Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 56994 |
|---|---|
| ensemblid | ENSG00000111666.11 |
| hgncid | 17852 |
| symbol | CHPT1 |
| name | choline phosphotransferase 1 |
| refseq_nuc | NM_020244.3 |
| refseq_prot | NP_064629.2 |
| ensembl_nuc | ENST00000229266.8 |
| ensembl_prot | ENSP00000229266.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 101697640 |
| end | 101729074 |
| strand | + |
| ver | v1.2 |
| region | chr12:101697640-101729074 |
| region5000 | chr12:101692640-101734074 |
| regionname0 | CHPT1_chr12_101697640_101729074 |
| regionname5000 | CHPT1_chr12_101692640_101734074 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 406 | 282 | 82 | 46 | 119 | 10 | 23 | 96 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002 | 0/0 | 406 | 105 | 6 | 20 | 64 | 4 | 11 | 53 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0003 | 0/0 | 406 | 9 | 0 | 1 | 8 | 0 | 0 | 4 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0004 | 0/0 | 406 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0005 | 0/0 | 406 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0006 | 0/0 | 406 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1221 | 144 | 62 | 9 | 59 | 3 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0002 | 0/0 | 1221 | 104 | 6 | 20 | 63 | 4 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0003 | 1/1 | 1221 | 89 | 17 | 26 | 27 | 6 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0004 | 0/0 | 1221 | 37 | 2 | 11 | 22 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0005 | 0/0 | 1221 | 10 | 0 | 0 | 10 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0006 | 0/0 | 1221 | 9 | 0 | 1 | 8 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0007 | 0/0 | 1221 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0008 | 0/0 | 1221 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0009 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0010 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0011 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| c0012 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 352 | 355 | 83 | 68 | 162 | 11 | 29 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| t0002 | 0/0 | 352 | 27 | 5 | 2 | 12 | 3 | 5 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| t0003 | 0/0 | 352 | 9 | 0 | 0 | 9 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| t0004 | 0/0 | 352 | 5 | 0 | 0 | 5 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| t0005 | 0/0 | 352 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| t0006 | 0/0 | 352 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| t0007 | 0/0 | 352 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 18 | 2 | 5 | 8 | 2 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0002 | 0/0 | 17 | 0 | 7 | 7 | 0 | 3 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0003 | 0/0 | 15 | 1 | 1 | 10 | 0 | 3 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0004 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0005 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0006 | 0/0 | 9 | 1 | 4 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0015 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0044 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1221 | 144 | 62 | 9 | 59 | 3 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0003 | 1/1 | 1221 | 89 | 17 | 26 | 27 | 6 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0004 | 0/0 | 1221 | 37 | 2 | 11 | 22 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0005 | 0/0 | 1221 | 10 | 0 | 0 | 10 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0010 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0012 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0002 | 0/0 | 1221 | 104 | 6 | 20 | 63 | 4 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0009 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0003c0006 | 0/0 | 1221 | 9 | 0 | 1 | 8 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0004c0007 | 0/0 | 1221 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0005c0008 | 0/0 | 1221 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0006c0011 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1572 | 117 | 55 | 7 | 47 | 1 | 7 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0001t0002 | 0/0 | 1572 | 13 | 5 | 2 | 0 | 2 | 4 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0001t0003 | 0/0 | 1572 | 9 | 0 | 0 | 9 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0001t0004 | 0/0 | 1572 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0001t0007 | 0/0 | 1572 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0003t0001 | 1/1 | 1572 | 85 | 17 | 26 | 24 | 5 | 11 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0003t0002 | 0/0 | 1572 | 2 | 0 | 0 | 1 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0003t0005 | 0/0 | 1572 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0004t0001 | 0/0 | 1572 | 37 | 2 | 11 | 22 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0005t0002 | 0/0 | 1572 | 10 | 0 | 0 | 10 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0010t0001 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0001c0012t0001 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0002t0001 | 0/0 | 1572 | 99 | 6 | 20 | 59 | 4 | 10 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0002t0002 | 0/0 | 1572 | 2 | 0 | 0 | 1 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0002t0004 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0002t0006 | 0/0 | 1572 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0002c0009t0001 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0003c0006t0001 | 0/0 | 1572 | 8 | 0 | 1 | 7 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0003c0006t0004 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0004c0007t0001 | 0/0 | 1572 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0005c0008t0001 | 0/0 | 1572 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| a0006c0011t0001 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | copy fasta | chr12 | 101692640 | 101734074 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0001 | 0/0 | 18 | 2 | 5 | 8 | 2 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0006 | 0/0 | 8 | 1 | 4 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0015 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0044 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0005t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0010t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0001c0012t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0002 | 0/0 | 17 | 0 | 7 | 7 | 0 | 3 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0003 | 0/0 | 15 | 1 | 1 | 10 | 0 | 3 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0002t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0002c0009t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0003c0006t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0004c0007t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0004c0007t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0005c0008t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0005c0008t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| a0006c0011t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0030 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0001 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0238 | EUR | GBR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0134 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0162 | EUR | FIN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0129 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00423 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00597 | hp1 | a0003 | c0006 | t0001 | g0005 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00609 | hp2 | a0001 | c0005 | t0002 | g0132 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00621 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | CHS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00639 | hp1 | a0004 | c0007 | t0001 | g0036 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0217 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01069 | hp1 | a0004 | c0007 | t0001 | g0154 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01071 | hp2 | a0004 | c0007 | t0001 | g0036 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0042 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0155 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0231 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0030 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0175 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0213 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0042 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0214 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0182 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0216 | EUR | IBS | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01928 | hp2 | a0003 | c0006 | t0001 | g0005 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0069 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02027 | hp1 | a0001 | c0005 | t0002 | g0014 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02040 | hp1 | a0001 | c0005 | t0002 | g0133 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02055 | hp1 | a0005 | c0008 | t0001 | g0253 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02074 | hp2 | a0002 | c0002 | t0006 | g0193 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02080 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0167 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02155 | hp1 | a0003 | c0006 | t0001 | g0243 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02165 | hp2 | a0001 | c0003 | t0005 | g0006 | EAS | CDX | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PEL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0172 | EAS | KHV | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0106 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02717 | hp1 | a0005 | c0008 | t0001 | g0254 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0135 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0241 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0179 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0221 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03209 | hp1 | a0001 | c0012 | t0001 | g0102 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0218 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0163 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0229 | SAS | PJL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0084 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0171 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0160 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18612 | hp2 | a0003 | c0006 | t0001 | g0225 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18747 | hp1 | a0003 | c0006 | t0004 | g0086 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18941 | hp1 | a0001 | c0005 | t0002 | g0131 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18944 | hp1 | a0002 | c0009 | t0001 | g0180 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18945 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18956 | hp1 | a0003 | c0006 | t0001 | g0223 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18957 | hp1 | a0001 | c0005 | t0002 | g0137 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18968 | hp2 | a0001 | c0003 | t0005 | g0068 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18969 | hp2 | a0003 | c0006 | t0001 | g0230 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18977 | hp1 | a0002 | c0002 | t0004 | g0097 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0233 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18978 | hp1 | a0002 | c0002 | t0006 | g0198 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18988 | hp2 | a0001 | c0005 | t0002 | g0128 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18993 | hp1 | a0001 | c0005 | t0002 | g0130 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18997 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0236 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19003 | hp1 | a0003 | c0006 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19004 | hp1 | a0006 | c0011 | t0001 | g0076 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0117 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19066 | hp1 | a0001 | c0010 | t0001 | g0092 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19075 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19081 | hp1 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19084 | hp1 | a0003 | c0006 | t0001 | g0224 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | YRI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | ASW | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0039 | EUR | TSI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0166 | EUR | TSI | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | ACB | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0054 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0235 | EAS | JPT | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0244 | AFR | LWK | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0161 | REF | REF | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0044 | REF | REF | CHPT1_chr12_101692640_101734074 | CHPT1 | chr12 | 101692640 | 101734074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101697970
|
G | A | 1 | a0005 | 2 | HG02055.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.109G>A | p.Ala37Thr | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 331/1572 | 109/1221 | 37/406 | chr12 | 101697970 | ||
| chr12:101714153
|
A | G | 1 | a0006 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.337A>G | p.Ile113Val | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 2/9 | 559/1572 | 337/1221 | 113/406 | chr12 | 101714153 | ||
| chr12:101714567
|
T | C | 2 | a0002a0006 | 106 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(103): Show |
missense_variant | MODERATE | c.485T>C | p.Phe162Ser | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/9 | 707/1572 | 485/1221 | 162/406 | chr12 | 101714567 | ||
| chr12:101720157
|
C | T | 1 | a0004 | 3 | HG00639.hp1 HG01069.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.683C>T | p.Pro228Leu | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/9 | 905/1572 | 683/1221 | 228/406 | chr12 | 101720157 | ||
| chr12:101723803
|
T | C | 1 | a0003 | 9 | HG00597.hp1 HG01928.hp2 HG02155.hp1 others(6): Show |
missense_variant | MODERATE | c.1021T>C | p.Phe341Leu | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/9 | 1243/1572 | 1021/1221 | 341/406 | chr12 | 101723803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101698053
|
C | T | 1 | a0001c0012 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.192C>T | p.Asn64Asn | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 414/1572 | 192/1221 | 64/406 | chr12 | 101698053 | ||
| chr12:101714523
|
T | C | 3 | a0001c0004a0001c0005a0003c0006 | 56 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
synonymous_variant | LOW | c.441T>C | p.Ala147Ala | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/9 | 663/1572 | 441/1221 | 147/406 | chr12 | 101714523 | ||
| chr12:101723811
|
C | T | 9 | a0001c0001a0001c0004a0001c0005others(6): Show | 309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
synonymous_variant | LOW | c.1029C>T | p.Asn343Asn | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/9 | 1251/1572 | 1029/1221 | 343/406 | chr12 | 101723811 | ||
| chr12:101726374
|
C | T | 2 | a0001c0005a0001c0010 | 11 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(8): Show |
synonymous_variant | LOW | c.1146C>T | p.Phe382Phe | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/9 | 1368/1572 | 1146/1221 | 382/406 | chr12 | 101726374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101697643
|
C | T | 5 | a0001c0001t0002a0001c0001t0007a0001c0003t0002others(2): Show | 29 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-219C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 219 | chr12 | 101697643 | |||||
| chr12:101697647
|
C | T | 1 | a0001c0001t0007 | 2 | HG02280.hp1 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-215C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 215 | chr12 | 101697647 | |||||
| chr12:101697682
|
G | A | 3 | a0001c0001t0004a0002c0002t0004a0003c0006t0004 | 5 | NA18747.hp1 NA18971.hp1 NA18977.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | 180 | chr12 | 101697682 | |||||
| chr12:101697712
|
C | T | 1 | a0002c0002t0006 | 2 | HG02074.hp2 NA18978.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-150C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | chr12 | 101697712 | ||||||
| chr12:101697726
|
C | T | 1 | a0001c0001t0003 | 9 | HG00609.hp1 HG00621.hp1 NA18942.hp1 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/9 | chr12 | 101697726 | ||||||
| chr12:101728972
|
T | C | 1 | a0001c0003t0005 | 2 | HG02165.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*27T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 9/9 | 27 | chr12 | 101728972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101698180
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.273+46G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698180 | ||||||
| chr12:101698206
|
G | C | 1 | a0001c0001t0003g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.273+72G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698206 | ||||||
| chr12:101698248
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.273+114G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698248 | ||||||
| chr12:101698256
|
T | G | 1 | a0001c0003t0001g0049 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.273+122T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698256 | ||||||
| chr12:101698457
|
G | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG01081.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+323G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698457 | ||||||
| chr12:101698490
|
T | C | 216 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(213): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.273+356T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698490 | ||||||
| chr12:101698608
|
G | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.273+474G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698608 | ||||||
| chr12:101698623
|
C | T | 1 | a0002c0002t0001g0041 | 2 | HG02074.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.273+489C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698623 | ||||||
| chr12:101698664
|
C | G | 24 | a0001c0001t0002g0018a0001c0001t0002g0118a0001c0001t0002g0120others(21): Show | 29 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+530C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698664 | ||||||
| chr12:101698920
|
A | T | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.273+786A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698920 | ||||||
| chr12:101698965
|
C | A | 2 | a0001c0001t0001g0139a0002c0002t0001g0031 | 3 | HG02109.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.273+831C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101698965 | ||||||
| chr12:101699054
|
A | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(212): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.273+920A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699054 | ||||||
| chr12:101699173
|
C | T | 7 | a0001c0001t0001g0249a0001c0001t0003g0023a0001c0001t0003g0045others(4): Show | 10 | HG00609.hp1 HG00621.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+1039C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699173 | ||||||
| chr12:101699211
|
C | A | 104 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0032others(101): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.273+1077C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699211 | ||||||
| chr12:101699248
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.273+1114C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699248 | ||||||
| chr12:101699278
|
A | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(212): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.273+1144A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699278 | ||||||
| chr12:101699307
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.273+1173A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699307 | ||||||
| chr12:101699334
|
G | A | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.273+1200G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699334 | ||||||
| chr12:101699353
|
TTGTCAAT others(15): Show |
T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1221_273+1242d others(24): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101699353 | |||||
| chr12:101699378
|
A | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1244A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699378 | ||||||
| chr12:101699380
|
G | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1246G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699380 | ||||||
| chr12:101699382
|
A | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1248A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699382 | ||||||
| chr12:101699386
|
C | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1252C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699386 | ||||||
| chr12:101699391
|
C | CT | 98 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0032others(95): Show | 168 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.273+1271dupT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101699391 | |||||
| chr12:101699391
|
C | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1257C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699391 | ||||||
| chr12:101699391
|
CT | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(88): Show | 126 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.273+1271delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101699391 | |||||
| chr12:101699411
|
A | G | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+1277A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699411 | ||||||
| chr12:101699418
|
C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0217a0001c0003t0001g0218 | 4 | HG00738.hp1 HG00738.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1284C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699418 | ||||||
