Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84698 |
|---|---|
| ensemblid | ENSG00000180881.21 |
| hgncid | 16471 |
| symbol | CAPS2 |
| name | calcyphosine 2 |
| refseq_nuc | NM_001355024.4 |
| refseq_prot | NP_001341953.2 |
| ensembl_nuc | ENST00000699294.1 |
| ensembl_prot | ENSP00000514274.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 75275979 |
| end | 75330324 |
| strand | - |
| ver | v1.2 |
| region | chr12:75275979-75330324 |
| region5000 | chr12:75270979-75335324 |
| regionname0 | CAPS2_chr12_75275979_75330324 |
| regionname5000 | CAPS2_chr12_75270979_75335324 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 557 | 289 | 69 | 53 | 118 | 10 | 37 | 86 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002 | 0/0 | 557 | 70 | 12 | 15 | 36 | 5 | 2 | 27 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0003 | 0/0 | 557 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0004 | 0/0 | 557 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0005 | 0/0 | 557 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0006 | 0/0 | 557 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0007 | 0/0 | 557 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0008 | 0/0 | 557 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0009 | 0/0 | 557 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1674 | 280 | 66 | 52 | 115 | 9 | 36 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0002 | 0/0 | 1674 | 63 | 10 | 11 | 36 | 4 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0003 | 0/0 | 1674 | 6 | 3 | 1 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0004 | 0/0 | 1674 | 5 | 0 | 4 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0005 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0006 | 0/0 | 1674 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0007 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0008 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0009 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0010 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0011 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0012 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0013 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0014 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0015 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| c0016 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3398 | 172 | 28 | 40 | 83 | 10 | 11 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0002 | 0/0 | 3398 | 76 | 13 | 4 | 39 | 0 | 20 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0003 | 1/0 | 3399 | 26 | 0 | 17 | 1 | 3 | 4 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0004 | 0/0 | 3398 | 19 | 13 | 1 | 0 | 2 | 3 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0005 | 0/0 | 3397 | 16 | 0 | 1 | 14 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0006 | 0/0 | 3398 | 10 | 0 | 0 | 9 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0007 | 0/0 | 3398 | 7 | 7 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0008 | 0/0 | 3398 | 5 | 5 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0009 | 0/1 | 3399 | 4 | 0 | 2 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0010 | 0/0 | 3397 | 4 | 4 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0011 | 0/0 | 3398 | 4 | 0 | 2 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0012 | 0/0 | 3398 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0013 | 0/0 | 3398 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0014 | 0/0 | 3398 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0015 | 0/0 | 3398 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0016 | 0/0 | 3395 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0017 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0018 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0019 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0020 | 0/0 | 3399 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0021 | 0/0 | 3399 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0022 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0023 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0024 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0025 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0026 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0027 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0028 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0029 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0030 | 0/0 | 3398 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0031 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0032 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| t0033 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0011 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0318 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1674 | 280 | 66 | 52 | 115 | 9 | 36 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0003 | 0/0 | 1674 | 6 | 3 | 1 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0010 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0013 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0014 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002 | 0/0 | 1674 | 63 | 10 | 11 | 36 | 4 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0004 | 0/0 | 1674 | 5 | 0 | 4 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0008 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0003c0007 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0004c0006 | 0/0 | 1674 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0005c0009 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0005c0016 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0006c0005 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0007c0011 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0008c0012 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0009c0015 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5071 | 104 | 20 | 24 | 50 | 3 | 7 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0002 | 0/0 | 5071 | 69 | 11 | 4 | 37 | 0 | 17 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0003 | 1/0 | 5072 | 25 | 0 | 16 | 1 | 3 | 4 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0004 | 0/0 | 5071 | 19 | 13 | 1 | 0 | 2 | 3 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0005 | 0/0 | 5070 | 16 | 0 | 1 | 14 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0006 | 0/0 | 5071 | 10 | 0 | 0 | 9 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0007 | 0/0 | 5071 | 7 | 7 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0008 | 0/0 | 5071 | 4 | 4 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0009 | 0/1 | 5072 | 4 | 0 | 2 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0010 | 0/0 | 5070 | 3 | 3 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0011 | 0/0 | 5071 | 4 | 0 | 2 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0012 | 0/0 | 5071 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0013 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0014 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0018 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0020 | 0/0 | 5072 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0021 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0022 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0024 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0026 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0027 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0029 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0030 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0001t0033 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0003t0001 | 0/0 | 5071 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0003t0002 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0003t0014 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0003t0031 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0003t0032 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0010t0001 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0013t0001 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0001c0014t0002 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0001 | 0/0 | 5071 | 51 | 6 | 10 | 30 | 4 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0002 | 0/0 | 5071 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0003 | 0/0 | 5072 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0008 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0010 | 0/0 | 5070 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0015 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0017 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0019 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0023 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0025 | 0/0 | 5070 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0002t0028 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0004t0001 | 0/0 | 5071 | 5 | 0 | 4 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0002c0008t0001 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0003c0007t0001 | 0/0 | 5071 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0004c0006t0016 | 0/0 | 5068 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0005c0009t0001 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0005c0016t0001 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0006c0005t0002 | 0/0 | 5071 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0007c0011t0001 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0008c0012t0001 | 0/0 | 5071 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| a0009c0015t0001 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | copy fasta | chr12 | 75270979 | 75335324 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0318 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0011 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0011g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0013g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0018g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0020g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0021g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0022g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0024g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0026g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0027g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0029g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0030g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0033g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0031g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0032g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0010t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0013t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0014t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0015g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0015g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0017g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0019g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0023g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0025g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0028g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0008t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0008t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0003c0007t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0003c0007t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0004c0006t0016g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0004c0006t0016g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0005c0009t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0005c0016t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0006c0005t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0007c0011t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0008c0012t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0009c0015t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0186 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0101 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0149 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00280 | hp2 | a0001 | c0010 | t0001 | g0066 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0187 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00738 | hp2 | a0002 | c0004 | t0001 | g0184 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00741 | hp2 | a0008 | c0012 | t0001 | g0078 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01071 | hp1 | a0002 | c0002 | t0003 | g0188 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0092 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01168 | hp2 | a0001 | c0001 | t0011 | g0127 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01243 | hp1 | a0004 | c0006 | t0016 | g0330 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0018 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01258 | hp2 | a0002 | c0004 | t0001 | g0018 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01261 | hp2 | a0002 | c0004 | t0001 | g0185 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0128 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0118 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0125 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0167 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01516 | hp1 | a0002 | c0004 | t0001 | g0209 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01516 | hp2 | a0009 | c0015 | t0001 | g0163 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01884 | hp1 | a0002 | c0002 | t0010 | g0181 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0079 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02004 | hp2 | a0001 | c0001 | t0020 | g0249 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0316 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02056 | hp2 | a0001 | c0003 | t0032 | g0328 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02083 | hp2 | a0001 | c0013 | t0001 | g0080 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | CDX | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02257 | hp2 | a0002 | c0008 | t0001 | g0219 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0231 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0046 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02683 | hp2 | a0001 | c0014 | t0002 | g0157 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02717 | hp2 | a0002 | c0008 | t0001 | g0218 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0132 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0119 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02735 | hp2 | a0003 | c0007 | t0001 | g0310 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0129 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02818 | hp1 | a0001 | c0001 | t0029 | g0143 