Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84260 |
| ensemblid | ENSG00000139437.18 |
| hgncid | 28135 |
| symbol | TCHP |
| name | trichoplein keratin filament binding |
| refseq_nuc | NM_001143852.2 |
| refseq_prot | NP_001137324.1 |
| ensembl_nuc | ENST00000405876.9 |
| ensembl_prot | ENSP00000384520.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109900274 |
| end | 109918069 |
| strand | + |
| ver | v1.2 |
| region | chr12:109900274-109918069 |
| region5000 | chr12:109895274-109923069 |
| regionname0 | TCHP_chr12_109900274_109918069 |
| regionname5000 | TCHP_chr12_109895274_109923069 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 498 | 210 | 27 | 41 | 93 | 15 | 32 | 72 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0002 | 0/0 | 498 | 57 | 22 | 10 | 22 | 1 | 2 | 16 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0003 | 0/0 | 498 | 50 | 34 | 6 | 6 | 0 | 4 | 6 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0004 | 0/0 | 498 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0005 | 0/0 | 498 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0006 | 0/0 | 498 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0007 | 0/0 | 498 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0008 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0009 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0010 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0011 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(493): Show |
chr12 | 109895274 | 109923069 |
| a0012 | 0/0 | 266 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | MALPT others(261): Show |
chr12 | 109895274 | 109923069 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1494 | 196 | 27 | 41 | 79 | 15 | 32 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0001c0004 | 0/0 | 1494 | 13 | 0 | 0 | 13 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0001c0013 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0002c0002 | 0/0 | 1494 | 43 | 18 | 1 | 22 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0002c0005 | 0/0 | 1494 | 12 | 4 | 7 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0002c0011 | 0/0 | 1494 | 2 | 0 | 2 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0003c0003 | 0/0 | 1494 | 41 | 26 | 5 | 6 | 0 | 4 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0003c0006 | 0/0 | 1494 | 9 | 8 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0004c0007 | 0/0 | 1494 | 3 | 2 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0005c0008 | 0/0 | 1494 | 3 | 3 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0006c0010 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0007c0009 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0008c0014 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0009c0017 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0010c0012 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0011c0016 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 | ||
| a0012c0015 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | ATGGC others(1489): Show |
chr12 | 109895274 | 109923069 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3096 | 176 | 23 | 30 | 76 | 14 | 31 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0003 | 0/0 | 3096 | 6 | 0 | 5 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0005 | 0/0 | 3096 | 3 | 0 | 3 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0007 | 0/0 | 3096 | 3 | 3 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0008 | 0/0 | 3096 | 2 | 1 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0009 | 0/0 | 3096 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0010 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0011 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0012 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0013 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0001t0014 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0004t0001 | 0/0 | 3096 | 13 | 0 | 0 | 13 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0001c0013t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0002c0002t0001 | 0/0 | 3096 | 43 | 18 | 1 | 22 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0002c0005t0002 | 0/0 | 3096 | 12 | 4 | 7 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0002c0011t0001 | 0/0 | 3096 | 2 | 0 | 2 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0003c0003t0001 | 0/0 | 3096 | 35 | 25 | 3 | 5 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0003c0003t0004 | 0/0 | 3096 | 5 | 0 | 2 | 1 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0003c0003t0015 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0003c0006t0001 | 0/0 | 3096 | 9 | 8 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0004c0007t0006 | 0/0 | 3096 | 3 | 2 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0005c0008t0001 | 0/0 | 3096 | 3 | 3 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0006c0010t0001 | 0/0 | 3096 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0007c0009t0001 | 0/0 | 3096 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0008c0014t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0009c0017t0001 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0010c0012t0002 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0011c0016t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| a0012c0015t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | GTCGT others(3091): Show |
chr12 | 109895274 | 109923069 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 61 | 11 | 10 | 27 | 5 | 6 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0002 | 0/0 | 24 | 3 | 3 | 10 | 0 | 8 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 1 | 4 | 2 | 6 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0005g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0007g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0001t0014g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0004t0001g0003 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0001c0013t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0008 | 0/0 | 9 | 5 | 0 | 4 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0005t0002g0006 | 0/0 | 10 | 4 | 5 | 0 | 1 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0005t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0005t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0011t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0002c0011t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0004 | 0/0 | 13 | 8 | 0 | 4 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0009 | 0/0 | 9 | 6 | 3 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0004g0015 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0003t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0003c0006t0001g0007 