Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 840 |
|---|---|
| ensemblid | ENSG00000165806.21 |
| hgncid | 1508 |
| symbol | CASP7 |
| name | caspase 7 |
| refseq_nuc | NM_001227.5 |
| refseq_prot | NP_001218.1 |
| ensembl_nuc | ENST00000369318.8 |
| ensembl_prot | ENSP00000358324.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 113679912 |
| end | 113730905 |
| strand | + |
| ver | v1.2 |
| region | chr10:113679912-113730905 |
| region5000 | chr10:113674912-113735905 |
| regionname0 | CASP7_chr10_113679912_113730905 |
| regionname5000 | CASP7_chr10_113674912_113735905 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 250 | 68 | 42 | 99 | 9 | 30 | 70 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002 | 0/0 | 303 | 112 | 14 | 24 | 62 | 3 | 9 | 48 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0003 | 0/0 | 303 | 39 | 10 | 11 | 14 | 2 | 2 | 11 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0004 | 0/0 | 303 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0005 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0006 | 0/0 | 303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 912 | 243 | 64 | 41 | 99 | 9 | 28 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0002 | 0/0 | 912 | 110 | 12 | 24 | 62 | 3 | 9 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0003 | 0/0 | 912 | 39 | 10 | 11 | 14 | 2 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0004 | 0/0 | 912 | 3 | 1 | 0 | 1 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0005 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0006 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0007 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0008 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0009 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0010 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0012 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| c0013 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1433 | 113 | 15 | 23 | 62 | 3 | 10 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0002 | 0/0 | 1433 | 76 | 17 | 14 | 33 | 4 | 8 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0003 | 0/0 | 1433 | 72 | 27 | 6 | 25 | 2 | 12 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0004 | 0/1 | 1433 | 61 | 17 | 21 | 14 | 3 | 5 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0005 | 1/0 | 1433 | 57 | 11 | 11 | 25 | 2 | 7 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0006 | 0/0 | 1433 | 6 | 0 | 0 | 6 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0007 | 0/0 | 1433 | 6 | 0 | 0 | 6 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0008 | 0/0 | 1433 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0009 | 0/0 | 1433 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0010 | 0/0 | 1433 | 2 | 1 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0011 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0012 | 0/0 | 1433 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0013 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0014 | 0/0 | 1433 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0015 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0016 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0017 | 0/0 | 1433 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0018 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| t0019 | 0/0 | 1433 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 912 | 243 | 64 | 41 | 99 | 9 | 28 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0005 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0008 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0010 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0012 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0013 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002c0002 | 0/0 | 912 | 110 | 12 | 24 | 62 | 3 | 9 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002c0006 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0003c0003 | 0/0 | 912 | 39 | 10 | 11 | 14 | 2 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0004c0004 | 0/0 | 912 | 3 | 1 | 0 | 1 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0005c0009 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0006c0007 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2344 | 39 | 10 | 3 | 19 | 2 | 5 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0003 | 0/0 | 2344 | 71 | 26 | 6 | 25 | 2 | 12 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0004 | 0/1 | 2344 | 60 | 17 | 20 | 14 | 3 | 5 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0005 | 1/0 | 2344 | 50 | 6 | 10 | 25 | 2 | 6 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0006 | 0/0 | 2344 | 6 | 0 | 0 | 6 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0007 | 0/0 | 2344 | 6 | 0 | 0 | 6 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0008 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0009 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0010 | 0/0 | 2344 | 2 | 1 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0011 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0014 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0015 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0016 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0001t0018 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0005t0002 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0008t0002 | 0/0 | 2344 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0010t0005 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0011t0017 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0012t0002 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0001c0013t0005 | 0/0 | 2344 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002c0002t0001 | 0/0 | 2344 | 108 | 12 | 23 | 61 | 3 | 9 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002c0002t0012 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002c0002t0013 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0002c0006t0001 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0003c0003t0002 | 0/0 | 2344 | 33 | 4 | 11 | 14 | 2 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0003c0003t0005 | 0/0 | 2344 | 5 | 5 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0003c0003t0019 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0004c0004t0001 | 0/0 | 2344 | 3 | 1 | 0 | 1 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0005c0009t0003 | 0/0 | 2362 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| a0006c0007t0004 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | copy fasta | chr10 | 113674912 | 113735905 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0009g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0009g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0010g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0014g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0015g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0016g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0018g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0005t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0008t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0010t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0011t0017g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0012t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0013t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0012g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0006t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0019g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0004c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0004c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0004c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0005c0009t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0006c0007t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0342 | EUR | GBR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0100 | EUR | GBR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0073 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0078 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0385 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0377 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0361 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0136 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0090 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0357 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0140 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00735 | hp1 | a0006 | c0007 | t0004 | g0061 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0372 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0121 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0122 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0108 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01106 | hp1 | a0003 | c0003 | t0002 | g0137 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0351 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0383 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0151 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01168 | hp1 | a0003 | c0003 | t0002 | g0007 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0007 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0366 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0142 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0141 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0235 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0356 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0367 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0146 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0143 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0057 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0083 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0371 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0263 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01515 | hp2 | a0003 | c0003 | t0002 | g0139 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01517 | hp1 | a0003 | c0003 | t0002 | g0147 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0295 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01928 | hp2 | a0002 | c0002 | t0012 | g0358 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0313 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01952 | hp1 | a0001 | c0010 | t0005 | g0098 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0376 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0360 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0343 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0370 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0339 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0349 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02129 | hp2 | a0003 | c0003 | t0002 | g0120 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02132 | hp2 | a0001 | c0001 | t0018 | g0179 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02257 | hp1 | a0004 | c0004 | t0001 | g0109 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0381 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0303 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0228 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0304 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0387 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0378 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02630 | hp1 | a0003 | c0003 | t0019 | g0144 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02647 | hp1 | a0003 | c0003 | t0005 | g0134 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02647 | hp2 | a0002 | c0006 | t0001 | g0105 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02717 | hp1 | a0003 | c0003 | t0005 | g0133 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0347 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0380 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0379 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02922 | hp1 | a0003 | c0003 | t0005 | g0126 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02922 | hp2 | a0003 | c0003 | t0002 | g0123 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0310 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02976 | hp1 | a0001 | c0011 | t0017 | g0386 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03017 | hp1 | a0001 | c0008 | t0002 | g0253 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0157 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03041 | hp1 | a0003 | c0003 | t0002 | g0111 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03098 | hp1 | a0001 | c0012 | t0002 | g0107 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0348 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0110 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0362 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03139 | hp1 | a0005 | c0009 | t0003 | g0204 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03225 | hp1 | a0003 | c0003 | t0005 | g0115 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0215 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0042 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0334 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0374 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0337 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0353 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03516 | hp2 | a0001 | c0005 | t0002 | g0264 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03540 | hp2 | a0002 | c0006 | t0001 | g0104 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0345 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0129 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0373 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03688 | hp2 | a0001 | c0013 | t0005 | g0044 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0125 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0331 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0344 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0325 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0055 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0071 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0340 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0118 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0117 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18945 | hp2 | a0003 | c0003 | t0002 | g0114 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0375 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0132 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18964 | hp2 | a0003 | c0003 | t0002 | g0138 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0365 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0119 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18979 | hp1 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18981 | hp1 | a0001 | c0001 | t0015 | g0010 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18981 | hp2 | a0003 | c0003 | t0002 | g0148 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18986 | hp2 | a0003 | c0003 | t0002 | g0127 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0145 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0369 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18998 | hp1 | a0002 | c0002 | t0013 | g0276 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0364 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19007 | hp1 | a0001 | c0001 | t0016 | g0037 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19012 | hp2 | a0003 | c0003 | t0002 | g0113 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0382 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0131 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19055 | hp1 | a0003 | c0003 | t0002 | g0116 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0359 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19077 | hp1 | a0004 | c0004 | t0001 | g0130 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19080 | hp2 | a0003 | c0003 | t0002 | g0128 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ASW | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ASW | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0368 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0101 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0005 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0087 | SAS | GIH | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | GIH | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0363 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0135 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0346 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02559 | hp1 | a0001 | c0005 | t0002 | g0020 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0384 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0112 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG06807 | hp1 | a0003 | c0003 | t0005 | g0124 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0341 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0354 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0155 | REF | REF | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0035 | REF | REF | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113697505
|
T | G | 2 | a0003a0004 | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
missense_variant | MODERATE | c.12T>G | p.Asp4Glu | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/7 | 79/2344 | 12/912 | 4/303 | chr10 | 113697505 | ||
| chr10:113726320
|
G | A | 1 | a0006 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.568G>A | p.Glu190Lys | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/7 | 635/2344 | 568/912 | 190/303 | chr10 | 113726320 | ||
| chr10:113729393
|
C | G | 2 | a0002a0004 | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
missense_variant | MODERATE | c.765C>G | p.Asp255Glu | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 832/2344 | 765/912 | 255/303 | chr10 | 113729393 | ||
| chr10:113729503
|
T | TCTCCATG others(11): Show |
1 | a0005 | 1 | HG03139.hp1 | conservative_inframe_insertion | MODERATE | c.885_886insCGCAGGTA others(10): Show |
p.Leu295_Thr296insAr others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 953/2344 | 886/912 | 296/303 | INFO_REALIGN_3_PRIME | chr10 | 113729503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113721712
|
C | T | 1 | a0002c0006 | 2 | HG02647.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.309C>T | p.Ser103Ser | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/7 | 376/2344 | 309/912 | 103/303 | chr10 | 113721712 | ||
| chr10:113725399
|
C | T | 1 | a0001c0013 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.414C>T | p.Ala138Ala | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/7 | 481/2344 | 414/912 | 138/303 | chr10 | 113725399 | ||
| chr10:113725480
|
C | T | 1 | a0001c0012 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.495C>T | p.His165His | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/7 | 562/2344 | 495/912 | 165/303 | chr10 | 113725480 | ||
| chr10:113725519
|
C | T | 1 | a0001c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.534C>T | p.Pro178Pro | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/7 | 601/2344 | 534/912 | 178/303 | chr10 | 113725519 | ||
| chr10:113729321
|
G | A | 1 | a0001c0005 | 2 | HG02559.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.693G>A | p.Ser231Ser | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 760/2344 | 693/912 | 231/303 | chr10 | 113729321 | ||
| chr10:113729408
|
G | A | 3 | a0002c0002a0002c0006a0004c0004 | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
synonymous_variant | LOW | c.780G>A | p.Gln260Gln | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 847/2344 | 780/912 | 260/303 | chr10 | 113729408 | ||
| chr10:113729495
|