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02818 | hp2 | a0001 | c0003 | t0014 | g0045 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02965 | hp1 | a0004 | c0006 | t0016 | g0331 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03017 | hp1 | a0006 | c0005 | t0002 | g0026 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0237 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03195 | hp2 | a0002 | c0002 | t0008 | g0166 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0313 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0146 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0015 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03491 | hp1 | a0006 | c0005 | t0002 | g0026 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0015 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0315 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0220 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03669 | hp1 | a0003 | c0007 | t0001 | g0309 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0256 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0148 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03927 | hp2 | a0007 | c0011 | t0001 | g0050 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0124 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04115 | hp1 | a0002 | c0002 | t0025 | g0199 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04184 | hp2 | a0001 | c0001 | t0021 | g0226 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0126 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18747 | hp1 | a0005 | c0009 | t0001 | g0058 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18747 | hp2 | a0001 | c0001 | t0033 | g0329 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18941 | hp2 | a0001 | c0001 | t0024 | g0033 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18942 | hp1 | a0002 | c0002 | t0028 | g0227 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18963 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18985 | hp1 | a0002 | c0002 | t0017 | g0212 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18990 | hp2 | a0001 | c0001 | t0018 | g0088 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19006 | hp1 | a0002 | c0002 | t0023 | g0179 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19010 | hp2 | a0001 | c0001 | t0030 | g0324 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19078 | hp2 | a0002 | c0002 | t0019 | g0216 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19081 | hp1 | a0001 | c0003 | t0031 | g0327 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19087 | hp2 | a0005 | c0016 | t0001 | g0111 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0011 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0165 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0153 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0170 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02109 | hp1 | a0002 | c0002 | t0015 | g0326 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02559 | hp1 | a0002 | c0002 | t0015 | g0325 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0048 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0162 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0009 | g0011 | REF | REF | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0318 | REF | REF | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75289632
|
C | G | 1 | a0004 | 2 | HG01243.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.1270G>C | p.Val424Leu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/17 | 1757/5072 | 1270/1674 | 424/557 | chr12 | 75289632 | ||
| chr12:75293259
|
C | T | 1 | a0008 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.1039G>A | p.Asp347Asn | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/17 | 1526/5072 | 1039/1674 | 347/557 | chr12 | 75293259 | ||
| chr12:75298772
|
A | G | 2 | a0003a0007 | 3 | HG02735.hp2 HG03669.hp1 HG03927.hp2 |
missense_variant | MODERATE | c.845T>C | p.Val282Ala | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/17 | 1332/5072 | 845/1674 | 282/557 | chr12 | 75298772 | ||
| chr12:75312889
|
T | G | 1 | a0009 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.504A>C | p.Lys168Asn | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/17 | 991/5072 | 504/1674 | 168/557 | chr12 | 75312889 | ||
| chr12:75316434
|
A | G | 1 | a0005 | 2 | NA18747.hp1 NA19087.hp2 |
missense_variant&splice_region_variant | MODERATE | c.355T>C | p.Cys119Arg | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/17 | 842/5072 | 355/1674 | 119/557 | chr12 | 75316434 | ||
| chr12:75321550
|
C | A | 2 | a0002a0003 | 72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
missense_variant | MODERATE | c.204G>T | p.Leu68Phe | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/17 | 691/5072 | 204/1674 | 68/557 | chr12 | 75321550 | ||
| chr12:75321574
|
A | T | 1 | a0006 | 2 | HG03017.hp1 HG03491.hp1 |
missense_variant&splice_region_variant | MODERATE | c.180T>A | p.Asp60Glu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/17 | 667/5072 | 180/1674 | 60/557 | chr12 | 75321574 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75289725
|
A | G | 1 | a0001c0013 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1177T>C | p.Leu393Leu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/17 | 1664/5072 | 1177/1674 | 393/557 | chr12 | 75289725 | ||
| chr12:75299911
|
C | T | 2 | a0001c0010a0002c0004 | 6 | HG00280.hp2 HG00738.hp2 HG01256.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.666G>A | p.Lys222Lys | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/17 | 1153/5072 | 666/1674 | 222/557 | chr12 | 75299911 | ||
| chr12:75304768
|
T | C | 1 | a0001c0014 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.654A>G | p.Leu218Leu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/17 | 1141/5072 | 654/1674 | 218/557 | chr12 | 75304768 | ||
| chr12:75304855
|
C | T | 2 | a0001c0003a0004c0006 | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
synonymous_variant | LOW | c.567G>A | p.Glu189Glu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/17 | 1054/5072 | 567/1674 | 189/557 | chr12 | 75304855 | ||
| chr12:75323198
|
G | A | 2 | a0002c0008a0005c0016 | 3 | HG02257.hp2 HG02717.hp2 NA19087.hp2 |
synonymous_variant | LOW | c.156C>T | p.Ser52Ser | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/17 | 643/5072 | 156/1674 | 52/557 | chr12 | 75323198 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75275986
|
T | TA | 1 | a0001c0001t0009 | 4 | HG01109.hp2 HG01952.hp1 NA20752.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2903_*2904insT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2903 | chr12 | 75275986 | |||||
| chr12:75276003
|
A | C | 1 | a0001c0001t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2887T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2887 | chr12 | 75276003 | |||||
| chr12:75276048
|
C | A | 2 | a0001c0001t0013a0001c0003t0031 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2842G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2842 | chr12 | 75276048 | |||||
| chr12:75276229
|
T | A | 1 | a0002c0002t0023 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2661A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2661 | chr12 | 75276229 | |||||
| chr12:75276667
|
T | G | 2 | a0001c0001t0008a0002c0002t0008 | 5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2223A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2223 | chr12 | 75276667 | |||||
| chr12:75276733
|
G | A | 1 | a0001c0001t0021 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2157C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2157 | chr12 | 75276733 | |||||
| chr12:75276769
|
G | C | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(11): Show | 123 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2121C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2121 | chr12 | 75276769 | |||||
| chr12:75276783
|
C | T | 1 | a0001c0001t0030 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2107 | chr12 | 75276783 | |||||
| chr12:75276938
|
T | C | 1 | a0001c0001t0024 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1952 | chr12 | 75276938 | |||||
| chr12:75277186
|
C | T | 2 | a0001c0001t0010a0002c0002t0010 | 4 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1704G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1704 | chr12 | 75277186 | |||||
| chr12:75277210
|
CT | C | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*1679delA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1679 | chr12 | 75277210 | |||||
| chr12:75277210
|
CTT | C | 4 | a0001c0001t0005a0001c0001t0010a0002c0002t0010others(1): Show | 21 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1678_*1679delAA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1678 | chr12 | 75277210 | |||||
| chr12:75277326
|
T | A | 2 | a0001c0001t0014a0001c0003t0014 | 2 | HG02818.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1564A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1564 | chr12 | 75277326 | |||||
| chr12:75277342
|
C | T | 1 | a0004c0006t0016 | 2 | HG01243.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1548G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1548 | chr12 | 75277342 | |||||
| chr12:75277491
|
T | C | 2 | a0001c0001t0004a0001c0001t0011 | 23 | HG00280.hp1 HG01109.hp1 HG01168.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1399A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1399 | chr12 | 75277491 | |||||
| chr12:75277519
|
A | T | 1 | a0001c0001t0020 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1371 | chr12 | 75277519 | |||||
| chr12:75277603
|
A | G | 1 | a0002c0002t0019 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1287 | chr12 | 75277603 | |||||
| chr12:75277880
|
A | G | 2 | a0001c0001t0013a0001c0003t0031 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1010T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1010 | chr12 | 75277880 | |||||
| chr12:75278051
|
T | C | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 839 | chr12 | 75278051 | |||||
| chr12:75278092
|
G | A | 1 | a0001c0001t0011 | 4 | HG01168.hp2 HG01361.hp1 HG03490.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*798C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 798 | chr12 | 75278092 | |||||
| chr12:75278158
|
G | T | 1 | a0001c0001t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 732 | chr12 | 75278158 | |||||
| chr12:75278159
|
G | T | 1 | a0001c0001t0012 | 2 | HG01496.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*731C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 731 | chr12 | 75278159 | |||||
| chr12:75278397
|
T | A | 3 | a0001c0001t0006a0001c0001t0030a0001c0001t0033 | 12 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*493A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 493 | chr12 | 75278397 | |||||
| chr12:75278434
|
C | T | 1 | a0001c0001t0018 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*456G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 456 | chr12 | 75278434 | |||||
| chr12:75278606
|
C | T | 1 | a0002c0002t0017 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 284 | chr12 | 75278606 | |||||
| chr12:75278645
|
T | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 245 | chr12 | 75278645 | |||||
| chr12:75278833
|
T | C | 1 | a0002c0002t0028 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 57 | chr12 | 75278833 | |||||
| chr12:75278883
|
T | C | 2 | a0001c0001t0007a0001c0001t0029 | 8 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 7 | chr12 | 75278883 | |||||
| chr12:75329979
|
T | C | 1 | a0001c0001t0030 | 1 | NA19010.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-142A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/17 | chr12 | 75329979 | ||||||
| chr12:75330099
|
T | C | 1 | a0002c0002t0015 | 2 | HG02109.hp1 HG02559.hp1 |
5_prime_UTR_variant | MODIFIER | c.-262A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/17 | 3601 | chr12 | 75330099 | |||||
| chr12:75330286
|
ACCT | A | 4 | a0001c0001t0033a0001c0003t0031a0001c0003t0032others(1): Show | 5 | HG01243.hp1 HG02056.hp2 HG02965.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-452_-450delAGG | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/17 | 3789 | chr12 | 75330286 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75279325
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1499-260A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279325 | ||||||
| chr12:75279413
|
T | C | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-348A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279413 | ||||||
| chr12:75279515
|
C | G | 2 | a0002c0002t0001g0189a0002c0002t0001g0195 | 2 | HG02071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1499-450G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279515 | ||||||
| chr12:75279599
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1499-534T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279599 | ||||||
| chr12:75279758
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1499-693G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279758 | ||||||
| chr12:75279967
|
T | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(14): Show | 18 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1499-902A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279967 | ||||||
| chr12:75279996
|
C | T | 1 | a0001c0001t0004g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1499-931G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279996 | ||||||
| chr12:75280177
|
G | C | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-1112C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280177 | ||||||
| chr12:75280254
|
G | T | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-1189C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280254 | ||||||
| chr12:75280287
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0235 | 3 | HG02647.hp2 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1499-1222C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280287 | ||||||
| chr12:75280547
|
T | C | 1 | a0002c0002t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1499-1482A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280547 | ||||||
| chr12:75280565
|
G | GAA | 6 | a0001c0010t0001g0066a0002c0004t0001g0018a0002c0004t0001g0184others(3): Show | 7 | HG00280.hp2 HG00738.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499-1502_1499-150 others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280565 | ||||||
| chr12:75280638
|
G | A | 1 | a0001c0013t0001g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1499-1573C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280638 | ||||||
| chr12:75280655
|
A | C | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-1590T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280655 | ||||||
| chr12:75281028
|