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0004c0007t0006g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0005c0008t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0006c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0006c0010t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0007c0009t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0008c0014t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0009c0017t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0010c0012t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0011c0016t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| a0012c0015t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00323 | hp1 | a0002 | c0005 | t0002 | g0006 | EUR | FIN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | CHS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00642 | hp2 | a0002 | c0005 | t0002 | g0006 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00735 | hp1 | a0003 | c0003 | t0004 | g0015 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00738 | hp2 | a0002 | c0011 | t0001 | g0096 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01069 | hp2 | a0002 | c0011 | t0001 | g0097 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01081 | hp1 | a0002 | c0005 | t0002 | g0006 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01099 | hp1 | a0002 | c0005 | t0002 | g0006 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01099 | hp2 | a0004 | c0007 | t0006 | g0018 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01106 | hp1 | a0003 | c0003 | t0004 | g0015 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01167 | hp2 | a0003 | c0006 | t0001 | g0007 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01175 | hp1 | a0002 | c0005 | t0002 | g0006 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01243 | hp1 | a0002 | c0005 | t0002 | g0006 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01361 | hp1 | a0002 | c0005 | t0002 | g0045 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0094 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01943 | hp2 | a0002 | c0005 | t0002 | g0046 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG01952 | hp2 | a0001 | c0001 | t0014 | g0011 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02071 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02080 | hp2 | a0008 | c0014 | t0001 | g0079 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02145 | hp2 | a0004 | c0007 | t0006 | g0018 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | CDX | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | CDX | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0093 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02280 | hp2 | a0003 | c0006 | t0001 | g0007 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02451 | hp1 | a0003 | c0006 | t0001 | g0007 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02572 | hp1 | a0005 | c0008 | t0001 | g0021 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02615 | hp1 | a0003 | c0006 | t0001 | g0007 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02622 | hp2 | a0003 | c0006 | t0001 | g0007 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02630 | hp1 | a0003 | c0006 | t0001 | g0007 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02647 | hp1 | a0002 | c0005 | t0002 | g0006 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02735 | hp1 | a0003 | c0003 | t0004 | g0015 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02809 | hp1 | a0002 | c0005 | t0002 | g0006 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02818 | hp1 | a0003 | c0006 | t0001 | g0007 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03041 | hp2 | a0010 | c0012 | t0002 | g0006 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03130 | hp1 | a0002 | c0005 | t0002 | g0006 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03130 | hp2 | a0003 | c0006 | t0001 | g0007 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03139 | hp2 | a0002 | c0005 | t0002 | g0006 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03209 | hp2 | a0004 | c0007 | t0006 | g0018 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0009 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03486 | hp1 | a0005 | c0008 | t0001 | g0021 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0038 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0042 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03927 | hp1 | a0001 | c0001 | t0009 | g0053 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03942 | hp1 | a0003 | c0003 | t0004 | g0015 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | YRI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18906 | hp2 | a0003 | c0006 | t0001 | g0007 | AFR | YRI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18939 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18944 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18952 | hp2 | a0001 | c0013 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18962 | hp1 | a0006 | c0010 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18979 | hp2 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18982 | hp1 | a0003 | c0003 | t0004 | g0043 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18995 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19007 | hp1 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19012 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | LWK | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19043 | hp1 | a0003 | c0003 | t0015 | g0041 | AFR | LWK | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19077 | hp1 | a0011 | c0016 | t0001 | g0017 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19078 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19083 | hp1 | a0006 | c0010 | t0001 | g0010 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19083 | hp2 | a0012 | c0015 | t0001 | g0048 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19085 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | YRI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA19240 | hp2 | a0005 | c0008 | t0001 | g0021 | AFR | YRI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0009 | AFR | ASW | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | ASW | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02486 | hp2 | a0009 | c0017 | t0001 | g0035 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0107 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | MSL | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | USA | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | USA | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | LWK | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TCHP_chr12_109895274_109923069 | TCHP | chr12 | 109895274 | 109923069 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109904128 | A | G | 7 | a0002 a0003 a0004 others(4): Show |
