Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1638 |
| ensemblid | ENSG00000080166.16 |
| hgncid | 2709 |
| symbol | DCT |
| name | dopachrome tautomerase |
| refseq_nuc | NM_001922.5 |
| refseq_prot | NP_001913.2 |
| ensembl_nuc | ENST00000377028.10 |
| ensembl_prot | ENSP00000366227.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 94436811 |
| end | 94479682 |
| strand | - |
| ver | v1.2 |
| region | chr13:94436811-94479682 |
| region5000 | chr13:94431811-94484682 |
| regionname0 | DCT_chr13_94436811_94479682 |
| regionname5000 | DCT_chr13_94431811_94484682 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 519 | 323 | 88 | 58 | 115 | 18 | 42 | 80 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0002 | 0/0 | 519 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0003 | 0/0 | 519 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0004 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0005 | 0/0 | 519 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0006 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0007 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0008 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| a0009 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | MSPLW others(514): Show |
chr13 | 94431811 | 94484682 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1557 | 314 | 81 | 57 | 114 | 18 | 42 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0001c0003 | 0/0 | 1557 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0001c0004 | 0/0 | 1557 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0001c0007 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0001c0011 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0001c0012 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0002c0002 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0003c0005 | 0/0 | 1557 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0004c0013 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0005c0010 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0006c0009 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0007c0014 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0008c0008 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 | ||
| a0009c0006 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | ATGAG others(1552): Show |
chr13 | 94431811 | 94484682 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5074 | 91 | 2 | 19 | 59 | 2 | 8 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0002 | 0/0 | 5073 | 62 | 11 | 16 | 15 | 5 | 15 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0003 | 0/0 | 5072 | 46 | 2 | 6 | 29 | 2 | 7 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0004 | 0/0 | 5073 | 20 | 4 | 6 | 1 | 5 | 4 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0005 | 0/0 | 5074 | 20 | 14 | 3 | 0 | 1 | 2 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0006 | 0/0 | 5073 | 13 | 10 | 1 | 1 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0007 | 0/0 | 5070 | 12 | 10 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5065): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0008 | 0/0 | 5072 | 8 | 7 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0009 | 0/0 | 5072 | 5 | 5 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0010 | 0/0 | 5069 | 4 | 0 | 3 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5064): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0011 | 0/0 | 5073 | 3 | 3 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0012 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0013 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0014 | 0/0 | 5072 | 2 | 0 | 0 | 0 | 0 | 2 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0015 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0017 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0018 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0019 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0020 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0021 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0022 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0023 | 0/0 | 5072 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0024 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0025 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0026 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0027 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0028 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0029 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0030 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0031 | 0/0 | 5141 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5136): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0032 | 0/1 | 5072 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0033 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0034 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0035 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0036 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0001t0037 | 0/0 | 5072 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0001c0003t0004 | 0/0 | 5073 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0004t0006 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0001c0007t0005 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0001c0011t0001 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0001c0012t0002 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0002c0002t0006 | 0/0 | 5073 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0002c0002t0008 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5067): Show |
chr13 | 94431811 | 94484682 |
| a0003c0005t0016 | 0/0 | 5073 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0004c0013t0001 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0005c0010t0002 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0006c0009t0002 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5068): Show |
chr13 | 94431811 | 94484682 |
| a0007c0014t0001 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0008c0008t0001 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| a0009c0006t0001 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | AACTG others(5069): Show |
chr13 | 94431811 | 94484682 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0002 | 0/0 | 6 | 2 | 3 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0011g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0014g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0014g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0017g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0018g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0019g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0020g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0022g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0023g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0024g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0025g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0026g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0027g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0028g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0029g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0030g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0031g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0032g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0033g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0034g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0035g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0036g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0001t0037g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0003t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0004t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0004t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0007t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0011t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0001c0012t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0002c0002t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0002c0002t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0002c0002t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0002c0002t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0002c0002t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0003c0005t0016g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0003c0005t0016g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0004c0013t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0005c0010t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0006c0009t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0007c0014t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0008c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| a0009c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0030 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00140 | hp2 | a0001 | c0001 | t0026 | g0128 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00280 | hp1 | a0001 | c0001 | t0025 | g0125 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0085 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00323 | hp2 | a0001 | c0001 | t0021 | g0083 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00609 | hp2 | a0004 | c0013 | t0001 | g0047 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0260 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0171 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0028 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01243 | hp2 | a0003 | c0005 | t0016 | g0253 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0236 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0237 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0257 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01496 | hp2 | a0001 | c0007 | t0005 | g0256 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0106 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0269 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0175 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01952 | hp2 | a0005 | c0010 | t0002 | g0159 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02055 | hp1 | a0001 | c0001 | t0028 | g0231 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02055 | hp2 | a0001 | c0001 | t0034 | g0262 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02135 | hp1 | a0001 | c0001 | t0033 | g0147 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0244 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | CDX | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0102 