C | T | 1 | a0001c0010 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.867C>T | p.Pro289Pro | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 934/2344 | 867/912 | 289/303 | chr10 | 113729495 | ||
| chr10:113729537
|
A | G | 1 | a0001c0008 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.909A>G | p.Gln303Gln | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 976/2344 | 909/912 | 303/303 | chr10 | 113729537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113679932
|
C | A | 1 | a0001c0001t0011 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/7 | 17562 | chr10 | 113679932 | |||||
| chr10:113679959
|
G | T | 1 | a0003c0003t0019 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/7 | 17535 | chr10 | 113679959 | |||||
| chr10:113729705
|
A | G | 1 | a0001c0001t0018 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 165 | chr10 | 113729705 | |||||
| chr10:113729725
|
A | G | 1 | a0001c0001t0010 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*185A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 185 | chr10 | 113729725 | |||||
| chr10:113729830
|
T | C | 5 | a0002c0002t0001a0002c0002t0012a0002c0002t0013others(2): Show | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*290T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 290 | chr10 | 113729830 | |||||
| chr10:113729891
|
T | G | 11 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(8): Show | 151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 351 | chr10 | 113729891 | |||||
| chr10:113729913
|
C | T | 1 | a0001c0011t0017 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 373 | chr10 | 113729913 | |||||
| chr10:113729923
|
C | G | 1 | a0001c0001t0016 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 383 | chr10 | 113729923 | |||||
| chr10:113730102
|
G | A | 1 | a0001c0001t0008 | 2 | HG02258.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*562G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 562 | chr10 | 113730102 | |||||
| chr10:113730228
|
G | A | 1 | a0001c0001t0006 | 6 | HG00597.hp2 NA18612.hp1 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*688G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 688 | chr10 | 113730228 | |||||
| chr10:113730247
|
A | G | 1 | a0002c0002t0013 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*707A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 707 | chr10 | 113730247 | |||||
| chr10:113730301
|
G | A | 5 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(2): Show | 81 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*761G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 761 | chr10 | 113730301 | |||||
| chr10:113730306
|
G | A | 1 | a0001c0001t0015 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 766 | chr10 | 113730306 | |||||
| chr10:113730314
|
A | G | 1 | a0001c0001t0014 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 774 | chr10 | 113730314 | |||||
| chr10:113730350
|
G | A | 9 | a0001c0001t0002a0001c0001t0009a0001c0001t0015others(6): Show | 81 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*810G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 810 | chr10 | 113730350 | |||||
| chr10:113730540
|
A | G | 1 | a0001c0001t0007 | 6 | NA18969.hp1 NA18971.hp2 NA18973.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1000A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 1000 | chr10 | 113730540 | |||||
| chr10:113730665
|
A | G | 1 | a0001c0001t0009 | 2 | HG02572.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1125A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 1125 | chr10 | 113730665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113680019
|
G | T | 1 | a0001c0001t0008g0016 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1+41G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680019 | ||||||
| chr10:113680025
|
C | T | 1 | a0001c0001t0009g0387 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1+47C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680025 | ||||||
| chr10:113680160
|
G | T | 299 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(296): Show | 312 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(309): Show |
intron_variant | MODIFIER | c.-1+182G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680160 | ||||||
| chr10:113680174
|
A | G | 1 | a0001c0001t0005g0101 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-1+196A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680174 | ||||||
| chr10:113680321
|
C | T | 1 | a0001c0011t0017g0386 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1+343C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680321 | ||||||
| chr10:113680349
|
C | G | 1 | a0002c0002t0001g0385 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-1+371C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680349 | ||||||
| chr10:113680654
|
T | G | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+676T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680654 | ||||||
| chr10:113680663
|
A | G | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+685A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680663 | ||||||
| chr10:113680828
|
G | T | 3 | a0001c0001t0005g0382a0001c0001t0005g0384a0002c0002t0001g0383 | 3 | HG01109.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1+850G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680828 | ||||||
| chr10:113680846
|
A | G | 4 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0001t0002g0381others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+868A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680846 | ||||||
| chr10:113680897
|
A | C | 1 | a0001c0001t0009g0378 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1+919A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680897 | ||||||
| chr10:113680898
|
G | C | 1 | a0001c0001t0009g0378 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1+920G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680898 | ||||||
| chr10:113680907
|
T | G | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+929T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680907 | ||||||
| chr10:113680934
|
C | T | 2 | a0001c0001t0004g0099a0001c0001t0004g0100 | 2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-1+956C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680934 | ||||||
| chr10:113681032
|
T | C | 10 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(7): Show | 11 | HG02258.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1+1054T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681032 | ||||||
| chr10:113681084
|
G | T | 4 | a0001c0001t0002g0103a0001c0001t0002g0106a0002c0006t0001g0104others(1): Show | 4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+1106G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681084 | ||||||
| chr10:113681172
|
T | C | 2 | a0001c0001t0005g0108a0001c0012t0002g0107 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+1194T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681172 | ||||||
| chr10:113681283
|
G | A | 10 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(7): Show | 11 | HG02258.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1+1305G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681283 | ||||||
| chr10:113681323
|
A | G | 112 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(109): Show | 118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-1+1345A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681323 | ||||||
| chr10:113681363
|
A | G | 1 | a0002c0002t0001g0377 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-1+1385A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681363 | ||||||
| chr10:113681370
|
C | T | 1 | a0001c0001t0003g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1+1392C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681370 | ||||||
| chr10:113681383
|
G | A | 41 | a0003c0003t0002g0007a0003c0003t0002g0110a0003c0003t0002g0111others(38): Show | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+1405G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681383 | ||||||
| chr10:113681472
|
A | T | 1 | a0001c0001t0005g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-1+1494A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681472 | ||||||
| chr10:113681545
|
G | C | 1 | a0004c0004t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-1+1567G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681545 | ||||||
| chr10:113681562
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-1+1584T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681562 | ||||||
| chr10:113681601
|
A | G | 294 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(291): Show | 306 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.-1+1623A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681601 | ||||||
| chr10:113681716
|
A | G | 1 | a0002c0002t0001g0376 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-1+1738A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681716 | ||||||
| chr10:113681904
|
T | C | 1 | a0002c0002t0001g0272 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-1+1926T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681904 | ||||||
| chr10:113681924
|
A | C | 288 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(285): Show | 300 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-1+1946A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681924 | ||||||
| chr10:113681954
|
T | C | 2 | a0001c0001t0005g0018a0001c0001t0005g0101 | 2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-1+1976T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681954 | ||||||
| chr10:113682076
|
A | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0272a0002c0002t0001g0375 | 5 | NA18946.hp1 NA18955.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+2098A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682076 | ||||||
| chr10:113682111
|
A | G | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2133A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682111 | ||||||
| chr10:113682112
|
G | A | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2134G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682112 | ||||||
| chr10:113682338
|
G | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2360G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682338 | ||||||
| chr10:113682339
|
C | G | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2361C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682339 | ||||||
| chr10:113682343
|
A | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2365A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682343 | ||||||
| chr10:113682456
|
T | TTCTCTCT others(5): Show |
1 | a0003c0003t0002g0148 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-1+2479_-1+2490dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113682456 | |||||
| chr10:113682481
|
C | G | 1 | a0001c0001t0003g0270 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+2503C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682481 | ||||||
| chr10:113682485
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-1+2507C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682485 | ||||||
| chr10:113682578
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+2600A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682578 | ||||||
| chr10:113682612
|
C | A | 2 | a0001c0001t0004g0099a0001c0001t0004g0100 | 2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-1+2634C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682612 | ||||||
| chr10:113682627
|
A | G | 87 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(84): Show | 91 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-1+2649A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682627 | ||||||
| chr10:113682651
|
T | C | 2 | a0001c0001t0005g0108a0001c0012t0002g0107 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+2673T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682651 | ||||||
| chr10:113682767
|
A | T | 1 | a0001c0010t0005g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-1+2789A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682767 | ||||||
| chr10:113682814
|
T | G | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2836T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682814 | ||||||
| chr10:113682924
|
A | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2946A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682924 | ||||||
| chr10:113682943
|
T | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2965T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682943 | ||||||
| chr10:113682944
|
C | T | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2966C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682944 | ||||||
| chr10:113682945
|
A | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2967A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682945 | ||||||
| chr10:113682995
|
A | G | 4 | a0001c0001t0004g0015a0001c0001t0004g0267a0001c0001t0004g0268others(1): Show | 5 | HG02572.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+3017A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682995 | ||||||
| chr10:113683039
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-1+3061G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683039 | ||||||
| chr10:113683160
|
A | G | 288 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(285): Show | 300 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-1+3182A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683160 | ||||||
| chr10:113683268
|
C | T | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3290C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683268 | ||||||
| chr10:113683269
|
T | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3291T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683269 | ||||||
| chr10:113683284
|
A | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3306A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683284 | ||||||
| chr10:113683298
|
C | G | 1 | a0001c0001t0004g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+3320C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683298 | ||||||
| chr10:113683331
|
G | A | 89 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(86): Show | 91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1+3353G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683331 | ||||||
| chr10:113683404
|
G | A | 2 | a0001c0001t0005g0019a0001c0005t0002g0020 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-1+3426G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683404 | ||||||
| chr10:113683431
|
A | G | 89 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(86): Show | 91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1+3453A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683431 | ||||||
| chr10:113683629
|
C | T | 1 | a0001c0001t0003g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1+3651C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683629 | ||||||
| chr10:113683630
|
G | A | 1 | a0001c0001t0006g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-1+3652G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683630 | ||||||
| chr10:113683636
|
T | C | 288 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(285): Show | 300 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-1+3658T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683636 | ||||||
| chr10:113683673
|
T | C | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3695T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683673 | ||||||
| chr10:113683731
|
TTATC | T | 42 | a0002c0002t0001g0265a0003c0003t0002g0007a0003c0003t0002g0110others(39): Show | 43 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-1+3757_-1+3760del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113683731 | |||||
| chr10:113683770
|
A | G | 1 | a0001c0001t0004g0096 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-1+3792A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683770 | ||||||
| chr10:113684054
|
T | TAC | 244 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0181others(241): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-1+4094_-1+4095dup others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684054 | |||||
| chr10:113684054
|
T | TACAC | 43 | a0001c0001t0002g0241a0001c0001t0005g0266a0003c0003t0002g0007others(40): Show | 44 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-1+4092_-1+4095dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684054 | |||||
| chr10:113684135
|
C | T | 156 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(153): Show | 163 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.-1+4157C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684135 | ||||||
| chr10:113684239
|
A | AT | 67 | a0001c0001t0002g0362a0001c0001t0004g0023a0001c0001t0004g0060others(64): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-1+4285dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | |||||
| chr10:113684239
|
A | ATT | 13 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(10): Show | 14 | HG00597.hp2 HG01192.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1+4284_-1+4285dup others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | |||||
| chr10:113684239
|
AT | A | 42 | a0001c0001t0003g0236a0001c0001t0004g0008a0001c0001t0005g0266others(39): Show | 44 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-1+4285delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | |||||
| chr10:113684239
|
ATT | A | 28 | a0001c0001t0002g0106a0001c0001t0002g0222a0001c0001t0002g0234others(25): Show | 31 | HG00438.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1+4284_-1+4285del others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | |||||
| chr10:113684239
|
ATTT | A | 73 | a0001c0001t0002g0010a0001c0001t0002g0103a0001c0001t0002g0181others(70): Show | 74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1+4283_-1+4285del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | |||||
| chr10:113684239
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0005g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1+4276_-1+4285del others(10): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | |||||
| chr10:113684349
|
A | G | 1 | a0001c0001t0003g0239 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-1+4371A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684349 | ||||||
| chr10:113684362
|
T | C | 293 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(290): Show | 306 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.-1+4384T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684362 | ||||||
| chr10:113684364
|
G | A | 41 | a0003c0003t0002g0007a0003c0003t0002g0110a0003c0003t0002g0111others(38): Show | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+4386G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684364 | ||||||
| chr10:113684408
|
T | A | 108 | a0001c0001t0002g0010a0001c0001t0002g0103a0001c0001t0002g0106others(105): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-1+4430T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684408 | ||||||
| chr10:113684522
|
T | G | 1 | a0001c0001t0005g0024 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1+4544T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684522 | ||||||
| chr10:113684586
|
G | A | 60 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(57): Show | 62 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-1+4608G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684586 | ||||||
| chr10:113684660
|
A | G | 68 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(65): Show | 70 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-1+4682A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684660 | ||||||
| chr10:113684715
|
T | C | 6 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(3): Show | 6 | HG02451.hp2 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+4737T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684715 | ||||||
| chr10:113684994
|
T | A | 1 | a0001c0001t0005g0024 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1+5016T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684994 | ||||||