T | G | 9 | a0001c0001t0007g0116a0001c0001t0007g0141a0001c0001t0007g0142others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498+1223A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281028 | ||||||
| chr12:75281215
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1498+1036C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281215 | ||||||
| chr12:75281225
|
A | C | 1 | a0005c0016t0001g0111 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1498+1026T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281225 | ||||||
| chr12:75281319
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1498+932A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281319 | ||||||
| chr12:75281407
|
A | G | 1 | a0002c0002t0008g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1498+844T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281407 | ||||||
| chr12:75281414
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1498+837C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281414 | ||||||
| chr12:75281549
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1498+702A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281549 | ||||||
| chr12:75281894
|
T | A | 1 | a0001c0001t0001g0014 | 2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1498+357A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281894 | ||||||
| chr12:75281993
|
A | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0144 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1498+258T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281993 | ||||||
| chr12:75282050
|
A | G | 1 | a0001c0001t0024g0033 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1498+201T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75282050 | ||||||
| chr12:75282380
|
T | C | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1402-33A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282380 | ||||||
| chr12:75282460
|
C | A | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1402-113G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282460 | ||||||
| chr12:75282475
|
C | A | 1 | a0001c0001t0004g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1402-128G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282475 | ||||||
| chr12:75282518
|
C | T | 6 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(3): Show | 7 | HG01168.hp2 HG01361.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1402-171G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282518 | ||||||
| chr12:75282536
|
G | A | 105 | a0001c0001t0002g0005a0001c0001t0002g0021a0001c0001t0002g0022others(102): Show | 118 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1402-189C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282536 | ||||||
| chr12:75282826
|
A | G | 1 | a0001c0001t0012g0119 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1402-479T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282826 | ||||||
| chr12:75282866
|
A | C | 2 | a0001c0003t0002g0046a0001c0003t0002g0047 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1402-519T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282866 | ||||||
| chr12:75283509
|
C | G | 2 | a0001c0003t0002g0046a0001c0003t0002g0047 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1402-1162G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283509 | ||||||
| chr12:75283619
|
G | C | 3 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0003t0031g0327 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1402-1272C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283619 | ||||||
| chr12:75283654
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1401+1307T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283654 | ||||||
| chr12:75283655
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1401+1306T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283655 | ||||||
| chr12:75284057
|
G | A | 1 | a0002c0002t0001g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1401+904C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284057 | ||||||
| chr12:75284234
|
T | A | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1401+727A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284234 | ||||||
| chr12:75284239
|
C | A | 3 | a0001c0001t0002g0302a0001c0001t0014g0131a0001c0003t0014g0045 | 3 | HG02280.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1401+722G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284239 | ||||||
| chr12:75284404
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1401+557A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284404 | ||||||
| chr12:75284435
|
T | C | 5 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0288others(2): Show | 5 | HG02683.hp1 HG03017.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1401+526A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284435 | ||||||
| chr12:75284688
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0001g0235others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+273C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284688 | ||||||
| chr12:75284754
|
T | C | 1 | a0001c0003t0032g0328 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1401+207A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284754 | ||||||
| chr12:75284788
|
T | C | 2 | a0001c0003t0002g0046a0001c0003t0002g0047 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1401+173A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284788 | ||||||
| chr12:75284800
|
G | A | 7 | a0001c0001t0002g0217a0001c0001t0002g0228a0001c0001t0002g0229others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1401+161C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284800 | ||||||
| chr12:75285232
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1282-152G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75285232 | ||||||
| chr12:75285245
|
G | T | 3 | a0001c0001t0002g0302a0001c0001t0014g0131a0001c0003t0014g0045 | 3 | HG02280.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1282-165C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75285245 | ||||||
| chr12:75285462
|
G | A | 1 | a0002c0002t0001g0174 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1282-382C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75285462 | ||||||
| chr12:75286001
|
T | C | 1 | a0001c0001t0007g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1282-921A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286001 | ||||||
| chr12:75286148
|
AAAT | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18944.hp1 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1282-1071_1282-106 others(7): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286148 | ||||||
| chr12:75286367
|
T | C | 1 | a0001c0001t0003g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1282-1287A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286367 | ||||||
| chr12:75286454
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1282-1374T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286454 | ||||||
| chr12:75286553
|
G | T | 4 | a0001c0001t0008g0028a0001c0001t0008g0313a0001c0001t0008g0315others(1): Show | 5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-1473C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286553 | ||||||
| chr12:75286895
|
A | G | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1282-1815T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286895 | ||||||
| chr12:75286973
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1282-1893A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286973 | ||||||
| chr12:75287155
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1282-2075T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287155 | ||||||
| chr12:75287158
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1282-2078C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287158 | ||||||
| chr12:75287258
|
C | T | 3 | a0001c0001t0002g0302a0001c0001t0014g0131a0001c0003t0014g0045 | 3 | HG02280.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1282-2178G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287258 | ||||||
| chr12:75287537
|
T | C | 1 | a0001c0001t0002g0250 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1281+2084A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287537 | ||||||
| chr12:75287600
|
G | A | 4 | a0001c0001t0008g0028a0001c0001t0008g0313a0001c0001t0008g0315others(1): Show | 5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+2021C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287600 | ||||||
| chr12:75287945
|
T | A | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1281+1676A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287945 | ||||||
| chr12:75288008
|
G | C | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1281+1613C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288008 | ||||||
| chr12:75288200
|
G | C | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1281+1421C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288200 | ||||||
| chr12:75288226
|
G | T | 75 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0225others(72): Show | 80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1281+1395C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288226 | ||||||
| chr12:75288327
|
C | G | 1 | a0001c0001t0003g0281 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1281+1294G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288327 | ||||||
| chr12:75288423
|
C | G | 1 | a0001c0001t0007g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1281+1198G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288423 | ||||||
| chr12:75288927
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1281+694G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288927 | ||||||
| chr12:75288983
|
G | C | 12 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0032others(9): Show | 16 | HG01257.hp2 NA18960.hp2 NA18965.hp1 others(13): Show |
intron_variant | MODIFIER | c.1281+638C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288983 | ||||||
| chr12:75289016
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 235 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.1281+605A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289016 | ||||||
| chr12:75289058
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1281+563A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289058 | ||||||
| chr12:75289167
|
A | C | 4 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0001t0021g0226others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+454T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289167 | ||||||
| chr12:75289190
|
T | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0096 | 2 | HG02074.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1281+431A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289190 | ||||||
| chr12:75289234
|
C | T | 82 | a0001c0001t0002g0005a0001c0001t0002g0021a0001c0001t0002g0022others(79): Show | 94 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1281+387G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289234 | ||||||
| chr12:75289803
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1127-28T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75289803 | ||||||
| chr12:75289853
|
A | C | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1127-78T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75289853 | ||||||
| chr12:75289946
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1127-171G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75289946 | ||||||
| chr12:75290223
|
A | C | 2 | a0001c0003t0002g0046a0001c0003t0002g0047 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1127-448T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290223 | ||||||
| chr12:75290331
|
C | G | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1127-556G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290331 | ||||||
| chr12:75290369
|
C | T | 1 | a0006c0005t0002g0026 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1127-594G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290369 | ||||||
| chr12:75290442
|
A | G | 1 | a0002c0002t0001g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1127-667T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290442 | ||||||
| chr12:75290466
|
A | G | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1127-691T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290466 | ||||||
| chr12:75290546
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1127-771C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290546 | ||||||
| chr12:75290654
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1127-879C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290654 | ||||||
| chr12:75290761
|
A | T | 3 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0003t0031g0327 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1126+983T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290761 | ||||||
| chr12:75290935
|
C | A | 1 | a0001c0001t0002g0260 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+809G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290935 | ||||||
| chr12:75290936
|
A | AAAAAAAA others(3): Show |
4 | a0001c0001t0006g0073a0001c0001t0013g0129a0001c0001t0013g0132others(1): Show | 4 | HG02723.hp1 HG02809.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126+798_1126+807d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290936 | ||||||
| chr12:75290936
|
A | AAAAAAAA others(2): Show |
195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1126+807_1126+808i others(11): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290936 | ||||||
| chr12:75290936
|
A | C | 1 | a0001c0001t0002g0260 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+808T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290936 | ||||||
| chr12:75291155
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1126+589T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291155 | ||||||
| chr12:75291294
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1126+450C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291294 | ||||||
| chr12:75291454
|
C | G | 1 | a0001c0001t0002g0306 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1126+290G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291454 | ||||||
| chr12:75291480
|
C | CAT | 31 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0064others(28): Show | 33 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126+262_1126+263d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
C | CATAT | 8 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0068others(5): Show | 8 | HG00280.hp2 HG00544.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126+260_1126+263d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CAT | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(40): Show | 53 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1126+262_1126+263d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATAT | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0040others(33): Show | 37 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1126+260_1126+263d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATATAT | C | 53 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0060others(50): Show | 60 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1126+258_1126+263d others(8): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATATATA others(1): Show |