| chr12:101699457
|
G | A | 123 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.273+1323G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699457 | ||||||
| chr12:101699681
|
G | A | 114 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0032others(111): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.273+1547G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699681 | ||||||
| chr12:101699696
|
T | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(44): Show | 75 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.273+1562T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699696 | ||||||
| chr12:101699746
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG01081.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+1612A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699746 | ||||||
| chr12:101699920
|
C | A | 212 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(209): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.273+1786C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699920 | ||||||
| chr12:101699976
|
G | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(212): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.273+1842G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101699976 | ||||||
| chr12:101700005
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+1871G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700005 | ||||||
| chr12:101700065
|
A | G | 1 | a0001c0003t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.273+1931A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700065 | ||||||
| chr12:101700318
|
CAT | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(55): Show | 84 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.273+2185_273+2186d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700318 | ||||||
| chr12:101700319
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0055others(21): Show | 35 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.273+2185A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700319 | ||||||
| chr12:101700321
|
GT | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0055others(18): Show | 32 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.273+2188delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700321 | ||||||
| chr12:101700322
|
T | A | 1 | a0001c0003t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+2188T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700322 | ||||||
| chr12:101700323
|
G | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0055others(19): Show | 33 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+2189G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700323 | ||||||
| chr12:101700323
|
GA | G | 103 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(100): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.273+2205delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101700323 | |||||
| chr12:101700581
|
A | G | 4 | a0002c0002t0001g0039a0002c0002t0001g0214a0002c0002t0001g0215others(1): Show | 5 | HG01192.hp1 HG01258.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+2447A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700581 | ||||||
| chr12:101700591
|
C | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+2457C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700591 | ||||||
| chr12:101700598
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0101 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.273+2464C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700598 | ||||||
| chr12:101700703
|
C | A | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+2569C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700703 | ||||||
| chr12:101700715
|
GT | G | 69 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(66): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.273+2583delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101700715 | |||||
| chr12:101700728
|
G | T | 4 | a0002c0002t0001g0020a0002c0002t0001g0208a0002c0002t0001g0209others(1): Show | 6 | NA18966.hp2 NA18968.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+2594G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700728 | ||||||
| chr12:101700745
|
C | T | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+2611C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700745 | ||||||
| chr12:101700800
|
G | C | 26 | a0001c0001t0001g0222a0001c0001t0001g0237a0001c0003t0001g0034others(23): Show | 47 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.273+2666G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700800 | ||||||
| chr12:101700865
|
A | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 192 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.273+2731A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700865 | ||||||
| chr12:101700948
|
A | G | 204 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(201): Show | 311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.273+2814A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700948 | ||||||
| chr12:101700994
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(4): Show | 13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+2860A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101700994 | ||||||
| chr12:101701023
|
G | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG02486.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.273+2889G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701023 | ||||||
| chr12:101701097
|
C | A | 2 | a0005c0008t0001g0253a0005c0008t0001g0254 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.273+2963C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701097 | ||||||
| chr12:101701162
|
A | T | 70 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.273+3028A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701162 | ||||||
| chr12:101701293
|
A | G | 8 | a0001c0003t0002g0129a0001c0005t0002g0014a0001c0005t0002g0128others(5): Show | 11 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+3159A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701293 | ||||||
| chr12:101701400
|
A | G | 204 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(201): Show | 311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.273+3266A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701400 | ||||||
| chr12:101701592
|
T | G | 25 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(22): Show | 30 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.273+3458T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701592 | ||||||
| chr12:101701716
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.273+3582T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701716 | ||||||
| chr12:101701738
|
A | G | 1 | a0002c0002t0001g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.273+3604A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701738 | ||||||
| chr12:101701768
|
A | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0101others(7): Show | 13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+3634A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701768 | ||||||
| chr12:101701789
|
A | G | 1 | a0001c0003t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.273+3655A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701789 | ||||||
| chr12:101701823
|
C | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(186): Show | 290 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.273+3689C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701823 | ||||||
| chr12:101701843
|
G | A | 1 | a0001c0012t0001g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.273+3709G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101701843 | ||||||
| chr12:101702042
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.273+3908C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702042 | ||||||
| chr12:101702120
|
G | A | 1 | a0001c0001t0007g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.273+3986G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702120 | ||||||
| chr12:101702234
|
A | T | 155 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(152): Show | 236 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.273+4100A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702234 | ||||||
| chr12:101702356
|
C | G | 1 | a0001c0003t0001g0175 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.273+4222C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702356 | ||||||
| chr12:101702644
|
CT | C | 20 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0042others(17): Show | 34 | HG00544.hp2 HG00597.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.273+4518delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101702644 | |||||
| chr12:101702712
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.273+4578C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702712 | ||||||
| chr12:101702759
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.273+4625C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702759 | ||||||
| chr12:101702827
|
G | T | 1 | a0002c0002t0001g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.273+4693G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702827 | ||||||
| chr12:101702889
|
G | A | 1 | a0001c0003t0001g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+4755G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702889 | ||||||
| chr12:101702924
|
C | A | 24 | a0001c0001t0001g0237a0001c0004t0001g0005a0001c0004t0001g0009others(21): Show | 44 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.273+4790C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702924 | ||||||
| chr12:101702998
|
T | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(29): Show | 54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.273+4864T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101702998 | ||||||
| chr12:101703025
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(95): Show | 164 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.273+4891A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703025 | ||||||
| chr12:101703049
|
G | A | 1 | a0002c0002t0001g0031 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+4915G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703049 | ||||||
| chr12:101703053
|
C | T | 25 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(22): Show | 30 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.273+4919C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703053 | ||||||
| chr12:101703234
|
T | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 86 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.273+5100T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703234 | ||||||
| chr12:101703300
|
G | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(106): Show | 181 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.273+5166G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703300 | ||||||
| chr12:101703363
|
G | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(107): Show | 182 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.273+5229G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703363 | ||||||