| chr10:113684995
|
G | T | 1 | a0001c0001t0005g0024 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1+5017G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684995 | ||||||
| chr10:113685077
|
G | T | 2 | a0002c0002t0001g0349a0002c0002t0001g0350 | 2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-1+5099G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685077 | ||||||
| chr10:113685425
|
G | T | 41 | a0003c0003t0002g0007a0003c0003t0002g0110a0003c0003t0002g0111others(38): Show | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+5447G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685425 | ||||||
| chr10:113685455
|
A | C | 1 | a0001c0001t0010g0235 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1+5477A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685455 | ||||||
| chr10:113685650
|
G | C | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+5672G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685650 | ||||||
| chr10:113685767
|
G | T | 35 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(32): Show | 36 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-1+5789G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685767 | ||||||
| chr10:113685919
|
C | T | 2 | a0001c0001t0005g0058a0001c0001t0005g0059 | 2 | NA19006.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-1+5941C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685919 | ||||||
| chr10:113686251
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1+6273G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686251 | ||||||
| chr10:113686510
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1+6532A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686510 | ||||||
| chr10:113686589
|
T | C | 41 | a0001c0001t0004g0060a0001c0001t0004g0066a0001c0001t0004g0067others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.-1+6611T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686589 | ||||||
| chr10:113686617
|
G | A | 193 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(190): Show | 201 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.-1+6639G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686617 | ||||||
| chr10:113686759
|
C | T | 1 | a0001c0005t0002g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-1+6781C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686759 | ||||||
| chr10:113686839
|
T | C | 1 | a0001c0001t0004g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1+6861T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686839 | ||||||
| chr10:113687144
|
T | C | 3 | a0003c0003t0002g0110a0003c0003t0002g0111a0003c0003t0002g0112 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-1+7166T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687144 | ||||||
| chr10:113687344
|
G | GTGTATGT others(27): Show |
1 | a0001c0001t0004g0083 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-1+7405_-1+7438dup others(34): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687344 | |||||
| chr10:113687344
|
GTGTATGT others(27): Show |
G | 292 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(289): Show | 305 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.-1+7405_-1+7438del others(34): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687344 | |||||
| chr10:113687378
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+7400A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687378 | ||||||
| chr10:113687383
|
T | C | 1 | a0001c0001t0003g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+7405T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687383 | ||||||
| chr10:113687415
|
T | C | 1 | a0002c0002t0001g0277 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-1+7437T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687415 | ||||||
| chr10:113687417
|
C | T | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+7439C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687417 | ||||||
| chr10:113687424
|
A | G | 6 | a0001c0001t0003g0199a0001c0001t0004g0095a0001c0001t0005g0382others(3): Show | 6 | HG01109.hp1 HG01346.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+7446A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687424 | ||||||
| chr10:113687448
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1+7470A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687448 | ||||||
| chr10:113687580
|
T | G | 1 | a0001c0001t0004g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1+7602T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687580 | ||||||
| chr10:113687721
|
C | A | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1+7743C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687721 | ||||||
| chr10:113687729
|
A | G | 41 | a0003c0003t0002g0007a0003c0003t0002g0110a0003c0003t0002g0111others(38): Show | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+7751A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687729 | ||||||
| chr10:113687794
|
C | CTCTT | 7 | a0001c0001t0003g0206a0001c0001t0003g0232a0001c0001t0004g0089others(4): Show | 8 | HG00733.hp2 HG02559.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+7855_-1+7858dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTCTT others(8): Show |
1 | a0001c0001t0004g0060 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-1+7820_-1+7821ins others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTTCT others(1): Show |
24 | a0001c0001t0003g0207a0001c0001t0004g0066a0001c0001t0004g0154others(21): Show | 24 | HG00597.hp2 HG01109.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1+7851_-1+7858dup others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTTCT others(5): Show |
31 | a0001c0001t0002g0234a0001c0001t0002g0307a0001c0001t0002g0308others(28): Show | 33 | HG00280.hp2 HG00544.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1+7847_-1+7858dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTTCT others(9): Show |
26 | a0001c0001t0002g0010a0001c0001t0002g0326a0001c0001t0003g0183others(23): Show | 26 | HG00140.hp2 HG00597.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+7843_-1+7858dup others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTTCT others(13): Show |
11 | a0001c0001t0003g0190a0001c0001t0004g0079a0001c0001t0004g0080others(8): Show | 11 | HG00558.hp1 HG01123.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+7839_-1+7858dup others(20): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTTCT others(17): Show |
10 | a0001c0001t0003g0195a0001c0001t0003g0229a0001c0001t0003g0230others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+7835_-1+7858dup others(24): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTCTTTCT others(21): Show |
2 | a0001c0001t0003g0198a0001c0001t0005g0339 | 2 | HG02074.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-1+7831_-1+7858dup others(28): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTTTCTTT others(7): Show |
1 | a0002c0002t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+7817_-1+7818ins others(14): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTTTCTTT others(11): Show |
1 | a0001c0001t0003g0346 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+7817_-1+7818ins others(18): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
C | CTTTCTTT others(15): Show |
2 | a0001c0001t0003g0348a0001c0001t0004g0347 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-1+7817_-1+7818ins others(22): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
CTCTT | C | 6 | a0001c0001t0004g0025a0001c0001t0004g0027a0001c0001t0004g0097others(3): Show | 7 | HG01952.hp1 HG01975.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+7855_-1+7858del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
CTCTTTCT others(1): Show |
C | 4 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 5 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7851_-1+7858del others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687794
|
CTCTTTCT others(5): Show |
C | 1 | a0001c0001t0002g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-1+7847_-1+7858del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | |||||
| chr10:113687800
|
C | CTTT | 3 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247 | 3 | HG00408.hp1 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-1+7823_-1+7825dup others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687800 | |||||
| chr10:113687803
|
TC | T | 7 | a0001c0001t0002g0241a0001c0001t0002g0249a0001c0001t0002g0250others(4): Show | 7 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+7826delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687803 | ||||||
| chr10:113687803
|
TCTTTCTT others(2): Show |
T | 16 | a0001c0001t0002g0012a0001c0001t0002g0242a0001c0001t0002g0243others(13): Show | 17 | HG01081.hp1 HG01168.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+7826_-1+7834del others(9): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687803 | ||||||
| chr10:113687812
|
C | CTTTCTTT others(3): Show |
2 | a0002c0002t0001g0344a0002c0002t0001g0372 | 2 | HG00735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-1+7836_-1+7845dup others(10): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687812 | |||||
| chr10:113687816
|
C | CTTTCTT | 4 | a0002c0002t0001g0341a0002c0002t0001g0342a0002c0002t0001g0343others(1): Show | 4 | HG00140.hp1 HG01361.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7840_-1+7845dup others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687816 | |||||
| chr10:113687823
|
T | TC | 3 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247 | 3 | HG00408.hp1 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-1+7846dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687823 | |||||
| chr10:113687827
|
T | TC | 9 | a0001c0001t0002g0241a0001c0001t0002g0249a0001c0001t0002g0250others(6): Show | 9 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+7850dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687827 | |||||
| chr10:113687827
|
T | TCTTTC | 3 | a0001c0001t0004g0031a0001c0001t0005g0032a0001c0001t0005g0058 | 3 | HG01361.hp2 NA19006.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-1+7850_-1+7854dup others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687827 | |||||
| chr10:113687833
|
T | C | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0030others(9): Show | 13 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+7855T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687833 | ||||||
| chr10:113687835
|
TC | T | 39 | a0001c0001t0003g0149a0001c0001t0003g0161a0001c0001t0003g0163others(36): Show | 41 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-1+7859delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687835 | |||||
| chr10:113687836
|
C | CTTT | 72 | a0001c0001t0002g0222a0001c0001t0002g0328a0001c0001t0003g0160others(69): Show | 72 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT | 29 | a0001c0001t0002g0181a0001c0001t0003g0188a0001c0001t0003g0191others(26): Show | 31 | HG01081.hp2 HG01123.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(7): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT others(4): Show |
21 | a0001c0001t0002g0193a0001c0001t0003g0189a0001c0001t0003g0192others(18): Show | 23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(11): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT others(18): Show |
1 | a0001c0001t0004g0093 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(25): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT others(22): Show |
1 | a0001c0001t0004g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(29): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT others(8): Show |
6 | a0001c0001t0002g0335a0001c0001t0003g0196a0001c0001t0003g0197others(3): Show | 6 | HG00558.hp2 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT others(12): Show |
1 | a0001c0001t0004g0095 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(19): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | CTTTCTTT others(34): Show |
1 | a0001c0001t0004g0338 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(41): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687836
|
C | T | 15 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247others(12): Show | 16 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+7858C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | ||||||
| chr10:113687837
|
C | T | 23 | a0001c0001t0002g0106a0001c0001t0002g0241a0001c0001t0002g0249others(20): Show | 25 | HG00140.hp1 HG00544.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1+7859C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687837 | ||||||
| chr10:113687840
|
T | C | 8 | a0001c0001t0005g0054a0002c0002t0001g0002a0002c0002t0001g0279others(5): Show | 10 | HG00140.hp1 HG01361.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+7862T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687840 | ||||||
| chr10:113687840
|
T | TC | 4 | a0001c0001t0005g0382a0002c0002t0001g0281a0002c0002t0001g0287others(1): Show | 4 | HG00735.hp1 NA18984.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7863dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687840 | |||||
| chr10:113687845
|
C | T | 16 | a0001c0001t0002g0106a0001c0001t0002g0379a0001c0001t0002g0380others(13): Show | 17 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+7867C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687845 | ||||||
| chr10:113687845
|
CT | C | 14 | a0001c0001t0002g0241a0001c0001t0002g0246a0001c0001t0002g0247others(11): Show | 16 | HG00408.hp1 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+7871delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687845 | |||||
| chr10:113687846
|
T | C | 122 | a0001c0001t0002g0106a0001c0001t0002g0181a0001c0001t0002g0222others(119): Show | 127 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-1+7868T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687846 | ||||||
| chr10:113687846
|
T | TTTC | 5 | a0001c0001t0002g0245a0001c0001t0004g0074a0001c0001t0004g0338others(2): Show | 5 | HG01515.hp2 HG02083.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTCCTTT others(14): Show |
1 | a0001c0001t0002g0328 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(21): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTCTTTC others(14): Show |
1 | a0002c0002t0001g0370 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(21): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTCTTTC others(22): Show |
1 | a0002c0002t0001g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(29): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTCTTTC others(26): Show |
1 | a0002c0002t0001g0350 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(33): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTTC | 29 | a0001c0001t0002g0311a0001c0001t0002g0326a0001c0001t0003g0346others(26): Show | 31 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1+7909_-1+7912dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTTCTTT others(1): Show |
9 | a0001c0001t0003g0348a0001c0001t0005g0050a0001c0001t0005g0051others(6): Show | 9 | HG02523.hp1 HG03098.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+7905_-1+7912dup others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
T | TTTTCTTT others(5): Show |
4 | a0001c0001t0004g0060a0001c0001t0004g0066a0001c0001t0005g0052others(1): Show | 4 | HG02135.hp1 NA18943.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7901_-1+7912dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687846
|
TTTTCTTT others(1): Show |
T | 2 | a0001c0001t0004g0015a0002c0002t0001g0278 | 3 | HG00423.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+7905_-1+7912del others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | |||||
| chr10:113687849
|
T | C | 64 | a0001c0001t0002g0193a0001c0001t0003g0165a0001c0001t0003g0166others(61): Show | 66 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-1+7871T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687849 | ||||||
| chr10:113687850
|
C | CTT | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1+7874_-1+7875dup others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687850 | |||||
| chr10:113687850
|
C | CTTTCT | 24 | a0001c0001t0003g0324a0001c0001t0004g0067a0001c0001t0004g0068others(21): Show | 24 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.-1+7875_-1+7879dup others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687850 | |||||
| chr10:113687850
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0054a0001c0001t0005g0382others(8): Show | 11 | HG00140.hp1 HG00735.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+7872C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687850 | ||||||
| chr10:113687851
|
TTTC | T | 2 | a0002c0002t0001g0002a0002c0002t0001g0279 | 4 | NA18943.hp1 NA18962.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7876_-1+7878del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687851 | |||||
| chr10:113687853
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1+7875T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687853 | ||||||
| chr10:113687853
|
TC | T | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+7876delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687853 | ||||||
| chr10:113687854
|
C | CT | 71 | a0001c0001t0002g0181a0001c0001t0002g0222a0001c0001t0002g0335others(68): Show | 74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1+7879dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687854 | |||||
| chr10:113687855
|
TTTC | T | 7 | a0001c0001t0003g0149a0001c0001t0003g0161a0001c0001t0003g0163others(4): Show | 7 | HG00741.hp1 HG01069.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+7880_-1+7882del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687855 | |||||
| chr10:113687858
|
C | CT | 49 | a0001c0001t0002g0193a0001c0001t0003g0165a0001c0001t0003g0166others(46): Show | 51 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-1+7883dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687858 | |||||
| chr10:113687859
|
TTTC | T | 4 | a0001c0001t0003g0208a0001c0001t0003g0209a0003c0003t0002g0121others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7884_-1+7886del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687859 | |||||
| chr10:113687870
|
C | CT | 3 | a0001c0001t0002g0106a0001c0001t0003g0187a0001c0001t0003g0191 | 3 | HG02602.hp1 HG03704.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-1+7895dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687870 | |||||
| chr10:113687889
|
TC | T | 76 | a0001c0001t0002g0010a0001c0001t0002g0244a0001c0001t0003g0009others(73): Show | 78 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-1+7913delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687889 | |||||
| chr10:113687890
|
C | CTTT | 60 | a0001c0001t0002g0181a0001c0001t0002g0193a0001c0001t0002g0222others(57): Show | 62 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | ||||||
| chr10:113687890
|
C | CTTTCTTT | 4 | a0001c0001t0004g0077a0003c0003t0002g0118a0003c0003t0002g0119others(1): Show | 4 | HG00738.hp2 HG04199.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(7): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | ||||||
| chr10:113687890
|
C | CTTTCTTT others(4): Show |
1 | a0003c0003t0002g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(11): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | ||||||
| chr10:113687890
|
C | CTTTCTTT others(8): Show |
1 | a0003c0003t0002g0131 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | ||||||
| chr10:113687890
|
C | T | 8 | a0001c0001t0002g0103a0001c0001t0004g0008a0001c0001t0004g0152others(5): Show | 9 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+7912C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | ||||||
| chr10:113687891
|
C | T | 39 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0245others(36): Show | 40 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1+7913C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687891 | ||||||
| chr10:113687894
|
T | C | 20 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(17): Show | 20 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+7916T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687894 | ||||||