C | 52 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(49): Show | 55 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1126+256_1126+263d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATATATA others(3): Show |
C | 31 | a0001c0001t0001g0029a0001c0001t0001g0074a0001c0001t0002g0217others(28): Show | 33 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126+254_1126+263d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATATATA others(5): Show |
C | 18 | a0001c0001t0001g0082a0001c0001t0001g0322a0001c0001t0002g0241others(15): Show | 19 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1126+252_1126+263d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATATATA others(7): Show |
C | 3 | a0001c0001t0001g0122a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1126+250_1126+263d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291480
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0003g0160a0001c0001t0004g0117 | 2 | HG01993.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1126+248_1126+263d others(18): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | ||||||
| chr12:75291509
|
A | ATATATAT others(16): Show |
1 | a0002c0002t0001g0213 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1126+234_1126+235i others(25): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291509 | ||||||
| chr12:75291523
|
A | G | 3 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0003t0031g0327 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1126+221T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291523 | ||||||
| chr12:75291533
|
A | T | 4 | a0001c0001t0004g0151a0001c0001t0004g0152a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+211T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291533 | ||||||
| chr12:75291538
|
G | GTA | 115 | a0001c0001t0002g0005a0001c0001t0002g0021a0001c0001t0002g0022others(112): Show | 128 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1126+204_1126+205d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291538 | ||||||
| chr12:75291566
|
AGTATATA others(1): Show |
A | 3 | a0001c0001t0003g0067a0001c0001t0003g0101a0001c0001t0003g0102 | 3 | HG00140.hp2 HG00639.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1126+170_1126+177d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291566 | ||||||
| chr12:75291567
|
G | GTA | 34 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0043others(31): Show | 35 | HG00544.hp2 HG00609.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1126+175_1126+176d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
G | GTATA | 26 | a0001c0001t0001g0037a0001c0001t0002g0022a0001c0001t0002g0242others(23): Show | 28 | HG00673.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+173_1126+176d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
G | GTATATA | 7 | a0001c0001t0001g0029a0001c0001t0001g0099a0001c0001t0002g0243others(4): Show | 9 | HG00438.hp1 HG00621.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1126+171_1126+176d others(8): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0320a0001c0001t0002g0230a0001c0001t0002g0246others(1): Show | 4 | HG02129.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+169_1126+176d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0002g0290a0002c0002t0001g0174 | 2 | NA18984.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1126+167_1126+176d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
G | GTATATAT others(7): Show |
1 | a0002c0002t0001g0210 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1126+163_1126+176d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTA | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0084a0001c0001t0001g0120others(34): Show | 41 | HG00323.hp1 HG00738.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1126+175_1126+176d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATA | G | 25 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0164others(22): Show | 27 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1126+173_1126+176d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATA | G | 9 | a0001c0001t0001g0138a0001c0001t0001g0154a0001c0001t0002g0304others(6): Show | 10 | HG01496.hp2 HG01952.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126+171_1126+176d others(8): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(1): Show |
G | 8 | a0001c0001t0003g0093a0001c0001t0008g0028a0001c0001t0008g0313others(5): Show | 9 | HG01192.hp2 HG02647.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1126+169_1126+176d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(3): Show |
G | 7 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126+167_1126+176d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0267a0001c0001t0003g0160 | 2 | HG01993.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1126+165_1126+176d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(7): Show |
G | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1126+163_1126+176d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(9): Show |
G | 4 | a0001c0001t0002g0021a0001c0001t0010g0016a0001c0001t0021g0226others(1): Show | 6 | HG00099.hp1 HG02257.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126+161_1126+176d others(18): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(11): Show |
G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 10 | HG01069.hp2 HG02055.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126+159_1126+176d others(20): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(17): Show |
G | 1 | a0001c0001t0005g0256 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1126+153_1126+176d others(26): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0321 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1126+149_1126+176d others(30): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(23): Show |
G | 1 | a0001c0001t0004g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1126+147_1126+176d others(32): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(25): Show |
G | 1 | a0001c0001t0002g0239 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1126+145_1126+176d others(34): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291567
|
GTATATAT others(27): Show |
G | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1126+143_1126+176d others(36): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | ||||||
| chr12:75291579
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1126+164_1126+165i others(25): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291579 | ||||||
| chr12:75291591
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1126+131_1126+152d others(24): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291591 | ||||||
| chr12:75291593
|
ATATATAT others(13): Show |
A | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 80 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1126+131_1126+150d others(22): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291593 | ||||||
| chr12:75291595
|
ATATATAT others(11): Show |
A | 8 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0059others(5): Show | 9 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1126+131_1126+148d others(20): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291595 | ||||||
| chr12:75291598
|
T | G | 3 | a0002c0002t0001g0019a0002c0002t0001g0195a0002c0002t0001g0201 | 4 | HG00408.hp2 HG02132.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126+146A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291598 | ||||||
| chr12:75291598
|
T | TATATATA others(1): Show |
2 | a0001c0001t0002g0023a0001c0001t0002g0255 | 3 | HG02074.hp1 NA18951.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1126+145_1126+146i others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291598 | ||||||
| chr12:75291598
|
T | TATATATA others(3): Show |
1 | a0001c0001t0002g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1126+145_1126+146i others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291598 | ||||||
| chr12:75291686
|
T | C | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1126+58A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291686 | ||||||
| chr12:75291903
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1050-83A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75291903 | ||||||
| chr12:75292052
|
T | C | 36 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(33): Show | 44 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1050-232A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292052 | ||||||
| chr12:75292221
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 227 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1050-401G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292221 | ||||||
| chr12:75292223
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0148a0001c0001t0004g0149 | 3 | HG00280.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1050-403G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292223 | ||||||
| chr12:75292308
|
C | T | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1050-488G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292308 | ||||||
| chr12:75292455
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1050-635C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292455 | ||||||
| chr12:75292489
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1050-669G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292489 | ||||||
| chr12:75292588
|
TATATTAT others(6): Show |
T | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1049+648_1049+660d others(15): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292588 | ||||||
| chr12:75292614
|
T | C | 4 | a0001c0001t0008g0028a0001c0001t0008g0313a0001c0001t0008g0315others(1): Show | 5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049+635A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292614 | ||||||
| chr12:75292614
|
T | TATCTATA others(18): Show |
1 | a0001c0001t0006g0090 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1049+610_1049+634d others(27): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292614 | ||||||
| chr12:75293405
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.931-38C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293405 | ||||||
| chr12:75293465
|
G | A | 2 | a0001c0001t0013g0129a0001c0001t0013g0132 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.931-98C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293465 | ||||||
| chr12:75293492
|
T | C | 1 | a0001c0013t0001g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.931-125A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293492 | ||||||
| chr12:75293542
|
T | A | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.931-175A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293542 | ||||||
| chr12:75293743
|
C | T | 1 | a0001c0001t0024g0033 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.931-376G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293743 | ||||||
| chr12:75293873
|
T | C | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.931-506A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293873 | ||||||
| chr12:75294134
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.931-767G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294134 | ||||||
| chr12:75294208
|
C | T | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.931-841G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294208 | ||||||
| chr12:75294608
|
C | T | 1 | a0001c0001t0002g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.931-1241G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294608 | ||||||
| chr12:75294667
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.931-1300C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294667 | ||||||
| chr12:75294707
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931-1340C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294707 | ||||||
| chr12:75294755
|
ATG | A | 5 | a0002c0002t0001g0020a0002c0002t0001g0196a0002c0002t0001g0197others(2): Show | 6 | HG02257.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.931-1390_931-1389d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294755 | ||||||
| chr12:75294868
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.931-1501G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294868 | ||||||
| chr12:75294899
|
A | T | 1 | a0001c0001t0004g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.931-1532T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294899 | ||||||
| chr12:75295318
|
T | C | 4 | a0001c0001t0002g0023a0001c0001t0002g0240a0001c0001t0002g0254others(1): Show | 5 | HG00597.hp1 HG02074.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-1951A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75295318 | ||||||
| chr12:75295470
|
C | T | 1 | a0001c0013t0001g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.931-2103G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75295470 | ||||||
| chr12:75295991
|
T | C | 1 | a0001c0001t0004g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.931-2624A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75295991 | ||||||
| chr12:75296209
|
T | TTA | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.930+2477_930+2478i others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296209 | ||||||
| chr12:75296273
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.930+2414A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296273 | ||||||
| chr12:75296453
|
A | G | 4 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0001t0021g0226others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+2234T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296453 | ||||||
| chr12:75296867
|
C | T | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.930+1820G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296867 | ||||||
| chr12:75297007
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 89 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.930+1680A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297007 | ||||||
| chr12:75297178
|
T | C | 3 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0003t0031g0327 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.930+1509A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297178 | ||||||
| chr12:75297443
|
C | T | 1 | a0001c0001t0005g0247 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.930+1244G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297443 | ||||||
| chr12:75297456
|
T | C | 3 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0003t0031g0327 | 3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.930+1231A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297456 | ||||||