| chr12:101703419
|
C | T | 1 | a0002c0002t0001g0178 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.273+5285C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703419 | ||||||
| chr12:101703504
|
A | G | 2 | a0005c0008t0001g0253a0005c0008t0001g0254 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.273+5370A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703504 | ||||||
| chr12:101703648
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0093others(3): Show | 12 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+5514C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703648 | ||||||
| chr12:101703691
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0101 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.273+5557C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703691 | ||||||
| chr12:101703711
|
C | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(8): Show | 17 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+5577C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703711 | ||||||
| chr12:101703774
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(8): Show | 17 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+5640C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703774 | ||||||
| chr12:101703814
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.273+5680T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101703814 | ||||||
| chr12:101704175
|
AG | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(4): Show | 13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+6043delG | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704175 | |||||
| chr12:101704177
|
G | T | 4 | a0001c0001t0001g0047a0001c0012t0001g0102a0005c0008t0001g0253others(1): Show | 4 | HG01167.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+6043G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704177 | ||||||
| chr12:101704196
|
GT | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(8): Show | 17 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+6070delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704196 | |||||
| chr12:101704244
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0212a0001c0003t0001g0030 | 4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+6110G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704244 | ||||||
| chr12:101704404
|
C | CT | 64 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(61): Show | 108 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.273+6284dupT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704404 | |||||
| chr12:101704514
|
G | GCCTCAGC others(655): Show |
1 | a0001c0003t0001g0029 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+7058_273+7719d others(664): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704514 | |||||
| chr12:101704514
|
GCCTCAGC others(655): Show |
G | 26 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0028others(23): Show | 35 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.273+7058_273+7719d others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101704514 | |||||
| chr12:101704748
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.273+6614C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704748 | ||||||
| chr12:101704903
|
A | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(2): Show | 7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+6769A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704903 | ||||||
| chr12:101704970
|
C | A | 1 | a0002c0002t0001g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.273+6836C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101704970 | ||||||
| chr12:101705035
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(2): Show | 7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+6901C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705035 | ||||||
| chr12:101705061
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+6927G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705061 | ||||||
| chr12:101705177
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0003g0252 | 2 | NA18984.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.273+7043C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705177 | ||||||
| chr12:101705224
|
TGGCTAAT others(655): Show |
T | 70 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.273+7101_273+7762d others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101705224 | |||||
| chr12:101705283
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.273+7149G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705283 | ||||||
| chr12:101705296
|
C | T | 3 | a0001c0001t0001g0047a0001c0012t0001g0102a0002c0002t0001g0145 | 3 | HG01167.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.273+7162C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705296 | ||||||
| chr12:101705423
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.273+7289T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705423 | ||||||
| chr12:101705565
|
A | T | 66 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(63): Show | 110 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.273+7431A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705565 | ||||||
| chr12:101705664
|
A | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0004g0087others(3): Show | 6 | NA18747.hp1 NA18971.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+7530A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705664 | ||||||
| chr12:101705697
|
C | T | 74 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0025others(71): Show | 121 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(118): Show |
intron_variant | MODIFIER | c.273+7563C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705697 | ||||||
| chr12:101705719
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.273+7585C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705719 | ||||||
| chr12:101705752
|
T | TTTTG | 6 | a0001c0001t0004g0087a0001c0001t0004g0088a0001c0001t0004g0089others(3): Show | 6 | HG03471.hp1 HG03579.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+7638_273+7641d others(6): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101705752 | |||||
| chr12:101705871
|
A | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG02486.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.273+7737A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705871 | ||||||
| chr12:101705882
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.273+7748C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101705882 | ||||||
| chr12:101706270
|
A | C | 1 | a0005c0008t0001g0254 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274-7820A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706270 | ||||||
| chr12:101706327
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.274-7763G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706327 | ||||||
| chr12:101706352
|
GA | G | 68 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(65): Show | 112 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(109): Show |
intron_variant | MODIFIER | c.274-7726delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101706352 | |||||
| chr12:101706395
|
C | G | 1 | a0001c0001t0001g0025 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.274-7695C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706395 | ||||||
| chr12:101706458
|
A | G | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-7632A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706458 | ||||||
| chr12:101706486
|
T | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(29): Show | 54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.274-7604T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706486 | ||||||
| chr12:101706653
|
C | T | 23 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(20): Show | 43 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.274-7437C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706653 | ||||||
| chr12:101706762
|
A | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-7328A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706762 | ||||||
| chr12:101706780
|
G | A | 1 | a0002c0002t0001g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.274-7310G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706780 | ||||||
| chr12:101706809
|
TCTTTA | T | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-7276_274-7272d others(7): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101706809 | |||||
| chr12:101706810
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-7280C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101706810 | ||||||
| chr12:101707112
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.274-6978G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707112 | ||||||
| chr12:101707168
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.274-6922G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707168 | ||||||
| chr12:101707409
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-6681C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707409 | ||||||
| chr12:101707411
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-6679T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707411 | ||||||
| chr12:101707615
|
A | G | 1 | a0001c0012t0001g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274-6475A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707615 | ||||||
| chr12:101707671
|
A | G | 1 | a0002c0002t0001g0177 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274-6419A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707671 | ||||||
| chr12:101707848
|
C | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(44): Show | 58 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.274-6242C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707848 | ||||||
| chr12:101707872
|
G | A | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-6218G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707872 | ||||||
| chr12:101707949
|
C | T | 3 | a0001c0004t0001g0043a0001c0004t0001g0235a0001c0004t0001g0236 | 4 | NA18955.hp2 NA18999.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-6141C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707949 | ||||||
| chr12:101707976
|
C | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0058others(33): Show | 59 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.274-6114C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101707976 | ||||||
| chr12:101708337
|
G | T | 26 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(23): Show | 31 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.274-5753G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708337 | ||||||
| chr12:101708356
|
G | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 9 | HG01884.hp1 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-5734G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708356 | ||||||
| chr12:101708492
|
G | A | 2 | a0001c0001t0001g0017a0006c0011t0001g0076 | 4 | NA18945.hp1 NA18954.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-5598G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708492 | ||||||
| chr12:101708509
|
