Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6910 |
|---|---|
| ensemblid | ENSG00000089225.20 |
| hgncid | 11604 |
| symbol | TBX5 |
| name | T-box transcription factor 5 |
| refseq_nuc | NM_181486.4 |
| refseq_prot | NP_852259.1 |
| ensembl_nuc | ENST00000405440.7 |
| ensembl_prot | ENSP00000384152.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 114353911 |
| end | 114406144 |
| strand | - |
| ver | v1.2 |
| region | chr12:114353911-114406144 |
| region5000 | chr12:114348911-114411144 |
| regionname0 | TBX5_chr12_114353911_114406144 |
| regionname5000 | TBX5_chr12_114348911_114411144 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 518 | 382 | 86 | 77 | 153 | 16 | 48 | 115 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0002 | 0/0 | 518 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0003 | 0/0 | 518 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0004 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0005 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0006 | 0/0 | 518 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0007 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1557 | 360 | 69 | 72 | 153 | 16 | 48 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0002 | 0/0 | 1557 | 15 | 11 | 4 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0003 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0004 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0005 | 0/0 | 1557 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0006 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0007 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0008 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0009 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0010 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| c0011 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2176 | 142 | 42 | 24 | 51 | 9 | 16 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0002 | 0/1 | 2176 | 54 | 4 | 10 | 30 | 0 | 9 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0003 | 0/0 | 2176 | 42 | 0 | 0 | 41 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0004 | 1/0 | 2177 | 35 | 5 | 6 | 6 | 4 | 13 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0005 | 0/0 | 2177 | 24 | 1 | 11 | 12 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0006 | 0/0 | 2176 | 17 | 6 | 8 | 3 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0007 | 0/0 | 2177 | 12 | 9 | 3 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0008 | 0/0 | 2176 | 9 | 0 | 5 | 0 | 1 | 3 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0009 | 0/0 | 2177 | 5 | 1 | 2 | 0 | 1 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0010 | 0/0 | 2176 | 5 | 0 | 0 | 5 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0011 | 0/0 | 2176 | 4 | 0 | 1 | 0 | 0 | 3 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0012 | 0/0 | 2176 | 4 | 3 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0013 | 0/0 | 2176 | 2 | 0 | 0 | 1 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0014 | 0/0 | 2176 | 2 | 1 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0015 | 0/0 | 2176 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0016 | 0/0 | 2180 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0017 | 0/0 | 2180 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0018 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0019 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0020 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0021 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0022 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0023 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0024 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0025 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0026 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0027 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0028 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0029 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0030 | 0/0 | 2177 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0031 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0032 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0033 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0034 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0035 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0036 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0037 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0038 | 0/0 | 2188 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0039 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0040 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0041 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0042 | 0/0 | 2180 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0043 | 0/0 | 2180 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| t0044 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0349 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1557 | 360 | 69 | 72 | 153 | 16 | 48 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002 | 0/0 | 1557 | 15 | 11 | 4 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0003 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0006 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0009 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0002c0004 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0003c0005 | 0/0 | 1557 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0004c0007 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0005c0010 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0006c0008 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0007c0011 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3732 | 125 | 29 | 22 | 49 | 9 | 16 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0002 | 0/1 | 3732 | 51 | 2 | 10 | 29 | 0 | 9 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0003 | 0/0 | 3732 | 42 | 0 | 0 | 41 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0004 | 1/0 | 3733 | 33 | 4 | 5 | 6 | 4 | 13 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0005 | 0/0 | 3733 | 24 | 1 | 11 | 12 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0006 | 0/0 | 3732 | 16 | 5 | 8 | 3 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0007 | 0/0 | 3733 | 12 | 9 | 3 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0008 | 0/0 | 3732 | 7 | 0 | 3 | 0 | 1 | 3 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0009 | 0/0 | 3733 | 5 | 1 | 2 | 0 | 1 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0010 | 0/0 | 3732 | 5 | 0 | 0 | 5 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0011 | 0/0 | 3732 | 4 | 0 | 1 | 0 | 0 | 3 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0012 | 0/0 | 3732 | 4 | 3 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0013 | 0/0 | 3732 | 2 | 0 | 0 | 1 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0014 | 0/0 | 3732 | 2 | 1 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0015 | 0/0 | 3732 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0016 | 0/0 | 3736 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0018 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0020 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0021 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0022 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0023 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0024 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0025 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0026 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0027 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0028 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0029 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0031 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0032 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0033 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0034 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0035 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0036 | 0/0 | 3732 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0037 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0038 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0039 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0040 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0041 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0042 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0001t0044 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002t0001 | 0/0 | 3732 | 7 | 6 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002t0002 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002t0004 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002t0008 | 0/0 | 3732 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002t0017 | 0/0 | 3736 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0002t0043 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0003t0001 | 0/0 | 3732 | 5 | 5 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0006t0019 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0001c0009t0001 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0002c0004t0001 | 0/0 | 3732 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0003c0005t0001 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0003c0005t0006 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0004c0007t0002 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0005c0010t0001 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0006c0008t0030 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| a0007c0011t0002 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | copy fasta | chr12 | 114348911 | 114411144 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0349 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0013g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0014g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0015g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0015g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0016g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0018g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0020g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0021g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0022g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0023g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0024g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0025g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0026g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0027g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0028g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0029g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0031g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0032g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0033g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0034g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0035g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0036g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0037g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0038g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0039g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0040g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0041g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0042g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0044g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0017g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0017g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0043g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0006t0019g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0009t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0002c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0002c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0003c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0003c0005t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0004c0007t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0005c0010t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0006c0008t0030g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0007c0011t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0009 | g0022 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0112 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0331 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0326 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0113 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0111 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0352 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0042 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0325 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0334 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0333 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0351 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01099 | hp2 | a0001 | c0009 | t0001 | g0295 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0041 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01109 | hp1 | a0001 | c0001 | t0029 | g0344 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0140 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0005 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01168 | hp1 | a0001 | c0002 | t0008 | g0116 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01168 | hp2 | a0001 | c0001 | t0039 | g0363 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01169 | hp1 | a0001 | c0002 | t0008 | g0115 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0005 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01192 | hp1 | a0001 | c0001 | t0020 | g0021 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0308 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0301 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0350 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0276 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0176 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0129 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01496 | hp2 | a0001 | c0001 | t0021 | g0016 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0338 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0320 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0340 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01884 | hp1 | a0001 | c0001 | t0034 | g0289 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0036 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01928 | hp1 | a0001 | c0001 | t0044 | g0370 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0126 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01978 | hp1 | a0006 | c0008 | t0030 | g0322 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02015 | hp1 | a0001 | c0001 | t0040 | g0364 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02027 | hp1 | a0001 | c0001 | t0023 | g0038 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02055 | hp2 | a0005 | c0010 | t0001 | g0108 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0128 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0071 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0133 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02165 | hp1 | a0001 | c0001 | t0038 | g0237 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02257 | hp1 | a0001 | c0002 | t0017 | g0368 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02300 | hp1 | a0001 | c0001 | t0041 | g0365 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02622 | hp2 | a0001 | c0001 | t0027 | g0147 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02683 | hp2 | a0001 | c0001 | t0011 | g0046 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0169 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0087 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0357 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02809 | hp1 | a0001 | c0001 | t0032 | g0077 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0144 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0123 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0141 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0014 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02965 | hp2 | a0003 | c0005 | t0001 | g0078 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02976 | hp1 | a0001 | c0001 | t0028 | g0192 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02976 | hp2 | a0003 | c0005 | t0006 | g0033 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0045 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0306 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0014 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0110 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03139 | hp2 | a0001 | c0002 | t0017 | g0369 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0088 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03209 | hp2 | a0001 | c0006 | t0019 | g0035 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0329 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0324 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0310 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03486 | hp2 | a0007 | c0011 | t0002 | g0315 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0229 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0070 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03540 | hp2 | a0001 | c0001 | t0025 | g0270 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0039 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0304 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0024 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0097 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03927 | hp1 | a0001 | c0001 | t0036 | g0328 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0167 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0337 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0040 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0290 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18906 | hp1 | a0001 | c0002 | t0043 | g0367 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18949 | hp1 | a0001 | c0001 | t0024 | g0262 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18949 | hp2 | a0001 | c0001 | t0033 | g0264 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18954 | hp2 | a0001 | c0001 | t0010 | g0247 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0241 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18973 | hp1 | a0004 | c0007 | t0002 | g0217 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18979 | hp1 | a0002 | c0004 | t0001 | g0165 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18986 | hp1 | a0001 | c0001 | t0037 | g0059 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18988 | hp2 | a0001 | c0001 | t0010 | g0135 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0255 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18991 | hp1 | a0001 | c0001 | t0031 | g0278 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0317 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0292 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19089 | hp1 | a0001 | c0001 | t0013 | g0029 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19091 | hp2 | a0002 | c0004 | t0001 | g0164 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0034 | AFR | ASW | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0336 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | GIH | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | GIH | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0152 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02109 | hp1 | a0001 | c0001 | t0042 | g0366 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0143 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0291 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0052 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0072 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG06807 | hp2 | a0001 | c0001 | t0035 | g0281 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0179 | REF | REF | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0349 | REF | REF | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114355855
|
C | T | 1 | a0003 | 2 | HG02965.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.1234G>A | p.Val412Ile | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1789/3733 | 1234/1557 | 412/518 | chr12 | 114355855 | ||
| chr12:114355938
|
G | A | 1 | a0005 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1151C>T | p.Ala384Val | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1706/3733 | 1151/1557 | 384/518 | chr12 | 114355938 | ||
| chr12:114366356
|
C | T | 1 | a0002 | 2 | NA18979.hp1 NA19091.hp2 |
missense_variant | MODERATE | c.791G>A | p.Arg264Lys | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/9 | 1346/3733 | 791/1557 | 264/518 | chr12 | 114366356 | ||
| chr12:114385502
|
C | A | 1 | a0004 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.729G>T | p.Glu243Asp | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/9 | 1284/3733 | 729/1557 | 243/518 | chr12 | 114385502 | ||
| chr12:114399544
|
C | A | 1 | a0006 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.331G>T | p.Asp111Tyr | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/9 | 886/3733 | 331/1557 | 111/518 | chr12 | 114399544 | ||
| chr12:114403844
|
C | A | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.55G>T | p.Ala19Ser | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/9 | 610/3733 | 55/1557 | 19/518 | chr12 | 114403844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114355808
|
G | A | 2 | a0001c0003a0001c0009 | 6 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
synonymous_variant | LOW | c.1281C>T | p.Ser427Ser | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1836/3733 | 1281/1557 | 427/518 | chr12 | 114355808 | ||
| chr12:114394786
|
A | G | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.618T>C | p.Phe206Phe | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/9 | 1173/3733 | 618/1557 | 206/518 | chr12 | 114394786 | ||
| chr12:114399566
|
G | A | 3 | a0001c0002a0001c0009a0005c0010 | 17 | HG01081.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
synonymous_variant | LOW | c.309C>T | p.Leu103Leu | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/9 | 864/3733 | 309/1557 | 103/518 | chr12 | 114399566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114354146
|
GA | G | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*1385delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1385 | chr12 | 114354146 | |||||
| chr12:114354152