| chr12:75297719
|
C | T | 1 | a0001c0001t0003g0284 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.930+968G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297719 | ||||||
| chr12:75297795
|
T | C | 1 | a0001c0001t0002g0260 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.930+892A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297795 | ||||||
| chr12:75297992
|
T | G | 1 | a0001c0001t0003g0284 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.930+695A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297992 | ||||||
| chr12:75298018
|
A | C | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.930+669T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298018 | ||||||
| chr12:75298101
|
A | G | 2 | a0001c0001t0001g0285a0001c0001t0001g0298 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.930+586T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298101 | ||||||
| chr12:75298222
|
T | G | 1 | a0001c0001t0014g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.930+465A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298222 | ||||||
| chr12:75298225
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.930+462G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298225 | ||||||
| chr12:75298481
|
A | C | 78 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(75): Show | 88 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.930+206T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298481 | ||||||
| chr12:75298618
|
C | T | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.930+69G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298618 | ||||||
| chr12:75298808
|
A | G | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.837-28T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 10/16 | chr12 | 75298808 | ||||||
| chr12:75298827
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 90 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.836+44C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 10/16 | chr12 | 75298827 | ||||||
| chr12:75298975
|
A | T | 140 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(137): Show | 155 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.741-9T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75298975 | ||||||
| chr12:75299085
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.741-119C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299085 | ||||||
| chr12:75299188
|
T | G | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.741-222A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299188 | ||||||
| chr12:75299206
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.741-240G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299206 | ||||||
| chr12:75299271
|
G | A | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.741-305C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299271 | ||||||
| chr12:75299349
|
A | G | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.741-383T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299349 | ||||||
| chr12:75299520
|
C | T | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.740+317G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299520 | ||||||
| chr12:75299692
|
A | G | 1 | a0009c0015t0001g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.740+145T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299692 | ||||||
| chr12:75299722
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.740+115C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299722 | ||||||
| chr12:75299740
|
C | T | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.740+97G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299740 | ||||||
| chr12:75299751
|
A | C | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.740+86T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299751 | ||||||
| chr12:75299971
|
G | A | 120 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(117): Show | 134 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.666-60C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75299971 | ||||||
| chr12:75299981
|
A | G | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.666-70T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75299981 | ||||||
| chr12:75300034
|
T | TA | 6 | a0001c0001t0013g0129a0001c0001t0013g0132a0001c0003t0031g0327others(3): Show | 6 | HG00609.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-124dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300034 | ||||||
| chr12:75300043
|
A | C | 1 | a0001c0001t0003g0153 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.666-132T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300043 | ||||||
| chr12:75300101
|
G | T | 35 | a0001c0001t0002g0217a0001c0001t0002g0228a0001c0001t0002g0229others(32): Show | 37 | HG00280.hp1 HG01109.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.666-190C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300101 | ||||||
| chr12:75300226
|
T | C | 35 | a0001c0001t0002g0217a0001c0001t0002g0228a0001c0001t0002g0229others(32): Show | 37 | HG00280.hp1 HG01109.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.666-315A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300226 | ||||||
| chr12:75300276
|
G | T | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.666-365C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300276 | ||||||
| chr12:75300282
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 112 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.666-371G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300282 | ||||||
| chr12:75300328
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-417C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300328 | ||||||
| chr12:75300339
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-428C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300339 | ||||||
| chr12:75300353
|
G | A | 2 | a0001c0001t0014g0131a0001c0003t0014g0045 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.666-442C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300353 | ||||||
| chr12:75300414
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 90 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.666-503C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300414 | ||||||
| chr12:75300425
|
G | A | 120 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(117): Show | 134 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.666-514C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300425 | ||||||
| chr12:75300439
|
T | C | 120 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(117): Show | 134 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.666-528A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300439 | ||||||
| chr12:75300543
|
C | G | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.666-632G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300543 | ||||||
| chr12:75300555
|
C | CA | 62 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(59): Show | 67 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.666-645dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
C | CAA | 13 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0081others(10): Show | 13 | HG01243.hp2 HG01952.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.666-646_666-645dup others(2): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CA | C | 6 | a0001c0001t0001g0014a0001c0001t0009g0011a0001c0001t0009g0079others(3): Show | 8 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-645delT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CAA | C | 13 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0051others(10): Show | 13 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.666-646_666-645del others(2): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CAAA | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(51): Show | 69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.666-647_666-645del others(3): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0246a0001c0001t0002g0301a0001c0001t0005g0257 | 3 | HG02129.hp1 NA18941.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.666-654_666-645del others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CAAAAAAA others(4): Show |
C | 101 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(98): Show | 113 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.666-655_666-645del others(11): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CAAAAAAA others(5): Show |
C | 15 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(12): Show | 17 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-656_666-645del others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300555
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.666-657_666-645del others(13): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | ||||||
| chr12:75300759
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.666-848A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300759 | ||||||
| chr12:75300764
|
C | T | 1 | a0002c0002t0001g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.666-853G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300764 | ||||||
| chr12:75300945
|
T | C | 1 | a0001c0001t0002g0295 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.666-1034A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300945 | ||||||
| chr12:75300971
|
G | C | 85 | a0001c0001t0001g0261a0001c0001t0002g0005a0001c0001t0002g0021others(82): Show | 97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.666-1060C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300971 | ||||||
| chr12:75301051
|
C | A | 1 | a0001c0001t0021g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.666-1140G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301051 | ||||||
| chr12:75301100
|
A | G | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-1189T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301100 | ||||||
| chr12:75301106
|
A | G | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-1195T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301106 | ||||||
| chr12:75301234
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.666-1323T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301234 | ||||||
| chr12:75301326
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.666-1415T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301326 | ||||||
| chr12:75301432
|
T | G | 1 | a0001c0001t0001g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666-1521A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301432 | ||||||
| chr12:75301434
|
G | T | 5 | a0001c0001t0004g0151a0001c0001t0004g0152a0001c0001t0004g0158others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-1523C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301434 | ||||||
| chr12:75301662
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(71): Show | 91 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.666-1751A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301662 | ||||||
| chr12:75301797
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 228 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.666-1886T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301797 | ||||||
| chr12:75301860
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18944.hp1 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.666-1949T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301860 | ||||||
| chr12:75301884
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.666-1973G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301884 | ||||||
| chr12:75301894
|
A | G | 6 | a0001c0001t0010g0016a0001c0001t0013g0129a0001c0001t0013g0132others(3): Show | 7 | HG01884.hp1 HG02056.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-1983T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301894 | ||||||
| chr12:75302147
|
T | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(99): Show | 114 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.666-2236A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302147 | ||||||
| chr12:75302185
|
G | A | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.666-2274C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302185 | ||||||
| chr12:75302298
|
G | A | 2 | a0001c0001t0004g0311a0001c0001t0004g0312 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.666-2387C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302298 | ||||||
| chr12:75302628
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(14): Show | 18 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.665+2129C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302628 | ||||||
| chr12:75302633
|
G | A | 6 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(3): Show | 6 | HG01243.hp1 HG02004.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+2124C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302633 | ||||||
| chr12:75302650
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.665+2107C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302650 | ||||||
| chr12:75302945
|
A | G | 1 | a0002c0002t0001g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.665+1812T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302945 | ||||||
| chr12:75303021
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.665+1736T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303021 | ||||||
| chr12:75303112
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.665+1645G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303112 | ||||||
| chr12:75303176
|
A | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+1581T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303176 | ||||||
| chr12:75303275
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.665+1482G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303275 | ||||||
| chr12:75303487
|
G | A | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.665+1270C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303487 | ||||||
| chr12:75303616
|
G | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+1141C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303616 | ||||||
| chr12:75303659
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.665+1098C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303659 | ||||||
| chr12:75303720
|
G | A | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+1037C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303720 | ||||||
| chr12:75303798
|
C | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+959G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303798 | ||||||
| chr12:75303859
|
G | A | 4 | a0001c0001t0003g0017a0001c0001t0003g0139a0001c0001t0003g0140others(1): Show | 5 | HG01496.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+898C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303859 | ||||||
| chr12:75303877
|