T | C | 2 | a0002c0002t0001g0182a0002c0002t0001g0183 | 2 | HG01517.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.274-5581T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708509 | ||||||
| chr12:101708628
|
GACAGGGT others(4673): Show |
G | 24 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(21): Show | 44 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.274-5457_274-778de others(1): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101708628 | |||||
| chr12:101708642
|
C | T | 2 | a0001c0001t0001g0237a0001c0003t0001g0104 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.274-5448C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708642 | ||||||
| chr12:101708818
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0101others(5): Show | 11 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-5272A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708818 | ||||||
| chr12:101708833
|
G | A | 3 | a0001c0003t0001g0158a0001c0003t0001g0159a0001c0003t0001g0160 | 3 | HG01361.hp2 HG01928.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.274-5257G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708833 | ||||||
| chr12:101708840
|
G | A | 1 | a0001c0003t0001g0066 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.274-5250G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101708840 | ||||||
| chr12:101709002
|
A | G | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-5088A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709002 | ||||||
| chr12:101709210
|
G | A | 123 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 198 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.274-4880G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709210 | ||||||
| chr12:101709388
|
C | CA | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0032others(50): Show | 71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.274-4680dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101709388 | |||||
| chr12:101709388
|
C | CAA | 8 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0002g0118others(5): Show | 9 | HG00408.hp1 HG00621.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-4681_274-4680d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101709388 | |||||
| chr12:101709388
|
CA | C | 67 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0025others(64): Show | 109 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.274-4680delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101709388 | |||||
| chr12:101709410
|
A | C | 1 | a0001c0003t0001g0072 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.274-4680A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709410 | ||||||
| chr12:101709481
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.274-4609A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709481 | ||||||
| chr12:101709608
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.274-4482C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709608 | ||||||
| chr12:101709710
|
G | A | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-4380G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709710 | ||||||
| chr12:101709864
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0101others(5): Show | 11 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-4226G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709864 | ||||||
| chr12:101709959
|
G | A | 1 | a0001c0001t0001g0011 | 4 | HG02165.hp1 NA18947.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-4131G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101709959 | ||||||
| chr12:101710125
|
A | G | 1 | a0002c0002t0001g0191 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.274-3965A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710125 | ||||||
| chr12:101710557
|
C | T | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-3533C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710557 | ||||||
| chr12:101710774
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-3316G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710774 | ||||||
| chr12:101710863
|
A | G | 2 | a0001c0001t0001g0047a0001c0012t0001g0102 | 2 | HG01167.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.274-3227A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710863 | ||||||
| chr12:101710889
|
G | A | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-3201G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101710889 | ||||||
| chr12:101711027
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-3063G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711027 | ||||||
| chr12:101711179
|
G | C | 14 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0037others(11): Show | 20 | HG00735.hp2 HG01106.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.274-2911G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711179 | ||||||
| chr12:101711211
|
G | T | 1 | a0002c0002t0001g0245 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.274-2879G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711211 | ||||||
| chr12:101711228
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-2862G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711228 | ||||||
| chr12:101711421
|
C | G | 1 | a0001c0001t0002g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.274-2669C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711421 | ||||||
| chr12:101711460
|
C | T | 1 | a0002c0002t0001g0204 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.274-2630C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711460 | ||||||
| chr12:101711566
|
T | TACA | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(29): Show | 54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.274-2523_274-2521d others(5): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101711566 | |||||
| chr12:101711581
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-2509C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711581 | ||||||
| chr12:101711769
|
C | T | 1 | a0001c0003t0001g0218 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.274-2321C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711769 | ||||||
| chr12:101711783
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274-2307C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711783 | ||||||
| chr12:101711851
|
T | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.274-2239T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101711851 | ||||||
| chr12:101712053
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.274-2037C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712053 | ||||||
| chr12:101712122
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-1968G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712122 | ||||||
| chr12:101712195
|
T | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 13 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.274-1895T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712195 | ||||||
| chr12:101712260
|
A | G | 4 | a0001c0001t0001g0114a0001c0003t0001g0163a0004c0007t0001g0036others(1): Show | 5 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-1830A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712260 | ||||||
| chr12:101712362
|
C | T | 1 | a0002c0002t0001g0188 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.274-1728C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712362 | ||||||
| chr12:101712406
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0101 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.274-1684G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712406 | ||||||
| chr12:101712563
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-1527C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712563 | ||||||
| chr12:101712887
|
A | G | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-1203A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712887 | ||||||
| chr12:101712891
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.274-1199G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101712891 | ||||||
| chr12:101713134
|
G | C | 1 | a0001c0001t0002g0124 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-956G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713134 | ||||||
| chr12:101713249
|
T | C | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-841T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713249 | ||||||
| chr12:101713549
|
A | G | 4 | a0001c0001t0001g0157a0001c0001t0003g0045a0001c0001t0003g0251others(1): Show | 5 | HG00609.hp1 NA18943.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-541A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713549 | ||||||
| chr12:101713556
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 9 | HG01884.hp1 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-534A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713556 | ||||||
| chr12:101713600
|
C | T | 4 | a0001c0001t0001g0026a0001c0001t0003g0023a0001c0001t0003g0048others(1): Show | 7 | HG00621.hp1 NA18942.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-490C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713600 | ||||||
| chr12:101713650
|
T | G | 4 | a0003c0006t0001g0223a0003c0006t0001g0224a0003c0006t0001g0225others(1): Show | 4 | NA18612.hp2 NA18747.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-440T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713650 | ||||||
| chr12:101713687
|
A | AATCTAGT others(14): Show |
24 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(21): Show | 44 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.274-396_274-395ins others(21): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 101713687 | |||||
| chr12:101713847
|
A | G | 12 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(9): Show | 14 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-243A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713847 | ||||||
| chr12:101713955
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG02486.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.274-135C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713955 | ||||||
| chr12:101713956
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-134G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713956 | ||||||
| chr12:101713971
|
G | A | 3 | a0001c0003t0001g0158a0001c0003t0001g0159a0001c0003t0001g0160 | 3 | HG01361.hp2 HG01928.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.274-119G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 1/8 | chr12 | 101713971 | ||||||
| chr12:101714414
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.422-90C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 2/8 | chr12 | 101714414 | ||||||
| chr12:101714486
|
A | T | 2 | a0001c0003t0001g0171a0001c0003t0001g0213 | 2 | HG01358.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.422-18A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 2/8 | chr12 | 101714486 | ||||||
| chr12:101714683
|
A | G | 1 | a0001c0003t0001g0084 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.563+38A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714683 | ||||||
| chr12:101714764
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.563+119C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714764 | ||||||
| chr12:101714807
|