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02523 | hp2 | a0001 | c0001 | t0013 | g0061 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0201 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0184 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0275 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02630 | hp2 | a0001 | c0001 | t0029 | g0242 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02723 | hp2 | a0001 | c0001 | t0018 | g0129 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0202 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02818 | hp2 | a0001 | c0003 | t0004 | g0105 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0172 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02886 | hp2 | a0001 | c0001 | t0020 | g0230 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02895 | hp1 | a0002 | c0002 | t0006 | g0247 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02897 | hp2 | a0002 | c0002 | t0006 | g0238 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02922 | hp1 | a0003 | c0005 | t0016 | g0245 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0092 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0108 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03098 | hp2 | a0001 | c0001 | t0035 | g0270 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0169 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03209 | hp2 | a0001 | c0001 | t0030 | g0140 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03225 | hp1 | a0001 | c0004 | t0006 | g0195 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0176 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0185 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0104 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03492 | hp1 | a0001 | c0001 | t0014 | g0193 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0251 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03579 | hp1 | a0001 | c0001 | t0027 | g0177 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03688 | hp2 | a0006 | c0009 | t0002 | g0214 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0261 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03831 | hp2 | a0007 | c0014 | t0001 | g0255 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03927 | hp1 | a0001 | c0001 | t0022 | g0155 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04184 | hp2 | a0001 | c0001 | t0010 | g0234 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04204 | hp1 | a0001 | c0001 | t0024 | g0188 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0276 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18522 | hp1 | a0001 | c0012 | t0002 | g0224 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0246 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18906 | hp2 | a0002 | c0002 | t0006 | g0248 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18948 | hp1 | a0008 | c0008 | t0001 | g0156 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18975 | hp1 | a0009 | c0006 | t0001 | g0036 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18978 | hp1 | a0001 | c0001 | t0012 | g0098 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18978 | hp2 | a0001 | c0001 | t0031 | g0057 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18998 | hp1 | a0001 | c0011 | t0001 | g0043 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA18998 | hp2 | a0001 | c0001 | t0012 | g0099 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19030 | hp2 | a0001 | c0003 | t0004 | g0205 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0198 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19064 | hp2 | a0001 | c0001 | t0023 | g0186 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19067 | hp2 | a0001 | c0001 | t0036 | g0277 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19068 | hp1 | a0001 | c0001 | t0013 | g0048 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19080 | hp1 | a0001 | c0001 | t0037 | g0278 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0025 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0029 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0079 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0103 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0096 | SAS | GIH | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | GIH | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0235 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02486 | hp1 | a0001 | c0004 | t0006 | g0194 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0197 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG03471 | hp2 | a0002 | c0002 | t0008 | g0240 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG06807 | hp1 | a0002 | c0002 | t0006 | g0239 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0254 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0252 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0130 | REF | REF | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0055 | REF | REF | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94460111 | C | T | 1 | a0005 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.1159G>A | p.Ala387Thr | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/8 | 1586/5074 | 1159/1560 | 387/519 | chr13 | 94460111 | |||
| chr13:94465646 | T | C | 1 | a0004 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.850A>G | p.Thr284Ala | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/8 | 1277/5074 | 850/1560 | 284/519 | chr13 | 94465646 | |||
| chr13:94465672 | C | T | 1 | a0002 | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
missense_variant | MODERATE | c.824G>A | p.Arg275Gln | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/8 | 1251/5074 | 824/1560 | 275/519 | chr13 | 94465672 | |||
| chr13:94465739 | C | T | 1 | a0006 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.757G>A | p.Glu253Lys | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/8 | 1184/5074 | 757/1560 | 253/519 | chr13 | 94465739 | |||
| chr13:94466616 | C | T | 1 | a0008 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.638G>A | p.Gly213Glu | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/8 | 1065/5074 | 638/1560 | 213/519 | chr13 | 94466616 | |||
| chr13:94468832 | T | C | 1 | a0003 | 2 | HG01243.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.509A>G | p.Asn170Ser | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/8 | 936/5074 | 509/1560 | 170/519 | chr13 | 94468832 | |||
| chr13:94479033 | A | C | 1 | a0009 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.223T>G | p.Tyr75Asp | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 650/5074 | 223/1560 | 75/519 | chr13 | 94479033 | |||
| chr13:94479110 | G | A | 1 | a0007 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.146C>T | p.Ala49Val | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 573/5074 | 146/1560 | 49/519 | chr13 | 94479110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94440033 | T | G | 1 | a0001c0011 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.1425A>C | p.Val475Val | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1852/5074 | 1425/1560 | 475/519 | chr13 | 94440033 | |||
| chr13:94440039 | G | C | 1 | a0001c0012 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1419C>G | p.Leu473Leu | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1846/5074 | 1419/1560 | 473/519 | chr13 | 94440039 | |||
| chr13:94462144 | A | G | 1 | a0001c0004 | 2 | HG02486.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.909T>C | p.Tyr303Tyr | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/8 | 1336/5074 | 909/1560 | 303/519 | chr13 | 94462144 | |||
| chr13:94468999 | G | A | 1 | a0001c0003 | 4 | HG02559.hp1 HG02818.hp2 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.342C>T | p.Thr114Thr | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/8 | 769/5074 | 342/1560 | 114/519 | chr13 | 94468999 | |||
| chr13:94479007 | A | C | 1 | a0001c0007 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.249T>G | p.Arg83Arg | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 676/5074 | 249/1560 | 83/519 | chr13 | 94479007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94436864 | A | G | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(33): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*3034T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 3034 | chr13 | 94436864 | ||||||
| chr13:94436900 | G | A | 1 | a0001c0001t0022 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2998C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2998 | chr13 | 94436900 | ||||||
| chr13:94437026 | C | T | 1 | a0001c0001t0029 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2872 | chr13 | 94437026 | ||||||
| chr13:94437052 | GA | G | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(33): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2845delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2845 | chr13 | 94437052 | ||||||
| chr13:94437354 | ACTT | A | 1 | a0001c0001t0007 | 12 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2541_*2543delAAG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2541 | chr13 | 94437354 | ||||||
| chr13:94437481 | T | C | 3 | a0001c0001t0004 a0001c0001t0021 a0001c0003t0004 |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2417A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2417 | chr13 | 94437481 | ||||||
| chr13:94437753 | A | G | 1 | a0001c0001t0007 | 12 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2145T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2145 | chr13 | 94437753 | ||||||
| chr13:94437764 | G | A | 1 | a0001c0001t0025 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2134 | chr13 | 94437764 | ||||||
| chr13:94437964 | A | G | 2 | a0001c0001t0015 a0001c0001t0027 |
3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1934T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1934 | chr13 | 94437964 | ||||||
| chr13:94438437 | T | C | 1 | a0001c0001t0019 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1461A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1461 | chr13 | 94438437 | ||||||
| chr13:94438438 | T | A | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(37): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1460A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1460 | chr13 | 94438438 | ||||||
| chr13:94438574 | C | CCTATGCT others(60): Show |
1 | a0001c0001t0031 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323_*1324insCTTT others(63): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1323 | chr13 | 94438574 | ||||||