| chr10:113687894
|
T | TC | 6 | a0001c0001t0004g0077a0001c0001t0005g0005a0001c0001t0005g0018others(3): Show | 7 | HG00733.hp2 HG00738.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+7917dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687894 | |||||
| chr10:113687895
|
C | T | 5 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(2): Show | 5 | HG01433.hp2 HG03017.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+7917C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687895 | ||||||
| chr10:113687896
|
TTTCTTTC others(5): Show |
T | 1 | a0001c0001t0002g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-1+7922_-1+7933del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687896 | |||||
| chr10:113687898
|
T | TC | 5 | a0001c0001t0003g0205a0001c0001t0004g0268a0002c0002t0001g0320others(2): Show | 5 | HG01358.hp1 HG03453.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7921dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687898 | |||||
| chr10:113687900
|
T | C | 1 | a0001c0012t0002g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1+7922T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687900 | ||||||
| chr10:113687902
|
T | TC | 9 | a0001c0001t0002g0222a0001c0001t0003g0169a0001c0001t0003g0172others(6): Show | 9 | HG01243.hp2 HG02040.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+7925dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687902 | |||||
| chr10:113687904
|
T | C | 4 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0005t0002g0264others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7926T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687904 | ||||||
| chr10:113687908
|
C | CT | 102 | a0001c0001t0002g0010a0001c0001t0002g0103a0001c0001t0002g0181others(99): Show | 105 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-1+7932dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687908 | |||||
| chr10:113687908
|
C | CTTTCT | 4 | a0001c0001t0003g0176a0001c0001t0003g0192a0002c0006t0001g0104others(1): Show | 4 | HG02647.hp2 HG03239.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7932_-1+7933ins others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687908 | |||||
| chr10:113687908
|
C | T | 53 | a0001c0001t0002g0222a0001c0001t0002g0244a0001c0001t0002g0255others(50): Show | 54 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-1+7930C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687908 | ||||||
| chr10:113687909
|
TTCC | T | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 29 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1+7933_-1+7935del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687909 | |||||
| chr10:113687911
|
CCTT | C | 4 | a0001c0001t0002g0255a0002c0002t0001g0254a0003c0003t0005g0115others(1): Show | 4 | HG03225.hp1 HG06807.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7937_-1+7939del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687911 | |||||
| chr10:113687912
|
C | CT | 9 | a0001c0001t0002g0381a0001c0001t0003g0182a0001c0001t0003g0188others(6): Show | 9 | HG01106.hp1 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+7936dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687912 | |||||
| chr10:113687912
|
C | T | 123 | a0001c0001t0002g0010a0001c0001t0002g0103a0001c0001t0002g0181others(120): Show | 126 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-1+7934C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687912 | ||||||
| chr10:113687913
|
TTCTTTCC others(4): Show |
T | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-1+7937_-1+7947del others(11): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687913 | |||||
| chr10:113687914
|
T | TC | 3 | a0003c0003t0005g0126a0003c0003t0005g0133a0003c0003t0005g0134 | 3 | HG02647.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-1+7937dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687914 | |||||
| chr10:113687916
|
T | C | 36 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0312others(33): Show | 37 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-1+7938T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687916 | ||||||
| chr10:113687916
|
T | TTTCC | 32 | a0001c0001t0002g0326a0001c0001t0003g0348a0001c0001t0004g0025others(29): Show | 36 | HG00639.hp2 HG00642.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.-1+7985_-1+7988dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687916
|
T | TTTCCTTC others(1): Show |
6 | a0001c0001t0004g0156a0001c0001t0004g0157a0001c0001t0005g0085others(3): Show | 6 | HG01081.hp2 HG01123.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+7981_-1+7988dup others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687916
|
T | TTTCCTTC others(5): Show |
2 | a0001c0001t0004g0155a0001c0001t0005g0384 | 2 | HG03471.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-1+7977_-1+7988dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687916
|
T | TTTCCTTC others(9): Show |
1 | a0001c0001t0005g0382 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1+7973_-1+7988dup others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687916
|
TTTCC | T | 6 | a0001c0001t0004g0080a0001c0001t0004g0083a0001c0001t0005g0057others(3): Show | 6 | HG01192.hp1 HG01346.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+7985_-1+7988del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687916
|
TTTCCTTC others(5): Show |
T | 1 | a0001c0001t0005g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1+7977_-1+7988del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687916
|
TTTCCTTC others(9): Show |
T | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+7973_-1+7988del others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | |||||
| chr10:113687920
|
C | T | 114 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(111): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-1+7942C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687920 | ||||||
| chr10:113687924
|
C | T | 13 | a0001c0001t0003g0182a0001c0001t0003g0188a0001c0001t0003g0205others(10): Show | 13 | HG01358.hp1 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+7946C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687924 | ||||||
| chr10:113687928
|
C | T | 39 | a0001c0001t0002g0222a0001c0001t0002g0244a0001c0001t0002g0256others(36): Show | 40 | HG00558.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1+7950C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687928 | ||||||
| chr10:113687932
|
C | T | 83 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(80): Show | 85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-1+7954C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687932 | ||||||
| chr10:113687936
|
C | T | 8 | a0001c0001t0003g0182a0001c0001t0003g0188a0002c0002t0001g0168others(5): Show | 8 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+7958C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687936 | ||||||
| chr10:113687955
|
CCTTCCTT others(5): Show |
C | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0263others(2): Show | 5 | HG01081.hp1 HG01515.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7981_-1+7992del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687955 | |||||
| chr10:113687959
|
CCTTCCTT others(1): Show |
C | 12 | a0001c0001t0002g0335a0002c0002t0001g0002a0002c0002t0001g0273others(9): Show | 14 | HG00423.hp1 HG00438.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+7985_-1+7992del others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687959 | |||||
| chr10:113687963
|
CCTTT | C | 52 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0247others(49): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+7998_-1+8001del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687963 | |||||
| chr10:113687967
|
T | C | 71 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0246others(68): Show | 75 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-1+7989T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687967 | ||||||
| chr10:113688035
|
C | T | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+8057C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688035 | ||||||
| chr10:113688410
|
T | C | 1 | a0001c0001t0003g0169 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1+8432T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688410 | ||||||
| chr10:113688419
|
C | G | 1 | a0001c0001t0003g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1+8441C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688419 | ||||||
| chr10:113688422
|
T | C | 13 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(10): Show | 14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+8444T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688422 | ||||||
| chr10:113688506
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+8528A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688506 | ||||||
| chr10:113688546
|
A | G | 2 | a0001c0001t0005g0038a0001c0001t0005g0046 | 2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-1+8568A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688546 | ||||||
| chr10:113688552
|
A | G | 1 | a0001c0001t0002g0335 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1+8574A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688552 | ||||||
| chr10:113688604
|
T | C | 40 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(37): Show | 42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+8626T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688604 | ||||||
| chr10:113688644
|
T | C | 40 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(37): Show | 42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+8666T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688644 | ||||||
| chr10:113688699
|
C | T | 89 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(86): Show | 91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1+8721C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688699 | ||||||
| chr10:113688824
|
T | C | 2 | a0002c0006t0001g0104a0002c0006t0001g0105 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-8670T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688824 | ||||||
| chr10:113689005
|
GT | G | 5 | a0002c0002t0001g0281a0002c0002t0001g0283a0002c0002t0001g0293others(2): Show | 5 | NA18947.hp1 NA18951.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-8488delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689005 | ||||||
| chr10:113689057
|
C | T | 3 | a0002c0002t0001g0304a0002c0002t0001g0306a0002c0002t0001g0353 | 3 | HG01891.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1-8437C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689057 | ||||||
| chr10:113689081
|
T | C | 1 | a0002c0002t0001g0351 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1-8413T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689081 | ||||||
| chr10:113689085
|
A | C | 3 | a0001c0001t0003g0161a0001c0001t0003g0166a0001c0001t0003g0167 | 3 | HG00323.hp2 HG03927.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1-8409A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689085 | ||||||
| chr10:113689180
|
C | T | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-8314C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689180 | ||||||
| chr10:113689210
|
T | C | 1 | a0004c0004t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1-8284T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689210 | ||||||
| chr10:113689238
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1-8256C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689238 | ||||||
| chr10:113689432
|
G | A | 2 | a0003c0003t0002g0121a0003c0003t0002g0122 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1-8062G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689432 | ||||||
| chr10:113689573
|
T | C | 3 | a0001c0001t0003g0346a0001c0001t0003g0348a0001c0001t0004g0347 | 3 | HG02109.hp2 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1-7921T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689573 | ||||||
| chr10:113689576
|
T | C | 1 | a0001c0001t0002g0381 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1-7918T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689576 | ||||||
| chr10:113689681
|
A | C | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-7813A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689681 | ||||||
| chr10:113689717
|
G | A | 95 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(92): Show | 99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1-7777G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689717 | ||||||
| chr10:113690040
|
C | CCCGAAGG others(118): Show |
66 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(63): Show | 68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1-7454_1-7453insCC others(123): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690040 | ||||||
| chr10:113690058
|
G | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-7436G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690058 | ||||||
| chr10:113690096
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1-7398T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690096 | ||||||
| chr10:113690198
|
T | C | 1 | a0003c0003t0019g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-7296T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690198 | ||||||
| chr10:113690264
|
G | GT | 167 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0307others(164): Show | 175 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.1-7221dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113690264 | |||||
| chr10:113690264
|
GT | G | 5 | a0001c0001t0005g0108a0001c0001t0005g0382a0001c0001t0005g0384others(2): Show | 5 | HG01081.hp2 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-7221delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113690264 | |||||
| chr10:113690265
|
T | G | 2 | a0001c0001t0005g0041a0001c0001t0005g0050 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1-7229T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690265 | ||||||
| chr10:113690288
|
A | G | 89 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(86): Show | 91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1-7206A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690288 | ||||||
| chr10:113690368
|
C | T | 1 | a0003c0003t0002g0123 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-7126C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690368 | ||||||
| chr10:113690400
|
A | G | 2 | a0001c0001t0005g0085a0001c0001t0005g0087 | 2 | HG01981.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1-7094A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690400 | ||||||
| chr10:113690755
|
C | G | 381 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(378): Show | 399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.1-6739C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690755 | ||||||
| chr10:113691013
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1-6481G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691013 | ||||||
| chr10:113691424
|
A | T | 4 | a0002c0002t0001g0356a0002c0002t0001g0357a0002c0002t0001g0363others(1): Show | 4 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-6070A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691424 | ||||||
| chr10:113691464
|
G | T | 1 | a0003c0003t0002g0123 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-6030G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691464 | ||||||
| chr10:113691641
|
C | A | 3 | a0001c0001t0005g0382a0001c0001t0005g0384a0002c0002t0001g0383 | 3 | HG01109.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1-5853C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691641 | ||||||
| chr10:113691673
|
G | A | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-5821G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691673 | ||||||
| chr10:113691702
|
C | T | 1 | a0001c0001t0006g0063 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1-5792C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691702 | ||||||
| chr10:113691878
|
T | C | 2 | a0001c0001t0004g0154a0001c0001t0004g0159 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1-5616T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691878 | ||||||
| chr10:113691887
|
G | A | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-5607G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691887 | ||||||
| chr10:113691941
|
G | T | 1 | a0002c0002t0001g0375 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1-5553G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691941 | ||||||
| chr10:113691946
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-5548A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691946 | ||||||
| chr10:113692022
|
C | T | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-5472C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692022 | ||||||
| chr10:113692245
|
G | T | 1 | a0002c0002t0001g0336 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1-5249G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692245 | ||||||
| chr10:113692246
|
G | A | 2 | a0001c0001t0005g0028a0001c0001t0005g0040 | 2 | HG02080.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1-5248G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692246 | ||||||
| chr10:113692269
|
G | A | 1 | a0001c0001t0008g0016 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-5225G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692269 | ||||||
| chr10:113692525
|
G | C | 7 | a0001c0001t0004g0374a0002c0002t0001g0313a0002c0002t0001g0355others(4): Show | 7 | HG01099.hp2 HG01928.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-4969G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692525 | ||||||
| chr10:113692543
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1-4951G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692543 | ||||||
| chr10:113692624
|
G | A | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-4870G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692624 | ||||||
| chr10:113692684
|
T | A | 35 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(32): Show | 36 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1-4810T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692684 | ||||||
| chr10:113692693
|
A | T | 1 | a0001c0001t0003g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1-4801A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692693 | ||||||
| chr10:113692914
|
C | T | 2 | a0001c0001t0005g0382a0001c0001t0005g0384 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1-4580C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692914 | ||||||
| chr10:113693366
|
G | A | 1 | a0001c0001t0005g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1-4128G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693366 | ||||||
| chr10:113693366
|
G | C | 40 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(37): Show | 42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1-4128G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693366 | ||||||
| chr10:113693492
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1-4002C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693492 | ||||||
| chr10:113693509
|
T | C | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-3985T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693509 | ||||||
| chr10:113693590
|
G | A | 41 | a0003c0003t0002g0007a0003c0003t0002g0110a0003c0003t0002g0111others(38): Show | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1-3904G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693590 | ||||||
| chr10:113693610
|
T | A | 1 | a0001c0001t0002g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1-3884T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693610 | ||||||
| chr10:113693682
|
G | A | 1 | a0003c0003t0002g0148 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1-3812G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693682 | ||||||
| chr10:113693922
|