C | T | 168 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 252 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.563+162C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714807 | ||||||
| chr12:101714966
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.563+321C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714966 | ||||||
| chr12:101714996
|
G | A | 135 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(132): Show | 207 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.563+351G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101714996 | ||||||
| chr12:101715168
|
T | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(4): Show | 9 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.563+523T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715168 | ||||||
| chr12:101715497
|
A | ACATGTTT others(1): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0111others(3): Show | 9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.563+853_563+860dup others(8): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 101715497 | |||||
| chr12:101715569
|
TG | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0143others(5): Show | 10 | HG01496.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.563+927delG | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 101715569 | |||||
| chr12:101715663
|
A | G | 1 | a0002c0002t0001g0031 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.563+1018A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715663 | ||||||
| chr12:101715708
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.564-1020T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715708 | ||||||
| chr12:101715951
|
C | A | 1 | a0001c0001t0002g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.564-777C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101715951 | ||||||
| chr12:101716026
|
G | A | 1 | a0001c0003t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.564-702G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716026 | ||||||
| chr12:101716097
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564-631A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716097 | ||||||
| chr12:101716115
|
T | C | 34 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(31): Show | 57 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.564-613T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716115 | ||||||
| chr12:101716231
|
C | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0112others(1): Show | 7 | HG01884.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.564-497C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716231 | ||||||
| chr12:101716291
|
T | A | 12 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(9): Show | 14 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.564-437T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716291 | ||||||
| chr12:101716327
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(156): Show | 242 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.564-401A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716327 | ||||||
| chr12:101716523
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.564-205G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716523 | ||||||
| chr12:101716557
|
T | C | 167 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 251 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.564-171T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716557 | ||||||
| chr12:101716698
|
C | T | 1 | a0001c0010t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.564-30C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 3/8 | chr12 | 101716698 | ||||||
| chr12:101716835
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.648+23A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101716835 | ||||||
| chr12:101716914
|
A | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.648+102A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101716914 | ||||||
| chr12:101716914
|
AT | A | 108 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(105): Show | 167 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.648+114delT | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101716914 | |||||
| chr12:101716914
|
ATT | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0099a0001c0001t0001g0100others(27): Show | 35 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.648+113_648+114del others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101716914 | |||||
| chr12:101717106
|
T | C | 1 | a0002c0002t0006g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.648+294T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717106 | ||||||
| chr12:101717145
|
T | A | 20 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 26 | HG00609.hp1 HG00621.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.648+333T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717145 | ||||||
| chr12:101717364
|
T | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0101a0001c0001t0001g0237 | 3 | HG02451.hp1 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.648+552T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717364 | ||||||
| chr12:101717395
|
G | C | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.648+583G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717395 | ||||||
| chr12:101717639
|
G | T | 2 | a0001c0003t0001g0159a0001c0003t0001g0160 | 2 | HG01928.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.648+827G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717639 | ||||||
| chr12:101717652
|
G | A | 32 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(29): Show | 55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.648+840G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717652 | ||||||
| chr12:101717924
|
T | C | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 9 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.648+1112T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717924 | ||||||
| chr12:101717969
|
A | G | 2 | a0001c0004t0001g0009a0001c0004t0001g0234 | 6 | NA18945.hp2 NA18946.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.648+1157A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717969 | ||||||
| chr12:101717976
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.648+1164T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101717976 | ||||||
| chr12:101718072
|
G | T | 20 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 26 | HG00609.hp1 HG00621.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.648+1260G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718072 | ||||||
| chr12:101718092
|
A | G | 1 | a0001c0003t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.648+1280A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718092 | ||||||
| chr12:101718233
|
T | A | 1 | a0002c0002t0001g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.648+1421T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718233 | ||||||
| chr12:101718289
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.648+1477G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718289 | ||||||
| chr12:101718410
|
T | A | 1 | a0001c0003t0001g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.648+1598T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718410 | ||||||
| chr12:101718513
|
A | T | 32 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(29): Show | 55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.649-1610A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718513 | ||||||
| chr12:101718529
|
A | G | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02257.hp1 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.649-1594A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718529 | ||||||
| chr12:101718565
|
C | T | 1 | a0002c0002t0001g0202 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.649-1558C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718565 | ||||||
| chr12:101718606
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.649-1517G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718606 | ||||||
| chr12:101718664
|
T | TA | 7 | a0001c0001t0001g0060a0001c0001t0001g0101a0001c0001t0001g0249others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-1441dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101718664 | |||||
| chr12:101718664
|
TA | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0099others(16): Show | 19 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.649-1441delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101718664 | |||||
| chr12:101718687
|
T | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02486.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-1436T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718687 | ||||||
| chr12:101718739
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02486.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-1384C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718739 | ||||||
| chr12:101718775
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.649-1348A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101718775 | ||||||
| chr12:101719021
|
G | T | 1 | a0001c0003t0001g0106 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.649-1102G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719021 | ||||||
| chr12:101719148
|
C | T | 1 | a0001c0003t0001g0167 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.649-975C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719148 | ||||||
| chr12:101719156
|
G | GA | 71 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(68): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.649-946dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | |||||
| chr12:101719156
|
G | GAA | 81 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(78): Show | 138 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.649-947_649-946dup others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | |||||
| chr12:101719156
|
G | GAAA | 34 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(31): Show | 44 | HG00735.hp2 HG01081.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.649-948_649-946dup others(3): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | |||||
| chr12:101719156
|
G | GAAAA | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 8 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.649-949_649-946dup others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719156 | |||||
| chr12:101719156
|
G | GGAA | 10 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0020others(7): Show | 17 | NA18944.hp1 NA18954.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.649-967_649-966ins others(3): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719156 | ||||||
| chr12:101719413
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0111others(3): Show | 9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.649-710A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719413 | ||||||
| chr12:101719474
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0101 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.649-649T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719474 | ||||||
| chr12:101719524