116 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(113): Show |
missense_variant | MODERATE | c.380A>G | p.Lys127Arg | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 3/13 | 533/3096 | 380/1497 | 127/498 | chr12 | 109904128 | |||
| chr12:109904756 | A | G | 1 | a0010 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.419A>G | p.Tyr140Cys | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/13 | 572/3096 | 419/1497 | 140/498 | chr12 | 109904756 | |||
| chr12:109904789 | G | A | 1 | a0007 | 2 | NA18979.hp2 NA19007.hp1 |
missense_variant | MODERATE | c.452G>A | p.Arg151Gln | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/13 | 605/3096 | 452/1497 | 151/498 | chr12 | 109904789 | |||
| chr12:109908587 | C | T | 1 | a0009 | 1 | HG02486.hp2 | missense_variant&splice_region_variant | MODERATE | c.701C>T | p.Ala234Val | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 854/3096 | 701/1497 | 234/498 | chr12 | 109908587 | |||
| chr12:109908593 | A | G | 1 | a0004 | 3 | HG01099.hp2 HG02145.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.707A>G | p.Lys236Arg | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 860/3096 | 707/1497 | 236/498 | chr12 | 109908593 | |||
| chr12:109908605 | A | T | 1 | a0012 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.719A>T | p.Glu240Val | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 872/3096 | 719/1497 | 240/498 | chr12 | 109908605 | |||
| chr12:109908628 | C | T | 1 | a0008 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.742C>T | p.Arg248Trp | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 895/3096 | 742/1497 | 248/498 | chr12 | 109908628 | |||
| chr12:109908667 | A | G | 1 | a0011 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.781A>G | p.Met261Val | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 934/3096 | 781/1497 | 261/498 | chr12 | 109908667 | |||
| chr12:109908685 | A | T | 1 | a0012 | 1 | NA19083.hp2 | stop_gained | HIGH | c.799A>T | p.Lys267* | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 952/3096 | 799/1497 | 267/498 | chr12 | 109908685 | |||
| chr12:109913043 | C | T | 1 | a0006 | 2 | NA18962.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.1105C>T | p.Arg369Cys | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/13 | 1258/3096 | 1105/1497 | 369/498 | chr12 | 109913043 | |||
| chr12:109914556 | G | A | 3 | a0003 a0005 a0009 |
54 | HG00735.hp1 HG01106.hp1 HG01167.hp2 others(51): Show |
missense_variant | MODERATE | c.1249G>A | p.Glu417Lys | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/13 | 1402/3096 | 1249/1497 | 417/498 | chr12 | 109914556 | |||
| chr12:109914565 | C | T | 1 | a0005 | 3 | HG02572.hp1 HG03486.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1258C>T | p.Arg420Cys | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/13 | 1411/3096 | 1258/1497 | 420/498 | chr12 | 109914565 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109903047 | G | A | 4 | a0002c0005 a0003c0006 a0004c0007 others(1): Show |
25 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(22): Show |
synonymous_variant | LOW | c.21G>A | p.Pro7Pro | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/13 | 174/3096 | 21/1497 | 7/498 | chr12 | 109903047 | |||
| chr12:109904793 | G | A | 2 | a0001c0004 a0001c0013 |
14 | HG00423.hp1 HG02040.hp1 HG02056.hp2 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.456G>A | p.Glu152Glu | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/13 | 609/3096 | 456/1497 | 152/498 | chr12 | 109904793 | |||
| chr12:109907675 | G | A | 1 | a0002c0011 | 2 | HG00738.hp2 HG01069.hp2 |
synonymous_variant | LOW | c.675G>A | p.Glu225Glu | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/13 | 828/3096 | 675/1497 | 225/498 | chr12 | 109907675 | |||
| chr12:109908687 | G | A | 1 | a0012c0015 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.801G>A | p.Lys267Lys | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/13 | 954/3096 | 801/1497 | 267/498 | chr12 | 109908687 | |||
| chr12:109911134 | G | A | 1 | a0001c0013 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.951G>A | p.Arg317Arg | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/13 | 1104/3096 | 951/1497 | 317/498 | chr12 | 109911134 | |||
| chr12:109911152 | C | T | 1 | a0009c0017 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.969C>T | p.Ala323Ala | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/13 | 1122/3096 | 969/1497 | 323/498 | chr12 | 109911152 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109916718 | C | G | 1 | a0003c0003t0004 | 5 | HG00735.hp1 HG01106.hp1 HG02735.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*95C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 95 | chr12 | 109916718 | ||||||
| chr12:109916731 | C | T | 1 | a0001c0001t0003 | 6 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*108C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 108 | chr12 | 109916731 | ||||||
| chr12:109916775 | C | T | 1 | a0003c0003t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 152 | chr12 | 109916775 | ||||||
| chr12:109916831 | C | A | 2 | a0002c0005t0002 a0010c0012t0002 |
13 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*208C>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 208 | chr12 | 109916831 | ||||||
| chr12:109916954 | G | T | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*331G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 331 | chr12 | 109916954 | ||||||
| chr12:109917191 | G | A | 1 | a0001c0001t0009 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 568 | chr12 | 109917191 | ||||||
| chr12:109917228 | G | A | 1 | a0001c0001t0010 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 605 | chr12 | 109917228 | ||||||
| chr12:109917235 | C | T | 1 | a0001c0001t0014 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*612C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 612 | chr12 | 109917235 | ||||||
| chr12:109917380 | C | T | 1 | a0004c0007t0006 | 3 | HG01099.hp2 HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*757C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 757 | chr12 | 109917380 | ||||||
| chr12:109917626 | C | T | 1 | a0001c0001t0005 | 3 | HG01069.hp1 HG01071.hp1 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1003C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 1003 | chr12 | 109917626 | ||||||
| chr12:109917674 | T | A | 1 | a0001c0001t0011 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1051T>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 1051 | chr12 | 109917674 | ||||||
| chr12:109917899 | T | G | 1 | a0001c0001t0008 | 2 | HG00642.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1276T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 1276 | chr12 | 109917899 | ||||||