A | G | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+880T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303877 | ||||||
| chr12:75303951
|
T | A | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.665+806A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303951 | ||||||
| chr12:75304017
|
C | T | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.665+740G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304017 | ||||||
| chr12:75304139
|
T | G | 1 | a0002c0002t0001g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.665+618A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304139 | ||||||
| chr12:75304148
|
A | G | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+609T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304148 | ||||||
| chr12:75304177
|
G | A | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+580C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304177 | ||||||
| chr12:75304353
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0007g0116 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.665+404A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304353 | ||||||
| chr12:75304427
|
T | G | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+330A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304427 | ||||||
| chr12:75304448
|
A | G | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.665+309T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304448 | ||||||
| chr12:75304473
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.665+284C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304473 | ||||||
| chr12:75304514
|
G | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+243C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304514 | ||||||
| chr12:75304515
|
T | G | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+242A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304515 | ||||||
| chr12:75304551
|
T | A | 2 | a0001c0001t0001g0138a0001c0001t0007g0116 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.665+206A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304551 | ||||||
| chr12:75304552
|
C | A | 2 | a0001c0001t0001g0138a0001c0001t0007g0116 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.665+205G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304552 | ||||||
| chr12:75304614
|
A | C | 15 | a0002c0002t0001g0006a0002c0002t0001g0168a0002c0002t0001g0171others(12): Show | 17 | HG00558.hp1 NA18942.hp1 NA18954.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+143T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304614 | ||||||
| chr12:75304747
|
A | G | 1 | a0001c0001t0002g0267 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.665+10T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304747 | ||||||
| chr12:75305029
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.546-153A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305029 | ||||||
| chr12:75305079
|
C | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-203G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305079 | ||||||
| chr12:75305196
|
C | T | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.546-320G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305196 | ||||||
| chr12:75305292
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.546-416C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305292 | ||||||
| chr12:75305582
|
C | G | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-706G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305582 | ||||||
| chr12:75305600
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.546-724G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305600 | ||||||
| chr12:75305607
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.546-731G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305607 | ||||||
| chr12:75305647
|
C | T | 27 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(24): Show | 29 | HG00280.hp1 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.546-771G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305647 | ||||||
| chr12:75305706
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.546-830G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305706 | ||||||
| chr12:75305901
|
C | T | 3 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045 | 3 | HG02622.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.546-1025G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305901 | ||||||
| chr12:75305953
|
CA | C | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-1078delT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305953 | ||||||
| chr12:75305984
|
G | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-1108C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305984 | ||||||
| chr12:75306144
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.546-1268G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306144 | ||||||
| chr12:75306316
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0061a0001c0001t0001g0087others(2): Show | 6 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-1440G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306316 | ||||||
| chr12:75306322
|
C | A | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.546-1446G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306322 | ||||||
| chr12:75306883
|
C | T | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.546-2007G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306883 | ||||||
| chr12:75306911
|
T | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.546-2035A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306911 | ||||||
| chr12:75306925
|
A | C | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2049T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306925 | ||||||
| chr12:75306948
|
C | G | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2072G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306948 | ||||||
| chr12:75307125
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.546-2249C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307125 | ||||||
| chr12:75307158
|
G | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2282C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307158 | ||||||
| chr12:75307691
|
G | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.546-2815C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307691 | ||||||
| chr12:75307995
|
A | C | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.546-3119T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307995 | ||||||
| chr12:75308065
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.546-3189G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308065 | ||||||
| chr12:75308333
|
G | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0108 | 3 | HG01255.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.546-3457C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308333 | ||||||
| chr12:75308380
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.546-3504G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308380 | ||||||
| chr12:75308466
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.546-3590A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308466 | ||||||
| chr12:75308496
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546-3620C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308496 | ||||||
| chr12:75308677
|
G | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-3801C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308677 | ||||||
| chr12:75308687
|
T | C | 2 | a0001c0001t0002g0229a0001c0001t0026g0231 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.546-3811A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308687 | ||||||
| chr12:75308723
|
T | C | 2 | a0001c0001t0002g0290a0001c0001t0002g0296 | 2 | HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.546-3847A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308723 | ||||||
| chr12:75308803
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.546-3927T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308803 | ||||||
| chr12:75308818
|
T | TA | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-3943_546-3942i others(3): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308818 | ||||||
| chr12:75308819
|
T | A | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-3943A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308819 | ||||||
| chr12:75308830
|
A | G | 1 | a0001c0001t0007g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.546-3954T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308830 | ||||||
| chr12:75308890
|
G | A | 4 | a0001c0001t0004g0151a0001c0001t0004g0152a0001c0001t0004g0158others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+3958C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308890 | ||||||
| chr12:75308902
|
C | CA | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.545+3945dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308902 | ||||||
| chr12:75308902
|
C | CAA | 17 | a0001c0001t0001g0060a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01175.hp2 HG01361.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.545+3944_545+3945d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308902 | ||||||
| chr12:75308925
|
G | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.545+3923C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308925 | ||||||
| chr12:75308930
|
A | T | 8 | a0001c0003t0001g0135a0001c0003t0002g0046a0001c0003t0002g0047others(5): Show | 8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+3918T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308930 | ||||||
| chr12:75309077
|
A | T | 3 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045 | 3 | HG02622.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.545+3771T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309077 | ||||||
| chr12:75309218
|
C | T | 1 | a0002c0002t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.545+3630G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309218 | ||||||
| chr12:75309789
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.545+3059G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309789 | ||||||
| chr12:75309805
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.545+3043C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309805 | ||||||
| chr12:75310190
|
G | T | 1 | a0002c0002t0001g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.545+2658C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310190 | ||||||
| chr12:75310266
|
C | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.545+2582G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310266 | ||||||
| chr12:75310284
|
G | A | 1 | a0001c0001t0002g0297 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.545+2564C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310284 | ||||||
| chr12:75310371
|
T | A | 2 | a0001c0001t0001g0285a0001c0001t0001g0298 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.545+2477A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310371 | ||||||
| chr12:75310472
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.545+2376C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310472 | ||||||
| chr12:75310697
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(327): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.545+2151A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310697 | ||||||
| chr12:75310742
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.545+2106C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310742 | ||||||
| chr12:75310769
|
G | T | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.545+2079C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310769 | ||||||
| chr12:75310787
|
G | C | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+2061C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310787 | ||||||
| chr12:75310834
|
A | G | 2 | a0001c0001t0002g0270a0001c0001t0002g0286 | 2 | NA18991.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.545+2014T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310834 | ||||||
| chr12:75310969
|
A | T | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.545+1879T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310969 | ||||||
| chr12:75310991
|
G | A | 76 | a0001c0001t0001g0144a0001c0001t0007g0141a0001c0001t0007g0142others(73): Show | 81 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.545+1857C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310991 | ||||||
| chr12:75311086
|
T | C | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.545+1762A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311086 | ||||||
| chr12:75311149
|
G | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0002g0005others(2): Show | 7 | HG01069.hp2 HG01243.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+1699C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311149 | ||||||
| chr12:75311158
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.545+1690G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311158 | ||||||
| chr12:75311366
|
A | G | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1482T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311366 | ||||||
| chr12:75311429
|
G | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18944.hp1 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.545+1419C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311429 | ||||||
| chr12:75311685
|
C | A | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.545+1163G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311685 | ||||||
| chr12:75311699
|
GGAAAAAA others(3): Show |
G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02040.hp1 NA18942.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+1139_545+1148d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(4): Show |
G | 22 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0053others(19): Show | 23 | HG00544.hp1 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.545+1138_545+1148d others(13): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(5): Show |
G | 67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(64): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.545+1137_545+1148d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(6): Show |
G | 7 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | HG01081.hp2 HG01256.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1136_545+1148d others(15): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(7): Show |
G | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.545+1135_545+1148d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(17): Show |
G | 1 | a0001c0003t0032g0328 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.545+1125_545+1148d others(26): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(18): Show |
G | 1 | a0001c0003t0031g0327 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.545+1124_545+1148d others(27): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311699