| chr13:94438583 | A | T | 1 | a0001c0001t0031 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1315 | chr13 | 94438583 | ||||||
| chr13:94438656 | C | G | 1 | a0001c0001t0031 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1242 | chr13 | 94438656 | ||||||
| chr13:94438679 | T | C | 1 | a0001c0001t0030 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1219 | chr13 | 94438679 | ||||||
| chr13:94438700 | A | G | 1 | a0001c0001t0007 | 12 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1198T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1198 | chr13 | 94438700 | ||||||
| chr13:94438741 | A | G | 3 | a0001c0001t0009 a0001c0001t0034 a0003c0005t0016 |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1157 | chr13 | 94438741 | ||||||
| chr13:94438948 | A | G | 3 | a0001c0001t0004 a0001c0001t0021 a0001c0003t0004 |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*950T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 950 | chr13 | 94438948 | ||||||
| chr13:94439042 | C | G | 7 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0011 others(4): Show |
21 | HG01243.hp2 HG01981.hp2 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 856 | chr13 | 94439042 | ||||||
| chr13:94439093 | C | T | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*805G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 805 | chr13 | 94439093 | ||||||
| chr13:94439103 | A | G | 1 | a0001c0001t0024 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*795T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 795 | chr13 | 94439103 | ||||||
| chr13:94439107 | A | G | 2 | a0001c0001t0020 a0001c0001t0028 |
2 | HG02055.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*791T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 791 | chr13 | 94439107 | ||||||
| chr13:94439173 | G | C | 1 | a0001c0001t0026 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 725 | chr13 | 94439173 | ||||||
| chr13:94439185 | A | G | 7 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0011 others(4): Show |
21 | HG01243.hp2 HG01981.hp2 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*713T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 713 | chr13 | 94439185 | ||||||
| chr13:94439206 | G | A | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 692 | chr13 | 94439206 | ||||||
| chr13:94439485 | A | G | 13 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0015 others(10): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*413T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 413 | chr13 | 94439485 | ||||||
| chr13:94439554 | G | A | 1 | a0001c0001t0023 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 344 | chr13 | 94439554 | ||||||
| chr13:94439612 | G | A | 1 | a0001c0001t0014 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 286 | chr13 | 94439612 | ||||||
| chr13:94439625 | TG | T | 15 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(12): Show |
74 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*272delC | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 272 | chr13 | 94439625 | ||||||
| chr13:94439667 | ATCTT | A | 1 | a0001c0001t0010 | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*227_*230delAAGA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 227 | chr13 | 94439667 | ||||||
| chr13:94439847 | G | A | 1 | a0001c0001t0033 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 51 | chr13 | 94439847 | ||||||
| chr13:94479309 | T | C | 4 | a0001c0001t0005 a0001c0001t0034 a0001c0001t0035 others(1): Show |
23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 54 | chr13 | 94479309 | ||||||
| chr13:94479437 | T | C | 1 | a0001c0001t0036 | 1 | NA19067.hp2 | 5_prime_UTR_variant | MODIFIER | c.-182A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 182 | chr13 | 94479437 | ||||||
| chr13:94479536 | G | A | 1 | a0001c0001t0037 | 1 | NA19080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-281C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 281 | chr13 | 94479536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94440642 | T | A | 197 | a0001c0001t0001g0192 a0001c0001t0002g0002 a0001c0001t0002g0004 others(194): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1382-566A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440642 | |||||||
| chr13:94440676 | G | GT | 121 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0067 others(118): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1382-601dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | |||||||
| chr13:94440676 | G | GTT | 33 | a0001c0001t0001g0074 a0001c0001t0001g0162 a0001c0001t0002g0032 others(30): Show |
35 | HG00140.hp2 HG01123.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1382-602_1382-601d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | |||||||
| chr13:94440676 | G | GTTT | 45 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0080 others(42): Show |
48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1382-603_1382-601d others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | |||||||
| chr13:94440676 | G | GTTTT | 9 | a0001c0001t0004g0079 a0001c0001t0004g0082 a0001c0001t0005g0258 others(6): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1382-604_1382-601d others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | |||||||
| chr13:94440676 | G | T | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1382-600C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | |||||||
| chr13:94441050 | T | C | 1 | a0001c0004t0006g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1382-974A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441050 | |||||||
| chr13:94441065 | C | T | 24 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(21): Show |
26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1382-989G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441065 | |||||||
| chr13:94441337 | T | A | 17 | a0001c0001t0001g0221 a0001c0001t0002g0004 a0001c0001t0002g0031 others(14): Show |
23 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1382-1261A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441337 | |||||||
| chr13:94441720 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1382-1644T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441720 | |||||||
| chr13:94441872 | G | T | 11 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381+1564C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441872 | |||||||
| chr13:94441920 | T | C | 1 | a0001c0001t0009g0254 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1381+1516A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441920 | |||||||
| chr13:94441921 | A | T | 1 | a0001c0001t0008g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1381+1515T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441921 | |||||||
| chr13:94442017 | A | AT | 12 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381+1418dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442017 | |||||||
| chr13:94442018 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0022g0155 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1381+1418A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442018 | |||||||
| chr13:94442131 | C | T | 179 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(176): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1381+1305G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442131 | |||||||
| chr13:94442153 | G | T | 1 | a0001c0001t0011g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1381+1283C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442153 | |||||||
| chr13:94442461 | T | C | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1381+975A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442461 | |||||||
| chr13:94442485 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0157 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1381+951A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442485 | |||||||
| chr13:94442498 | A | G | 6 | a0001c0001t0007g0092 a0001c0001t0007g0093 a0001c0001t0007g0094 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381+938T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442498 | |||||||
| chr13:94442732 | G | A | 4 | a0001c0001t0006g0039 a0001c0001t0006g0137 a0001c0001t0006g0141 others(1): Show |
4 | HG01891.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+704C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442732 | |||||||
| chr13:94442742 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1381+694A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442742 | |||||||
| chr13:94442762 | T | C | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1381+674A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442762 | |||||||
| chr13:94442814 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0017g0169 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1381+622G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442814 | |||||||
| chr13:94442824 | A | G | 191 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(188): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1381+612T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442824 | |||||||
| chr13:94443022 | C | A | 12 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381+414G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443022 | |||||||
| chr13:94443077 | T | C | 179 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(176): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1381+359A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443077 | |||||||
| chr13:94443137 | A | T | 191 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(188): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1381+299T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443137 | |||||||
| chr13:94443228 | CA | C | 4 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+207delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443228 | |||||||
| chr13:94443275 | A | G | 190 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1381+161T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443275 | |||||||
| chr13:94443288 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1381+148G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443288 | |||||||
| chr13:94443674 | A | C | 2 | a0001c0001t0006g0037 a0001c0001t0006g0038 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1180-37T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443674 | |||||||
| chr13:94443759 | T | C | 179 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(176): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1180-122A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443759 | |||||||