|
A | G | 1 | a0001c0001t0020 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1380 | chr12 | 114354152 | |||||
| chr12:114354159
|
C | A | 1 | a0001c0001t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1373 | chr12 | 114354159 | |||||
| chr12:114354196
|
GA | G | 3 | a0001c0001t0012a0001c0001t0015a0001c0001t0022 | 7 | HG01167.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1335delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1335 | chr12 | 114354196 | |||||
| chr12:114354204
|
C | CA | 5 | a0001c0001t0018a0001c0001t0026a0001c0001t0035others(2): Show | 5 | HG01928.hp1 HG01978.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1327dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1327 | chr12 | 114354204 | |||||
| chr12:114354431
|
T | C | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1101 | chr12 | 114354431 | |||||
| chr12:114354696
|
T | G | 1 | a0001c0001t0031 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 836 | chr12 | 114354696 | |||||
| chr12:114354720
|
G | A | 2 | a0001c0001t0015a0001c0001t0022 | 3 | HG01884.hp2 HG02723.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*812C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 812 | chr12 | 114354720 | |||||
| chr12:114354749
|
G | A | 1 | a0001c0001t0036 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 783 | chr12 | 114354749 | |||||
| chr12:114354774
|
G | GAATAAGA others(5): Show |
1 | a0001c0001t0038 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*757_*758insTGGGCT others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 757 | chr12 | 114354774 | |||||
| chr12:114354793
|
A | G | 1 | a0001c0001t0010 | 5 | NA18952.hp1 NA18954.hp2 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*739T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 739 | chr12 | 114354793 | |||||
| chr12:114354850
|
C | G | 1 | a0001c0001t0027 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 682 | chr12 | 114354850 | |||||
| chr12:114354931
|
C | T | 5 | a0001c0001t0014a0001c0001t0018a0001c0001t0026others(2): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*601G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 601 | chr12 | 114354931 | |||||
| chr12:114354969
|
C | T | 1 | a0001c0001t0033 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 563 | chr12 | 114354969 | |||||
| chr12:114355052
|
C | T | 1 | a0001c0001t0025 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 480 | chr12 | 114355052 | |||||
| chr12:114355148
|
A | G | 3 | a0001c0001t0005a0001c0001t0033a0001c0001t0044 | 26 | HG00408.hp2 HG01081.hp1 HG01256.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*384T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 384 | chr12 | 114355148 | |||||
| chr12:114355237
|
A | G | 1 | a0001c0001t0024 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 295 | chr12 | 114355237 | |||||
| chr12:114355388
|
G | A | 1 | a0001c0001t0032 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 144 | chr12 | 114355388 | |||||
| chr12:114355435
|
C | T | 28 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(25): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*97G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 97 | chr12 | 114355435 | |||||
| chr12:114355455
|
T | C | 3 | a0001c0001t0008a0001c0001t0011a0001c0002t0008 | 13 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*77A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 77 | chr12 | 114355455 | |||||
| chr12:114355492
|
T | C | 4 | a0001c0001t0003a0001c0001t0013a0001c0001t0037others(1): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 40 | chr12 | 114355492 | |||||
| chr12:114355503
|
G | A | 1 | a0001c0001t0023 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 29 | chr12 | 114355503 | |||||
| chr12:114405655
|
C | A | 1 | a0001c0001t0039 | 1 | HG01168.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | chr12 | 114405655 | ||||||
| chr12:114405731
|
G | A | 1 | a0001c0001t0040 | 1 | HG02015.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-142C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | chr12 | 114405731 | ||||||
| chr12:114405757
|
G | C | 1 | a0001c0001t0041 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-168C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 1859 | chr12 | 114405757 | |||||
| chr12:114405788
|
G | A | 1 | a0001c0001t0042 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-199C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 1890 | chr12 | 114405788 | |||||
| chr12:114405801
|
C | T | 11 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(8): Show | 34 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-212G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 1903 | chr12 | 114405801 | |||||
| chr12:114405941
|
C | T | 2 | a0001c0001t0016a0001c0001t0042 | 3 | HG02109.hp1 HG02922.hp2 HG03041.hp1 |
5_prime_UTR_variant | MODIFIER | c.-352G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 2043 | chr12 | 114405941 | |||||
| chr12:114406061
|
T | TCTCC | 4 | a0001c0001t0016a0001c0001t0042a0001c0002t0017others(1): Show | 6 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-476_-473dupGGAG | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 2164 | chr12 | 114406061 | |||||
| chr12:114406103
|
G | A | 1 | a0001c0001t0044 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-514C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 2205 | chr12 | 114406103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114356252
|
T | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.983-146A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356252 | ||||||
| chr12:114356398
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(29): Show | 37 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.983-292A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356398 | ||||||
| chr12:114356446
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.983-340G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356446 | ||||||
| chr12:114356794
|
C | G | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.983-688G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356794 | ||||||
| chr12:114356852
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.983-746C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356852 | ||||||
| chr12:114356990
|
C | CGATG | 35 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0105others(32): Show | 35 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.983-888_983-885dup others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | ||||||
| chr12:114356990
|
C | CGATGGAT others(1): Show |
8 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0022g0036others(5): Show | 8 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.983-892_983-885dup others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | ||||||
| chr12:114356990
|
C | CGATGGAT others(5): Show |
3 | a0001c0003t0001g0122a0001c0003t0001g0290a0001c0003t0001g0291 | 3 | HG02280.hp2 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.983-896_983-885dup others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | ||||||
| chr12:114356990
|
C | CGATGGAT others(9): Show |
1 | a0001c0003t0001g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.983-900_983-885dup others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | ||||||
| chr12:114356990
|
CGATG | C | 134 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0079others(131): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.983-888_983-885del others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | ||||||
| chr12:114356990
|
CGATGGAT others(1): Show |
C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 106 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.983-892_983-885del others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | ||||||
| chr12:114357028
|
A | G | 60 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0054others(57): Show | 62 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.983-922T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357028 | ||||||
| chr12:114357221
|
G | A | 22 | a0001c0001t0005g0003a0001c0001t0005g0007a0001c0001t0005g0057others(19): Show | 25 | HG00408.hp2 HG01081.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.983-1115C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357221 | ||||||
| chr12:114357264
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.983-1158G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357264 | ||||||
| chr12:114357314
|
A | G | 43 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.983-1208T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357314 | ||||||
| chr12:114357549
|
G | A | 1 | a0001c0001t0010g0255 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.983-1443C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357549 | ||||||
| chr12:114357586
|
T | C | 43 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.983-1480A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357586 | ||||||
| chr12:114357614
|
T | C | 1 | a0001c0002t0004g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.983-1508A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357614 | ||||||
| chr12:114357638
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.983-1532C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357638 | ||||||
| chr12:114357740
|
C | G | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.983-1634G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357740 | ||||||
| chr12:114357931
|
C | T | 1 | a0001c0001t0009g0022 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.983-1825G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357931 | ||||||
| chr12:114357965
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.983-1859A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357965 | ||||||
| chr12:114358122
|
G | A | 5 | a0001c0001t0003g0205a0001c0001t0003g0210a0001c0001t0003g0215others(2): Show | 5 | HG02056.hp2 HG02135.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.983-2016C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358122 | ||||||
| chr12:114358272
|
C | T | 1 | a0001c0001t0011g0041 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.983-2166G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358272 | ||||||
| chr12:114358479
|
G | T | 58 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0054others(55): Show | 60 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.983-2373C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358479 | ||||||
| chr12:114358545
|
A | C | 1 | a0007c0011t0002g0315 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.983-2439T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358545 | ||||||
| chr12:114358582
|
T | G | 58 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0054others(55): Show | 60 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.983-2476A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358582 | ||||||
| chr12:114358777
|
T | TTTTG | 85 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(82): Show | 88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.983-2675_983-2672d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | ||||||
| chr12:114358777
|
T | TTTTGTTT others(1): Show |
58 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0054others(55): Show | 60 | HG00140.hp1 HG00408.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.983-2679_983-2672d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | ||||||
| chr12:114358777
|
T | TTTTGTTT others(5): Show |
4 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0002g0222others(1): Show | 4 | HG04115.hp2 NA18991.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-2683_983-2672d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | ||||||
| chr12:114358777
|
TTTTGTTT others(1): Show |
T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 107 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.983-2679_983-2672d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | ||||||
| chr12:114358781
|
G | T | 1 | a0001c0001t0035g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.983-2675C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358781 | ||||||
| chr12:114358854
|
C | A | 5 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0026g0072others(2): Show | 5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-2748G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358854 | ||||||
| chr12:114358883
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 260 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.983-2777A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358883 | ||||||
| chr12:114358897
|
C | T | 5 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG01515.hp1 HG02040.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-2791G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358897 | ||||||
| chr12:114359136
|
C | T | 2 | a0001c0001t0034g0289a0001c0006t0019g0035 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.983-3030G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359136 | ||||||
| chr12:114359254
|
G | C | 1 | a0001c0001t0040g0364 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.983-3148C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359254 | ||||||
| chr12:114359288
|
G | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 189 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.983-3182C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359288 | ||||||
| chr12:114359501
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.983-3395T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359501 | ||||||
| chr12:114359542
|
A | G | 10 | a0001c0001t0007g0051a0001c0001t0007g0082a0001c0001t0007g0123others(7): Show | 10 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-3436T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359542 | ||||||
| chr12:114359624
|
C | A | 1 | a0001c0001t0001g0356 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.983-3518G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359624 | ||||||
| chr12:114359756
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.983-3650C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359756 | ||||||
| chr12:114359760
|
G | A | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.983-3654C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359760 | ||||||
| chr12:114359809
|
T | C | 58 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0054others(55): Show | 60 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.983-3703A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359809 | ||||||
| chr12:114359878
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0024g0262 | 2 | NA18949.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.983-3772T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359878 | ||||||
| chr12:114359922
|
C | A | 56 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0054others(53): Show | 58 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.983-3816G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359922 | ||||||
| chr12:114360060
|
T | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 108 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.983-3954A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360060 | ||||||
| chr12:114360068
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.983-3962T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360068 | ||||||
| chr12:114360124
|
G | A | 6 | a0001c0003t0001g0122a0001c0003t0001g0225a0001c0003t0001g0290others(3): Show | 6 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.983-4018C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360124 | ||||||
| chr12:114360194
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0342 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.983-4088C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360194 | ||||||
| chr12:114360277
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 260 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.983-4171G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360277 | ||||||
| chr12:114360284
|
C | T | 2 | a0001c0001t0001g0346a0001c0001t0006g0027 | 2 | HG00738.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.983-4178G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360284 | ||||||
| chr12:114360419
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0001g0321a0001c0001t0001g0359others(1): Show | 4 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-4313C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360419 | ||||||
| chr12:114360570
|
G | A | 1 | a0001c0001t0041g0365 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.983-4464C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360570 | ||||||
| chr12:114360668
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.983-4562C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360668 | ||||||
| chr12:114360679
|
G | A | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.983-4573C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360679 | ||||||
| chr12:114360723
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.983-4617T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360723 | ||||||
| chr12:114360768
|
G | A | 2 | a0001c0001t0002g0204a0001c0001t0002g0218 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.983-4662C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360768 | ||||||
| chr12:114360840
|
C | T | 2 | a0001c0001t0034g0289a0001c0006t0019g0035 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.983-4734G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360840 | ||||||
| chr12:114361049
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.983-4943G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361049 | ||||||
| chr12:114361191
|
A | G | 1 | a0001c0001t0024g0262 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.982+4974T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361191 | ||||||
| chr12:114361235
|
G | A | 1 | a0001c0001t0025g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.982+4930C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361235 | ||||||
| chr12:114361415
|
T | C | 1 | a0002c0004t0001g0164 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.982+4750A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361415 | ||||||
| chr12:114361452
|
A | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(50): Show | 56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.982+4713T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361452 | ||||||
| chr12:114361599
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0146a0001c0001t0016g0014 | 4 | HG02922.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+4566G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361599 | ||||||
| chr12:114361647
|
C | T | 2 | a0001c0001t0007g0143a0001c0001t0007g0352 | 2 | HG00639.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.982+4518G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361647 | ||||||
| chr12:114361651
|
T | C | 43 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.982+4514A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361651 | ||||||
| chr12:114361761
|
C | A | 4 | a0001c0001t0003g0068a0001c0001t0003g0230a0001c0001t0003g0233others(1): Show | 4 | HG00438.hp2 HG02135.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+4404G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361761 | ||||||
| chr12:114361883
|
G | T | 4 | a0001c0001t0002g0124a0001c0001t0002g0166a0001c0001t0002g0203others(1): Show | 4 | HG01123.hp1 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+4282C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361883 | ||||||
| chr12:114361986
|
C | T | 1 | a0001c0001t0004g0155 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.982+4179G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361986 | ||||||
| chr12:114362058
|
A | T | 39 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0094others(36): Show | 39 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.982+4107T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362058 | ||||||
| chr12:114362121
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.982+4044G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362121 | ||||||
| chr12:114362169
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(228): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.982+3996C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362169 | ||||||
| chr12:114362315
|
T | C | 28 | a0001c0001t0001g0275a0001c0001t0002g0054a0001c0001t0002g0066others(25): Show | 28 | HG00408.hp1 HG01123.hp1 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.982+3850A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362315 | ||||||
| chr12:114362575
|
C | T | 1 | a0001c0001t0028g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982+3590G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362575 | ||||||
| chr12:114362584
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+3581G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362584 | ||||||
| chr12:114362731
|
C | T | 25 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(22): Show | 25 | HG01081.hp2 HG01943.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.982+3434G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362731 | ||||||
| chr12:114362749
|
C | G | 1 | a0001c0001t0008g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.982+3416G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362749 | ||||||
| chr12:114362833
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0076 | 5 | HG01109.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.982+3332A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362833 | ||||||
| chr12:114362858
|
T | A | 1 | a0001c0001t0009g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.982+3307A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362858 | ||||||
| chr12:114362999
|
A | G | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(366): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.982+3166T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362999 | ||||||
| chr12:114363008
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(228): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.982+3157T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363008 | ||||||
| chr12:114363022
|
C | T | 15 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(12): Show | 15 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.982+3143G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363022 | ||||||
| chr12:114363206
|
C | T | 1 | a0001c0001t0042g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.982+2959G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363206 | ||||||
| chr12:114363420
|
A | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(50): Show | 56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.982+2745T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363420 | ||||||
| chr12:114363492
|
C | G | 1 | a0001c0001t0003g0104 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.982+2673G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363492 | ||||||
| chr12:114363494
|
T | C | 1 | a0001c0001t0003g0104 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.982+2671A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363494 | ||||||
| chr12:114363529
|
C | T | 51 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 54 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.982+2636G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363529 | ||||||
| chr12:114363588
|
T | G | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.982+2577A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363588 | ||||||
| chr12:114363670
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.982+2495C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363670 | ||||||
| chr12:114363728
|
C | A | 2 | a0001c0001t0035g0281a0001c0002t0004g0052 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.982+2437G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363728 | ||||||
| chr12:114363805
|
T | C | 43 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0089others(40): Show | 43 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.982+2360A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363805 | ||||||
| chr12:114363930
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982+2235C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363930 | ||||||
| chr12:114363967
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 188 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.982+2198C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363967 | ||||||
| chr12:114364259
|
G | A | 43 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.982+1906C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364259 | ||||||
| chr12:114364290
|
C | G | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+1875G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364290 | ||||||
| chr12:114364333
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.982+1832T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364333 | ||||||
| chr12:114364382
|
T | C | 1 | a0001c0002t0002g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982+1783A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364382 | ||||||
| chr12:114364438
|
C | T | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.982+1727G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364438 | ||||||
| chr12:114364468
|
A | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+1697T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364468 | ||||||
| chr12:114364510
|
T | G | 2 | a0001c0001t0034g0289a0001c0006t0019g0035 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.982+1655A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364510 | ||||||
| chr12:114364525
|
T | C | 1 | a0001c0001t0002g0296 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.982+1640A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364525 | ||||||
| chr12:114364556
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.982+1609T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364556 | ||||||
| chr12:114364568
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.982+1597A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364568 | ||||||
| chr12:114364584
|
C | T | 3 | a0001c0001t0011g0039a0001c0001t0011g0040a0001c0001t0011g0046 | 3 | HG02683.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.982+1581G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364584 | ||||||
| chr12:114364753
|
G | A | 1 | a0001c0001t0003g0298 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.982+1412C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364753 | ||||||
| chr12:114364928
|
C | T | 15 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(12): Show | 15 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.982+1237G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364928 | ||||||
| chr12:114364955
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 188 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.982+1210C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364955 | ||||||
| chr12:114365065
|
GA | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(170): Show | 184 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.982+1099delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365065 | ||||||
| chr12:114365150
|
C | T | 8 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(5): Show | 8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.982+1015G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365150 | ||||||
| chr12:114365167
|
G | C | 1 | a0001c0001t0006g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.982+998C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365167 | ||||||
| chr12:114365168
|
A | ATG | 7 | a0001c0001t0002g0206a0001c0001t0004g0157a0001c0001t0007g0051others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.982+995_982+996dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | ||||||
| chr12:114365168
|
ATG | A | 43 | a0001c0001t0001g0224a0001c0001t0003g0006a0001c0001t0003g0009others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.982+995_982+996del others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | ||||||
| chr12:114365168
|
ATGTG | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.982+993_982+996del others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | ||||||
| chr12:114365168
|
ATGTGTG | A | 64 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(61): Show | 64 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.982+991_982+996del others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | ||||||
| chr12:114365198
|
G | C | 51 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 54 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.982+967C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365198 | ||||||
| chr12:114365209
|
GA | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(50): Show | 56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.982+955delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365209 | ||||||
| chr12:114365539
|
A | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0307a0001c0001t0001g0316others(4): Show | 7 | HG00741.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.982+626T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365539 | ||||||
| chr12:114365622
|
A | T | 2 | a0001c0001t0034g0289a0001c0006t0019g0035 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.982+543T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365622 | ||||||
| chr12:114365646
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+519G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365646 | ||||||
| chr12:114365759
|
G | C | 1 | a0001c0001t0004g0357 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.982+406C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365759 | ||||||
| chr12:114365829
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(81): Show | 91 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.982+335dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | ||||||
| chr12:114365829
|
C | CAA | 55 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0055others(52): Show | 59 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.982+334_982+335dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | ||||||
| chr12:114365829
|
CA | C | 64 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(61): Show | 67 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.982+335delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | ||||||
| chr12:114365829
|
CAAAAAAA | C | 40 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0094others(37): Show | 40 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.982+329_982+335del others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | ||||||
| chr12:114365888
|
C | T | 2 | a0001c0001t0003g0232a0001c0001t0003g0234 | 2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.982+277G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365888 | ||||||
| chr12:114366021
|
T | A | 1 | a0001c0001t0014g0331 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.982+144A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366021 | ||||||
| chr12:114366085
|
C | G | 2 | a0001c0001t0034g0289a0001c0006t0019g0035 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.982+80G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366085 | ||||||
| chr12:114366122
|
A | G | 3 | a0001c0001t0004g0160a0001c0001t0004g0161a0001c0001t0004g0162 | 3 | NA18968.hp2 NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.982+43T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366122 | ||||||
| chr12:114366149
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.982+16C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366149 | ||||||
| chr12:114366417
|
C | A | 1 | a0001c0002t0004g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.756-26G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114366417 | ||||||
| chr12:114366775
|
A | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 112 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.756-384T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114366775 | ||||||
| chr12:114366881
|
T | A | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.756-490A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114366881 | ||||||
| chr12:114367093
|
G | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(228): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.756-702C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367093 | ||||||
| chr12:114367113
|
G | A | 1 | a0001c0001t0002g0296 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.756-722C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367113 | ||||||
| chr12:114367252
|
G | GGAAAGAA others(12): Show |
149 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0069others(146): Show | 152 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.756-862_756-861ins others(19): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367252 | ||||||
| chr12:114367257
|
G | GAAAGAAA others(13): Show |
94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 105 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.756-867_756-866ins others(20): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367257 | ||||||
| chr12:114367278
|
T | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(318): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.756-887A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367278 | ||||||
| chr12:114367278
|
T | G | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-887A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367278 | ||||||
| chr12:114367391
|
G | C | 14 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0096others(11): Show | 14 | HG01361.hp1 HG01981.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-1000C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367391 | ||||||
| chr12:114367397
|
T | A | 1 | a0001c0001t0027g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.756-1006A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367397 | ||||||
| chr12:114367400
|
G | A | 1 | a0001c0001t0027g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.756-1009C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367400 | ||||||
| chr12:114367401
|
C | T | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-1010G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367401 | ||||||
| chr12:114367402
|
A | G | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-1011T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367402 | ||||||
| chr12:114367447
|
G | A | 14 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0084others(11): Show | 14 | HG01943.hp2 HG02258.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-1056C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367447 | ||||||
| chr12:114367463
|
C | T | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-1072G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367463 | ||||||
| chr12:114367738
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.756-1347G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367738 | ||||||
| chr12:114367788
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.756-1397A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367788 | ||||||
| chr12:114367820
|
C | T | 3 | a0001c0001t0001g0346a0001c0001t0006g0027a0006c0008t0030g0322 | 3 | HG00738.hp1 HG01978.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.756-1429G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367820 | ||||||
| chr12:114367843
|
T | C | 134 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0069others(131): Show | 137 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.756-1452A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367843 | ||||||
| chr12:114368014
|
G | A | 1 | a0001c0003t0001g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.756-1623C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368014 | ||||||
| chr12:114368030
|
A | G | 5 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0026g0072others(2): Show | 5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-1639T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368030 | ||||||
| chr12:114368036
|
A | C | 1 | a0001c0001t0039g0363 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.756-1645T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368036 | ||||||
| chr12:114368042
|
T | C | 1 | a0001c0001t0005g0125 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.756-1651A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368042 | ||||||
| chr12:114368155
|
G | A | 57 | a0001c0001t0001g0321a0001c0001t0002g0008a0001c0001t0002g0012others(54): Show | 59 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.756-1764C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368155 | ||||||
| chr12:114368189
|
T | A | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-1798A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368189 | ||||||
| chr12:114368196
|
G | A | 43 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.756-1805C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368196 | ||||||
| chr12:114368332
|
C | CTCAA | 37 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0079others(34): Show | 37 | HG00639.hp2 HG01081.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.756-1945_756-1942d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368332 | ||||||
| chr12:114368332
|
CTCAA | C | 3 | a0001c0001t0001g0282a0001c0001t0018g0034a0001c0001t0042g0366 | 3 | HG02109.hp1 HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.756-1945_756-1942d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368332 | ||||||
| chr12:114368332
|
CTCAATCA others(1): Show |
C | 5 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0026g0072others(2): Show | 5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-1949_756-1942d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368332 | ||||||
| chr12:114368344
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.756-1953T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368344 | ||||||
| chr12:114368411
|
G | A | 13 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0096others(10): Show | 13 | HG01361.hp1 HG01981.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.756-2020C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368411 | ||||||
| chr12:114368411
|
G | T | 5 | a0001c0001t0007g0051a0001c0001t0007g0123a0001c0001t0007g0299others(2): Show | 5 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-2020C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368411 | ||||||
| chr12:114368429
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-2038G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368429 | ||||||
| chr12:114368645
|
T | G | 45 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(42): Show | 48 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.756-2254A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368645 | ||||||
| chr12:114368716
|
C | T | 11 | a0001c0001t0007g0051a0001c0001t0007g0082a0001c0001t0007g0123others(8): Show | 11 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-2325G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368716 | ||||||
| chr12:114368730
|
T | C | 16 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(13): Show | 17 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.756-2339A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368730 | ||||||
| chr12:114368736
|
C | T | 53 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(50): Show | 56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.756-2345G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368736 | ||||||
| chr12:114369079
|
G | A | 1 | a0001c0002t0004g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.756-2688C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369079 | ||||||
| chr12:114369080
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.756-2689T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369080 | ||||||
| chr12:114369230
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.756-2839C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369230 | ||||||
| chr12:114369358
|
T | A | 1 | a0007c0011t0002g0315 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.756-2967A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369358 | ||||||
| chr12:114369418
|
T | A | 1 | a0001c0003t0001g0225 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.756-3027A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369418 | ||||||
| chr12:114369421
|
C | T | 12 | a0001c0001t0007g0051a0001c0001t0007g0082a0001c0001t0007g0092others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.756-3030G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369421 | ||||||
| chr12:114369462
|
G | A | 1 | a0001c0001t0022g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.756-3071C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369462 | ||||||
| chr12:114369498
|
G | A | 1 | a0001c0002t0001g0309 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.756-3107C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369498 | ||||||
| chr12:114369573
|
A | C | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3182T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369573 | ||||||
| chr12:114369583
|
G | A | 3 | a0001c0001t0001g0307a0001c0001t0001g0316a0001c0001t0001g0342 | 3 | HG00741.hp1 HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.756-3192C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369583 | ||||||
| chr12:114369689
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0006g0023 | 2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.756-3298T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369689 | ||||||
| chr12:114369821
|
A | G | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-3430T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369821 | ||||||
| chr12:114369850
|
A | AG | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.756-3460_756-3459i others(3): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369850 | ||||||
| chr12:114369874
|
G | A | 1 | a0001c0002t0004g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.756-3483C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369874 | ||||||
| chr12:114369995
|
C | T | 11 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0195others(8): Show | 11 | HG02027.hp2 NA18946.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.756-3604G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369995 | ||||||
| chr12:114370060
|
G | C | 1 | a0001c0001t0009g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.756-3669C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370060 | ||||||
| chr12:114370195
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.756-3804G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370195 | ||||||
| chr12:114370231
|
C | CAGAAA | 13 | a0001c0001t0002g0218a0001c0001t0004g0336a0001c0001t0004g0357others(10): Show | 13 | HG02071.hp1 HG02738.hp2 HG04228.hp1 others(10): Show |
intron_variant | MODIFIER | c.756-3845_756-3841d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
C | CAGAAAAG others(3): Show |
19 | a0001c0001t0002g0206a0001c0001t0002g0213a0001c0001t0002g0220others(16): Show | 21 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.756-3850_756-3841d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
C | CAGAAAAG others(8): Show |
22 | a0001c0001t0002g0054a0001c0001t0002g0066a0001c0001t0002g0204others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.756-3855_756-3841d others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
C | CAGAAAAG others(13): Show |
9 | a0001c0001t0002g0166a0001c0001t0002g0203a0001c0001t0002g0211others(6): Show | 9 | HG01123.hp1 HG02027.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.756-3860_756-3841d others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
C | CAGAAAAG others(18): Show |
4 | a0001c0001t0002g0124a0001c0001t0002g0285a0001c0001t0002g0302others(1): Show | 4 | HG01993.hp1 HG02300.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-3865_756-3841d others(27): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
C | CAGAAAAG others(23): Show |
1 | a0001c0001t0040g0364 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.756-3870_756-3841d others(32): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
C | CAGAAAAG others(28): Show |
1 | a0001c0001t0001g0318 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.756-3875_756-3841d others(37): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370231
|
CAGAAAAG others(13): Show |
C | 42 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(39): Show | 45 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.756-3860_756-3841d others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | ||||||
| chr12:114370248
|
G | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(88): Show | 102 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.756-3857C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370248 | ||||||
| chr12:114370259
|
A | C | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3868T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370259 | ||||||
| chr12:114370265
|
AAAGAAAA others(20): Show |
A | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3901_756-3875d others(29): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370265 | ||||||