|
GGAAAAAA others(19): Show |
G | 3 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045 | 3 | HG02622.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.545+1123_545+1148d others(28): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | ||||||
| chr12:75311700
|
G | A | 2 | a0001c0001t0002g0302a0001c0001t0004g0232 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.545+1148C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | ||||||
| chr12:75311700
|
G | GA | 8 | a0001c0001t0002g0025a0001c0001t0002g0269a0001c0001t0002g0286others(5): Show | 9 | HG00673.hp1 HG02015.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.545+1147dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | ||||||
| chr12:75311700
|
G | GAA | 8 | a0001c0001t0001g0298a0001c0001t0002g0291a0001c0001t0002g0292others(5): Show | 8 | HG02523.hp1 HG02683.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+1146_545+1147d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | ||||||
| chr12:75311700
|
GAAAAAAA others(5): Show |
G | 1 | a0002c0002t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.545+1136_545+1147d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | ||||||
| chr12:75311701
|
AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0010g0016 | 4 | HG02257.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+1136_545+1146d others(13): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311701 | ||||||
| chr12:75311701
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0002g0270 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.545+1124_545+1146d others(25): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311701 | ||||||
| chr12:75311702
|
AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0003g0275a0001c0001t0004g0136a0001c0001t0004g0151others(2): Show | 5 | HG01109.hp1 HG01255.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+1136_545+1145d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311702 | ||||||
| chr12:75311702
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.545+1124_545+1145d others(24): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311702 | ||||||
| chr12:75311703
|
A | G | 2 | a0002c0002t0001g0210a0002c0002t0001g0211 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.545+1145T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311703 | ||||||
| chr12:75311703
|
AAAAAAAA others(2): Show |
A | 27 | a0001c0001t0001g0122a0001c0001t0001g0154a0001c0001t0001g0161others(24): Show | 28 | HG00280.hp1 HG01168.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.545+1136_545+1144d others(11): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311703 | ||||||
| chr12:75311704
|
AAAAAAAA others(1): Show |
A | 14 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0003g0017others(11): Show | 16 | HG01243.hp2 HG01361.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.545+1136_545+1143d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311704 | ||||||
| chr12:75311705
|
AAAAAAAC | A | 5 | a0001c0001t0002g0005a0001c0001t0002g0133a0001c0001t0002g0134others(2): Show | 7 | HG01069.hp2 HG02004.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+1136_545+1142d others(9): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311705 | ||||||
| chr12:75311705
|
AAAAAAAC others(12): Show |
A | 1 | a0001c0001t0003g0271 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.545+1124_545+1142d others(21): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311705 | ||||||
| chr12:75311707
|
AAAAACAA others(10): Show |
A | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(2): Show | 5 | HG00609.hp2 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1124_545+1140d others(19): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311707 | ||||||
| chr12:75311708
|
AAAACAAA others(9): Show |
A | 32 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(29): Show | 40 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.545+1124_545+1139d others(18): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311708 | ||||||
| chr12:75311709
|
AAACAAAA others(8): Show |
A | 11 | a0001c0001t0001g0261a0001c0001t0002g0259a0001c0001t0002g0260others(8): Show | 11 | HG01106.hp1 HG01175.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.545+1124_545+1138d others(17): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311709 | ||||||
| chr12:75311710
|
AACAAAAA others(7): Show |
A | 56 | a0001c0001t0001g0144a0001c0001t0007g0141a0001c0001t0007g0142others(53): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.545+1124_545+1137d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311710 | ||||||
| chr12:75311711
|
AC | A | 4 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0276others(1): Show | 4 | HG01099.hp1 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+1136delG | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311711 | ||||||
| chr12:75311711
|
ACAAAAAA others(6): Show |
A | 15 | a0001c0001t0004g0124a0001c0001t0007g0146a0001c0001t0007g0147others(12): Show | 15 | HG00544.hp2 HG00621.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+1124_545+1136d others(15): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311711 | ||||||
| chr12:75311712
|
C | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.545+1136G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311712 | ||||||
| chr12:75311720
|
A | C | 1 | a0001c0001t0001g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.545+1128T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311720 | ||||||
| chr12:75311724
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.545+1124G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311724 | ||||||
| chr12:75311761
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.545+1087C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311761 | ||||||
| chr12:75311796
|
G | A | 2 | a0001c0001t0003g0101a0001c0001t0003g0102 | 2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.545+1052C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311796 | ||||||
| chr12:75311801
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.545+1047G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311801 | ||||||
| chr12:75311935
|
G | C | 2 | a0001c0003t0002g0046a0001c0003t0002g0047 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.545+913C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311935 | ||||||
| chr12:75311951
|
G | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.545+897C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311951 | ||||||
| chr12:75312349
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.545+499G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75312349 | ||||||
| chr12:75312573
|
AT | A | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+274delA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75312573 | ||||||
| chr12:75312940
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.478-25A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75312940 | ||||||
| chr12:75313017
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.478-102C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313017 | ||||||
| chr12:75313026
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.478-111T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313026 | ||||||
| chr12:75313127
|
G | C | 1 | a0001c0001t0002g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.478-212C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313127 | ||||||
| chr12:75313154
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0003g0027 | 3 | HG01070.hp2 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.478-239T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313154 | ||||||
| chr12:75313201
|
T | G | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.478-286A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313201 | ||||||
| chr12:75313429
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.478-514T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313429 | ||||||
| chr12:75313616
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.478-701T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313616 | ||||||
| chr12:75313697
|
T | C | 2 | a0001c0001t0012g0118a0001c0001t0012g0119 | 2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.478-782A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313697 | ||||||
| chr12:75314139
|
C | T | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1224G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314139 | ||||||
| chr12:75314192
|
C | T | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1277G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314192 | ||||||
| chr12:75314303
|
T | C | 3 | a0001c0001t0001g0104a0005c0009t0001g0058a0005c0016t0001g0111 | 3 | NA18747.hp1 NA19079.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.478-1388A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314303 | ||||||
| chr12:75314357
|
T | C | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.478-1442A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314357 | ||||||
| chr12:75314626
|
AT | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.477+1685delA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314626 | ||||||
| chr12:75314728
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.477+1584G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314728 | ||||||
| chr12:75314812
|
T | C | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+1500A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314812 | ||||||
| chr12:75315110
|
A | G | 2 | a0001c0001t0004g0311a0001c0001t0004g0312 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+1202T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315110 | ||||||
| chr12:75315290
|
G | T | 8 | a0001c0001t0004g0117a0001c0001t0004g0311a0001c0001t0004g0312others(5): Show | 9 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.477+1022C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315290 | ||||||
| chr12:75315378
|
C | A | 1 | a0001c0001t0001g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.477+934G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315378 | ||||||
| chr12:75315687
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.477+625G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315687 | ||||||
| chr12:75315700
|
T | C | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+612A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315700 | ||||||
| chr12:75315907
|
T | TTGCTTCA | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+404_477+405ins others(7): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315907 | ||||||
| chr12:75315988
|
C | T | 1 | a0001c0001t0026g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.477+324G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315988 | ||||||
| chr12:75316104
|
C | A | 4 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(1): Show | 4 | HG02572.hp2 HG02895.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+208G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75316104 | ||||||
| chr12:75316224
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.477+88G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75316224 | ||||||
| chr12:75316479
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18612.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.355-45T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316479 | ||||||
| chr12:75316582
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.355-148T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316582 | ||||||
| chr12:75316607
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.355-173G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316607 | ||||||
| chr12:75316865
|
A | G | 2 | a0002c0002t0015g0325a0002c0002t0015g0326 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.355-431T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316865 | ||||||
| chr12:75316941
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.355-507G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316941 | ||||||
| chr12:75317082
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0105 | 4 | HG02040.hp1 NA18944.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-648A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317082 | ||||||
| chr12:75317133
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.355-699A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317133 | ||||||
| chr12:75317219
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0115 | 4 | HG01261.hp1 HG01358.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-785C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317219 | ||||||
| chr12:75317370
|
C | T | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(4): Show | 7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.355-936G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317370 | ||||||
| chr12:75317650
|
T | C | 2 | a0001c0003t0031g0327a0001c0003t0032g0328 | 2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.355-1216A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317650 | ||||||
| chr12:75317774
|
T | C | 1 | a0002c0004t0001g0209 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.355-1340A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317774 | ||||||
| chr12:75317794
|
CAT | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 8 | HG00544.hp1 HG01255.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-1362_355-1361d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317794 | ||||||
| chr12:75318006
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.355-1572G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318006 | ||||||
| chr12:75318220
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.355-1786C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318220 | ||||||
| chr12:75318341
|
C | T | 1 | a0002c0002t0008g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.355-1907G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318341 | ||||||
| chr12:75318390
|
C | T | 1 | a0001c0003t0031g0327 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.355-1956G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318390 | ||||||
| chr12:75318440
|
C | T | 6 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(3): Show | 7 | HG01168.hp2 HG01361.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-2006G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318440 | ||||||
| chr12:75318766
|
A | AT | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.355-2333dupA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318766 | ||||||
| chr12:75318797
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.355-2363A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318797 | ||||||
| chr12:75318882
|
A | G | 75 | a0001c0001t0001g0144a0001c0001t0007g0141a0001c0001t0007g0142others(72): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.355-2448T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318882 | ||||||