| chr13:94443773 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-136G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443773 | |||||||
| chr13:94443857 | A | G | 46 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(43): Show |
56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1180-220T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443857 | |||||||
| chr13:94443868 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1180-231A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443868 | |||||||
| chr13:94444021 | C | T | 3 | a0001c0001t0015g0175 a0001c0001t0015g0176 a0001c0001t0027g0177 |
3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1180-384G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444021 | |||||||
| chr13:94444033 | G | C | 12 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-396C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444033 | |||||||
| chr13:94444155 | C | T | 191 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(188): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1180-518G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444155 | |||||||
| chr13:94444251 | G | A | 191 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(188): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1180-614C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444251 | |||||||
| chr13:94444348 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1180-711C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444348 | |||||||
| chr13:94444383 | C | T | 12 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-746G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444383 | |||||||
| chr13:94444422 | C | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0058 others(1): Show |
5 | NA18942.hp2 NA18965.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-785G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444422 | |||||||
| chr13:94444518 | T | C | 1 | a0001c0001t0005g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-881A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444518 | |||||||
| chr13:94444549 | A | T | 1 | a0001c0001t0005g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-912T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444549 | |||||||
| chr13:94444670 | G | A | 1 | a0001c0001t0006g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1180-1033C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444670 | |||||||
| chr13:94444762 | T | C | 2 | a0001c0001t0006g0039 a0001c0001t0006g0137 |
2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1180-1125A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444762 | |||||||
| chr13:94444797 | T | C | 188 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(185): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1180-1160A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444797 | |||||||
| chr13:94444941 | A | G | 191 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(188): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1180-1304T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444941 | |||||||
| chr13:94444945 | T | C | 57 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(54): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.1180-1308A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444945 | |||||||
| chr13:94444979 | G | A | 1 | a0001c0001t0004g0204 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1180-1342C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444979 | |||||||
| chr13:94445087 | T | C | 12 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-1450A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445087 | |||||||
| chr13:94445210 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1180-1573A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445210 | |||||||
| chr13:94445336 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1180-1699A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445336 | |||||||
| chr13:94445407 | A | G | 188 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(185): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1180-1770T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445407 | |||||||
| chr13:94445479 | C | T | 2 | a0001c0001t0002g0216 a0001c0001t0003g0199 |
2 | HG04184.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1180-1842G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445479 | |||||||
| chr13:94445702 | C | T | 176 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(173): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1180-2065G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445702 | |||||||
| chr13:94445750 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1180-2113C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445750 | |||||||
| chr13:94445892 | C | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-2255G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445892 | |||||||
| chr13:94445944 | T | G | 3 | a0001c0001t0002g0118 a0001c0001t0002g0133 a0001c0001t0002g0218 |
3 | HG02559.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1180-2307A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445944 | |||||||
| chr13:94446004 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1180-2367C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446004 | |||||||
| chr13:94446189 | A | G | 1 | a0001c0001t0007g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1180-2552T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446189 | |||||||
| chr13:94446352 | G | T | 1 | a0001c0001t0029g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1180-2715C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446352 | |||||||
| chr13:94446422 | G | C | 1 | a0001c0001t0006g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1180-2785C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446422 | |||||||
| chr13:94446449 | T | A | 1 | a0001c0001t0002g0123 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1180-2812A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446449 | |||||||
| chr13:94446550 | C | T | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1180-2913G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446550 | |||||||
| chr13:94446584 | T | C | 3 | a0001c0001t0015g0175 a0001c0001t0015g0176 a0001c0001t0027g0177 |
3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1180-2947A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446584 | |||||||
| chr13:94446744 | C | T | 45 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(42): Show |
48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1180-3107G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446744 | |||||||
| chr13:94446805 | T | C | 22 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(19): Show |
24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.1180-3168A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446805 | |||||||
| chr13:94446853 | A | C | 3 | a0001c0001t0002g0118 a0001c0001t0002g0133 a0001c0001t0002g0218 |
3 | HG02559.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1180-3216T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446853 | |||||||
| chr13:94447255 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1180-3618C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447255 | |||||||
| chr13:94447323 | A | G | 33 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(30): Show |
35 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.1180-3686T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447323 | |||||||
| chr13:94447355 | C | T | 46 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(43): Show |
56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1180-3718G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447355 | |||||||
| chr13:94447653 | C | T | 4 | a0001c0001t0003g0190 a0001c0001t0006g0096 a0001c0001t0014g0104 others(1): Show |
4 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-4016G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447653 | |||||||
| chr13:94447657 | T | C | 1 | a0001c0001t0008g0012 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1180-4020A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447657 | |||||||
| chr13:94447659 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1180-4022T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447659 | |||||||
| chr13:94447676 | G | T | 1 | a0001c0001t0004g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180-4039C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447676 | |||||||
| chr13:94447886 | G | C | 78 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(75): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1180-4249C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447886 | |||||||
| chr13:94448050 | C | G | 1 | a0001c0001t0023g0186 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1180-4413G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448050 | |||||||
| chr13:94448114 | G | T | 1 | a0001c0001t0003g0233 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1180-4477C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448114 | |||||||
| chr13:94448228 | G | C | 10 | a0001c0001t0007g0028 a0001c0001t0007g0076 a0001c0001t0007g0092 others(7): Show |
11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180-4591C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448228 | |||||||
| chr13:94448243 | T | TCAA | 10 | a0001c0001t0007g0028 a0001c0001t0007g0076 a0001c0001t0007g0092 others(7): Show |
11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180-4609_1180-460 others(7): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448243 | |||||||
| chr13:94448502 | T | C | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1180-4865A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448502 | |||||||
| chr13:94448587 | A | G | 190 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1180-4950T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448587 | |||||||
| chr13:94448797 | G | A | 4 | a0001c0001t0006g0039 a0001c0001t0006g0137 a0001c0001t0006g0141 others(1): Show |
4 | HG01891.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-5160C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448797 | |||||||
| chr13:94448809 | C | G | 7 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(4): Show |
8 | HG01981.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180-5172G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448809 | |||||||
| chr13:94448903 | CA | C | 11 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1180-5267delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448903 | |||||||