| chr12:109917921 | C | G | 1 | a0001c0001t0013 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1298C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 1298 | chr12 | 109917921 | ||||||
| chr12:109917932 | G | A | 1 | a0001c0001t0012 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1309G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 13/13 | 1309 | chr12 | 109917932 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109900721 | G | C | 11 | a0002c0002t0001g0036 a0003c0003t0001g0004 a0003c0003t0001g0037 others(8): Show |
26 | HG00735.hp1 HG01106.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+295G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109900721 | |||||||
| chr12:109900951 | G | T | 1 | a0003c0003t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+525G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109900951 | |||||||
| chr12:109901071 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1+645A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901071 | |||||||
| chr12:109901084 | A | T | 11 | a0002c0002t0001g0036 a0003c0003t0001g0004 a0003c0003t0001g0037 others(8): Show |
26 | HG00735.hp1 HG01106.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+658A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901084 | |||||||
| chr12:109901217 | G | A | 1 | a0009c0017t0001g0035 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-1+791G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901217 | |||||||
| chr12:109901281 | G | GTTGTTTT others(28): Show |
36 | a0001c0001t0001g0022 a0002c0002t0001g0008 a0002c0002t0001g0014 others(33): Show |
79 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.-1+874_-1+908dupTT others(33): Show |
TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 109901281 | ||||||
| chr12:109901607 | G | T | 37 | a0001c0001t0001g0022 a0002c0002t0001g0008 a0002c0002t0001g0014 others(34): Show |
80 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.-1+1181G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901607 | |||||||
| chr12:109901612 | C | T | 2 | a0003c0003t0004g0015 a0003c0003t0004g0043 |
5 | HG00735.hp1 HG01106.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+1186C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901612 | |||||||
| chr12:109901838 | T | G | 1 | a0002c0002t0001g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1-1189T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901838 | |||||||
| chr12:109901894 | C | G | 37 | a0001c0001t0001g0022 a0002c0002t0001g0008 a0002c0002t0001g0014 others(34): Show |
80 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1-1133C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901894 | |||||||
| chr12:109901895 | T | C | 1 | a0002c0002t0001g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1-1132T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109901895 | |||||||
| chr12:109902080 | C | T | 2 | a0002c0002t0001g0013 a0002c0002t0001g0088 |
6 | HG01884.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-947C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902080 | |||||||
| chr12:109902248 | A | G | 37 | a0001c0001t0001g0022 a0002c0002t0001g0008 a0002c0002t0001g0014 others(34): Show |
80 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1-779A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902248 | |||||||
| chr12:109902332 | C | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18953.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1-695C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902332 | |||||||
| chr12:109902420 | CAA | C | 13 | a0002c0002t0001g0036 a0003c0003t0001g0004 a0003c0003t0001g0034 others(10): Show |
29 | HG00735.hp1 HG01106.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1-605_1-604delAA | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 109902420 | ||||||
| chr12:109902549 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1-478C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902549 | |||||||
| chr12:109902555 | C | T | 1 | a0003c0003t0001g0034 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1-472C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902555 | |||||||
| chr12:109902654 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1-373T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902654 | |||||||
| chr12:109902664 | A | G | 33 | a0001c0001t0001g0033 a0002c0002t0001g0008 a0002c0002t0001g0016 others(30): Show |
71 | HG00423.hp2 HG00735.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.1-363A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902664 | |||||||
| chr12:109902718 | C | T | 2 | a0003c0003t0001g0009 a0003c0003t0001g0105 |
10 | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-309C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902718 | |||||||
| chr12:109902815 | T | G | 4 | a0002c0005t0002g0006 a0002c0005t0002g0045 a0002c0005t0002g0046 others(1): Show |
13 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-212T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902815 | |||||||
| chr12:109902819 | G | A | 1 | a0003c0003t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-208G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 1/12 | chr12 | 109902819 | |||||||
| chr12:109903215 | G | T | 1 | a0002c0002t0001g0084 | 1 | HG02717.hp1 | splice_donor_variant&intron_variant | HIGH | c.188+1G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903215 | |||||||
| chr12:109903388 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.188+174G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903388 | |||||||
| chr12:109903512 | C | T | 39 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(36): Show |
87 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.188+298C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903512 | |||||||
| chr12:109903581 | C | A | 2 | a0001c0001t0007g0023 a0001c0001t0007g0047 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.189-356C>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903581 | |||||||
| chr12:109903756 | A | C | 1 | a0003c0003t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.189-181A>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903756 | |||||||
| chr12:109903759 | A | T | 1 | a0003c0003t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-178A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903759 | |||||||
| chr12:109903806 | G | A | 1 | a0003c0003t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-131G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903806 | |||||||
| chr12:109903834 | G | A | 4 | a0003c0003t0001g0004 a0003c0003t0001g0038 a0003c0003t0001g0039 others(1): Show |
16 | HG02055.hp1 HG02809.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.189-103G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 2/12 | chr12 | 109903834 | |||||||