| chr12:114370267
|
AGAAAAGA others(18): Show |
A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 103 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.756-3901_756-3877d others(27): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370267 | ||||||
| chr12:114370272
|
AGAAAAGA others(13): Show |
A | 4 | a0001c0001t0001g0279a0001c0001t0001g0323a0001c0001t0001g0340others(1): Show | 4 | HG00642.hp1 HG01516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-3901_756-3882d others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370272 | ||||||
| chr12:114370274
|
AAAAGAAA others(7): Show |
A | 4 | a0001c0001t0004g0074a0001c0001t0004g0161a0001c0001t0004g0228others(1): Show | 4 | HG01361.hp1 HG02965.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-3897_756-3884d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370274 | ||||||
| chr12:114370277
|
AGAAAAGA others(8): Show |
A | 5 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0002t0001g0114others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-3901_756-3887d others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370277 | ||||||
| chr12:114370278
|
GA | G | 3 | a0001c0001t0012g0070a0001c0001t0012g0140a0001c0001t0012g0141 | 3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.756-3888delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370278 | ||||||
| chr12:114370279
|
AAAAGAAA others(2): Show |
A | 7 | a0001c0001t0004g0073a0001c0001t0004g0096a0001c0001t0004g0159others(4): Show | 7 | HG02615.hp2 HG03017.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.756-3897_756-3889d others(11): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370279 | ||||||
| chr12:114370281
|
A | AAGAAAAG others(43): Show |
2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.756-3940_756-3891d others(52): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370281 | ||||||
| chr12:114370282
|
AGAAAAGA others(3): Show |
A | 18 | a0001c0001t0001g0089a0001c0001t0001g0105a0001c0001t0001g0106others(15): Show | 18 | HG00544.hp1 HG00741.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.756-3901_756-3892d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370282 | ||||||
| chr12:114370284
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.756-3893T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370284 | ||||||
| chr12:114370284
|
AAAAG | A | 3 | a0001c0001t0012g0070a0001c0001t0012g0140a0001c0001t0012g0141 | 3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.756-3897_756-3894d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370284 | ||||||
| chr12:114370287
|
A | G | 1 | a0001c0001t0012g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-3896T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370287 | ||||||
| chr12:114370287
|
AGAAAG | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0244others(15): Show | 18 | HG00735.hp1 HG01243.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.756-3901_756-3897d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370287 | ||||||
| chr12:114370288
|
G | A | 1 | a0001c0001t0012g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-3897C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | C | 49 | a0001c0001t0001g0224a0001c0001t0003g0006a0001c0001t0003g0009others(46): Show | 52 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.756-3897C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GA | 23 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0223others(20): Show | 23 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.756-3898dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGA | 6 | a0001c0001t0001g0080a0001c0001t0004g0157a0001c0001t0042g0366others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(3): Show |
1 | a0001c0006t0019g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.756-3898_756-3897i others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(4): Show |
5 | a0001c0001t0001g0139a0001c0001t0001g0275a0001c0001t0001g0294others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(13): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(8): Show |
2 | a0001c0001t0034g0289a0001c0002t0004g0052 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.756-3898_756-3897i others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(13): Show |
1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-3898_756-3897i others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(18): Show |
3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0021g0016 | 3 | HG01496.hp2 NA18946.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.756-3898_756-3897i others(27): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(13): Show |
4 | a0001c0001t0002g0095a0001c0001t0002g0127a0001c0001t0002g0191others(1): Show | 4 | HG01070.hp2 HG01192.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(8): Show |
11 | a0001c0001t0002g0109a0001c0001t0002g0171a0001c0001t0002g0179others(8): Show | 11 | HG01069.hp1 HG01168.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(13): Show |
1 | a0001c0001t0002g0287 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.756-3898_756-3897i others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(3): Show |
4 | a0001c0001t0002g0277a0001c0001t0002g0334a0001c0001t0002g0362others(1): Show | 4 | HG00733.hp2 HG03654.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAAGAA others(8): Show |
1 | a0001c0001t0002g0266 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.756-3898_756-3897i others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370288
|
G | GAAAGA | 6 | a0001c0001t0001g0321a0001c0001t0002g0008a0001c0001t0002g0012others(3): Show | 8 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-3902_756-3898d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | ||||||
| chr12:114370289
|
AAAGAAAA others(16): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.756-3921_756-3899d others(25): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370289 | ||||||
| chr12:114370292
|
G | A | 18 | a0001c0001t0001g0049a0001c0001t0001g0090a0001c0001t0001g0091others(15): Show | 19 | HG00558.hp2 HG00642.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.756-3901C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370292 | ||||||
| chr12:114370293
|
A | AAAAC | 30 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(27): Show | 30 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.756-3903_756-3902i others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370293 | ||||||
| chr12:114370293
|
A | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(152): Show | 167 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.756-3902T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370293 | ||||||
| chr12:114370293
|
A | G | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3902T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370293 | ||||||
| chr12:114370311
|
A | G | 13 | a0001c0001t0008g0097a0001c0001t0008g0152a0001c0001t0008g0176others(10): Show | 14 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-3920T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370311 | ||||||
| chr12:114370312
|
G | A | 13 | a0001c0001t0008g0097a0001c0001t0008g0152a0001c0001t0008g0176others(10): Show | 14 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-3921C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370312 | ||||||
| chr12:114370312
|
GAAAGA | G | 5 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0026g0072others(2): Show | 5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-3926_756-3922d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370312 | ||||||
| chr12:114370316
|
G | A | 1 | a0001c0001t0042g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.756-3925C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370316 | ||||||
| chr12:114370317
|
A | AAAAGAAA others(26): Show |
1 | a0001c0001t0018g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-3927_756-3926i others(35): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370317 | ||||||
| chr12:114370317
|
A | G | 1 | a0001c0001t0042g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.756-3926T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370317 | ||||||
| chr12:114370528
|
C | T | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-4137G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370528 | ||||||
| chr12:114370533
|
A | G | 6 | a0001c0001t0001g0271a0001c0001t0001g0346a0001c0001t0001g0359others(3): Show | 6 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.756-4142T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370533 | ||||||
| chr12:114370627
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.756-4236C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370627 | ||||||
| chr12:114370638
|
C | CCT | 78 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0094others(75): Show | 81 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.756-4249_756-4248d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | ||||||
| chr12:114370638
|
C | CCTCT | 44 | a0001c0001t0001g0050a0001c0001t0001g0069a0001c0001t0001g0080others(41): Show | 44 | HG00558.hp2 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.756-4251_756-4248d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | ||||||
| chr12:114370638
|
C | CCTCTCT | 4 | a0001c0001t0001g0049a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-4253_756-4248d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | ||||||
| chr12:114370638
|
CCTCT | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 99 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.756-4251_756-4248d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | ||||||
| chr12:114370638
|
CCTCTCTC others(1): Show |
C | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(1): Show | 4 | HG00733.hp1 HG01175.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-4255_756-4248d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | ||||||
| chr12:114370741
|
CT | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(232): Show | 250 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.756-4351delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370741 | ||||||
| chr12:114370833
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(288): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.756-4442C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370833 | ||||||
| chr12:114370894
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0146a0001c0001t0016g0014 | 4 | HG02922.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-4503T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370894 | ||||||
| chr12:114370918
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-4527G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370918 | ||||||
| chr12:114370979
|
C | T | 57 | a0001c0001t0001g0321a0001c0001t0002g0008a0001c0001t0002g0012others(54): Show | 59 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.756-4588G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370979 | ||||||
| chr12:114371125
|
C | T | 1 | a0001c0001t0005g0177 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.756-4734G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371125 | ||||||
| chr12:114371322
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.756-4931T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371322 | ||||||
| chr12:114371328
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0076 | 5 | HG01109.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.756-4937C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371328 | ||||||
| chr12:114371386
|
C | T | 1 | a0001c0001t0003g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.756-4995G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371386 | ||||||
| chr12:114371485
|
C | A | 3 | a0001c0001t0012g0070a0001c0001t0012g0140a0001c0001t0012g0141 | 3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.756-5094G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371485 | ||||||
| chr12:114371587
|
G | GT | 51 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0001g0154others(48): Show | 54 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.756-5197dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371587 | ||||||
| chr12:114371587
|
G | GTT | 6 | a0001c0001t0003g0068a0001c0001t0003g0136a0001c0001t0003g0205others(3): Show | 6 | HG02135.hp1 HG02135.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.756-5198_756-5197d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371587 | ||||||
| chr12:114371587
|
GT | G | 73 | a0001c0001t0001g0047a0001c0001t0001g0069a0001c0001t0001g0170others(70): Show | 75 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.756-5197delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371587 | ||||||
| chr12:114371589
|
T | G | 1 | a0001c0001t0001g0004 | 3 | HG02486.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.756-5198A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371589 | ||||||
| chr12:114371606
|
T | C | 1 | a0001c0002t0001g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.756-5215A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371606 | ||||||
| chr12:114371664
|
TG | T | 68 | a0001c0001t0001g0224a0001c0001t0002g0209a0001c0001t0002g0216others(65): Show | 72 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.756-5274delC | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371664 | ||||||
| chr12:114371668
|
G | C | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-5277C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371668 | ||||||
| chr12:114371669
|
C | A | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-5278G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371669 | ||||||
| chr12:114371844
|
G | C | 10 | a0001c0001t0001g0080a0001c0001t0001g0139a0001c0001t0001g0148others(7): Show | 10 | HG01081.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.756-5453C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371844 | ||||||
| chr12:114371878
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(83): Show | 97 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.756-5487C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371878 | ||||||
| chr12:114371888
|
G | C | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-5497C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371888 | ||||||
| chr12:114372043
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.756-5652C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372043 | ||||||
| chr12:114372165
|
C | A | 1 | a0001c0001t0001g0288 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.756-5774G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372165 | ||||||
| chr12:114372322
|
T | C | 2 | a0001c0001t0005g0101a0001c0001t0005g0186 | 2 | HG00408.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.756-5931A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372322 | ||||||
| chr12:114372391
|
G | A | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(366): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.756-6000C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372391 | ||||||
| chr12:114372417
|
G | T | 7 | a0001c0001t0012g0070a0001c0001t0012g0110a0001c0001t0012g0140others(4): Show | 7 | HG01167.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.756-6026C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372417 | ||||||
| chr12:114372479
|
A | AT | 76 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(73): Show | 78 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.756-6089dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372479 | ||||||
| chr12:114372479
|
AT | A | 68 | a0001c0001t0001g0224a0001c0001t0002g0209a0001c0001t0002g0216others(65): Show | 72 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.756-6089delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372479 | ||||||
| chr12:114372591
|
C | T | 61 | a0001c0001t0001g0224a0001c0001t0002g0209a0001c0001t0002g0216others(58): Show | 65 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.756-6200G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372591 | ||||||
| chr12:114372628
|
A | C | 1 | a0001c0001t0008g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.756-6237T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372628 | ||||||
| chr12:114372819
|
C | T | 1 | a0001c0002t0001g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.756-6428G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372819 | ||||||
| chr12:114372832
|
G | C | 70 | a0001c0001t0001g0224a0001c0001t0002g0209a0001c0001t0002g0216others(67): Show | 74 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-6441C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372832 | ||||||
| chr12:114372851
|
A | G | 70 | a0001c0001t0001g0224a0001c0001t0002g0209a0001c0001t0002g0216others(67): Show | 74 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-6460T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372851 | ||||||
| chr12:114372949
|
A | T | 16 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(13): Show | 17 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.756-6558T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372949 | ||||||
| chr12:114372969
|
AATATAT | A | 3 | a0001c0001t0003g0062a0001c0001t0003g0298a0001c0001t0038g0237 | 3 | HG02155.hp2 HG02165.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.756-6584_756-6579d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372969 | ||||||
| chr12:114372969
|
AATATATA others(3): Show |
A | 2 | a0001c0001t0003g0063a0001c0001t0003g0064 | 2 | NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.756-6588_756-6579d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372969 | ||||||
| chr12:114372971
|
TATATATA others(1): Show |
T | 38 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(35): Show | 41 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.756-6588_756-6581d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372971 | ||||||
| chr12:114372971
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0003g0136a0001c0001t0003g0258 | 2 | HG00438.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.756-6592_756-6581d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372971 | ||||||
| chr12:114372977
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156 | 3 | HG00733.hp1 HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.756-6586A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372977 | ||||||
| chr12:114372981
|
T | C | 45 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(42): Show | 48 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.756-6590A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
T | TAC | 19 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0294others(16): Show | 19 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.756-6592_756-6591d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
T | TACAC | 3 | a0001c0001t0007g0123a0001c0001t0007g0301a0001c0001t0009g0022 | 3 | HG00099.hp1 HG01243.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.756-6594_756-6591d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
TAC | T | 28 | a0001c0001t0001g0069a0001c0001t0001g0094a0001c0001t0001g0119others(25): Show | 28 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.756-6592_756-6591d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
TACAC | T | 79 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0170others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-6594_756-6591d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
TACACAC | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(66): Show | 73 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.756-6596_756-6591d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
TACACACA others(1): Show |
T | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(32): Show | 43 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.756-6598_756-6591d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0158a0001c0001t0001g0305a0001c0001t0001g0327others(4): Show | 7 | HG01943.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-6600_756-6591d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114372981
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0100a0001c0001t0004g0073a0001c0001t0004g0074 | 3 | HG02015.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.756-6602_756-6591d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | ||||||
| chr12:114373136
|
A | G | 1 | a0001c0001t0003g0232 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.756-6745T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373136 | ||||||
| chr12:114373164
|
G | C | 11 | a0001c0001t0007g0051a0001c0001t0007g0082a0001c0001t0007g0123others(8): Show | 11 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-6773C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373164 | ||||||
| chr12:114373237
|
A | G | 43 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0089others(40): Show | 43 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.756-6846T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373237 | ||||||
| chr12:114373247
|
C | T | 52 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(49): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-6856G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373247 | ||||||
| chr12:114373318
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-6927G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373318 | ||||||
| chr12:114373515
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0244a0001c0001t0006g0028others(1): Show | 4 | NA18963.hp2 NA18975.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-7124T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373515 | ||||||
| chr12:114373545
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.756-7154C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373545 | ||||||
| chr12:114373550
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(322): Show | 342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.756-7159A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373550 | ||||||
| chr12:114373590
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-7199G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373590 | ||||||
| chr12:114373612
|
T | C | 52 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(49): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7221A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373612 | ||||||
| chr12:114373615
|
T | A | 52 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(49): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7224A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373615 | ||||||
| chr12:114373708
|
C | T | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-7317G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373708 | ||||||