A | G | 2 | a0001c0001t0003g0324a0002c0002t0001g0310 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1-3572A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693922 | ||||||
| chr10:113693961
|
A | G | 1 | a0003c0003t0002g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1-3533A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693961 | ||||||
| chr10:113694004
|
G | A | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-3490G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694004 | ||||||
| chr10:113694140
|
C | T | 1 | a0001c0001t0008g0016 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-3354C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694140 | ||||||
| chr10:113694173
|
G | T | 1 | a0001c0001t0008g0016 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-3321G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694173 | ||||||
| chr10:113694226
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1-3268A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694226 | ||||||
| chr10:113694230
|
A | C | 337 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(334): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1-3264A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694230 | ||||||
| chr10:113694265
|
G | A | 10 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0210others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1-3229G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694265 | ||||||
| chr10:113694447
|
C | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1-3047C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694447 | ||||||
| chr10:113694554
|
G | A | 1 | a0003c0003t0019g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-2940G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694554 | ||||||
| chr10:113694779
|
T | C | 3 | a0001c0001t0003g0346a0001c0001t0003g0348a0001c0001t0004g0347 | 3 | HG02109.hp2 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1-2715T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694779 | ||||||
| chr10:113694784
|
T | G | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-2710T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694784 | ||||||
| chr10:113694789
|
T | C | 2 | a0001c0001t0005g0038a0001c0001t0005g0046 | 2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1-2705T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694789 | ||||||
| chr10:113694839
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1-2655G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694839 | ||||||
| chr10:113694879
|
G | A | 1 | a0001c0001t0004g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1-2615G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694879 | ||||||
| chr10:113694937
|
T | C | 4 | a0001c0001t0004g0015a0001c0001t0004g0267a0001c0001t0004g0268others(1): Show | 5 | HG02572.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-2557T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694937 | ||||||
| chr10:113694974
|
T | A | 4 | a0001c0001t0002g0103a0001c0001t0002g0106a0002c0006t0001g0104others(1): Show | 4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2520T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694974 | ||||||
| chr10:113695031
|
C | T | 2 | a0003c0003t0002g0114a0004c0004t0001g0130 | 2 | NA18945.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1-2463C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695031 | ||||||
| chr10:113695103
|
C | A | 112 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(109): Show | 118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1-2391C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695103 | ||||||
| chr10:113695278
|
C | T | 2 | a0003c0003t0002g0121a0003c0003t0002g0122 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1-2216C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695278 | ||||||
| chr10:113695407
|
C | T | 4 | a0001c0001t0002g0103a0001c0001t0002g0106a0002c0006t0001g0104others(1): Show | 4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2087C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695407 | ||||||
| chr10:113695455
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1-2039G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695455 | ||||||
| chr10:113695481
|
G | A | 1 | a0003c0003t0002g0123 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-2013G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695481 | ||||||
| chr10:113695494
|
T | C | 3 | a0001c0001t0004g0259a0001c0001t0004g0261a0001c0001t0004g0262 | 3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1-2000T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695494 | ||||||
| chr10:113695532
|
G | A | 35 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(32): Show | 36 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1-1962G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695532 | ||||||
| chr10:113695542
|
C | T | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1952C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695542 | ||||||
| chr10:113695777
|
G | T | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-1717G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695777 | ||||||
| chr10:113696122
|
G | A | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1372G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696122 | ||||||
| chr10:113696208
|
A | G | 1 | a0001c0001t0005g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-1286A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696208 | ||||||
| chr10:113696414
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1-1080C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696414 | ||||||
| chr10:113696469
|
C | A | 1 | a0002c0002t0001g0373 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1-1025C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696469 | ||||||
| chr10:113696507
|
A | C | 112 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(109): Show | 118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1-987A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696507 | ||||||
| chr10:113696623
|
C | A | 1 | a0001c0001t0005g0043 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1-871C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696623 | ||||||
| chr10:113697086
|
A | C | 1 | a0002c0002t0001g0353 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1-408A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697086 | ||||||
| chr10:113697088
|
A | G | 1 | a0001c0008t0002g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1-406A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697088 | ||||||
| chr10:113697134
|
C | T | 1 | a0003c0003t0002g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1-360C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697134 | ||||||
| chr10:113697208
|
C | T | 3 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0001t0002g0381 | 3 | HG02258.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1-286C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697208 | ||||||
| chr10:113697355
|
G | A | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-139G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697355 | ||||||
| chr10:113697410
|
C | A | 1 | a0001c0001t0003g0185 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1-84C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697410 | ||||||
| chr10:113697628
|
T | C | 2 | a0002c0002t0001g0300a0002c0002t0001g0319 | 2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.110+25T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697628 | ||||||
| chr10:113697691
|
G | A | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.110+88G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697691 | ||||||
| chr10:113697745
|
G | A | 1 | a0003c0003t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+142G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697745 | ||||||
| chr10:113697838
|
G | A | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.110+235G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697838 | ||||||
| chr10:113697930
|
T | C | 1 | a0003c0003t0002g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+327T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697930 | ||||||
| chr10:113698130
|
T | C | 38 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.110+527T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698130 | ||||||
| chr10:113698146
|
T | A | 1 | a0001c0001t0005g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.110+543T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698146 | ||||||
| chr10:113698209
|
C | A | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.110+606C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698209 | ||||||
| chr10:113698378
|
A | C | 6 | a0001c0001t0006g0021a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG00597.hp2 NA18612.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+775A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698378 | ||||||
| chr10:113698465
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+862C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698465 | ||||||
| chr10:113698513
|
G | A | 5 | a0001c0001t0003g0175a0001c0001t0003g0177a0001c0001t0003g0192others(2): Show | 5 | HG02074.hp1 HG02300.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+910G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698513 | ||||||
| chr10:113698555
|
G | A | 293 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(290): Show | 306 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.110+952G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698555 | ||||||
| chr10:113698610
|
A | T | 2 | a0002c0002t0001g0316a0002c0002t0001g0332 | 2 | NA18966.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.110+1007A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698610 | ||||||
| chr10:113698666
|
G | GT | 99 | a0001c0001t0002g0010a0001c0001t0002g0193a0001c0001t0002g0222others(96): Show | 104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.110+1074dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113698666 | |||||
| chr10:113698666
|
G | GTT | 42 | a0001c0001t0002g0181a0003c0003t0002g0007a0003c0003t0002g0110others(39): Show | 43 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+1073_110+1074d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113698666 | |||||
| chr10:113698666
|
G | T | 34 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(31): Show | 35 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.110+1063G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698666 | ||||||
| chr10:113698761
|
A | G | 1 | a0002c0002t0001g0343 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.110+1158A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698761 | ||||||
| chr10:113698866
|
G | A | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.110+1263G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698866 | ||||||
| chr10:113698927
|
G | T | 2 | a0001c0001t0005g0382a0001c0001t0005g0384 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110+1324G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698927 | ||||||
| chr10:113699177
|
A | G | 113 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(110): Show | 119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+1574A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699177 | ||||||
| chr10:113699222
|
A | G | 27 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.110+1619A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699222 | ||||||
| chr10:113699241
|
T | C | 1 | a0002c0002t0001g0288 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.110+1638T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699241 | ||||||
| chr10:113699280
|
C | G | 1 | a0005c0009t0003g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+1677C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699280 | ||||||
| chr10:113699347
|
T | C | 13 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(10): Show | 14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+1744T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699347 | ||||||
| chr10:113699536
|
A | G | 2 | a0003c0003t0002g0127a0003c0003t0002g0138 | 2 | NA18964.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.110+1933A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699536 | ||||||
| chr10:113699553
|
C | G | 1 | a0002c0002t0001g0313 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110+1950C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699553 | ||||||
| chr10:113699576
|
A | G | 1 | a0001c0001t0018g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.110+1973A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699576 | ||||||
| chr10:113699698
|
A | T | 1 | a0001c0012t0002g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.110+2095A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699698 | ||||||
| chr10:113699742
|
T | G | 1 | a0001c0001t0005g0266 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110+2139T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699742 | ||||||
| chr10:113699850
|
A | C | 1 | a0001c0005t0002g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+2247A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699850 | ||||||
| chr10:113699881
|
TA | T | 2 | a0001c0001t0005g0001a0001c0001t0005g0045 | 4 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+2279delA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699881 | ||||||
| chr10:113700020
|
T | C | 1 | a0001c0001t0004g0031 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.110+2417T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700020 | ||||||
| chr10:113700053
|
A | G | 4 | a0001c0001t0002g0103a0001c0001t0002g0106a0002c0006t0001g0104others(1): Show | 4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+2450A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700053 | ||||||
| chr10:113700054
|
T | A | 1 | a0003c0003t0002g0131 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.110+2451T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700054 | ||||||
| chr10:113700218
|
G | T | 1 | a0002c0002t0001g0275 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.110+2615G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700218 | ||||||
| chr10:113700432
|
A | G | 1 | a0001c0005t0002g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+2829A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700432 | ||||||
| chr10:113700449
|
C | T | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+2846C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700449 | ||||||
| chr10:113700701
|
G | C | 13 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(10): Show | 14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+3098G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700701 | ||||||
| chr10:113700729
|
CATG | C | 346 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(343): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.110+3127_110+3129d others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700729 | ||||||
| chr10:113700766
|
G | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.110+3163G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700766 | ||||||
| chr10:113700784
|
T | C | 1 | a0002c0002t0001g0301 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.110+3181T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700784 | ||||||
| chr10:113700815
|
G | A | 5 | a0001c0001t0005g0108a0001c0001t0005g0382a0001c0001t0005g0384others(2): Show | 5 | HG01081.hp2 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+3212G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700815 | ||||||
| chr10:113700844
|
C | T | 39 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(36): Show | 41 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.110+3241C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700844 | ||||||
| chr10:113700954
|
C | T | 26 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0004g0067others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.110+3351C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700954 | ||||||
| chr10:113700955
|
G | A | 113 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(110): Show | 119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+3352G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700955 | ||||||
| chr10:113701011
|
C | T | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+3408C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701011 | ||||||
| chr10:113701078
|
A | C | 1 | a0003c0003t0005g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.110+3475A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701078 | ||||||
| chr10:113701169
|
G | A | 194 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(191): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.110+3566G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701169 | ||||||
| chr10:113701207
|
C | CA | 95 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(92): Show | 99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.110+3605dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113701207 | |||||
| chr10:113701312
|
C | CT | 103 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0311others(100): Show | 109 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.110+3725dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113701312 | |||||
| chr10:113701312
|
CT | C | 40 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(37): Show | 42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.110+3725delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113701312 | |||||
| chr10:113701353
|
C | G | 1 | a0001c0001t0005g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.110+3750C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701353 | ||||||
| chr10:113701360
|
G | T | 1 | a0001c0001t0003g0165 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.110+3757G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701360 | ||||||
| chr10:113701466
|
C | T | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+3863C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701466 | ||||||
| chr10:113701509
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0106 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.110+3906T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701509 | ||||||
| chr10:113701698
|
C | G | 2 | a0003c0003t0002g0139a0003c0003t0002g0147 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.110+4095C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701698 | ||||||
| chr10:113701726
|
A | G | 113 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(110): Show | 119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+4123A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701726 | ||||||
| chr10:113701761
|
A | G | 1 | a0002c0002t0001g0351 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.110+4158A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701761 | ||||||
| chr10:113702038
|
A | G | 95 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(92): Show | 99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.110+4435A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702038 | ||||||
| chr10:113702055
|
A | G | 2 | a0002c0006t0001g0104a0002c0006t0001g0105 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.110+4452A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702055 | ||||||
| chr10:113702399
|
A | G | 1 | a0003c0003t0019g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110+4796A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702399 | ||||||
| chr10:113702415
|
C | A | 5 | a0001c0001t0005g0108a0001c0001t0005g0382a0001c0001t0005g0384others(2): Show | 5 | HG01081.hp2 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+4812C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702415 | ||||||
| chr10:113702655
|
A | G | 346 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(343): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.110+5052A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702655 | ||||||