| chr12:109904211 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.399+64A>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 3/12 | chr12 | 109904211 | |||||||
| chr12:109904338 | C | CCCCTTCA others(10): Show |
1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.399+193_399+209dup others(17): Show |
TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 109904338 | ||||||
| chr12:109904370 | T | C | 1 | a0003c0003t0004g0043 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.399+223T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 3/12 | chr12 | 109904370 | |||||||
| chr12:109904616 | T | G | 39 | a0001c0001t0001g0049 a0002c0002t0001g0008 a0002c0002t0001g0013 others(36): Show |
91 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.400-121T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 3/12 | chr12 | 109904616 | |||||||
| chr12:109904822 | T | C | 41 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
97 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.456+29T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109904822 | |||||||
| chr12:109904870 | T | C | 1 | a0003c0003t0001g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.456+77T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109904870 | |||||||
| chr12:109904880 | C | T | 41 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
97 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.456+87C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109904880 | |||||||
| chr12:109904923 | C | T | 2 | a0003c0003t0004g0015 a0003c0003t0004g0043 |
5 | HG00735.hp1 HG01106.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+130C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109904923 | |||||||
| chr12:109904952 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.456+159G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109904952 | |||||||
| chr12:109904997 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(24): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.456+204C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109904997 | |||||||
| chr12:109905197 | G | C | 1 | a0003c0003t0001g0034 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.456+404G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905197 | |||||||
| chr12:109905200 | A | T | 1 | a0001c0001t0001g0029 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.456+407A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905200 | |||||||
| chr12:109905225 | G | C | 2 | a0003c0003t0004g0015 a0003c0003t0004g0043 |
5 | HG00735.hp1 HG01106.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+432G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905225 | |||||||
| chr12:109905237 | T | C | 38 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(35): Show |
92 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.456+444T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905237 | |||||||
| chr12:109905295 | G | C | 40 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(37): Show |
94 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.456+502G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905295 | |||||||
| chr12:109905352 | C | T | 2 | a0001c0004t0001g0003 a0001c0013t0001g0003 |
14 | HG00423.hp1 HG02040.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.456+559C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905352 | |||||||
| chr12:109905691 | C | T | 1 | a0002c0005t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.457-881C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905691 | |||||||
| chr12:109905707 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.457-865A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905707 | |||||||
| chr12:109905851 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.457-721G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905851 | |||||||
| chr12:109905855 | G | A | 16 | a0002c0002t0001g0036 a0003c0003t0001g0004 a0003c0003t0001g0009 others(13): Show |
47 | HG00735.hp1 HG01106.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.457-717G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905855 | |||||||
| chr12:109905985 | G | A | 1 | a0003c0003t0001g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.457-587G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109905985 | |||||||
| chr12:109906073 | G | C | 38 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(35): Show |
92 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.457-499G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906073 | |||||||
| chr12:109906096 | A | G | 2 | a0001c0004t0001g0003 a0001c0013t0001g0003 |
14 | HG00423.hp1 HG02040.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.457-476A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906096 | |||||||
| chr12:109906154 | C | T | 1 | a0002c0002t0001g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.457-418C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906154 | |||||||
| chr12:109906169 | G | A | 2 | a0003c0003t0004g0015 a0003c0003t0004g0043 |
5 | HG00735.hp1 HG01106.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-403G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906169 | |||||||
| chr12:109906283 | C | T | 1 | a0001c0001t0001g0012 | 5 | HG02647.hp2 HG03516.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.457-289C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906283 | |||||||
| chr12:109906335 | C | G | 1 | a0003c0003t0001g0095 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.457-237C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906335 | |||||||
| chr12:109906338 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.457-234C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906338 | |||||||
| chr12:109906423 | C | T | 1 | a0005c0008t0001g0021 | 3 | HG02572.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.457-149C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906423 | |||||||
| chr12:109906435 | C | T | 36 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(33): Show |
90 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.457-137C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906435 | |||||||
| chr12:109906463 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.457-109G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906463 | |||||||
| chr12:109906463 | G | C | 1 | a0005c0008t0001g0021 | 3 | HG02572.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.457-109G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906463 | |||||||
| chr12:109906482 | C | A | 36 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(33): Show |
90 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.457-90C>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906482 | |||||||
| chr12:109906534 | T | C | 41 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