| chr12:114373815
|
C | T | 52 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(49): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7424G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373815 | ||||||
| chr12:114373849
|
T | C | 52 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(49): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7458A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373849 | ||||||
| chr12:114373934
|
G | C | 1 | a0001c0001t0001g0339 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.756-7543C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373934 | ||||||
| chr12:114374045
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.756-7654A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374045 | ||||||
| chr12:114374089
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.756-7698C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374089 | ||||||
| chr12:114374385
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756-7994T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374385 | ||||||
| chr12:114374429
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.756-8038C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374429 | ||||||
| chr12:114374582
|
C | T | 45 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(42): Show | 48 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.756-8191G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374582 | ||||||
| chr12:114374821
|
T | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(90): Show | 104 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.756-8430A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374821 | ||||||
| chr12:114374897
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.756-8506C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374897 | ||||||
| chr12:114375287
|
G | T | 43 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0010others(40): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.756-8896C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375287 | ||||||
| chr12:114375303
|
T | C | 53 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(50): Show | 56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.756-8912A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375303 | ||||||
| chr12:114375460
|
T | C | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-9069A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375460 | ||||||
| chr12:114375508
|
T | C | 43 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0089others(40): Show | 43 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.756-9117A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375508 | ||||||
| chr12:114375706
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.756-9315C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375706 | ||||||
| chr12:114375731
|
G | T | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-9340C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375731 | ||||||
| chr12:114375911
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.756-9520C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375911 | ||||||
| chr12:114375975
|
G | T | 2 | a0001c0001t0001g0282a0001c0001t0035g0281 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755+9501C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375975 | ||||||
| chr12:114375984
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.755+9492C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375984 | ||||||
| chr12:114376125
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755+9351A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376125 | ||||||
| chr12:114376188
|
C | T | 8 | a0001c0001t0004g0096a0001c0001t0004g0157a0001c0001t0004g0159others(5): Show | 8 | HG01981.hp1 HG03017.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.755+9288G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376188 | ||||||
| chr12:114376261
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9215C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376261 | ||||||
| chr12:114376262
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9214A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376262 | ||||||
| chr12:114376265
|
GTA | G | 108 | a0001c0001t0001g0170a0001c0001t0001g0282a0001c0001t0001g0321others(105): Show | 113 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.755+9209_755+9210d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376265 | ||||||
| chr12:114376267
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9209T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376267 | ||||||
| chr12:114376272
|
T | TAC | 14 | a0001c0001t0001g0293a0001c0001t0001g0319a0001c0001t0001g0330others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.755+9203_755+9204i others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376272 | ||||||
| chr12:114376274
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(133): Show | 143 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.755+9202A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376274 | ||||||
| chr12:114376274
|
TACAC | T | 24 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+9198_755+9201d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376274 | ||||||
| chr12:114376276
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9200G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376276 | ||||||
| chr12:114376344
|
C | G | 3 | a0001c0001t0001g0282a0001c0001t0035g0281a0001c0002t0004g0052 | 3 | HG02280.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755+9132G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376344 | ||||||
| chr12:114376481
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(224): Show | 242 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.755+8995A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376481 | ||||||
| chr12:114376564
|
G | C | 3 | a0001c0001t0001g0282a0001c0001t0035g0281a0001c0002t0004g0052 | 3 | HG02280.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755+8912C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376564 | ||||||
| chr12:114376594
|
GTT | G | 13 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0096others(10): Show | 13 | HG01361.hp1 HG01981.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.755+8880_755+8881d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376594 | ||||||
| chr12:114376611
|
G | A | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(21): Show | 24 | HG01081.hp2 HG01943.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.755+8865C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376611 | ||||||
| chr12:114376720
|
G | A | 2 | a0001c0001t0007g0144a0001c0001t0007g0149 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.755+8756C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376720 | ||||||
| chr12:114376966
|
T | C | 1 | a0001c0001t0020g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.755+8510A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376966 | ||||||
| chr12:114377256
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755+8220A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377256 | ||||||
| chr12:114377404
|
T | A | 1 | a0001c0001t0002g0296 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.755+8072A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377404 | ||||||
| chr12:114377459
|
C | T | 24 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+8017G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377459 | ||||||
| chr12:114377512
|
A | T | 8 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(5): Show | 8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+7964T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377512 | ||||||
| chr12:114377513
|
A | C | 8 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(5): Show | 8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+7963T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377513 | ||||||
| chr12:114377514
|
A | C | 8 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(5): Show | 8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+7962T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377514 | ||||||
| chr12:114377539
|
G | T | 24 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+7937C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377539 | ||||||
| chr12:114377559
|
C | CT | 6 | a0001c0001t0001g0271a0001c0001t0005g0131a0001c0001t0006g0044others(3): Show | 6 | HG00639.hp1 HG01074.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+7916dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377559 | ||||||
| chr12:114377559
|
CT | C | 35 | a0001c0001t0001g0183a0001c0001t0001g0224a0001c0001t0001g0318others(32): Show | 36 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.755+7916delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377559 | ||||||
| chr12:114377564
|
T | C | 45 | a0001c0001t0002g0209a0001c0001t0002g0216a0001c0001t0003g0006others(42): Show | 48 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.755+7912A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377564 | ||||||
| chr12:114377617
|
C | T | 25 | a0001c0001t0001g0224a0001c0001t0002g0194a0001c0001t0008g0097others(22): Show | 26 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.755+7859G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377617 | ||||||
| chr12:114377618
|
G | A | 3 | a0001c0001t0015g0087a0001c0001t0015g0088a0001c0001t0022g0036 | 3 | HG01884.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.755+7858C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377618 | ||||||
| chr12:114377670
|
CA | C | 7 | a0001c0001t0001g0120a0001c0001t0001g0307a0001c0001t0001g0316others(4): Show | 7 | HG00741.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+7805delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377670 | ||||||
| chr12:114377718
|
G | A | 8 | a0001c0001t0004g0096a0001c0001t0004g0157a0001c0001t0004g0159others(5): Show | 8 | HG01981.hp1 HG03017.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.755+7758C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377718 | ||||||
| chr12:114377719
|
A | T | 64 | a0001c0001t0001g0105a0001c0001t0001g0170a0001c0001t0001g0282others(61): Show | 66 | HG00140.hp2 HG00408.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.755+7757T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377719 | ||||||
| chr12:114377720
|
C | G | 24 | a0001c0001t0001g0224a0001c0001t0008g0097a0001c0001t0008g0152others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+7756G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377720 | ||||||
| chr12:114377951
|
G | A | 7 | a0001c0001t0014g0071a0001c0001t0014g0331a0001c0001t0018g0034others(4): Show | 7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.755+7525C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377951 | ||||||
| chr12:114378012
|
C | A | 1 | a0001c0001t0004g0329 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.755+7464G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378012 | ||||||
| chr12:114378244
|
G | A | 2 | a0001c0001t0003g0232a0001c0001t0003g0234 | 2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.755+7232C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378244 | ||||||
| chr12:114378261
|
C | T | 2 | a0001c0001t0034g0289a0001c0006t0019g0035 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.755+7215G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378261 | ||||||
| chr12:114378555
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(152): Show | 168 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.755+6921G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378555 | ||||||
| chr12:114378558
|
A | T | 62 | a0001c0001t0001g0105a0001c0001t0001g0170a0001c0001t0001g0321others(59): Show | 64 | HG00140.hp2 HG00408.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.755+6918T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378558 | ||||||
| chr12:114378631
|
G | GTTTGT | 46 | a0001c0001t0001g0269a0001c0001t0002g0209a0001c0001t0002g0216others(43): Show | 49 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.755+6840_755+6844d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378631 | ||||||
| chr12:114378743
|
G | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(311): Show | 331 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.755+6733C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378743 | ||||||
| chr12:114378975
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.755+6501G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378975 | ||||||
| chr12:114378976
|
G | A | 4 | a0001c0001t0012g0070a0001c0001t0012g0110a0001c0001t0012g0140others(1): Show | 4 | HG01167.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+6500C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378976 | ||||||
| chr12:114379015
|
A | T | 63 | a0001c0001t0001g0094a0001c0001t0001g0170a0001c0001t0001g0282others(60): Show | 65 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.755+6461T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379015 | ||||||
| chr12:114379044
|
C | T | 2 | a0001c0003t0001g0122a0001c0003t0001g0290 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.755+6432G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379044 | ||||||
| chr12:114379132
|
C | T | 4 | a0001c0001t0012g0070a0001c0001t0012g0110a0001c0001t0012g0140others(1): Show | 4 | HG01167.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+6344G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379132 | ||||||
| chr12:114379198
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.755+6278G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379198 | ||||||
| chr12:114379201
|
A | T | 1 | a0001c0001t0010g0135 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.755+6275T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379201 | ||||||
| chr12:114379257
|
A | G | 2 | a0001c0001t0001g0359a0001c0001t0039g0363 | 2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.755+6219T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379257 | ||||||
| chr12:114379261
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.755+6215G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379261 | ||||||
| chr12:114379310
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.755+6166T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379310 | ||||||
| chr12:114379440
|
C | T | 1 | a0001c0001t0007g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.755+6036G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379440 | ||||||
| chr12:114379515
|
T | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(263): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.755+5961A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379515 | ||||||
| chr12:114379527
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0103others(55): Show | 63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.755+5949C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379527 | ||||||
| chr12:114379703
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0321 | 2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.755+5773C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379703 | ||||||
| chr12:114379724
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(229): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.755+5752A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379724 | ||||||
| chr12:114379785
|
G | A | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.755+5691C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379785 | ||||||
| chr12:114380009
|
T | C | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+5467A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380009 | ||||||
| chr12:114380064
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0244a0001c0001t0010g0150others(3): Show | 6 | NA18952.hp1 NA18954.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+5412C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380064 | ||||||
| chr12:114380448
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(58): Show | 68 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.755+5028G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380448 | ||||||
| chr12:114380570
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0050others(46): Show | 50 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.755+4906A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380570 | ||||||
| chr12:114380622
|
G | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0034g0289 | 3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.755+4854C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380622 | ||||||
| chr12:114380656
|
AG | A | 109 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(106): Show | 113 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.755+4819delC | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380656 | ||||||
| chr12:114380664
|
T | A | 1 | a0001c0001t0010g0150 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.755+4812A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380664 | ||||||
| chr12:114380676
|
A | G | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+4800T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380676 | ||||||
| chr12:114380697
|
G | A | 24 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+4779C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380697 | ||||||
| chr12:114380850
|
T | TA | 104 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(101): Show | 108 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.755+4625dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | ||||||
| chr12:114380850
|
T | TAA | 66 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0158others(63): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.755+4624_755+4625d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | ||||||
| chr12:114380850
|
T | TAAA | 40 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0085others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.755+4623_755+4625d others(5): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | ||||||
| chr12:114380850
|
TA | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0343a0001c0001t0012g0070others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+4625delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | ||||||
| chr12:114380851
|
A | T | 1 | a0001c0001t0003g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.755+4625T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380851 | ||||||
| chr12:114380921
|
AT | A | 24 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+4554delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380921 | ||||||
| chr12:114380933
|
A | T | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(360): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.755+4543T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380933 | ||||||
| chr12:114380997
|
G | A | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+4479C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380997 | ||||||
| chr12:114381136
|
G | A | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.755+4340C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381136 | ||||||
| chr12:114381139
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.755+4337C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381139 | ||||||
| chr12:114381173
|
C | T | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+4303G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381173 | ||||||
| chr12:114381174
|
A | C | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+4302T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381174 | ||||||
| chr12:114381207
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.755+4269C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381207 | ||||||
| chr12:114381594
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0007g0051a0001c0001t0007g0299others(3): Show | 7 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+3882G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381594 | ||||||
| chr12:114381826
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.755+3650G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381826 | ||||||
| chr12:114381955
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0081others(101): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.755+3521T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381955 | ||||||
| chr12:114382052
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0190others(23): Show | 31 | HG00408.hp2 HG00544.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.755+3424A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382052 | ||||||
| chr12:114382182
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.755+3294A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382182 | ||||||
| chr12:114382294
|
A | G | 1 | a0001c0001t0031g0278 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.755+3182T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382294 | ||||||
| chr12:114382301
|
G | A | 1 | a0001c0001t0008g0324 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.755+3175C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382301 | ||||||
| chr12:114382445
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.755+3031G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382445 | ||||||
| chr12:114382458
|
G | T | 7 | a0001c0001t0001g0158a0001c0001t0001g0327a0001c0001t0004g0157others(4): Show | 7 | HG01943.hp1 HG02683.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+3018C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382458 | ||||||
| chr12:114382475
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0081others(100): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.755+3001C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382475 | ||||||
| chr12:114382537
|
G | A | 109 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(106): Show | 113 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.755+2939C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382537 | ||||||
| chr12:114382643
|
G | A | 24 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+2833C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382643 | ||||||
| chr12:114382655
|
G | C | 1 | a0001c0001t0042g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.755+2821C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382655 | ||||||
| chr12:114382751
|
C | T | 1 | a0001c0001t0004g0155 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.755+2725G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382751 | ||||||
| chr12:114382758