| chr10:113702684
|
C | T | 1 | a0002c0002t0001g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.110+5081C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702684 | ||||||
| chr10:113702714
|
C | T | 1 | a0001c0001t0004g0060 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.110+5111C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702714 | ||||||
| chr10:113702727
|
C | T | 2 | a0001c0001t0005g0108a0001c0012t0002g0107 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+5124C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702727 | ||||||
| chr10:113702770
|
A | G | 5 | a0001c0001t0003g0175a0001c0001t0003g0177a0001c0001t0003g0192others(2): Show | 5 | HG02074.hp1 HG02300.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+5167A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702770 | ||||||
| chr10:113703058
|
A | G | 2 | a0001c0001t0005g0018a0001c0001t0005g0101 | 2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.110+5455A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703058 | ||||||
| chr10:113703238
|
T | C | 9 | a0002c0002t0001g0273a0002c0002t0001g0278a0002c0002t0001g0285others(6): Show | 9 | HG00423.hp1 HG01257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+5635T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703238 | ||||||
| chr10:113703323
|
G | A | 346 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(343): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.110+5720G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703323 | ||||||
| chr10:113703493
|
C | T | 1 | a0002c0002t0001g0282 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.110+5890C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703493 | ||||||
| chr10:113703556
|
G | C | 1 | a0001c0001t0004g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.110+5953G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703556 | ||||||
| chr10:113703630
|
CT | C | 221 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0181others(218): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.110+6051delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113703630 | |||||
| chr10:113703654
|
T | A | 8 | a0001c0001t0004g0374a0002c0002t0001g0162a0002c0002t0001g0273others(5): Show | 8 | HG01255.hp1 HG01517.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+6051T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703654 | ||||||
| chr10:113703654
|
T | TA | 64 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(61): Show | 69 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.110+6053dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113703654 | |||||
| chr10:113703909
|
A | G | 23 | a0001c0001t0005g0315a0002c0002t0001g0002a0002c0002t0001g0274others(20): Show | 25 | HG00438.hp2 HG01433.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.110+6306A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703909 | ||||||
| chr10:113703920
|
G | A | 22 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(19): Show | 23 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.110+6317G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703920 | ||||||
| chr10:113703948
|
A | G | 1 | a0001c0001t0005g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.110+6345A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703948 | ||||||
| chr10:113703977
|
G | A | 1 | a0001c0001t0005g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.110+6374G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703977 | ||||||
| chr10:113704093
|
G | C | 1 | a0001c0001t0008g0016 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110+6490G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704093 | ||||||
| chr10:113704138
|
C | T | 4 | a0001c0001t0002g0258a0001c0001t0004g0259a0001c0001t0004g0261others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+6535C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704138 | ||||||
| chr10:113704260
|
C | T | 2 | a0002c0002t0001g0342a0002c0002t0001g0343 | 2 | HG00140.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.110+6657C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704260 | ||||||
| chr10:113704274
|
T | C | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+6671T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704274 | ||||||
| chr10:113704342
|
C | T | 1 | a0002c0002t0001g0357 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.110+6739C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704342 | ||||||
| chr10:113704373
|
G | A | 94 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(91): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.110+6770G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704373 | ||||||
| chr10:113704378
|
C | T | 1 | a0001c0001t0005g0086 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.110+6775C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704378 | ||||||
| chr10:113704412
|
A | G | 189 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(186): Show | 198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.110+6809A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704412 | ||||||
| chr10:113704517
|
A | G | 13 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(10): Show | 14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+6914A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704517 | ||||||
| chr10:113704677
|
A | G | 1 | a0001c0001t0004g0268 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.110+7074A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704677 | ||||||
| chr10:113704710
|
C | G | 2 | a0001c0001t0002g0311a0001c0001t0002g0326 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.110+7107C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704710 | ||||||
| chr10:113704716
|
C | A | 1 | a0001c0001t0002g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.110+7113C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704716 | ||||||
| chr10:113704782
|
T | C | 2 | a0001c0001t0005g0108a0001c0012t0002g0107 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+7179T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704782 | ||||||
| chr10:113704931
|
C | T | 111 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(108): Show | 117 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.110+7328C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704931 | ||||||
| chr10:113704952
|
G | GC | 229 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(226): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.110+7359dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113704952 | |||||
| chr10:113704952
|
G | GCC | 42 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0191others(39): Show | 42 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.110+7358_110+7359d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113704952 | |||||
| chr10:113705018
|
T | C | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7415T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705018 | ||||||
| chr10:113705109
|
C | T | 1 | a0002c0002t0001g0340 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+7506C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705109 | ||||||
| chr10:113705115
|
A | G | 1 | a0003c0003t0002g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.110+7512A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705115 | ||||||
| chr10:113705118
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.110+7515C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705118 | ||||||
| chr10:113705225
|
CT | C | 343 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(340): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.110+7631delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113705225 | |||||
| chr10:113705378
|
AC | A | 3 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0001t0002g0381 | 3 | HG02258.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.110+7776delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705378 | ||||||
| chr10:113705459
|
C | T | 1 | a0001c0005t0002g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+7856C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705459 | ||||||
| chr10:113705500
|
G | T | 1 | a0001c0001t0003g0195 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.110+7897G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705500 | ||||||
| chr10:113705727
|
G | T | 1 | a0003c0003t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+8124G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705727 | ||||||
| chr10:113705729
|
G | C | 1 | a0001c0001t0004g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+8126G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705729 | ||||||
| chr10:113705736
|
CAG | C | 7 | a0001c0001t0003g0208a0001c0001t0003g0212a0001c0001t0003g0214others(4): Show | 7 | HG01243.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+8134_110+8135d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705736 | ||||||
| chr10:113705805
|
G | T | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8202G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705805 | ||||||
| chr10:113705808
|
T | G | 2 | a0001c0001t0005g0028a0001c0001t0005g0040 | 2 | HG02080.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.110+8205T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705808 | ||||||
| chr10:113705840
|
G | A | 1 | a0003c0003t0002g0146 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.110+8237G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705840 | ||||||
| chr10:113705926
|
C | T | 2 | a0001c0001t0003g0169a0001c0001t0003g0199 | 2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.110+8323C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705926 | ||||||
| chr10:113705971
|
G | A | 4 | a0002c0002t0001g0356a0002c0002t0001g0357a0002c0002t0001g0363others(1): Show | 4 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+8368G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705971 | ||||||
| chr10:113706080
|
C | T | 1 | a0001c0001t0005g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.110+8477C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706080 | ||||||
| chr10:113706166
|
G | T | 74 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(71): Show | 79 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.110+8563G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706166 | ||||||
| chr10:113706408
|
C | T | 2 | a0002c0002t0001g0300a0002c0002t0001g0319 | 2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.110+8805C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706408 | ||||||
| chr10:113706409
|
G | A | 1 | a0001c0001t0003g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.110+8806G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706409 | ||||||
| chr10:113706557
|
G | A | 1 | a0002c0002t0001g0383 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110+8954G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706557 | ||||||
| chr10:113706696
|
T | C | 1 | a0003c0003t0002g0123 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.110+9093T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706696 | ||||||
| chr10:113706740
|
T | G | 14 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0379others(11): Show | 14 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+9137T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706740 | ||||||
| chr10:113706793
|
G | A | 1 | a0001c0001t0004g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+9190G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706793 | ||||||
| chr10:113706889
|
C | G | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+9286C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706889 | ||||||
| chr10:113707077
|
T | G | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+9474T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707077 | ||||||
| chr10:113707184
|
C | T | 3 | a0001c0001t0004g0259a0001c0001t0004g0261a0001c0001t0004g0262 | 3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.110+9581C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707184 | ||||||
| chr10:113707309
|
A | G | 139 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(136): Show | 146 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.110+9706A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707309 | ||||||
| chr10:113707506
|
C | G | 2 | a0002c0002t0001g0291a0002c0002t0001g0292 | 2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.110+9903C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707506 | ||||||
| chr10:113707549
|
C | G | 26 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+9946C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707549 | ||||||
| chr10:113707652
|
A | G | 1 | a0001c0001t0004g0338 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.110+10049A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707652 | ||||||
| chr10:113707862
|
G | C | 2 | a0001c0001t0005g0108a0001c0012t0002g0107 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+10259G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707862 | ||||||
| chr10:113707898
|
C | T | 39 | a0001c0001t0005g0001a0001c0001t0005g0004a0001c0001t0005g0005others(36): Show | 43 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+10295C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707898 | ||||||
| chr10:113707987
|
C | CAGATTAC others(6): Show |
3 | a0002c0002t0001g0304a0002c0002t0001g0306a0002c0002t0001g0353 | 3 | HG01891.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.110+10386_110+1038 others(17): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113707987 | |||||
| chr10:113708081
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.110+10478G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708081 | ||||||
| chr10:113708147
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0102a0003c0003t0002g0148 | 4 | HG02559.hp2 HG02717.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+10544C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708147 | ||||||
| chr10:113708239
|
A | G | 12 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.110+10636A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708239 | ||||||
| chr10:113708277
|
G | T | 4 | a0001c0001t0004g0015a0001c0001t0004g0267a0001c0001t0004g0268others(1): Show | 5 | HG02572.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+10674G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708277 | ||||||
| chr10:113708356
|
T | C | 1 | a0001c0001t0005g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.110+10753T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708356 | ||||||
| chr10:113708535
|
A | G | 1 | a0002c0002t0001g0360 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.110+10932A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708535 | ||||||
| chr10:113708567
|
C | T | 1 | a0003c0003t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+10964C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708567 | ||||||
| chr10:113708928
|
G | C | 54 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(51): Show | 54 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+11325G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708928 | ||||||
| chr10:113709009
|
T | C | 94 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(91): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.110+11406T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709009 | ||||||
| chr10:113709013
|
CCT | C | 94 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(91): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.110+11411_110+1141 others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709013 | ||||||
| chr10:113709018
|
C | T | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+11415C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709018 | ||||||
| chr10:113709049
|
C | T | 38 | a0001c0001t0005g0001a0001c0001t0005g0004a0001c0001t0005g0005others(35): Show | 42 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.110+11446C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709049 | ||||||
| chr10:113709090
|
C | G | 1 | a0001c0001t0004g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+11487C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709090 | ||||||
| chr10:113709184
|
G | A | 1 | a0001c0001t0004g0089 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.110+11581G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709184 | ||||||
| chr10:113709225
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.110+11622C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709225 | ||||||
| chr10:113709603
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-11429C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709603 | ||||||
| chr10:113709791
|
G | A | 1 | a0002c0002t0001g0299 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.111-11241G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709791 | ||||||
| chr10:113709866
|
C | G | 214 | a0001c0001t0002g0010a0001c0001t0002g0103a0001c0001t0002g0106others(211): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.111-11166C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709866 | ||||||
| chr10:113709951
|
G | A | 129 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(126): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.111-11081G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709951 | ||||||
| chr10:113710005
|
A | G | 3 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0231 | 3 | HG02451.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.111-11027A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710005 | ||||||
| chr10:113710131
|
G | A | 65 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(62): Show | 67 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.111-10901G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710131 | ||||||
| chr10:113710233
|
C | T | 56 | a0001c0001t0003g0346a0001c0001t0003g0348a0001c0001t0004g0022others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.111-10799C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710233 | ||||||
| chr10:113710309
|
C | T | 1 | a0001c0005t0002g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111-10723C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710309 | ||||||
| chr10:113710335
|
T | C | 2 | a0001c0001t0005g0038a0001c0001t0005g0046 | 2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.111-10697T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710335 | ||||||
| chr10:113710344
|
T | G | 1 | a0001c0001t0003g0177 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.111-10688T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710344 | ||||||
| chr10:113710685
|
G | A | 3 | a0001c0001t0005g0382a0001c0001t0005g0384a0002c0002t0001g0383 | 3 | HG01109.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.111-10347G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710685 | ||||||
| chr10:113710697
|
C | G | 2 | a0002c0002t0001g0291a0002c0002t0001g0292 | 2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.111-10335C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710697 | ||||||
| chr10:113710735
|
A | T | 1 | a0001c0001t0003g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.111-10297A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710735 | ||||||
| chr10:113710831
|
A | G | 5 | a0001c0001t0004g0068a0001c0001t0004g0080a0001c0001t0004g0094others(2): Show | 5 | HG00735.hp1 HG01070.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-10201A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710831 | ||||||
| chr10:113711257
|
T | G | 128 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(125): Show | 135 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.111-9775T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711257 | ||||||
| chr10:113711270
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-9762T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711270 | ||||||
| chr10:113711310
|