97 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.457-38T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 4/12 | chr12 | 109906534 | |||||||
| chr12:109906653 | G | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0083 a0002c0002t0001g0084 others(1): Show |
6 | HG01099.hp2 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+13G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109906653 | |||||||
| chr12:109906670 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.525+30G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109906670 | |||||||
| chr12:109906747 | G | A | 36 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(33): Show |
90 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.525+107G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109906747 | |||||||
| chr12:109906933 | G | A | 1 | a0001c0001t0001g0030 | 2 | NA18969.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.525+293G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109906933 | |||||||
| chr12:109906939 | T | C | 1 | a0002c0002t0001g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.525+299T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109906939 | |||||||
| chr12:109906944 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525+304A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109906944 | |||||||
| chr12:109907014 | C | T | 1 | a0003c0003t0001g0034 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.525+374C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907014 | |||||||
| chr12:109907116 | G | A | 1 | a0003c0003t0001g0038 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.526-410G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907116 | |||||||
| chr12:109907197 | G | A | 1 | a0003c0003t0015g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-329G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907197 | |||||||
| chr12:109907253 | C | T | 5 | a0001c0001t0001g0067 a0003c0003t0001g0004 a0003c0003t0001g0038 others(2): Show |
17 | HG02055.hp1 HG02523.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.526-273C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907253 | |||||||
| chr12:109907268 | A | G | 49 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(46): Show |
116 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.526-258A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907268 | |||||||
| chr12:109907322 | G | T | 3 | a0003c0003t0001g0093 a0003c0003t0001g0107 a0005c0008t0001g0021 |
5 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-204G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907322 | |||||||
| chr12:109907427 | A | T | 41 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
97 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.526-99A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | chr12 | 109907427 | |||||||
| chr12:109907500 | A | ACCT | 39 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(36): Show |
95 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.526-25_526-23dupCC others(1): Show |
TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 109907500 | ||||||
| chr12:109907791 | T | C | 1 | a0002c0005t0002g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.699+92T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109907791 | |||||||
| chr12:109907817 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.699+118C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109907817 | |||||||
| chr12:109907950 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.699+251C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109907950 | |||||||
| chr12:109908017 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.699+318C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908017 | |||||||
| chr12:109908042 | G | A | 2 | a0003c0003t0001g0009 a0003c0003t0001g0104 |
10 | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.699+343G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908042 | |||||||
| chr12:109908057 | C | T | 1 | a0001c0001t0003g0028 | 2 | HG00741.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.699+358C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908057 | |||||||
| chr12:109908131 | G | GAGTT | 41 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
97 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.699+434_699+435ins others(4): Show |
TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 109908131 | ||||||
| chr12:109908142 | A | G | 8 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0091 others(5): Show |
13 | HG02165.hp1 HG02165.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.699+443A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908142 | |||||||
| chr12:109908167 | C | A | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.700-419C>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908167 | |||||||
| chr12:109908294 | T | C | 1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.700-292T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908294 | |||||||
| chr12:109908295 | G | T | 1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.700-291G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908295 | |||||||
| chr12:109908296 | A | G | 1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.700-290A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908296 | |||||||
| chr12:109908345 | T | G | 1 | a0001c0001t0001g0019 | 3 | HG01167.hp1 HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.700-241T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908345 | |||||||
| chr12:109908473 | T | C | 18 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(15): Show |
40 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.700-113T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908473 | |||||||
| chr12:109908494 | A | G | 1 | a0008c0014t0001g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.700-92A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908494 | |||||||
| chr12:109908503 | G | A | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.700-83G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908503 | |||||||
| chr12:109908536 | A | T | 1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.700-50A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908536 | |||||||
| chr12:109908552 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.700-34A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908552 | |||||||
| chr12:109908580 | C | A | 1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | splice_region_variant&intron_variant | LOW | c.700-6C>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908580 | |||||||
| chr12:109908582 | A | C | 1 | a0012c0015t0001g0048 | 1 | NA19083.hp2 | splice_region_variant&intron_variant | LOW | c.700-4A>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 6/12 | chr12 | 109908582 | |||||||