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(4): Show | 13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.649-599T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719524 | ||||||
| chr12:101719558
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.649-565A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719558 | ||||||
| chr12:101719844
|
G | T | 2 | a0001c0005t0002g0133a0001c0010t0001g0092 | 2 | HG02040.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.649-279G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719844 | ||||||
| chr12:101719954
|
T | TTAAA | 170 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 254 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.649-168_649-165dup others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 101719954 | |||||
| chr12:101719959
|
A | T | 1 | a0003c0006t0001g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.649-164A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101719959 | ||||||
| chr12:101720007
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.649-116T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101720007 | ||||||
| chr12:101720023
|
G | T | 1 | a0001c0004t0001g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.649-100G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101720023 | ||||||
| chr12:101720053
|
T | A | 1 | a0001c0001t0001g0027 | 2 | HG02056.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.649-70T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 4/8 | chr12 | 101720053 | ||||||
| chr12:101720424
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.780+170T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720424 | ||||||
| chr12:101720659
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.780+405A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720659 | ||||||
| chr12:101720886
|
C | A | 1 | a0001c0003t0001g0034 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.780+632C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720886 | ||||||
| chr12:101720965
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.780+711C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720965 | ||||||
| chr12:101720997
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.780+743C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101720997 | ||||||
| chr12:101721004
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0212a0001c0003t0001g0030 | 4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+750G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721004 | ||||||
| chr12:101721036
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0111others(3): Show | 9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.780+782A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721036 | ||||||
| chr12:101721101
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0212a0001c0003t0001g0030 | 4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+847G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721101 | ||||||
| chr12:101721114
|
G | A | 1 | a0001c0004t0001g0233 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.780+860G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721114 | ||||||
| chr12:101721184
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.780+930G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721184 | ||||||
| chr12:101721242
|
G | T | 19 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(16): Show | 21 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.780+988G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721242 | ||||||
| chr12:101721455
|
C | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.780+1201C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721455 | ||||||
| chr12:101721487
|
C | T | 2 | a0001c0001t0004g0088a0001c0001t0004g0089 | 2 | NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.780+1233C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721487 | ||||||
| chr12:101721511
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.780+1257T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721511 | ||||||
| chr12:101721650
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0255 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.780+1396T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721650 | ||||||
| chr12:101721710
|
G | A | 2 | a0002c0002t0001g0096a0002c0002t0001g0196 | 2 | NA18951.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.780+1456G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721710 | ||||||
| chr12:101721991
|
G | A | 1 | a0001c0003t0001g0034 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.781-1177G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101721991 | ||||||
| chr12:101722036
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.781-1132G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722036 | ||||||
| chr12:101722058
|
C | CA | 33 | a0001c0001t0001g0060a0001c0001t0001g0101a0001c0001t0001g0237others(30): Show | 52 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.781-1098dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722058 | |||||
| chr12:101722058
|
C | CAA | 2 | a0001c0004t0001g0009a0001c0005t0002g0131 | 6 | NA18941.hp1 NA18945.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1099_781-1098d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722058 | |||||
| chr12:101722058
|
CA | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0003t0001g0029others(1): Show | 9 | HG01243.hp1 HG01257.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-1098delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722058 | |||||
| chr12:101722315
|
A | C | 1 | a0002c0002t0001g0195 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.781-853A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722315 | ||||||
| chr12:101722591
|
G | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(10): Show | 19 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-577G>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722591 | ||||||
| chr12:101722707
|
T | TA | 7 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0003t0001g0159others(4): Show | 7 | HG01928.hp1 HG02451.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-442dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | |||||
| chr12:101722707
|
T | TAA | 12 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(9): Show | 18 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-443_781-442dup others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | |||||
| chr12:101722707
|
TA | T | 14 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0093others(11): Show | 19 | HG00609.hp2 HG00639.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-442delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | |||||
| chr12:101722707
|
TAA | T | 20 | a0001c0001t0001g0055a0001c0001t0001g0099a0001c0001t0001g0100others(17): Show | 22 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.781-443_781-442del others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | |||||
| chr12:101722707
|
TAAA | T | 85 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(82): Show | 135 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.781-444_781-442del others(3): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | |||||
| chr12:101722707
|
TAAAAAAA | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0112others(2): Show | 8 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-448_781-442del others(7): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 101722707 | |||||
| chr12:101722878
|
G | A | 203 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.781-290G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722878 | ||||||
| chr12:101722973
|
T | A | 1 | a0002c0002t0001g0195 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.781-195T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101722973 | ||||||
| chr12:101723014
|
G | A | 108 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(105): Show | 160 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.781-154G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 5/8 | chr12 | 101723014 | ||||||
| chr12:101723371
|
G | A | 19 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(16): Show | 21 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.939+45G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723371 | ||||||
| chr12:101723448
|
T | A | 2 | a0001c0001t0004g0088a0001c0001t0004g0089 | 2 | NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.939+122T>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723448 | ||||||
| chr12:101723470
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.939+144G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723470 | ||||||
| chr12:101723472
|
TAA | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0003t0001g0074 | 3 | HG02486.hp2 HG03486.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.939+147_939+148del others(2): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 6/8 | chr12 | 101723472 | ||||||
| chr12:101723942
|
C | A | 2 | a0001c0001t0007g0117a0001c0001t0007g0119 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1065+95C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101723942 | ||||||
| chr12:101724150
|
C | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0212 | 2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1065+303C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724150 | ||||||
| chr12:101724218
|
C | CA | 39 | a0001c0001t0001g0013a0001c0001t0001g0063a0001c0001t0001g0078others(36): Show | 59 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.1065+387dupA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101724218 | |||||
| chr12:101724490
|
C | T | 32 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(29): Show | 55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1065+643C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724490 | ||||||
| chr12:101724744
|
C | T | 1 | a0001c0003t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1065+897C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724744 | ||||||
| chr12:101724754
|
A | ATAGATAT | 121 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(118): Show | 179 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1065+909_1065+910i others(9): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101724754 | |||||
| chr12:101724809
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1065+962C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724809 | ||||||
| chr12:101724841
|
T | C | 60 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0016others(57): Show | 102 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1065+994T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101724841 | ||||||
| chr12:101725021
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1065+1174C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725021 | ||||||
| chr12:101725061
|
T | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065+1214T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725061 | ||||||
| chr12:101725095
|
G | T | 254 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(251): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1066-1199G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725095 | ||||||