C | G | 1 | a0001c0001t0004g0338 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.111-9722C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711310 | ||||||
| chr10:113711523
|
G | A | 1 | a0003c0003t0019g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.111-9509G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711523 | ||||||
| chr10:113711802
|
A | G | 343 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(340): Show | 360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.111-9230A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711802 | ||||||
| chr10:113712014
|
A | G | 343 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(340): Show | 360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.111-9018A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712014 | ||||||
| chr10:113712039
|
C | T | 4 | a0001c0001t0004g0259a0001c0001t0004g0261a0001c0001t0004g0262others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-8993C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712039 | ||||||
| chr10:113712161
|
C | T | 1 | a0002c0002t0001g0356 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.111-8871C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712161 | ||||||
| chr10:113712354
|
G | C | 39 | a0001c0001t0005g0001a0001c0001t0005g0004a0001c0001t0005g0005others(36): Show | 43 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.111-8678G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712354 | ||||||
| chr10:113712523
|
T | C | 6 | a0003c0003t0002g0007a0003c0003t0002g0121a0003c0003t0002g0122others(3): Show | 7 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-8509T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712523 | ||||||
| chr10:113712562
|
C | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.111-8470C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712562 | ||||||
| chr10:113712575
|
C | G | 1 | a0002c0002t0001g0303 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.111-8457C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712575 | ||||||
| chr10:113712683
|
T | G | 1 | a0002c0002t0001g0320 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.111-8349T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712683 | ||||||
| chr10:113712691
|
C | T | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | NA18747.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.111-8341C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712691 | ||||||
| chr10:113712698
|
G | A | 1 | a0002c0002t0001g0367 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.111-8334G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712698 | ||||||
| chr10:113712802
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.111-8230G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712802 | ||||||
| chr10:113712833
|
A | G | 1 | a0001c0011t0017g0386 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.111-8199A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712833 | ||||||
| chr10:113712838
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-8194G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712838 | ||||||
| chr10:113712960
|
G | A | 280 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(277): Show | 293 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.111-8072G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712960 | ||||||
| chr10:113713029
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.111-8003C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713029 | ||||||
| chr10:113713153
|
C | G | 24 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.111-7879C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713153 | ||||||
| chr10:113713216
|
T | TA | 111 | a0001c0001t0002g0311a0001c0001t0002g0326a0001c0001t0002g0328others(108): Show | 118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.111-7807dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113713216 | |||||
| chr10:113713497
|
C | G | 90 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(87): Show | 94 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.111-7535C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713497 | ||||||
| chr10:113713628
|
C | CTGT | 37 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(34): Show | 38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7403_111-7402i others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113713628 | |||||
| chr10:113713628
|
CT | C | 345 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(342): Show | 362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.111-7394delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113713628 | |||||
| chr10:113713637
|
T | C | 1 | a0001c0001t0004g0268 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.111-7395T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713637 | ||||||
| chr10:113713736
|
G | C | 1 | a0001c0001t0004g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.111-7296G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713736 | ||||||
| chr10:113713832
|
A | C | 1 | a0001c0001t0005g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.111-7200A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713832 | ||||||
| chr10:113713933
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.111-7099T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713933 | ||||||
| chr10:113714206
|
C | T | 1 | a0002c0006t0001g0105 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.111-6826C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714206 | ||||||
| chr10:113714277
|
C | G | 37 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(34): Show | 38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-6755C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714277 | ||||||
| chr10:113714362
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.111-6670G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714362 | ||||||
| chr10:113714475
|
G | T | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-6557G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714475 | ||||||
| chr10:113714590
|
A | G | 92 | a0001c0001t0002g0010a0001c0001t0002g0181a0001c0001t0002g0193others(89): Show | 96 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.111-6442A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714590 | ||||||
| chr10:113714804
|
T | TA | 16 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0234others(13): Show | 17 | HG01081.hp2 HG01109.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.111-6228_111-6227i others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714804 | ||||||
| chr10:113714805
|
T | A | 104 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(101): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.111-6227T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714805 | ||||||
| chr10:113714806
|
T | A | 13 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0234others(10): Show | 14 | HG01081.hp2 HG01109.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-6226T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714806 | ||||||
| chr10:113714807
|
T | A | 101 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(98): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.111-6225T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714807 | ||||||
| chr10:113714808
|
T | A | 6 | a0001c0001t0002g0258a0001c0001t0004g0008a0001c0001t0004g0152others(3): Show | 7 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-6224T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714808 | ||||||
| chr10:113714809
|
T | A | 41 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(38): Show | 42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.111-6223T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714809 | ||||||
| chr10:113714811
|
T | A | 37 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(34): Show | 38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-6221T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714811 | ||||||
| chr10:113715033
|
G | A | 2 | a0001c0001t0004g0069a0001c0001t0004g0070 | 2 | NA18945.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.111-5999G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715033 | ||||||
| chr10:113715362
|
C | T | 5 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-5670C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715362 | ||||||
| chr10:113715363
|
G | A | 3 | a0001c0001t0005g0019a0001c0005t0002g0020a0002c0002t0001g0294 | 3 | HG02559.hp1 HG02895.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.111-5669G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715363 | ||||||
| chr10:113715455
|
G | A | 37 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(34): Show | 38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-5577G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715455 | ||||||
| chr10:113715472
|
A | C | 1 | a0003c0003t0002g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111-5560A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715472 | ||||||
| chr10:113715588
|
A | G | 382 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(379): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): Show |
intron_variant | MODIFIER | c.111-5444A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715588 | ||||||
| chr10:113715639
|
A | G | 2 | a0001c0001t0003g0171a0001c0001t0003g0190 | 2 | NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.111-5393A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715639 | ||||||
| chr10:113715682
|
G | A | 74 | a0001c0001t0004g0374a0001c0001t0005g0315a0002c0002t0001g0002others(71): Show | 79 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.111-5350G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715682 | ||||||
| chr10:113715748
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111-5284G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715748 | ||||||
| chr10:113715864
|
A | C | 60 | a0001c0001t0003g0210a0001c0001t0003g0216a0001c0001t0003g0218others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.111-5168A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715864 | ||||||
| chr10:113715869
|
T | C | 60 | a0001c0001t0003g0210a0001c0001t0003g0216a0001c0001t0003g0218others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.111-5163T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715869 | ||||||
| chr10:113715870
|
C | T | 60 | a0001c0001t0003g0210a0001c0001t0003g0216a0001c0001t0003g0218others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.111-5162C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715870 | ||||||
| chr10:113716043
|
C | T | 1 | a0003c0003t0002g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111-4989C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716043 | ||||||
| chr10:113716045
|
A | G | 36 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(33): Show | 37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-4987A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716045 | ||||||
| chr10:113716053
|
G | A | 1 | a0002c0002t0001g0367 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.111-4979G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716053 | ||||||
| chr10:113716069
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.111-4963A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716069 | ||||||
| chr10:113716283
|
C | T | 151 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(148): Show | 159 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.111-4749C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716283 | ||||||
| chr10:113716348
|
TTGTC | T | 151 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(148): Show | 159 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.111-4678_111-4675d others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113716348 | |||||
| chr10:113716379
|
C | T | 151 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(148): Show | 159 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.111-4653C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716379 | ||||||
| chr10:113716510
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111-4522G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716510 | ||||||
| chr10:113716642
|
G | A | 1 | a0001c0001t0004g0075 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.111-4390G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716642 | ||||||
| chr10:113716769
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.111-4263C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716769 | ||||||
| chr10:113716831
|
A | G | 1 | a0002c0002t0001g0351 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.111-4201A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716831 | ||||||
| chr10:113716849
|
T | C | 1 | a0002c0002t0001g0029 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.111-4183T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716849 | ||||||
| chr10:113716858
|
T | C | 1 | a0002c0002t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.111-4174T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716858 | ||||||
| chr10:113716860
|
T | C | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-4172T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716860 | ||||||
| chr10:113716931
|
C | T | 1 | a0002c0002t0001g0298 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.111-4101C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716931 | ||||||
| chr10:113717101
|
A | G | 11 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0234others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-3931A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717101 | ||||||
| chr10:113717404
|
G | A | 146 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(143): Show | 153 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.111-3628G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717404 | ||||||
| chr10:113717544
|
A | AAAAT | 6 | a0001c0001t0004g0049a0001c0001t0004g0067a0001c0001t0004g0075others(3): Show | 6 | HG00642.hp2 HG01358.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-3472_111-3469d others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113717544 | |||||
| chr10:113717680
|
T | A | 36 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(33): Show | 37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-3352T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717680 | ||||||
| chr10:113717811
|
T | C | 2 | a0002c0002t0001g0281a0002c0002t0001g0301 | 2 | NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.111-3221T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717811 | ||||||
| chr10:113717817
|
A | C | 1 | a0001c0012t0002g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111-3215A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717817 | ||||||
| chr10:113717860
|
T | C | 2 | a0001c0001t0005g0019a0001c0005t0002g0020 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-3172T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717860 | ||||||
| chr10:113717947
|
T | C | 1 | a0002c0002t0001g0343 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111-3085T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717947 | ||||||
| chr10:113718036
|
A | AG | 387 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(384): Show | 405 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.111-2995dupG | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113718036 | |||||
| chr10:113718049
|
A | C | 1 | a0001c0001t0005g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.111-2983A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718049 | ||||||
| chr10:113718095
|
C | A | 2 | a0002c0002t0001g0320a0004c0004t0001g0109 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.111-2937C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718095 | ||||||
| chr10:113718142
|
C | A | 1 | a0004c0004t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.111-2890C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718142 | ||||||
| chr10:113718255
|
A | G | 1 | a0001c0001t0005g0017 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.111-2777A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718255 | ||||||
| chr10:113718367
|
T | C | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2665T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718367 | ||||||
| chr10:113718411
|
C | G | 283 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(280): Show | 296 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.111-2621C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718411 | ||||||
| chr10:113718863
|
C | T | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2169C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718863 | ||||||
| chr10:113718864
|
A | C | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2168A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718864 | ||||||
| chr10:113718918
|
A | G | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2114A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718918 | ||||||
| chr10:113719069
|
G | A | 1 | a0002c0002t0001g0164 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.111-1963G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719069 | ||||||
| chr10:113719194
|
G | A | 2 | a0001c0001t0004g0008a0001c0001t0004g0153 | 3 | HG02486.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.111-1838G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719194 | ||||||
| chr10:113719221
|
G | A | 36 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(33): Show | 37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-1811G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719221 | ||||||
| chr10:113719232
|
G | A | 1 | a0003c0003t0002g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.111-1800G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719232 | ||||||
| chr10:113719402
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.111-1630G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719402 | ||||||
| chr10:113719509
|
C | T | 21 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(18): Show | 22 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.111-1523C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719509 | ||||||
| chr10:113719607
|
A | C | 1 | a0001c0001t0002g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-1425A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719607 | ||||||
| chr10:113720025
|
C | A | 24 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.111-1007C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720025 | ||||||
| chr10:113720316
|
C | G | 2 | a0002c0002t0001g0291a0002c0002t0001g0292 | 2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.111-716C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720316 | ||||||
| chr10:113720323
|
G | A | 2 | a0002c0002t0001g0342a0002c0002t0001g0343 | 2 | HG00140.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.111-709G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720323 | ||||||
| chr10:113720391
|
A | G | 1 | a0004c0004t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.111-641A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720391 | ||||||
| chr10:113720468
|
G | C | 1 | a0003c0003t0002g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.111-564G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720468 | ||||||
| chr10:113720501
|
C | T | 1 | a0002c0002t0001g0351 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.111-531C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720501 | ||||||
| chr10:113720764
|
C | T | 1 | a0002c0002t0001g0321 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111-268C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720764 | ||||||
| chr10:113720823
|
T | C | 283 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(280): Show | 296 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.111-209T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720823 | ||||||
| chr10:113720998
|
C | T | 5 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0234others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-34C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720998 | ||||||