| chr12:109908738 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.812+40G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/12 | chr12 | 109908738 | |||||||
| chr12:109908808 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.813-63A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 7/12 | chr12 | 109908808 | |||||||
| chr12:109908982 | T | A | 49 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(46): Show |
116 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.879+45T>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109908982 | |||||||
| chr12:109909067 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.879+130G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909067 | |||||||
| chr12:109909102 | G | C | 1 | a0001c0001t0009g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.879+165G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909102 | |||||||
| chr12:109909253 | G | C | 1 | a0002c0002t0001g0101 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.879+316G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909253 | |||||||
| chr12:109909267 | A | G | 15 | a0002c0002t0001g0008 a0002c0002t0001g0014 a0002c0002t0001g0016 others(12): Show |
32 | HG00423.hp2 HG00558.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+330A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909267 | |||||||
| chr12:109909333 | G | A | 41 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
97 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.879+396G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909333 | |||||||
| chr12:109909643 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.879+706A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909643 | |||||||
| chr12:109909644 | AC | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0090 |
6 | HG00558.hp2 NA18947.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+711delC | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 109909644 | ||||||
| chr12:109909676 | C | T | 2 | a0002c0002t0001g0013 a0002c0002t0001g0088 |
6 | HG01884.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+739C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909676 | |||||||
| chr12:109909677 | G | A | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.879+740G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909677 | |||||||
| chr12:109909926 | T | A | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.879+989T>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909926 | |||||||
| chr12:109909952 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0090 |
6 | HG00558.hp2 NA18947.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+1015C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909952 | |||||||
| chr12:109909997 | G | C | 1 | a0002c0002t0001g0099 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.879+1060G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109909997 | |||||||
| chr12:109910171 | T | A | 1 | a0001c0001t0009g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.880-892T>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109910171 | |||||||
| chr12:109910703 | G | A | 1 | a0003c0003t0001g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.880-360G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109910703 | |||||||
| chr12:109910707 | C | T | 18 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(15): Show |
40 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.880-356C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109910707 | |||||||
| chr12:109911027 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00408.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.880-36C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 8/12 | chr12 | 109911027 | |||||||
| chr12:109911378 | G | A | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1052+143G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109911378 | |||||||
| chr12:109911391 | C | T | 1 | a0002c0002t0001g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1052+156C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109911391 | |||||||
| chr12:109911412 | G | A | 2 | a0003c0003t0001g0037 a0005c0008t0001g0021 |
4 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+177G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109911412 | |||||||
| chr12:109911611 | C | CA | 16 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0052 others(13): Show |
27 | HG00738.hp1 HG01109.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1052+398dupA | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 109911611 | ||||||
| chr12:109911611 | CA | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0001c0001t0008g0063 others(5): Show |
8 | HG01069.hp2 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1052+398delA | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 109911611 | ||||||
| chr12:109911801 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1052+566A>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109911801 | |||||||
| chr12:109911801 | AT | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0071 a0003c0003t0004g0015 others(1): Show |
7 | HG00735.hp1 HG01106.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052+579delT | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 109911801 | ||||||
| chr12:109911831 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0064 |
3 | HG01496.hp2 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1052+596C>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109911831 | |||||||
| chr12:109912074 | G | A | 1 | a0001c0001t0009g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1052+839G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912074 | |||||||
| chr12:109912114 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1053-877A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912114 | |||||||
| chr12:109912254 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG00099.hp2 HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.1053-737C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912254 | |||||||
| chr12:109912349 | A | G | 2 | a0003c0003t0001g0034 a0003c0003t0001g0105 |
3 | HG02055.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1053-642A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912349 | |||||||
| chr12:109912357 | G | A | 1 | a0003c0003t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1053-634G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912357 | |||||||
| chr12:109912409 | T | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0014g0011 |
8 | HG01071.hp2 HG01081.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053-582T>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912409 | |||||||