| chr12:101725100
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1066-1194A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725100 | ||||||
| chr12:101725156
|
G | A | 18 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(15): Show | 20 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1066-1138G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725156 | ||||||
| chr12:101725236
|
T | G | 66 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0050others(63): Show | 110 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.1066-1058T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725236 | ||||||
| chr12:101725293
|
C | T | 2 | a0002c0002t0006g0193a0002c0002t0006g0198 | 2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1066-1001C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725293 | ||||||
| chr12:101725294
|
G | A | 1 | a0001c0001t0004g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1066-1000G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725294 | ||||||
| chr12:101725338
|
A | G | 1 | a0001c0003t0001g0069 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1066-956A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725338 | ||||||
| chr12:101725441
|
T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(4): Show | 13 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1066-853T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725441 | ||||||
| chr12:101725508
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1066-786T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725508 | ||||||
| chr12:101725535
|
G | A | 2 | a0001c0005t0002g0133a0001c0010t0001g0092 | 2 | HG02040.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1066-759G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725535 | ||||||
| chr12:101725565
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1066-729G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725565 | ||||||
| chr12:101725623
|
CA | C | 53 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0058others(50): Show | 79 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1066-654delA | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101725623 | |||||
| chr12:101725623
|
CAAAAAAA others(2): Show |
C | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1066-662_1066-654d others(11): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 101725623 | |||||
| chr12:101725629
|
A | C | 121 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(118): Show | 179 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1066-665A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725629 | ||||||
| chr12:101725630
|
A | C | 51 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0058others(48): Show | 77 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1066-664A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725630 | ||||||
| chr12:101725638
|
A | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(28): Show | 53 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(50): Show |
intron_variant | MODIFIER | c.1066-656A>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725638 | ||||||
| chr12:101725648
|
A | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(29): Show | 54 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(51): Show |
intron_variant | MODIFIER | c.1066-646A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725648 | ||||||
| chr12:101725671
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1066-623A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725671 | ||||||
| chr12:101725868
|
G | A | 3 | a0001c0004t0001g0042a0001c0004t0001g0229a0001c0004t0001g0231 | 4 | HG01106.hp1 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-426G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101725868 | ||||||
| chr12:101726109
|
A | G | 1 | a0003c0006t0001g0224 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1066-185A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726109 | ||||||
| chr12:101726131
|
A | T | 1 | a0001c0001t0001g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1066-163A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726131 | ||||||
| chr12:101726144
|
A | G | 1 | a0001c0005t0002g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1066-150A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726144 | ||||||
| chr12:101726200
|
G | A | 3 | a0001c0003t0001g0165a0001c0003t0001g0171a0001c0003t0001g0213 | 3 | HG01358.hp1 HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1066-94G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726200 | ||||||
| chr12:101726222
|
A | G | 12 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0058others(9): Show | 12 | HG00280.hp2 HG00741.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-72A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 7/8 | chr12 | 101726222 | ||||||
| chr12:101726418
|
TTGAC | T | 7 | a0001c0003t0001g0030a0001c0003t0001g0040a0001c0003t0001g0084others(4): Show | 9 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1176+20_1176+23del others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101726418 | |||||
| chr12:101726427
|
T | TAATA | 12 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0058others(9): Show | 12 | HG00280.hp2 HG00741.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1176+24_1176+27dup others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101726427 | |||||
| chr12:101726447
|
G | T | 1 | a0001c0003t0001g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1176+43G>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726447 | ||||||
| chr12:101726511
|
C | A | 104 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(101): Show | 156 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1176+107C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726511 | ||||||
| chr12:101726585
|
C | T | 32 | a0001c0004t0001g0005a0001c0004t0001g0009a0001c0004t0001g0010others(29): Show | 55 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1176+181C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726585 | ||||||
| chr12:101726586
|
A | G | 258 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(255): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1176+182A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726586 | ||||||
| chr12:101726630
|
C | A | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1176+226C>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101726630 | ||||||
| chr12:101726883
|
TTC | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(80): Show | 131 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1176+481_1176+482d others(4): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101726883 | |||||
| chr12:101727196
|
AACTT | A | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 308 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.1176+797_1176+800d others(6): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101727196 | |||||
| chr12:101727278
|
G | A | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG00280.hp2 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1176+874G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727278 | ||||||
| chr12:101727315
|
T | G | 38 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(35): Show | 61 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1176+911T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727315 | ||||||
| chr12:101727408
|
A | G | 1 | a0002c0002t0001g0156 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1176+1004A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727408 | ||||||
| chr12:101727488
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0143others(6): Show | 11 | HG01496.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1176+1084G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727488 | ||||||
| chr12:101727496
|
CAAA | C | 118 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(115): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1176+1104_1176+110 others(7): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101727496 | |||||
| chr12:101727496
|
CAAAA | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(79): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1176+1103_1176+110 others(8): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101727496 | |||||
| chr12:101727509
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1176+1105A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727509 | ||||||
| chr12:101727512
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1176+1108G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727512 | ||||||
| chr12:101727881
|
T | C | 20 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0099others(17): Show | 22 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1177-1020T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101727881 | ||||||
| chr12:101728090
|
A | G | 18 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(15): Show | 20 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1177-811A>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728090 | ||||||
| chr12:101728264
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG00280.hp2 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-637C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728264 | ||||||
| chr12:101728352
|
CATT | C | 20 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 26 | HG00609.hp1 HG00621.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1177-546_1177-544d others(5): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101728352 | |||||
| chr12:101728378
|
T | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(9): Show | 18 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1177-523T>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728378 | ||||||
| chr12:101728466
|
A | T | 1 | a0002c0002t0001g0190 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1177-435A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728466 | ||||||
| chr12:101728527
|
A | T | 1 | a0002c0002t0001g0190 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1177-374A>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728527 | ||||||
| chr12:101728578
|
TAAAG | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0143a0001c0001t0001g0147others(3): Show | 7 | HG01496.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-320_1177-317d others(6): Show |
CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 101728578 | |||||
| chr12:101728722
|
C | T | 2 | a0001c0004t0001g0010a0001c0004t0001g0021 | 8 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1177-179C>T | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728722 | ||||||
| chr12:101728744
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-157T>C | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728744 | ||||||
| chr12:101728760
|
C | G | 1 | a0001c0003t0001g0173 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1177-141C>G | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728760 | ||||||
| chr12:101728876
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1177-25G>A | CHPT1 | ENSG00000111666.11 | transcript | ENST00000229266.8 | protein_coding | 8/8 | chr12 | 101728876 |