| chr12:75319293
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+2107C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319293 | ||||||
| chr12:75319310
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.354+2090C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319310 | ||||||
| chr12:75319466
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.354+1934G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319466 | ||||||
| chr12:75319611
|
G | A | 5 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(2): Show | 5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+1789C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319611 | ||||||
| chr12:75319676
|
G | C | 1 | a0001c0001t0003g0165 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.354+1724C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319676 | ||||||
| chr12:75319720
|
C | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+1680G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319720 | ||||||
| chr12:75319881
|
T | C | 1 | a0001c0001t0026g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.354+1519A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319881 | ||||||
| chr12:75320339
|
C | A | 1 | a0001c0001t0004g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354+1061G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320339 | ||||||
| chr12:75320548
|
C | A | 38 | a0001c0001t0001g0285a0001c0001t0001g0298a0001c0001t0002g0024others(35): Show | 40 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.354+852G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320548 | ||||||
| chr12:75320640
|
T | C | 7 | a0002c0002t0001g0210a0002c0002t0001g0211a0002c0002t0001g0213others(4): Show | 7 | HG00544.hp2 HG00621.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+760A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320640 | ||||||
| chr12:75320771
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.354+629A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320771 | ||||||
| chr12:75320883
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.354+517A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320883 | ||||||
| chr12:75320916
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0004g0123a0001c0001t0004g0308 | 3 | HG01884.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.354+484G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320916 | ||||||
| chr12:75321119
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.354+281G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75321119 | ||||||
| chr12:75321235
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354+165G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75321235 | ||||||
| chr12:75321778
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.178-202G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75321778 | ||||||
| chr12:75322066
|
C | A | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.178-490G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322066 | ||||||
| chr12:75322183
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178-607T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322183 | ||||||
| chr12:75322304
|
A | T | 2 | a0001c0001t0003g0139a0001c0001t0003g0140 | 2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.178-728T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322304 | ||||||
| chr12:75322354
|
C | T | 5 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(2): Show | 5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-778G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322354 | ||||||
| chr12:75322358
|
C | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.178-782G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322358 | ||||||
| chr12:75322498
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.177+679C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322498 | ||||||
| chr12:75322532
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0007g0116 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.177+645G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322532 | ||||||
| chr12:75322586
|
T | C | 1 | a0001c0001t0005g0300 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.177+591A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322586 | ||||||
| chr12:75322681
|
A | G | 1 | a0001c0001t0004g0123 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+496T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322681 | ||||||
| chr12:75322822
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.177+355G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322822 | ||||||
| chr12:75322864
|
T | C | 1 | a0001c0001t0004g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.177+313A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322864 | ||||||
| chr12:75323223
|
C | A | 1 | a0001c0001t0007g0220 | 1 | HG03540.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.132-1G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323223 | ||||||
| chr12:75323231
|
C | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(20): Show | 24 | HG00438.hp2 HG00735.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132-9G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323231 | ||||||
| chr12:75323326
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-104A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323326 | ||||||
| chr12:75323330
|
G | A | 1 | a0002c0002t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132-108C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323330 | ||||||
| chr12:75323401
|
A | T | 1 | a0001c0003t0014g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.132-179T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323401 | ||||||
| chr12:75323527
|
T | C | 1 | a0002c0002t0001g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.132-305A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323527 | ||||||
| chr12:75323542
|
G | A | 3 | a0002c0002t0001g0223a0004c0006t0016g0330a0004c0006t0016g0331 | 3 | HG01074.hp2 HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.132-320C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323542 | ||||||
| chr12:75323572
|
T | C | 5 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(2): Show | 5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-350A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323572 | ||||||
| chr12:75323699
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.132-477G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323699 | ||||||
| chr12:75323943
|
A | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.132-721T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323943 | ||||||
| chr12:75324074
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.132-852A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324074 | ||||||
| chr12:75324162
|
C | T | 1 | a0002c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.132-940G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324162 | ||||||
| chr12:75324173
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | NA18951.hp2 NA18954.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.132-951A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324173 | ||||||
| chr12:75324506
|
A | G | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.131+733T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324506 | ||||||
| chr12:75324512
|
C | T | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.131+727G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324512 | ||||||
| chr12:75324643
|
G | T | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 34 | HG01069.hp2 HG01168.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.131+596C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324643 | ||||||
| chr12:75325308
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.82-20A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325308 | ||||||
| chr12:75325622
|
T | C | 1 | a0001c0001t0002g0301 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-334A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325622 | ||||||
| chr12:75325808
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.82-520C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325808 | ||||||
| chr12:75325904
|
A | G | 84 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0235others(81): Show | 94 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.81+514T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325904 | ||||||
| chr12:75326051
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0021g0226 | 2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.81+367A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75326051 | ||||||
| chr12:75326401
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+17T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75326401 | ||||||
| chr12:75326870
|
G | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-343C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75326870 | ||||||
| chr12:75326907
|
A | G | 2 | a0001c0001t0012g0118a0001c0001t0012g0119 | 2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-29-380T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75326907 | ||||||
| chr12:75327005
|
G | C | 1 | a0006c0005t0002g0026 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-29-478C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327005 | ||||||
| chr12:75327007
|
C | A | 1 | a0006c0005t0002g0026 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-29-480G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327007 | ||||||
| chr12:75327108
|
C | A | 1 | a0001c0001t0001g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-29-581G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327108 | ||||||
| chr12:75327212
|
G | A | 1 | a0002c0002t0028g0227 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-29-685C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327212 | ||||||
| chr12:75327255
|
G | T | 8 | a0001c0001t0004g0117a0001c0001t0004g0311a0001c0001t0004g0312others(5): Show | 9 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-728C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327255 | ||||||
| chr12:75327339
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.-29-812T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327339 | ||||||
| chr12:75327443
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-916T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327443 | ||||||
| chr12:75327478
|
C | T | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-29-951G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327478 | ||||||
| chr12:75327479
|
C | T | 1 | a0001c0001t0007g0116 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-952G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327479 | ||||||
| chr12:75327553
|
T | C | 5 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(2): Show | 5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-1026A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327553 | ||||||
| chr12:75327567
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.-29-1040A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327567 | ||||||
| chr12:75327769
|
T | C | 1 | a0001c0003t0032g0328 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-29-1242A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327769 | ||||||
| chr12:75327885
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.-29-1358T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327885 | ||||||
| chr12:75327919
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-29-1392T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327919 | ||||||
| chr12:75327926
|
T | C | 2 | a0004c0006t0016g0330a0004c0006t0016g0331 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-29-1399A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327926 | ||||||
| chr12:75328017
|
G | A | 81 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(78): Show | 91 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-29-1490C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328017 | ||||||
| chr12:75328060
|
A | C | 1 | a0001c0001t0027g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-29-1533T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328060 | ||||||
| chr12:75328141
|
C | A | 1 | a0001c0001t0003g0027 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-29-1614G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328141 | ||||||
| chr12:75328219
|
C | T | 5 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0014g0045others(2): Show | 5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+1648G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328219 | ||||||
| chr12:75328521
|
G | C | 1 | a0001c0001t0001g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-30+1346C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328521 | ||||||
| chr12:75328527
|
C | A | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-30+1340G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328527 | ||||||
| chr12:75328591
|
C | A | 1 | a0001c0001t0003g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-30+1276G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328591 | ||||||
| chr12:75328668
|
A | G | 2 | a0001c0003t0031g0327a0001c0003t0032g0328 | 2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-30+1199T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328668 | ||||||
| chr12:75328876
|
A | G | 2 | a0001c0003t0031g0327a0001c0003t0032g0328 | 2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-30+991T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328876 | ||||||
| chr12:75328881
|
T | C | 4 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(1): Show | 4 | NA18968.hp1 NA18974.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+986A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328881 | ||||||
| chr12:75328968
|
T | C | 1 | a0001c0001t0004g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30+899A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328968 | ||||||
| chr12:75328985
|
T | G | 2 | a0003c0007t0001g0309a0003c0007t0001g0310 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-30+882A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328985 | ||||||
| chr12:75329245
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-30+622G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329245 | ||||||
| chr12:75329427
|
T | C | 7 | a0001c0001t0004g0311a0001c0001t0004g0312a0001c0001t0004g0314others(4): Show | 8 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+440A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329427 | ||||||
| chr12:75329475
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30+392G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329475 | ||||||
| chr12:75329485
|
A | AT | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.-30+381dupA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329485 |