| chr13:94448914 | T | A | 21 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(18): Show |
22 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1180-5277A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448914 | |||||||
| chr13:94449021 | C | T | 56 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(53): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1180-5384G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449021 | |||||||
| chr13:94449084 | G | GA | 7 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 others(4): Show |
7 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-5448dupT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449084 | |||||||
| chr13:94449170 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1180-5533A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449170 | |||||||
| chr13:94449318 | T | A | 1 | a0001c0001t0006g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1180-5681A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449318 | |||||||
| chr13:94449379 | C | G | 1 | a0001c0001t0020g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1180-5742G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449379 | |||||||
| chr13:94449395 | C | T | 8 | a0001c0001t0009g0034 a0001c0001t0009g0246 a0001c0001t0009g0252 others(5): Show |
9 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-5758G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449395 | |||||||
| chr13:94449535 | C | G | 63 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(60): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.1180-5898G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449535 | |||||||
| chr13:94449776 | A | G | 13 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(10): Show |
14 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1180-6139T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449776 | |||||||
| chr13:94449822 | TATGTAAT others(4): Show |
T | 29 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(26): Show |
30 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.1180-6196_1180-618 others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449822 | |||||||
| chr13:94450150 | G | A | 11 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1180-6513C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450150 | |||||||
| chr13:94450181 | C | T | 2 | a0001c0001t0004g0081 a0001c0001t0004g0181 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1180-6544G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450181 | |||||||
| chr13:94450182 | G | T | 1 | a0008c0008t0001g0156 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1180-6545C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450182 | |||||||
| chr13:94450360 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1180-6723C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450360 | |||||||
| chr13:94450361 | C | T | 2 | a0001c0001t0005g0271 a0001c0001t0005g0273 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1180-6724G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450361 | |||||||
| chr13:94450423 | C | A | 5 | a0002c0002t0006g0238 a0002c0002t0006g0239 a0002c0002t0006g0247 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-6786G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450423 | |||||||
| chr13:94450443 | G | A | 190 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1180-6806C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450443 | |||||||
| chr13:94450495 | A | G | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1180-6858T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450495 | |||||||
| chr13:94450496 | T | C | 6 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0001t0005g0261 others(3): Show |
6 | HG01346.hp2 HG01358.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-6859A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450496 | |||||||
| chr13:94450592 | C | T | 2 | a0002c0002t0006g0238 a0002c0002t0006g0247 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1180-6955G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450592 | |||||||
| chr13:94450671 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1180-7034T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450671 | |||||||
| chr13:94450792 | C | T | 187 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(184): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1180-7155G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450792 | |||||||
| chr13:94451020 | A | T | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1180-7383T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451020 | |||||||
| chr13:94451030 | T | C | 3 | a0001c0001t0002g0118 a0001c0001t0002g0133 a0001c0001t0002g0218 |
3 | HG02559.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1180-7393A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451030 | |||||||
| chr13:94451230 | A | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-7593T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451230 | |||||||
| chr13:94451352 | C | T | 59 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(56): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1180-7715G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451352 | |||||||
| chr13:94451440 | T | C | 58 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(55): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1180-7803A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451440 | |||||||
| chr13:94451531 | A | T | 1 | a0001c0001t0009g0254 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1180-7894T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451531 | |||||||
| chr13:94451637 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1180-8000C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451637 | |||||||
| chr13:94451761 | A | C | 5 | a0002c0002t0006g0238 a0002c0002t0006g0239 a0002c0002t0006g0247 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-8124T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451761 | |||||||
| chr13:94451891 | C | G | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+8200G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451891 | |||||||
| chr13:94451919 | G | GT | 49 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(46): Show |
59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1179+8171dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451919 | |||||||
| chr13:94451952 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0009c0006t0001g0036 |
4 | HG02080.hp1 NA18970.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+8139G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451952 | |||||||
| chr13:94451992 | C | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0020 a0001c0001t0002g0115 others(3): Show |
9 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+8099G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451992 | |||||||
| chr13:94452039 | C | CT | 49 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(46): Show |
59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1179+8051dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452039 | |||||||
| chr13:94452206 | T | C | 3 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 |
3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1179+7885A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452206 | |||||||
| chr13:94452292 | C | T | 2 | a0001c0001t0004g0079 a0001c0001t0004g0080 |
2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1179+7799G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452292 | |||||||
| chr13:94452885 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1179+7206T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452885 | |||||||
| chr13:94452976 | T | C | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+7115A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452976 | |||||||
| chr13:94453145 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1179+6946A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453145 | |||||||
| chr13:94453172 | A | T | 1 | a0001c0001t0002g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1179+6919T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453172 | |||||||
| chr13:94453318 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(270): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1179+6773A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453318 | |||||||
| chr13:94453547 | T | C | 5 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(2): Show |
5 | HG02602.hp1 HG03669.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+6544A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453547 | |||||||
| chr13:94453595 | AC | A | 11 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+6495delG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453595 | |||||||
| chr13:94453654 | A | T | 1 | a0001c0001t0023g0186 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1179+6437T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453654 | |||||||
| chr13:94454229 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1179+5862T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454229 | |||||||
| chr13:94454240 | T | C | 3 | a0001c0001t0003g0078 a0001c0001t0003g0107 a0001c0001t0003g0199 |
3 | HG00438.hp2 HG02083.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1179+5851A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454240 | |||||||
| chr13:94454376 | G | A | 11 | a0001c0001t0008g0012 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+5715C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454376 | |||||||
| chr13:94454894 | C | G | 190 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1179+5197G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454894 | |||||||
| chr13:94454993 | G | C | 59 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(56): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1179+5098C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454993 | |||||||
| chr13:94455051 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0021 others(19): Show |
28 | HG00597.hp1 HG00609.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+5040T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455051 | |||||||
| chr13:94455324 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1179+4767C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455324 | |||||||
| chr13:94455336 | T | C | 190 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1179+4755A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455336 | |||||||