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.755+2718G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382758 | ||||||
| chr12:114382791
|
C | T | 16 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.755+2685G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382791 | ||||||
| chr12:114382903
|
G | A | 1 | a0001c0001t0007g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.755+2573C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382903 | ||||||
| chr12:114382977
|
C | CA | 6 | a0001c0001t0001g0076a0001c0001t0001g0256a0001c0001t0002g0287others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+2498dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382977 | ||||||
| chr12:114382977
|
CA | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0081others(103): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.755+2498delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382977 | ||||||
| chr12:114382977
|
CAA | C | 12 | a0001c0001t0001g0158a0001c0001t0001g0223a0001c0001t0001g0327others(9): Show | 12 | HG01943.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.755+2497_755+2498d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382977 | ||||||
| chr12:114382994
|
AAG | A | 88 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(85): Show | 92 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.755+2480_755+2481d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382994 | ||||||
| chr12:114382995
|
AG | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0353a0001c0001t0001g0355others(1): Show | 4 | HG01175.hp2 HG02148.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+2480delC | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382995 | ||||||
| chr12:114383007
|
A | G | 1 | a0001c0001t0006g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.755+2469T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383007 | ||||||
| chr12:114383016
|
C | T | 9 | a0001c0001t0001g0251a0001c0001t0003g0006a0001c0001t0003g0009others(6): Show | 11 | HG00673.hp1 NA18944.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.755+2460G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383016 | ||||||
| chr12:114383133
|
G | A | 1 | a0001c0001t0024g0262 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.755+2343C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383133 | ||||||
| chr12:114383180
|
T | G | 1 | a0001c0001t0004g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.755+2296A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383180 | ||||||
| chr12:114383341
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755+2135G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383341 | ||||||
| chr12:114383425
|
A | G | 5 | a0001c0001t0002g0066a0001c0001t0002g0239a0001c0001t0002g0250others(2): Show | 5 | HG00408.hp1 HG02129.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+2051T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383425 | ||||||
| chr12:114383466
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.755+2010T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383466 | ||||||
| chr12:114383508
|
A | T | 1 | a0001c0001t0040g0364 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.755+1968T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383508 | ||||||
| chr12:114383580
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.755+1896C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383580 | ||||||
| chr12:114383635
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.755+1841A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383635 | ||||||
| chr12:114383646
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(210): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.755+1830G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383646 | ||||||
| chr12:114383892
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.755+1584G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383892 | ||||||
| chr12:114383899
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.755+1577A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383899 | ||||||
| chr12:114384006
|
G | A | 2 | a0001c0001t0003g0233a0001c0001t0003g0236 | 2 | HG00438.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.755+1470C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384006 | ||||||
| chr12:114384063
|
G | T | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+1413C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384063 | ||||||
| chr12:114384273
|
GT | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(357): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.755+1202delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384273 | ||||||
| chr12:114384395
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.755+1081G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384395 | ||||||
| chr12:114384487
|
C | T | 12 | a0001c0001t0001g0158a0001c0001t0001g0223a0001c0001t0001g0327others(9): Show | 12 | HG01943.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.755+989G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384487 | ||||||
| chr12:114384592
|
T | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0034g0289 | 3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.755+884A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384592 | ||||||
| chr12:114384714
|
A | AAC | 14 | a0001c0001t0001g0004a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 16 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.755+760_755+761dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | AACACAC | 6 | a0001c0001t0001g0272a0001c0001t0003g0063a0001c0001t0004g0074others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+756_755+761dup others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | AACACACA others(1): Show |
30 | a0001c0001t0001g0011a0001c0001t0001g0100a0001c0001t0001g0271others(27): Show | 33 | HG00408.hp2 HG00639.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.755+754_755+761dup others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | AACACACA others(3): Show |
38 | a0001c0001t0001g0001a0001c0001t0001g0170a0001c0001t0001g0180others(35): Show | 41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.755+752_755+761dup others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | AACACACA others(5): Show |
10 | a0001c0001t0001g0168a0001c0001t0001g0307a0001c0001t0004g0073others(7): Show | 10 | HG00280.hp2 HG01106.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.755+750_755+761dup others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | AACACACA others(7): Show |
1 | a0001c0001t0004g0184 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.755+748_755+761dup others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | AACACACA others(9): Show |
2 | a0001c0002t0017g0368a0001c0002t0017g0369 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.755+746_755+761dup others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0346a0001c0001t0013g0029 | 2 | HG04204.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.755+761_755+762ins others(11): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
AAC | A | 30 | a0001c0001t0001g0146a0001c0001t0001g0235a0001c0001t0001g0269others(27): Show | 31 | HG00438.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+760_755+761del others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384714
|
AACAC | A | 5 | a0001c0001t0001g0249a0001c0001t0001g0256a0001c0001t0007g0123others(2): Show | 5 | HG01884.hp2 HG02071.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+758_755+761del others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | ||||||
| chr12:114384724
|
CACACACA others(14): Show |
C | 18 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(15): Show | 18 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.755+731_755+751del others(21): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384724 | ||||||
| chr12:114384726
|
CACACACA others(12): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.755+731_755+749del others(19): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384726 | ||||||
| chr12:114384745
|
A | ACACACAA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.755+730_755+731ins others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384745
|
A | ACACACAC others(3): Show |
9 | a0001c0001t0001g0354a0001c0001t0002g0008a0001c0001t0002g0054others(6): Show | 10 | HG01168.hp1 HG02132.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384745
|
A | ACACACAC others(5): Show |
6 | a0001c0001t0001g0327a0001c0001t0004g0157a0001c0001t0004g0159others(3): Show | 6 | HG02683.hp1 NA18966.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384745
|
A | ACACACAC others(5): Show |
65 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0094others(62): Show | 68 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384745
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0069 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.755+730_755+731ins others(11): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384745
|
A | ACACACAC others(7): Show |
19 | a0001c0001t0001g0083a0001c0001t0001g0153a0001c0001t0001g0154others(16): Show | 19 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384745
|
A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0353a0001c0001t0002g0222 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.755+730_755+731ins others(13): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | ||||||
| chr12:114384914
|
T | C | 24 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+562A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384914 | ||||||
| chr12:114384927
|
G | A | 1 | a0003c0005t0001g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.755+549C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384927 | ||||||
| chr12:114385091
|
C | T | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+385G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385091 | ||||||
| chr12:114385104
|
C | CA | 155 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0094others(152): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.755+371dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385104 | ||||||
| chr12:114385104
|
CA | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(138): Show | 151 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.755+371delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385104 | ||||||
| chr12:114385127
|
C | T | 1 | a0001c0001t0027g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.755+349G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385127 | ||||||
| chr12:114385284
|
G | A | 100 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(97): Show | 104 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.755+192C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385284 | ||||||
| chr12:114385286
|
C | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0034g0289 | 3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.755+190G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385286 | ||||||
| chr12:114385293
|
C | T | 54 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(51): Show | 54 | HG01070.hp1 HG01123.hp1 HG01192.hp1 others(51): Show |
intron_variant | MODIFIER | c.755+183G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385293 | ||||||
| chr12:114385382
|
G | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0050others(43): Show | 47 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.755+94C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385382 | ||||||
| chr12:114385389
|
G | A | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+87C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385389 | ||||||
| chr12:114385435
|
G | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG00323.hp2 HG00438.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+41C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385435 | ||||||
| chr12:114385664
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.664-97C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385664 | ||||||
| chr12:114385666
|
C | G | 1 | a0001c0001t0012g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.664-99G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385666 | ||||||
| chr12:114385670
|
G | A | 1 | a0001c0001t0003g0234 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.664-103C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385670 | ||||||
| chr12:114385712
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.664-145G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385712 | ||||||
| chr12:114385728
|
A | G | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.664-161T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385728 | ||||||
| chr12:114385840
|
C | CT | 100 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(97): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.664-274dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385840 | ||||||
| chr12:114385840
|
C | CTT | 98 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0100others(95): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.664-275_664-274dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385840 | ||||||
| chr12:114385962
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(59): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.664-395C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385962 | ||||||
| chr12:114386086
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0007g0051a0001c0001t0007g0299others(3): Show | 7 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-519C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386086 | ||||||
| chr12:114386127
|
C | T | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0285others(1): Show | 4 | HG02027.hp1 NA18957.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-560G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386127 | ||||||
| chr12:114386943
|
AT | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(178): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.664-1377delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386943 | ||||||
| chr12:114386945
|
TTA | T | 24 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(21): Show | 24 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.664-1380_664-1379d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386945 | ||||||
| chr12:114386946
|
T | A | 8 | a0001c0001t0001g0158a0001c0001t0001g0327a0001c0001t0004g0157others(5): Show | 8 | HG01243.hp1 HG01943.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-1379A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386946 | ||||||
| chr12:114386977
|
G | C | 1 | a0001c0001t0024g0262 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.664-1410C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386977 | ||||||
| chr12:114386983
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.664-1416T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386983 | ||||||
| chr12:114387108
|
A | G | 1 | a0001c0001t0005g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.664-1541T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387108 | ||||||
| chr12:114387114
|
A | C | 110 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(107): Show | 114 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.664-1547T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387114 | ||||||
| chr12:114387115
|
A | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(214): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.664-1548T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387115 | ||||||
| chr12:114387123
|
CAAAA | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0279others(8): Show | 12 | HG00735.hp1 HG00738.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.664-1560_664-1557d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387123 | ||||||
| chr12:114387124
|
A | C | 2 | a0001c0001t0004g0073a0001c0001t0004g0074 | 2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.664-1557T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387124 | ||||||
| chr12:114387205
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.664-1638G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387205 | ||||||
| chr12:114387216
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.664-1649A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387216 | ||||||
| chr12:114387236
|
GC | G | 24 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.664-1670delG | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387236 | ||||||
| chr12:114387490
|
T | C | 1 | a0001c0001t0005g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.664-1923A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387490 | ||||||
| chr12:114387492
|
G | A | 1 | a0001c0001t0004g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-1925C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387492 | ||||||
| chr12:114387524
|
T | C | 1 | a0001c0001t0002g0296 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.664-1957A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387524 | ||||||
| chr12:114387532
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.664-1965C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387532 | ||||||
| chr12:114387574
|
C | G | 1 | a0001c0001t0001g0242 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.664-2007G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387574 | ||||||
| chr12:114387614
|
C | T | 5 | a0001c0001t0006g0017a0001c0001t0006g0018a0001c0001t0006g0019others(2): Show | 5 | HG01070.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-2047G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387614 | ||||||
| chr12:114387680
|
G | A | 1 | a0001c0001t0005g0126 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.664-2113C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387680 | ||||||
| chr12:114387839
|
C | T | 10 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0075others(7): Show | 10 | HG01109.hp2 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.664-2272G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387839 | ||||||
| chr12:114387899
|
C | T | 1 | a0001c0001t0003g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664-2332G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387899 | ||||||
| chr12:114387915
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.664-2348G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387915 | ||||||
| chr12:114387962
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0007g0092 | 2 | HG03209.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.664-2395C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387962 | ||||||
| chr12:114388056
|
C | T | 20 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-2489G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388056 | ||||||
| chr12:114388097
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.664-2530G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388097 | ||||||
| chr12:114388239
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.664-2672G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388239 | ||||||
| chr12:114388292
|
G | C | 1 | a0001c0001t0010g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.664-2725C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388292 | ||||||
| chr12:114388318
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.664-2751A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388318 | ||||||
| chr12:114388472
|
A | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.664-2905T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388472 | ||||||
| chr12:114388473
|
A | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.664-2906T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388473 | ||||||
| chr12:114388569
|
C | G | 1 | a0001c0001t0039g0363 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.664-3002G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388569 | ||||||
| chr12:114388675
|
C | CGT | 43 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0081others(40): Show | 49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.664-3110_664-3109d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
C | CGTGT | 19 | a0001c0001t0001g0100a0001c0001t0001g0153a0001c0001t0001g0154others(16): Show | 19 | HG00140.hp2 HG00738.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.664-3112_664-3109d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
C | CGTGTGT | 5 | a0001c0001t0001g0156a0001c0001t0001g0346a0001c0001t0004g0169others(2): Show | 5 | HG00733.hp1 HG01934.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-3114_664-3109d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGT | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(109): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.664-3110_664-3109d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGTGT | C | 56 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(53): Show | 58 | HG00408.hp2 HG00673.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.664-3112_664-3109d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGTGTGT | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0079others(32): Show | 36 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.664-3114_664-3109d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGTGTGTG others(1): Show |
C | 27 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.664-3116_664-3109d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGTGTGTG others(3): Show |
C | 8 | a0001c0001t0001g0282a0001c0001t0004g0228a0001c0001t0004g0350others(5): Show | 8 | HG01257.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-3118_664-3109d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0003g0060 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.664-3122_664-3109d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388675
|
CGTGTGTG others(9): Show |
C | 23 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(20): Show | 23 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-3124_664-3109d others(18): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | ||||||
| chr12:114388739
|
C | CT | 207 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(204): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.664-3173dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388739 | ||||||
| chr12:114388765
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.664-3198C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388765 | ||||||
| chr12:114388843
|
C | T | 5 | a0001c0001t0001g0223a0001c0001t0004g0228a0001c0001t0042g0366others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-3276G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388843 | ||||||
| chr12:114388928
|