| chr10:113721005
|
T | C | 1 | a0003c0003t0002g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.111-27T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113721005 | ||||||
| chr10:113721171
|
G | A | 1 | a0001c0001t0005g0026 | 1 | NA18998.hp2 | splice_region_variant&intron_variant | LOW | c.247+3G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721171 | ||||||
| chr10:113721177
|
G | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0234others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+9G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721177 | ||||||
| chr10:113721259
|
C | T | 111 | a0001c0001t0002g0311a0001c0001t0002g0326a0001c0001t0002g0328others(108): Show | 117 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.247+91C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721259 | ||||||
| chr10:113721308
|
A | T | 2 | a0002c0002t0001g0330a0002c0002t0001g0369 | 2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.247+140A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721308 | ||||||
| chr10:113721537
|
G | T | 1 | a0001c0001t0006g0090 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.248-114G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721537 | ||||||
| chr10:113721547
|
G | A | 11 | a0002c0002t0001g0248a0002c0002t0001g0265a0002c0002t0001g0273others(8): Show | 11 | HG00423.hp1 HG01257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.248-104G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721547 | ||||||
| chr10:113721551
|
C | T | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.248-100C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721551 | ||||||
| chr10:113721586
|
G | A | 1 | a0004c0004t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.248-65G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721586 | ||||||
| chr10:113721599
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.248-52A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721599 | ||||||
| chr10:113721907
|
AT | A | 40 | a0001c0001t0003g0229a0001c0001t0004g0022a0001c0001t0004g0023others(37): Show | 40 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.376+143delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113721907 | |||||
| chr10:113722028
|
A | C | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.376+249A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722028 | ||||||
| chr10:113722069
|
G | A | 1 | a0001c0001t0004g0228 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.376+290G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722069 | ||||||
| chr10:113722099
|
C | T | 1 | a0002c0002t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.376+320C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722099 | ||||||
| chr10:113722138
|
G | T | 1 | a0001c0005t0002g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.376+359G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722138 | ||||||
| chr10:113722150
|
A | G | 1 | a0001c0001t0004g0095 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376+371A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722150 | ||||||
| chr10:113722229
|
G | T | 1 | a0002c0006t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.376+450G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722229 | ||||||
| chr10:113722233
|
A | G | 36 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(33): Show | 37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.376+454A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722233 | ||||||
| chr10:113722558
|
C | T | 1 | a0002c0002t0001g0376 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.376+779C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722558 | ||||||
| chr10:113722847
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.376+1068G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722847 | ||||||
| chr10:113722878
|
A | T | 1 | a0001c0001t0002g0307 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.376+1099A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722878 | ||||||
| chr10:113722897
|
AAAAAT | A | 8 | a0001c0001t0005g0017a0001c0001t0005g0051a0001c0001t0005g0052others(5): Show | 8 | HG02647.hp2 HG03540.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.376+1128_376+1132d others(7): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113722897 | |||||
| chr10:113722970
|
C | T | 2 | a0001c0001t0004g0008a0001c0001t0004g0153 | 3 | HG02486.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.376+1191C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722970 | ||||||
| chr10:113723145
|
C | G | 1 | a0001c0001t0004g0093 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.376+1366C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723145 | ||||||
| chr10:113723173
|
A | C | 1 | a0001c0001t0006g0064 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.376+1394A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723173 | ||||||
| chr10:113723174
|
C | A | 1 | a0001c0001t0006g0064 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.376+1395C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723174 | ||||||
| chr10:113723202
|
CT | C | 273 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(270): Show | 285 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.376+1436delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113723202 | |||||
| chr10:113723214
|
T | A | 1 | a0003c0003t0002g0138 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.376+1435T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723214 | ||||||
| chr10:113723215
|
T | A | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.376+1436T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723215 | ||||||
| chr10:113723224
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.376+1445G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723224 | ||||||
| chr10:113723363
|
G | A | 1 | a0001c0001t0006g0065 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.376+1584G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723363 | ||||||
| chr10:113723367
|
C | A | 1 | a0001c0001t0005g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.376+1588C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723367 | ||||||
| chr10:113723504
|
G | C | 3 | a0001c0001t0004g0259a0001c0001t0004g0261a0001c0001t0004g0262 | 3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.376+1725G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723504 | ||||||
| chr10:113723676
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.377-1686A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723676 | ||||||
| chr10:113723689
|
G | T | 1 | a0001c0001t0002g0242 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.377-1673G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723689 | ||||||
| chr10:113723725
|
A | ATTTT | 55 | a0001c0001t0003g0210a0001c0001t0003g0216a0001c0001t0003g0218others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.377-1622_377-1619d others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113723725 | |||||
| chr10:113723725
|
AT | A | 6 | a0001c0001t0003g0186a0001c0001t0004g0374a0001c0001t0005g0045others(3): Show | 6 | HG01069.hp1 HG01256.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-1619delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113723725 | |||||
| chr10:113723853
|
C | T | 39 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0312others(36): Show | 40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.377-1509C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723853 | ||||||
| chr10:113723854
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.377-1508G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723854 | ||||||
| chr10:113724247
|
C | T | 24 | a0001c0001t0002g0012a0001c0001t0002g0241a0001c0001t0002g0242others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.377-1115C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724247 | ||||||
| chr10:113724271
|
A | G | 5 | a0002c0002t0001g0248a0002c0002t0001g0265a0002c0002t0001g0273others(2): Show | 5 | HG00423.hp1 NA19003.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-1091A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724271 | ||||||
| chr10:113724370
|
C | T | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG01081.hp1 HG01168.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-992C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724370 | ||||||
| chr10:113724424
|
T | C | 186 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(183): Show | 194 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.377-938T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724424 | ||||||
| chr10:113724441
|
T | G | 147 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0002g0106others(144): Show | 154 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.377-921T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724441 | ||||||
| chr10:113724477
|
T | C | 1 | a0001c0001t0003g0324 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377-885T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724477 | ||||||
| chr10:113724667
|
TTTTG | T | 7 | a0001c0001t0004g0060a0001c0001t0004g0069a0001c0001t0004g0070others(4): Show | 7 | HG02083.hp2 NA18943.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-691_377-688del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113724667 | |||||
| chr10:113724690
|
C | T | 44 | a0001c0001t0002g0307a0001c0001t0002g0309a0001c0001t0002g0311others(41): Show | 45 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.377-672C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724690 | ||||||
| chr10:113724785
|
C | CT | 2 | a0001c0001t0004g0006a0001c0001t0004g0102 | 3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.377-574dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113724785 | |||||
| chr10:113724900
|
A | G | 44 | a0001c0001t0002g0103a0001c0001t0002g0307a0001c0001t0002g0309others(41): Show | 45 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.377-462A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724900 | ||||||
| chr10:113724901
|
G | A | 194 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(191): Show | 202 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.377-461G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724901 | ||||||
| chr10:113725017
|
G | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0153a0001c0001t0004g0259others(2): Show | 6 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-345G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113725017 | ||||||
| chr10:113725059
|
C | T | 1 | a0001c0001t0005g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.377-303C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113725059 | ||||||
| chr10:113725254
|
C | T | 1 | a0003c0003t0002g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.377-108C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113725254 | ||||||
| chr10:113725541
|
ATCTCTTT others(11): Show |
A | 1 | a0005c0009t0003g0204 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.552+5_552+22delTCT others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725541 | ||||||
| chr10:113725582
|
G | GCAGAGTG others(79): Show |
3 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0001t0002g0381 | 3 | HG02258.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.552+121_552+206dup others(86): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr10 | 113725582 | |||||
| chr10:113725641
|
T | C | 45 | a0001c0001t0002g0103a0001c0001t0002g0307a0001c0001t0002g0309others(42): Show | 46 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.552+104T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725641 | ||||||
| chr10:113725651
|
T | C | 3 | a0001c0001t0004g0015a0001c0001t0004g0267a0001c0001t0004g0268 | 4 | HG02886.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+114T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725651 | ||||||
| chr10:113725687
|
A | G | 2 | a0001c0001t0004g0022a0001c0001t0004g0023 | 2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.552+150A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725687 | ||||||
| chr10:113725695
|
T | C | 6 | a0002c0002t0001g0162a0002c0002t0001g0284a0002c0002t0001g0289others(3): Show | 6 | HG02027.hp1 NA18946.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+158T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725695 | ||||||
| chr10:113725728
|
A | G | 4 | a0001c0001t0003g0212a0001c0001t0003g0214a0001c0001t0003g0240others(1): Show | 4 | HG01884.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+191A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725728 | ||||||
| chr10:113725857
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.552+320G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725857 | ||||||
| chr10:113725961
|
A | G | 4 | a0001c0001t0004g0008a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 5 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-344A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725961 | ||||||
| chr10:113725966
|
T | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0050 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.553-339T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725966 | ||||||
| chr10:113726064
|
G | A | 6 | a0001c0001t0003g0225a0001c0001t0007g0011a0001c0001t0007g0221others(3): Show | 7 | NA18969.hp1 NA18971.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-241G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113726064 | ||||||
| chr10:113726131
|
T | C | 3 | a0001c0001t0004g0259a0001c0001t0004g0261a0001c0001t0004g0262 | 3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.553-174T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113726131 | ||||||
| chr10:113726269
|
C | G | 1 | a0001c0001t0004g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.553-36C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113726269 | ||||||
| chr10:113726475
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.682+41C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113726475 | ||||||
| chr10:113726837
|
A | C | 3 | a0001c0001t0004g0259a0001c0001t0004g0261a0001c0001t0004g0262 | 3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.682+403A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113726837 | ||||||
| chr10:113726851
|
G | A | 338 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(335): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.682+417G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113726851 | ||||||
| chr10:113727115
|
G | A | 50 | a0001c0001t0003g0009a0001c0001t0003g0149a0001c0001t0003g0160others(47): Show | 52 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.682+681G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727115 | ||||||
| chr10:113727194
|
G | A | 1 | a0001c0001t0005g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.682+760G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727194 | ||||||
| chr10:113727293
|
C | T | 1 | a0001c0001t0004g0096 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.682+859C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727293 | ||||||
| chr10:113727294
|
G | A | 1 | a0003c0003t0019g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.682+860G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727294 | ||||||
| chr10:113727318
|
CTATT | C | 193 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(190): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.682+887_682+890del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727318 | |||||
| chr10:113727712
|
C | T | 1 | a0001c0001t0004g0030 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.682+1278C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727712 | ||||||
| chr10:113727723
|
A | G | 340 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0103others(337): Show | 354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.682+1289A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727723 | ||||||
| chr10:113727734
|
C | G | 138 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0181others(135): Show | 145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.682+1300C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727734 | ||||||
| chr10:113727818
|
A | T | 1 | a0001c0001t0008g0016 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682+1384A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727818 | ||||||
| chr10:113727828
|
C | CA | 69 | a0001c0001t0002g0106a0001c0001t0002g0234a0001c0001t0002g0249others(66): Show | 71 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+1409dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727828 | |||||
| chr10:113727828
|
C | CAA | 6 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(3): Show | 6 | HG02451.hp2 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+1408_682+1409d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727828 | |||||
| chr10:113727991
|
C | CA | 174 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0106others(171): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.683-1299dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727991 | |||||
| chr10:113727991
|
C | CAA | 55 | a0001c0001t0002g0103a0001c0001t0002g0193a0001c0001t0002g0222others(52): Show | 56 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.683-1300_683-1299d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727991 | |||||
| chr10:113727991
|
CAA | C | 74 | a0001c0001t0003g0009a0001c0001t0003g0149a0001c0001t0003g0160others(71): Show | 77 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.683-1300_683-1299d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727991 | |||||
| chr10:113728456
|
A | T | 1 | a0001c0001t0003g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.683-855A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728456 | ||||||
| chr10:113728478
|
C | T | 1 | a0001c0012t0002g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-833C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728478 | ||||||
| chr10:113728572
|
G | A | 109 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0013others(106): Show | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.683-739G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728572 | ||||||
| chr10:113728613
|
G | C | 1 | a0001c0001t0007g0227 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.683-698G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728613 | ||||||
| chr10:113728691
|
G | A | 1 | a0003c0003t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.683-620G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728691 | ||||||
| chr10:113728815
|
A | G | 3 | a0002c0002t0001g0313a0002c0002t0001g0368a0002c0002t0012g0358 | 3 | HG01928.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.683-496A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728815 | ||||||
| chr10:113729056
|
G | A | 4 | a0001c0001t0005g0108a0001c0001t0005g0266a0001c0001t0005g0382others(1): Show | 4 | HG01081.hp2 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-255G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729056 | ||||||
| chr10:113729060
|
T | G | 2 | a0001c0005t0002g0020a0001c0005t0002g0264 | 2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.683-251T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729060 | ||||||
| chr10:113729172
|
A | T | 1 | a0001c0012t0002g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-139A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729172 | ||||||
| chr10:113729219
|
G | A | 1 | a0001c0001t0005g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.683-92G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729219 | ||||||
| chr10:113729259
|
A | T | 1 | a0001c0001t0003g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.683-52A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729259 | ||||||
| chr10:113729298
|
T | C | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.683-13T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729298 |