| chr13:94455381 | T | TAG | 38 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(35): Show |
44 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1179+4708_1179+470 others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAG | 51 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0002g0002 others(48): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.1179+4706_1179+470 others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAG | 4 | a0001c0001t0002g0127 a0001c0001t0003g0191 a0001c0001t0018g0129 others(1): Show |
4 | HG00597.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+4704_1179+470 others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(1): Show |
10 | a0001c0001t0002g0114 a0001c0001t0003g0107 a0001c0001t0003g0187 others(7): Show |
11 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1179+4702_1179+470 others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(3): Show |
30 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0002g0209 others(27): Show |
39 | HG00438.hp2 HG00621.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.1179+4700_1179+470 others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(5): Show |
16 | a0001c0001t0003g0103 a0001c0001t0005g0035 a0001c0001t0005g0257 others(13): Show |
17 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1179+4698_1179+470 others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(7): Show |
15 | a0001c0001t0005g0266 a0001c0001t0005g0273 a0001c0001t0006g0037 others(12): Show |
15 | HG02486.hp1 HG02622.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+4696_1179+470 others(18): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(9): Show |
3 | a0001c0001t0005g0276 a0001c0001t0010g0234 a0001c0001t0010g0235 |
3 | HG01123.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1179+4694_1179+470 others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(11): Show |
3 | a0001c0001t0005g0265 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01256.hp1 HG01257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1179+4692_1179+470 others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(13): Show |
1 | a0001c0001t0015g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1179+4690_1179+470 others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(17): Show |
1 | a0001c0001t0015g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1179+4686_1179+470 others(28): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | T | TAGAGAGA others(21): Show |
1 | a0001c0001t0027g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1179+4682_1179+470 others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455381 | TAGAGAG | T | 7 | a0001c0001t0003g0095 a0001c0001t0003g0097 a0001c0001t0003g0190 others(4): Show |
7 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+4704_1179+470 others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | |||||||
| chr13:94455561 | A | G | 1 | a0001c0003t0004g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1179+4530T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455561 | |||||||
| chr13:94456124 | G | A | 4 | a0001c0001t0006g0039 a0001c0001t0006g0137 a0001c0001t0006g0141 others(1): Show |
4 | HG01891.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+3967C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456124 | |||||||
| chr13:94456247 | C | T | 30 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(27): Show |
31 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.1179+3844G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456247 | |||||||
| chr13:94456291 | A | G | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+3800T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456291 | |||||||
| chr13:94456667 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0003g0100 |
2 | NA18939.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1179+3424G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456667 | |||||||
| chr13:94456723 | G | A | 14 | a0001c0001t0001g0221 a0001c0001t0002g0004 a0001c0001t0002g0031 others(11): Show |
20 | HG00438.hp1 HG00544.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.1179+3368C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456723 | |||||||
| chr13:94456862 | G | T | 46 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(43): Show |
56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1179+3229C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456862 | |||||||
| chr13:94456971 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0017g0169 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1179+3120T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456971 | |||||||
| chr13:94456990 | C | T | 1 | a0001c0001t0015g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1179+3101G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456990 | |||||||
| chr13:94457029 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1179+3062G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457029 | |||||||
| chr13:94457061 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1179+3030G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457061 | |||||||
| chr13:94457107 | A | G | 53 | a0001c0001t0001g0046 a0001c0001t0001g0154 a0001c0001t0001g0157 others(50): Show |
65 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1179+2984T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457107 | |||||||
| chr13:94457125 | G | A | 1 | a0001c0001t0029g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1179+2966C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457125 | |||||||
| chr13:94457229 | T | C | 190 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0217 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1179+2862A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457229 | |||||||
| chr13:94457358 | G | C | 13 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(10): Show |
14 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1179+2733C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457358 | |||||||
| chr13:94457378 | T | C | 2 | a0001c0001t0005g0271 a0001c0001t0005g0273 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1179+2713A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457378 | |||||||
| chr13:94457429 | G | A | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+2662C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457429 | |||||||
| chr13:94457504 | A | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0123 |
5 | HG01943.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+2587T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457504 | |||||||
| chr13:94457522 | C | G | 1 | a0001c0001t0030g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1179+2569G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457522 | |||||||
| chr13:94457522 | C | T | 1 | a0001c0004t0006g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1179+2569G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457522 | |||||||
| chr13:94457565 | A | G | 5 | a0002c0002t0006g0238 a0002c0002t0006g0239 a0002c0002t0006g0247 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+2526T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457565 | |||||||
| chr13:94457656 | C | T | 3 | a0001c0001t0015g0175 a0001c0001t0015g0176 a0001c0001t0027g0177 |
3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1179+2435G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457656 | |||||||
| chr13:94457764 | C | T | 2 | a0001c0001t0002g0134 a0001c0001t0002g0222 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1179+2327G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457764 | |||||||
| chr13:94457778 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1179+2313C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457778 | |||||||
| chr13:94457851 | T | C | 129 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(126): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1179+2240A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457851 | |||||||
| chr13:94457952 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1179+2139G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457952 | |||||||
| chr13:94457958 | C | T | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+2133G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457958 | |||||||
| chr13:94458000 | C | A | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+2091G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458000 | |||||||
| chr13:94458001 | G | A | 3 | a0001c0001t0006g0039 a0001c0001t0006g0141 a0001c0001t0030g0140 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+2090C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458001 | |||||||
| chr13:94458056 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0142 |
3 | NA18968.hp2 NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1179+2035A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458056 | |||||||
| chr13:94458066 | C | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+2025G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458066 | |||||||
| chr13:94458081 | C | T | 1 | a0001c0001t0007g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1179+2010G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458081 | |||||||
| chr13:94458290 | C | T | 50 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(47): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1179+1801G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458290 | |||||||
| chr13:94458299 | T | G | 2 | a0001c0001t0002g0116 a0001c0001t0002g0119 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1179+1792A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458299 | |||||||
| chr13:94458313 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1179+1778T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458313 | |||||||
| chr13:94458397 | C | G | 3 | a0001c0001t0015g0175 a0001c0001t0015g0176 a0001c0001t0027g0177 |
3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1179+1694G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458397 | |||||||
| chr13:94458457 | G | A | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+1634C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458457 | |||||||
| chr13:94458518 | T | G | 1 | a0001c0001t0030g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1179+1573A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458518 | |||||||
| chr13:94458646 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0052 |
3 | HG03654.hp1 HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1179+1445T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458646 | |||||||