T | A | 8 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0327others(5): Show | 8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-3361A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388928 | ||||||
| chr12:114388974
|
G | A | 96 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(93): Show | 100 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.664-3407C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388974 | ||||||
| chr12:114388990
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.664-3423C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388990 | ||||||
| chr12:114389082
|
A | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.664-3515T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389082 | ||||||
| chr12:114389220
|
G | A | 1 | a0001c0001t0004g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.664-3653C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389220 | ||||||
| chr12:114389230
|
A | C | 24 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.664-3663T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389230 | ||||||
| chr12:114389409
|
T | C | 1 | a0001c0001t0014g0331 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.664-3842A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389409 | ||||||
| chr12:114389450
|
T | A | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664-3883A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389450 | ||||||
| chr12:114389520
|
A | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.664-3953T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389520 | ||||||
| chr12:114389521
|
G | A | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.664-3954C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389521 | ||||||
| chr12:114389531
|
G | A | 1 | a0001c0001t0010g0150 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.664-3964C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389531 | ||||||
| chr12:114389547
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.664-3980C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389547 | ||||||
| chr12:114389550
|
C | A | 1 | a0001c0001t0001g0235 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.664-3983G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389550 | ||||||
| chr12:114389627
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(241): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.664-4060T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389627 | ||||||
| chr12:114389711
|
G | A | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664-4144C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389711 | ||||||
| chr12:114389729
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0002g0012 | 3 | HG02257.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.664-4162C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389729 | ||||||
| chr12:114389753
|
C | CA | 22 | a0001c0001t0001g0094a0001c0001t0001g0102a0001c0001t0001g0275others(19): Show | 23 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-4187dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
C | CAAAAA | 7 | a0001c0001t0001g0156a0001c0001t0002g0268a0001c0001t0008g0097others(4): Show | 7 | HG00280.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-4191_664-4187d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0224 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.664-4196_664-4187d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
C | CAAAAAAA others(168): Show |
1 | a0001c0001t0004g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.664-4187_664-4186i others(177): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CA | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0146others(22): Show | 26 | HG01070.hp2 HG01243.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.664-4187delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAA | C | 5 | a0001c0001t0003g0137a0001c0001t0007g0299a0001c0001t0007g0300others(2): Show | 6 | HG01346.hp2 HG02015.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-4188_664-4187d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAA | C | 14 | a0001c0001t0001g0163a0001c0001t0001g0251a0001c0001t0001g0254others(11): Show | 14 | HG02071.hp2 HG02129.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.664-4189_664-4187d others(5): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAA | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(41): Show | 50 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.664-4190_664-4187d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAA | C | 17 | a0001c0001t0001g0148a0001c0001t0001g0238a0001c0001t0001g0263others(14): Show | 17 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-4191_664-4187d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAA | C | 63 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0050others(60): Show | 64 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.664-4192_664-4187d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA | C | 11 | a0001c0001t0001g0139a0001c0001t0001g0269a0001c0001t0001g0327others(8): Show | 11 | HG02683.hp1 HG03017.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.664-4193_664-4187d others(9): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0001g0190a0001c0001t0001g0359a0001c0001t0002g0188others(4): Show | 7 | HG01256.hp1 HG02056.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-4197_664-4187d others(13): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA others(5): Show |
C | 75 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0100others(72): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.664-4198_664-4187d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0168a0001c0001t0005g0125 | 2 | HG01081.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.664-4199_664-4187d others(15): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA others(7): Show |
C | 10 | a0001c0001t0006g0042a0001c0001t0008g0152a0001c0001t0008g0324others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-4200_664-4187d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA others(8): Show |
C | 17 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(14): Show | 17 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-4201_664-4187d others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389753
|
CAAAAAAA others(11): Show |
C | 6 | a0001c0001t0001g0004a0001c0001t0006g0037a0001c0002t0001g0309others(3): Show | 8 | HG01081.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-4204_664-4187d others(20): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | ||||||
| chr12:114389857
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.664-4290C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389857 | ||||||
| chr12:114389878
|
C | T | 97 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(94): Show | 101 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.664-4311G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389878 | ||||||
| chr12:114389902
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0168others(58): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.664-4335T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389902 | ||||||
| chr12:114389931
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(59): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.664-4364G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389931 | ||||||
| chr12:114389932
|
A | G | 366 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(363): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.664-4365T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389932 | ||||||
| chr12:114390184
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0034g0289 | 2 | HG01884.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.663+4557G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390184 | ||||||
| chr12:114390566
|
C | T | 2 | a0001c0002t0008g0115a0001c0002t0008g0116 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.663+4175G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390566 | ||||||
| chr12:114390809
|
G | A | 8 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0327others(5): Show | 8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+3932C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390809 | ||||||
| chr12:114390876
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.663+3865G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390876 | ||||||
| chr12:114390877
|
G | A | 98 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(95): Show | 102 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.663+3864C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390877 | ||||||
| chr12:114390898
|
T | C | 1 | a0001c0001t0006g0043 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.663+3843A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390898 | ||||||
| chr12:114390971
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.663+3770C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390971 | ||||||
| chr12:114391020
|
T | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0259a0001c0001t0001g0260others(2): Show | 5 | HG00323.hp2 HG00438.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+3721A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391020 | ||||||
| chr12:114391067
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.663+3674C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391067 | ||||||
| chr12:114391130
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.663+3611C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391130 | ||||||
| chr12:114391146
|
C | T | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.663+3595G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391146 | ||||||
| chr12:114391158
|
G | A | 1 | a0001c0001t0004g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.663+3583C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391158 | ||||||
| chr12:114391166
|
A | G | 8 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0327others(5): Show | 8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+3575T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391166 | ||||||
| chr12:114391216
|
G | T | 23 | a0001c0001t0001g0011a0001c0001t0001g0271a0001c0001t0001g0272others(20): Show | 24 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.663+3525C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391216 | ||||||
| chr12:114391390
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.663+3351C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391390 | ||||||
| chr12:114391414
|
G | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0007g0317others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+3327C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391414 | ||||||
| chr12:114391490
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.663+3251G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391490 | ||||||
| chr12:114391512
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0034g0289 | 3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.663+3229G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391512 | ||||||
| chr12:114391586
|
G | T | 1 | a0001c0001t0037g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.663+3155C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391586 | ||||||
| chr12:114391882
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.663+2859G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391882 | ||||||
| chr12:114392022
|
A | G | 1 | a0001c0001t0003g0361 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.663+2719T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392022 | ||||||
| chr12:114392099
|
G | A | 1 | a0001c0001t0007g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.663+2642C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392099 | ||||||
| chr12:114392109
|
A | G | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.663+2632T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392109 | ||||||
| chr12:114392178
|
TA | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0056others(82): Show | 88 | HG00438.hp2 HG00673.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.663+2562delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | ||||||
| chr12:114392178
|
TAA | T | 102 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0050others(99): Show | 107 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.663+2561_663+2562d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | ||||||
| chr12:114392178
|
TAAA | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(56): Show | 65 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.663+2560_663+2562d others(5): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | ||||||
| chr12:114392178
|
TAAAA | T | 56 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0084others(53): Show | 57 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.663+2559_663+2562d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | ||||||
| chr12:114392178
|
TAAAAA | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0168others(55): Show | 63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.663+2558_663+2562d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | ||||||
| chr12:114392340
|
A | G | 1 | a0001c0001t0003g0286 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.663+2401T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392340 | ||||||
| chr12:114392353
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.663+2388A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392353 | ||||||
| chr12:114392475
|
C | G | 2 | a0001c0002t0017g0368a0001c0002t0017g0369 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.663+2266G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392475 | ||||||
| chr12:114392477
|
A | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0034g0289 | 3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.663+2264T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392477 | ||||||
| chr12:114392542
|
A | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.663+2199T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392542 | ||||||
| chr12:114392563
|
C | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.663+2178G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392563 | ||||||
| chr12:114392722
|
AT | A | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(360): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.663+2018delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392722 | ||||||
| chr12:114392843
|
G | A | 1 | a0001c0001t0004g0336 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.663+1898C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392843 | ||||||
| chr12:114392856
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.663+1885C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392856 | ||||||
| chr12:114392895
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(237): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.663+1846C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392895 | ||||||
| chr12:114392957
|
G | A | 22 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0280others(19): Show | 22 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.663+1784C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392957 | ||||||
| chr12:114392969
|
C | G | 19 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.663+1772G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392969 | ||||||
| chr12:114392976
|
T | C | 1 | a0001c0001t0038g0237 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.663+1765A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392976 | ||||||
| chr12:114392999
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.663+1742A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392999 | ||||||
| chr12:114393091
|
G | A | 3 | a0001c0001t0006g0028a0001c0001t0006g0030a0001c0001t0013g0029 | 3 | NA18963.hp2 NA19062.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.663+1650C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393091 | ||||||
| chr12:114393165
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0320a0001c0001t0029g0344 | 3 | HG01074.hp2 HG01109.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.663+1576C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393165 | ||||||
| chr12:114393184
|
A | G | 8 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0327others(5): Show | 8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+1557T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393184 | ||||||
| chr12:114393187
|
C | T | 1 | a0001c0001t0022g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.663+1554G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393187 | ||||||
| chr12:114393260
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.663+1481C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393260 | ||||||
| chr12:114393265
|
TAAGAAAA others(7): Show |
T | 99 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0047others(96): Show | 108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.663+1462_663+1475d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393265 | ||||||
| chr12:114393285
|
C | T | 1 | a0001c0001t0027g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.663+1456G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393285 | ||||||
| chr12:114393377
|
C | T | 3 | a0001c0001t0006g0025a0001c0001t0012g0110a0001c0002t0004g0052 | 3 | HG02559.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.663+1364G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393377 | ||||||
| chr12:114393414
|
G | A | 2 | a0001c0002t0017g0368a0001c0002t0017g0369 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.663+1327C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393414 | ||||||
| chr12:114393446
|
C | G | 2 | a0001c0001t0006g0025a0001c0002t0004g0052 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.663+1295G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393446 | ||||||
| chr12:114393497
|
C | T | 13 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0223others(10): Show | 13 | HG01943.hp1 HG02257.hp1 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.663+1244G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393497 | ||||||
| chr12:114393653
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(57): Show | 67 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.663+1088G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393653 | ||||||
| chr12:114393739
|
A | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(360): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.663+1002T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393739 | ||||||
| chr12:114393970
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0006g0037a0001c0002t0001g0309others(3): Show | 8 | HG01081.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+771T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393970 | ||||||
| chr12:114394135
|
C | T | 21 | a0001c0001t0001g0235a0001c0001t0001g0269a0001c0001t0001g0297others(18): Show | 21 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.663+606G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394135 | ||||||
| chr12:114394173
|
A | G | 44 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0084others(41): Show | 45 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.663+568T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394173 | ||||||
| chr12:114394222
|
A | G | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(360): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.663+519T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394222 | ||||||
| chr12:114394247
|
C | A | 1 | a0001c0001t0004g0337 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.663+494G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394247 | ||||||
| chr12:114394318
|
C | T | 1 | a0001c0001t0004g0229 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.663+423G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394318 | ||||||
| chr12:114394460
|
T | C | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.663+281A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394460 | ||||||
| chr12:114394527
|
A | T | 1 | a0001c0001t0004g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.663+214T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394527 | ||||||
| chr12:114394555
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(213): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.663+186A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394555 | ||||||
| chr12:114394705
|
C | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0055others(211): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.663+36G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394705 | ||||||
| chr12:114394707
|
G | A | 2 | a0001c0002t0017g0368a0001c0002t0017g0369 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.663+34C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394707 | ||||||
| chr12:114394981
|
G | A | 1 | a0001c0001t0025g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-88C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114394981 | ||||||
| chr12:114395015
|
T | C | 1 | a0006c0008t0030g0322 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.511-122A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395015 | ||||||
| chr12:114395033
|
G | T | 1 | a0001c0001t0036g0328 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.511-140C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395033 | ||||||
| chr12:114395389
|
G | A | 24 | a0001c0001t0001g0011a0001c0001t0001g0271a0001c0001t0001g0272others(21): Show | 25 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.511-496C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395389 | ||||||
| chr12:114395498
|
C | T | 11 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0223others(8): Show | 11 | HG01943.hp1 HG02257.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-605G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395498 | ||||||
| chr12:114395579
|
C | A | 2 | a0001c0001t0007g0317a0001c0001t0042g0366 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.511-686G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395579 | ||||||
| chr12:114395579
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(162): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.511-686G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395579 | ||||||
| chr12:114395700
|
T | C | 25 | a0001c0001t0001g0011a0001c0001t0001g0271a0001c0001t0001g0272others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.511-807A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395700 | ||||||
| chr12:114395810
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(162): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.511-917T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395810 | ||||||
