988 | ||||||
| chr12:117096064
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG00558.hp1 HG02083.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+3161A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096064 | ||||||
| chr12:117096593
|
AC | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 168 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.58+2631delG | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096593 | ||||||
| chr12:117096597
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+2628A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096597 | ||||||
| chr12:117096598
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0078others(1): Show | 6 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+2627C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096598 | ||||||
| chr12:117096792
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.58+2433C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096792 | ||||||
| chr12:117096843
|
C | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0203others(26): Show | 30 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.58+2382G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096843 | ||||||
| chr12:117096902
|
C | T | 34 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0206others(31): Show | 36 | HG00423.hp1 HG01109.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.58+2323G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096902 | ||||||
| chr12:117096904
|
C | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.58+2321G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117096904 | ||||||
| chr12:117097027
|
C | G | 9 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0204others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+2198G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097027 | ||||||
| chr12:117097031
|
C | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0074a0001c0001t0001g0075others(13): Show | 16 | HG01891.hp1 HG02647.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.58+2194G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097031 | ||||||
| chr12:117097076
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0283 | 2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.58+2149C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097076 | ||||||
| chr12:117097084
|
T | C | 5 | a0001c0001t0002g0284a0001c0001t0003g0285a0001c0001t0003g0286others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+2141A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097084 | ||||||
| chr12:117097233
|
G | C | 1 | a0001c0001t0007g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.58+1992C>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097233 | ||||||
| chr12:117097336
|
T | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(101): Show | 107 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.58+1889A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097336 | ||||||
| chr12:117097451
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.58+1774C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097451 | ||||||
| chr12:117097537
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.58+1688G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097537 | ||||||
| chr12:117097681
|
C | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01257.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.58+1544G>C | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097681 | ||||||
| chr12:117097748
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0060others(20): Show | 26 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.58+1477G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097748 | ||||||
| chr12:117097873
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.58+1352C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097873 | ||||||
| chr12:117097915
|
G | A | 3 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054 | 3 | HG01192.hp1 HG01358.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.58+1310C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097915 | ||||||
| chr12:117097919
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.58+1306G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117097919 | ||||||
| chr12:117098170
|
T | C | 5 | a0001c0001t0003g0055a0001c0001t0003g0056a0001c0001t0003g0057others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1055A>G | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098170 | ||||||
| chr12:117098187
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58+1038C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098187 | ||||||
| chr12:117098344
|
AG | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0060others(11): Show | 17 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+880delC | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098344 | ||||||
| chr12:117098487
|
G | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 63 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.58+738C>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098487 | ||||||
| chr12:117098497
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+728C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098497 | ||||||
| chr12:117098578
|
C | A | 1 | a0001c0001t0003g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58+647G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098578 | ||||||
| chr12:117098615
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+610G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098615 | ||||||
| chr12:117098689
|
C | A | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0002g0292others(1): Show | 4 | HG01175.hp2 HG01243.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+536G>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098689 | ||||||
| chr12:117098885
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0007g0299 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.58+340C>T | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098885 | ||||||
| chr12:117098979
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 7 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+246G>A | TESC | ENSG00000088992.18 | transcript | ENST00000335209.12 | protein_coding | 1/7 | chr12 | 117098979 |