| chr13:94458685 | C | T | 3 | a0001c0001t0006g0039 a0001c0001t0006g0141 a0001c0001t0030g0140 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+1406G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458685 | |||||||
| chr13:94458695 | G | A | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+1396C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458695 | |||||||
| chr13:94458790 | A | G | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1179+1301T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458790 | |||||||
| chr13:94458854 | G | A | 8 | a0001c0001t0005g0035 a0001c0001t0005g0259 a0001c0001t0005g0260 others(5): Show |
9 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+1237C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458854 | |||||||
| chr13:94458864 | G | T | 2 | a0001c0001t0008g0041 a0001c0001t0008g0136 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1179+1227C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458864 | |||||||
| chr13:94458918 | A | C | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+1173T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458918 | |||||||
| chr13:94458968 | C | G | 1 | a0001c0001t0002g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1179+1123G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458968 | |||||||
| chr13:94459052 | G | GT | 50 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(47): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1179+1038_1179+103 others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459052 | |||||||
| chr13:94459053 | G | T | 76 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(73): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1179+1038C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459053 | |||||||
| chr13:94459093 | G | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+998C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459093 | |||||||
| chr13:94459153 | A | G | 2 | a0001c0001t0011g0201 a0001c0001t0011g0202 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1179+938T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459153 | |||||||
| chr13:94459154 | C | T | 11 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(8): Show |
12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+937G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459154 | |||||||
| chr13:94459255 | T | C | 97 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(94): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1179+836A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459255 | |||||||
| chr13:94459341 | T | A | 1 | a0001c0001t0005g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1179+750A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459341 | |||||||
| chr13:94459405 | C | T | 50 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(47): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1179+686G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459405 | |||||||
| chr13:94459414 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1179+677C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459414 | |||||||
| chr13:94459544 | T | C | 60 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(57): Show |
64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1179+547A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459544 | |||||||
| chr13:94459578 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0044 others(11): Show |
23 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1179+513C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459578 | |||||||
| chr13:94459606 | G | A | 1 | a0001c0001t0027g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1179+485C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459606 | |||||||
| chr13:94460343 | C | T | 5 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0174 others(2): Show |
10 | NA18959.hp1 NA18962.hp2 NA18978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044-117G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460343 | |||||||
| chr13:94460726 | C | T | 21 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(18): Show |
22 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1044-500G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460726 | |||||||
| chr13:94460746 | T | C | 134 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(131): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1044-520A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460746 | |||||||
| chr13:94460916 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1044-690G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460916 | |||||||
| chr13:94461074 | G | A | 1 | a0001c0001t0006g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044-848C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461074 | |||||||
| chr13:94461292 | C | T | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1043+718G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461292 | |||||||
| chr13:94461505 | C | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0220 |
2 | HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1043+505G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461505 | |||||||
| chr13:94461606 | G | C | 13 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(10): Show |
14 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1043+404C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461606 | |||||||
| chr13:94461902 | A | C | 1 | a0001c0003t0004g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1043+108T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461902 | |||||||
| chr13:94461978 | C | T | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1043+32G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461978 | |||||||
| chr13:94462345 | C | T | 47 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(44): Show |
57 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.864-156G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462345 | |||||||
| chr13:94462380 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.864-191C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462380 | |||||||
| chr13:94462502 | GA | G | 14 | a0001c0001t0006g0039 a0001c0001t0006g0137 a0001c0001t0006g0141 others(11): Show |
15 | HG01891.hp1 HG01981.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.864-314delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462502 | |||||||
| chr13:94462612 | T | C | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-423A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462612 | |||||||
| chr13:94462635 | AC | A | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-447delG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462635 | |||||||
| chr13:94462742 | A | T | 2 | a0001c0001t0003g0178 a0001c0001t0024g0188 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.864-553T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462742 | |||||||
| chr13:94462820 | T | C | 1 | a0001c0001t0005g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.864-631A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462820 | |||||||
| chr13:94462921 | C | G | 26 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-732G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462921 | |||||||
| chr13:94463057 | G | A | 4 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-868C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463057 | |||||||
| chr13:94463078 | G | A | 21 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0212 others(18): Show |
28 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-889C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463078 | |||||||
| chr13:94463138 | T | A | 4 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-949A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463138 | |||||||
| chr13:94463243 | C | A | 10 | a0001c0001t0007g0028 a0001c0001t0007g0076 a0001c0001t0007g0092 others(7): Show |
11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.864-1054G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463243 | |||||||
| chr13:94463273 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.864-1084T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463273 | |||||||
| chr13:94463285 | C | CT | 8 | a0001c0001t0001g0050 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG00438.hp2 HG00597.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.864-1097dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463285 | |||||||
| chr13:94463285 | CT | C | 70 | a0001c0001t0001g0044 a0001c0001t0002g0122 a0001c0001t0002g0133 others(67): Show |
74 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.864-1097delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463285 | |||||||
| chr13:94463378 | C | T | 61 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0212 others(58): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.864-1189G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463378 | |||||||
| chr13:94463470 | TGTCAGGC others(18): Show |
T | 46 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(43): Show |
56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.864-1306_864-1282d others(27): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463470 | |||||||
| chr13:94463514 | T | C | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.864-1325A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463514 | |||||||
| chr13:94463526 | G | C | 1 | a0001c0001t0003g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.864-1337C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463526 | |||||||
| chr13:94463570 | G | A | 1 | a0001c0001t0004g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.864-1381C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463570 | |||||||
| chr13:94463574 | G | A | 26 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(23): Show |
27 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.864-1385C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463574 | |||||||
| chr13:94463579 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.864-1390G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463579 | |||||||
| chr13:94463651 | G | A | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.864-1462C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463651 | |||||||
| chr13:94464006 | G | C | 51 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0002g0114 others(48): Show |
61 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.863+1627C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464006 | |||||||