| chr12:114395830
|
G | C | 1 | a0001c0001t0006g0027 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.511-937C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395830 | ||||||
| chr12:114395847
|
C | T | 3 | a0001c0001t0012g0070a0001c0001t0012g0140a0001c0001t0012g0141 | 3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.511-954G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395847 | ||||||
| chr12:114395850
|
C | T | 1 | a0001c0001t0018g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.511-957G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395850 | ||||||
| chr12:114395874
|
C | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(148): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.511-981G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395874 | ||||||
| chr12:114395879
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.511-986C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395879 | ||||||
| chr12:114395975
|
T | G | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(360): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.511-1082A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395975 | ||||||
| chr12:114396023
|
C | T | 8 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0223others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-1130G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396023 | ||||||
| chr12:114396032
|
C | T | 6 | a0001c0001t0006g0042a0001c0001t0008g0152a0001c0001t0008g0324others(3): Show | 7 | HG00099.hp1 HG00642.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-1139G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396032 | ||||||
| chr12:114396037
|
G | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(15): Show | 18 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.511-1144C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396037 | ||||||
| chr12:114396115
|
A | G | 16 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(13): Show | 17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-1222T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396115 | ||||||
| chr12:114396177
|
C | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(15): Show | 18 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.511-1284G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396177 | ||||||
| chr12:114396239
|
G | C | 1 | a0001c0001t0042g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.511-1346C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396239 | ||||||
| chr12:114396261
|
G | A | 1 | a0001c0001t0004g0276 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.511-1368C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396261 | ||||||
| chr12:114396502
|
G | T | 1 | a0001c0001t0007g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-1609C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396502 | ||||||
| chr12:114396706
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.511-1813C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396706 | ||||||
| chr12:114397117
|
C | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.510+1456G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397117 | ||||||
| chr12:114397123
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510+1450A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397123 | ||||||
| chr12:114397240
|
A | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.510+1333T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397240 | ||||||
| chr12:114397325
|
A | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(349): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.510+1248T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397325 | ||||||
| chr12:114397379
|
G | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.510+1194C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397379 | ||||||
| chr12:114397408
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(163): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.510+1165G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397408 | ||||||
| chr12:114397433
|
T | A | 4 | a0001c0001t0001g0223a0001c0001t0004g0276a0001c0002t0017g0368others(1): Show | 4 | HG01361.hp1 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1140A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397433 | ||||||
| chr12:114397433
|
T | C | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0027g0147others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+1140A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397433 | ||||||
| chr12:114397445
|
C | T | 4 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0001g0284others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1128G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397445 | ||||||
| chr12:114397511
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.510+1062C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397511 | ||||||
| chr12:114397623
|
G | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(161): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.510+950C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397623 | ||||||
| chr12:114397683
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.510+890G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397683 | ||||||
| chr12:114397778
|
G | GA | 7 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0006g0037others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+794dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397778 | ||||||
| chr12:114398391
|
G | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.510+182C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114398391 | ||||||
| chr12:114398474
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.510+99A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114398474 | ||||||
| chr12:114398497
|
G | A | 1 | a0001c0001t0005g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.510+76C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114398497 | ||||||
| chr12:114398771
|
C | A | 1 | a0001c0001t0004g0350 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.363-51G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398771 | ||||||
| chr12:114398802
|
C | T | 2 | a0001c0001t0034g0289a0001c0002t0004g0052 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.363-82G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398802 | ||||||
| chr12:114398856
|
C | T | 1 | a0001c0001t0010g0150 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.363-136G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398856 | ||||||
| chr12:114398864
|
G | A | 2 | a0001c0001t0007g0149a0001c0001t0007g0317 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.363-144C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398864 | ||||||
| chr12:114399068
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.363-348C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399068 | ||||||
| chr12:114399188
|
A | T | 1 | a0001c0001t0011g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.362+325T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399188 | ||||||
| chr12:114399247
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.362+266T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399247 | ||||||
| chr12:114399280
|
G | A | 3 | a0001c0002t0017g0368a0001c0002t0017g0369a0001c0002t0043g0367 | 3 | HG02257.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.362+233C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399280 | ||||||
| chr12:114399414
|
T | A | 1 | a0001c0001t0006g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.362+99A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | ||||||
| chr12:114399414
|
T | C | 1 | a0001c0001t0007g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362+99A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | ||||||
| chr12:114399414
|
T | TA | 21 | a0001c0001t0001g0279a0001c0001t0001g0294a0001c0001t0001g0321others(18): Show | 21 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.362+98dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | ||||||
| chr12:114399414
|
TA | T | 30 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0146others(27): Show | 31 | HG00323.hp1 HG00642.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.362+98delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | ||||||
| chr12:114399916
|
A | G | 19 | a0001c0001t0001g0138a0001c0001t0002g0124a0001c0001t0002g0127others(16): Show | 21 | HG00544.hp1 HG01081.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.243-284T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114399916 | ||||||
| chr12:114399956
|
G | A | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(326): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.243-324C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114399956 | ||||||
| chr12:114400091
|
A | G | 3 | a0001c0002t0017g0368a0001c0002t0017g0369a0001c0002t0043g0367 | 3 | HG02257.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.243-459T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400091 | ||||||
| chr12:114400434
|
C | A | 3 | a0001c0001t0001g0316a0001c0001t0002g0351a0001c0001t0007g0352 | 3 | HG00639.hp2 HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.243-802G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400434 | ||||||
| chr12:114400477
|
C | A | 19 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0079others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.243-845G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400477 | ||||||
| chr12:114400601
|
G | T | 2 | a0001c0001t0007g0123a0001c0003t0001g0122 | 2 | HG02280.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.243-969C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400601 | ||||||
| chr12:114400602
|
C | T | 2 | a0001c0001t0007g0123a0001c0003t0001g0122 | 2 | HG02280.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.243-970G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400602 | ||||||
| chr12:114400813
|
C | A | 1 | a0001c0001t0003g0006 | 2 | HG00673.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.242+1013G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400813 | ||||||
| chr12:114400891
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.242+935C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400891 | ||||||
| chr12:114400895
|
G | A | 2 | a0001c0002t0001g0284a0001c0002t0002g0283 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.242+931C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400895 | ||||||
| chr12:114400903
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0035g0281 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.242+923C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400903 | ||||||
| chr12:114400931
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.242+895G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400931 | ||||||
| chr12:114400994
|
A | G | 5 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(2): Show | 5 | HG01081.hp2 HG01243.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+832T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400994 | ||||||
| chr12:114401183
|
T | A | 1 | a0001c0001t0001g0353 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.242+643A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401183 | ||||||
| chr12:114401186
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0002g0012 | 4 | HG01074.hp2 HG01358.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+640T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401186 | ||||||
| chr12:114401291
|
T | G | 5 | a0001c0002t0001g0114a0001c0002t0001g0117a0001c0002t0008g0115others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.242+535A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401291 | ||||||
| chr12:114401328
|
C | G | 1 | a0001c0001t0007g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242+498G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401328 | ||||||
| chr12:114401398
|
T | G | 16 | a0001c0002t0001g0114a0001c0002t0001g0117a0001c0002t0001g0284others(13): Show | 16 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.242+428A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401398 | ||||||
| chr12:114401409
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.242+417A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401409 | ||||||
| chr12:114401437
|
A | T | 19 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0079others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.242+389T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401437 | ||||||
| chr12:114401451
|
G | A | 14 | a0001c0002t0001g0114a0001c0002t0001g0117a0001c0002t0001g0309others(11): Show | 14 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.242+375C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401451 | ||||||
| chr12:114401641
|
C | T | 1 | a0001c0001t0005g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.242+185G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401641 | ||||||
| chr12:114401764
|
T | C | 1 | a0007c0011t0002g0315 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.242+62A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401764 | ||||||
| chr12:114401939
|
A | T | 9 | a0001c0002t0001g0114a0001c0002t0001g0117a0001c0002t0004g0052others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-19T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114401939 | ||||||
| chr12:114402126
|
T | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0288a0001c0001t0002g0287others(13): Show | 18 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.148-206A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402126 | ||||||
| chr12:114402151
|
C | A | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02148.hp2 HG02738.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-231G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402151 | ||||||
| chr12:114402151
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.148-231G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402151 | ||||||
| chr12:114402236
|
C | G | 18 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0079others(15): Show | 19 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.148-316G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402236 | ||||||
| chr12:114402262
|
C | A | 2 | a0001c0001t0001g0313a0001c0001t0003g0068 | 2 | HG01261.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.148-342G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402262 | ||||||
| chr12:114402270
|
A | C | 3 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113 | 3 | HG00099.hp2 HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.148-350T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402270 | ||||||
| chr12:114402280
|
C | CA | 37 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(34): Show | 38 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.148-361dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402280 | ||||||
| chr12:114402286
|
A | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.148-366T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402286 | ||||||
| chr12:114402287
|
A | T | 5 | a0001c0001t0001g0094a0001c0001t0007g0299a0001c0001t0007g0300others(2): Show | 6 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-367T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402287 | ||||||
| chr12:114402330
|
G | T | 19 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0079others(16): Show | 20 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.148-410C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402330 | ||||||
| chr12:114402342
|
T | C | 5 | a0001c0001t0002g0109a0001c0001t0005g0007a0001c0001t0042g0366others(2): Show | 6 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-422A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402342 | ||||||
| chr12:114402642
|
C | T | 5 | a0001c0001t0002g0109a0001c0001t0005g0007a0001c0001t0042g0366others(2): Show | 6 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-722G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402642 | ||||||
| chr12:114402683
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0007g0299a0001c0001t0007g0300others(2): Show | 6 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-763A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402683 | ||||||
| chr12:114402703
|
G | A | 2 | a0001c0001t0001g0303a0001c0001t0002g0302 | 2 | NA18747.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.148-783C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402703 | ||||||
| chr12:114402816
|
GA | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 299 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.148-897delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402816 | ||||||
| chr12:114402934
|
G | A | 8 | a0001c0001t0006g0042a0001c0001t0006g0043a0001c0001t0006g0044others(5): Show | 9 | HG00642.hp1 HG01074.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+818C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402934 | ||||||
| chr12:114402991
|
A | ACC | 28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(25): Show | 28 | HG00621.hp1 HG01175.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.147+759_147+760dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402991 | ||||||
| chr12:114403187
|
C | A | 3 | a0001c0002t0017g0368a0001c0002t0017g0369a0001c0002t0043g0367 | 3 | HG02257.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.147+565G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403187 | ||||||
| chr12:114403187
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02809.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.147+565G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403187 | ||||||
| chr12:114403305
|
G | A | 1 | a0001c0001t0009g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.147+447C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403305 | ||||||
| chr12:114403360
|
C | T | 1 | a0001c0002t0004g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+392G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403360 | ||||||
| chr12:114403388
|
G | T | 1 | a0001c0001t0008g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.147+364C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403388 | ||||||
| chr12:114403558
|
C | T | 5 | a0001c0001t0042g0366a0001c0002t0004g0052a0001c0002t0017g0368others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+194G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403558 | ||||||
| chr12:114403583
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.147+169C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403583 | ||||||
| chr12:114403739
|
G | T | 1 | a0001c0001t0004g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.147+13C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403739 | ||||||
| chr12:114404099
|
G | A | 1 | a0007c0011t0002g0315 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-38-163C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404099 | ||||||
| chr12:114404147
|
A | G | 6 | a0001c0001t0016g0014a0001c0001t0042g0366a0001c0002t0004g0052others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-211T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404147 | ||||||
| chr12:114404173
|
C | A | 1 | a0001c0001t0016g0014 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-38-237G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404173 | ||||||
| chr12:114404191
|
A | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(323): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.-38-255T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404191 | ||||||
| chr12:114404382
|
C | A | 1 | a0001c0001t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-38-446G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404382 | ||||||
| chr12:114404442
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-38-506C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404442 | ||||||
| chr12:114404453
|
T | C | 1 | a0001c0001t0011g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-517A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404453 | ||||||
| chr12:114404462
|
C | A | 1 | a0001c0001t0002g0360 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-38-526G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404462 | ||||||
| chr12:114404472
|
CA | C | 36 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0006g0015others(33): Show | 37 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38-537delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404472 | ||||||
| chr12:114404479
|
A | G | 36 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0006g0015others(33): Show | 37 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38-543T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404479 | ||||||
| chr12:114404590
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-38-654T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404590 | ||||||
| chr12:114404603
|
T | C | 5 | a0001c0001t0016g0014a0001c0001t0042g0366a0001c0002t0017g0368others(2): Show | 6 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38-667A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404603 | ||||||
| chr12:114404691
|
A | G | 4 | a0001c0001t0042g0366a0001c0002t0017g0368a0001c0002t0017g0369others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-755T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404691 | ||||||
| chr12:114404806
|
C | T | 4 | a0001c0001t0042g0366a0001c0002t0017g0368a0001c0002t0017g0369others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+822G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404806 | ||||||
| chr12:114404922
|
C | A | 1 | a0001c0001t0003g0361 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-39+706G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404922 | ||||||
| chr12:114405121
|
C | G | 83 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0055others(80): Show | 84 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.-39+507G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405121 | ||||||
| chr12:114405177
|
G | A | 1 | a0001c0001t0042g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-39+451C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405177 | ||||||
| chr12:114405483
|
G | A | 1 | a0001c0001t0002g0362 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-39+145C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405483 | ||||||
| chr12:114405583
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0003g0006 | 4 | HG00558.hp1 HG00673.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+45G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405583 |