| chr12:109912436 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1053-555G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912436 | |||||||
| chr12:109912514 | G | C | 1 | a0003c0003t0001g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1053-477G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912514 | |||||||
| chr12:109912740 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18975.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1053-251G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912740 | |||||||
| chr12:109912760 | T | G | 18 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(15): Show |
40 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1053-231T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912760 | |||||||
| chr12:109912777 | C | T | 4 | a0003c0003t0001g0004 a0003c0003t0001g0038 a0003c0003t0001g0039 others(1): Show |
16 | HG02055.hp1 HG02809.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.1053-214C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912777 | |||||||
| chr12:109912929 | C | T | 4 | a0002c0002t0001g0050 a0002c0002t0001g0083 a0002c0002t0001g0084 others(1): Show |
6 | HG01099.hp2 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053-62C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 9/12 | chr12 | 109912929 | |||||||
| chr12:109913076 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp2 | splice_region_variant&intron_variant | LOW | c.1134+4A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109913076 | |||||||
| chr12:109913422 | G | A | 18 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(15): Show |
40 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1134+350G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109913422 | |||||||
| chr12:109913485 | T | C | 1 | a0003c0003t0001g0034 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1134+413T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109913485 | |||||||
| chr12:109913635 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1134+563A>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109913635 | |||||||
| chr12:109914045 | C | T | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1135-397C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109914045 | |||||||
| chr12:109914140 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1135-302G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109914140 | |||||||
| chr12:109914316 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18977.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1135-126G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 10/12 | chr12 | 109914316 | |||||||
| chr12:109914704 | G | C | 32 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(29): Show |
66 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1320+77G>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109914704 | |||||||
| chr12:109914731 | C | A | 1 | a0003c0003t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1320+104C>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109914731 | |||||||
| chr12:109914743 | C | T | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1320+116C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109914743 | |||||||
| chr12:109915182 | A | C | 40 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(37): Show |
96 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1321-221A>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109915182 | |||||||
| chr12:109915183 | G | A | 40 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0014 others(37): Show |
96 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1321-220G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109915183 | |||||||
| chr12:109915275 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1321-128C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109915275 | |||||||
| chr12:109915320 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1321-83C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109915320 | |||||||
| chr12:109915367 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 |
15 | HG01516.hp1 HG01517.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1321-36T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 11/12 | chr12 | 109915367 | |||||||
| chr12:109915567 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1464+21T>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915567 | |||||||
| chr12:109915579 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1464+33G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915579 | |||||||
| chr12:109915706 | G | A | 2 | a0002c0011t0001g0096 a0002c0011t0001g0097 |
2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1464+160G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915706 | |||||||
| chr12:109915813 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1464+267T>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915813 | |||||||
| chr12:109915864 | A | C | 2 | a0003c0003t0001g0094 a0003c0003t0001g0095 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1464+318A>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915864 | |||||||
| chr12:109915904 | T | C | 4 | a0003c0003t0001g0093 a0003c0003t0001g0094 a0003c0003t0001g0095 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1464+358T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915904 | |||||||
| chr12:109915978 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1464+432C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109915978 | |||||||
| chr12:109916015 | G | T | 18 | a0001c0001t0001g0074 a0002c0002t0001g0008 a0002c0002t0001g0013 others(15): Show |
39 | HG00423.hp2 HG00558.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1464+469G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916015 | |||||||
| chr12:109916152 | T | C | 1 | a0003c0003t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1465-439T>C | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916152 | |||||||
| chr12:109916161 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1465-430G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916161 | |||||||
| chr12:109916224 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1465-367G>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916224 | |||||||
| chr12:109916313 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1465-278C>T | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916313 | |||||||
| chr12:109916323 | A | G | 1 | a0003c0003t0001g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1465-268A>G | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916323 | |||||||
| chr12:109916368 | G | A | 1 | a0003c0003t0001g0039 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1465-223G>A | TCHP | ENSG00000139437.18 | transcript | ENST00000405876.9 | protein_coding | 12/12 | chr12 | 109916368 |