| chr13:94464024 | T | C | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.863+1609A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464024 | |||||||
| chr13:94464099 | T | C | 54 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0002g0114 others(51): Show |
64 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.863+1534A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464099 | |||||||
| chr13:94464188 | C | T | 46 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(43): Show |
56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.863+1445G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464188 | |||||||
| chr13:94464243 | A | G | 21 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(18): Show |
23 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.863+1390T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464243 | |||||||
| chr13:94464244 | G | A | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.863+1389C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464244 | |||||||
| chr13:94464270 | C | T | 4 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+1363G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464270 | |||||||
| chr13:94464438 | G | A | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+1195C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464438 | |||||||
| chr13:94464468 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.863+1165A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464468 | |||||||
| chr13:94464476 | C | T | 10 | a0001c0001t0007g0028 a0001c0001t0007g0076 a0001c0001t0007g0092 others(7): Show |
11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.863+1157G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464476 | |||||||
| chr13:94464490 | A | C | 22 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(19): Show |
23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.863+1143T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464490 | |||||||
| chr13:94464556 | C | T | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.863+1077G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464556 | |||||||
| chr13:94464568 | A | C | 1 | a0001c0001t0006g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.863+1065T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464568 | |||||||
| chr13:94464576 | G | A | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.863+1057C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464576 | |||||||
| chr13:94464630 | C | G | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+1003G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464630 | |||||||
| chr13:94464661 | C | A | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+972G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464661 | |||||||
| chr13:94464736 | G | T | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+897C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464736 | |||||||
| chr13:94464769 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.863+864C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464769 | |||||||
| chr13:94464871 | C | T | 1 | a0001c0001t0007g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.863+762G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464871 | |||||||
| chr13:94465131 | C | A | 20 | a0001c0001t0006g0037 a0001c0001t0006g0038 a0001c0001t0006g0241 others(17): Show |
21 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.863+502G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465131 | |||||||
| chr13:94465142 | C | T | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+491G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465142 | |||||||
| chr13:94465171 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.863+462C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465171 | |||||||
| chr13:94465417 | CATAACCA | C | 44 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(41): Show |
54 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.863+209_863+215del others(7): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465417 | |||||||
| chr13:94465418 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.863+215T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465418 | |||||||
| chr13:94465422 | C | T | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+211G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465422 | |||||||
| chr13:94465443 | G | GAT | 36 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(33): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.863+188_863+189dup others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465443 | |||||||
| chr13:94465446 | A | AT | 59 | a0001c0001t0001g0021 a0001c0001t0001g0049 a0001c0001t0001g0131 others(56): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.863+186dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465446 | |||||||
| chr13:94465447 | T | TA | 91 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(88): Show |
103 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(100): Show |
intron_variant | MODIFIER | c.863+185_863+186ins others(1): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465447 | |||||||
| chr13:94465545 | AACAGCAC others(3): Show |
A | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.863+78_863+87delAT others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465545 | |||||||
| chr13:94465609 | C | T | 1 | a0003c0005t0016g0253 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.863+24G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465609 | |||||||
| chr13:94465966 | TTTTATAT others(7): Show |
T | 1 | a0001c0001t0002g0031 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.697-181_697-168del others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465966 | |||||||
| chr13:94465967 | TTTATATA others(6): Show |
T | 1 | a0001c0001t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.697-181_697-169del others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465967 | |||||||
| chr13:94465968 | T | TATATATA others(4): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18980.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.697-170_697-169ins others(11): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TATATATA others(6): Show |
1 | a0001c0001t0003g0006 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.697-170_697-169ins others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TATATATA others(10): Show |
1 | a0001c0001t0003g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.697-170_697-169ins others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(21): Show |
25 | HG00673.hp1 HG01099.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.697-171_697-170dup others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(17): Show |
20 | HG00673.hp2 HG01071.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.697-173_697-170dup others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0059 others(18): Show |
21 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.697-175_697-170dup others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0046 others(3): Show |
6 | HG00609.hp1 HG02523.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-177_697-170dup others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATAT others(3): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0050 others(11): Show |
15 | HG00558.hp1 HG01175.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.697-179_697-170dup others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0142 a0001c0001t0001g0154 a0001c0001t0002g0117 others(2): Show |
5 | HG02129.hp2 HG03834.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-181_697-170dup others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0008 a0001c0001t0003g0009 a0001c0001t0003g0068 |
3 | HG01069.hp2 NA18983.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.697-183_697-170dup others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATAT others(9): Show |
2 | a0001c0001t0015g0175 a0001c0001t0037g0278 |
2 | HG01884.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.697-185_697-170dup others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | T | TTATATAT others(11): Show |
1 | a0001c0001t0003g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.697-187_697-170dup others(18): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTA | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(20): Show |
24 | HG01358.hp1 HG01515.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.697-171_697-170del others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATA | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0023 others(17): Show |
20 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.697-173_697-170del others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATA | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0145 a0001c0001t0001g0228 others(9): Show |
12 | HG01168.hp2 HG02145.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.697-175_697-170del others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(1): Show |
T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0054 others(5): Show |
9 | HG01074.hp2 HG02055.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-177_697-170del others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(3): Show |
T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0131 others(15): Show |
19 | HG01109.hp2 HG02080.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.697-179_697-170del others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0212 a0001c0001t0002g0004 a0001c0001t0002g0032 others(5): Show |
10 | HG01516.hp2 HG01891.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.697-181_697-170del others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(7): Show |
T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0221 others(8): Show |
11 | HG00438.hp1 HG01261.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.697-183_697-170del others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(9): Show |
T | 7 | a0001c0001t0001g0152 a0001c0001t0002g0031 a0001c0001t0002g0113 others(4): Show |
7 | HG00544.hp2 HG00558.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.697-185_697-170del others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(11): Show |
T | 4 | a0001c0001t0001g0005 a0001c0001t0002g0118 a0001c0001t0002g0218 others(1): Show |
4 | HG02559.hp2 HG03516.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-187_697-170del others(18): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(13): Show |
T | 5 | a0001c0001t0001g0170 a0001c0001t0002g0002 a0001c0001t0005g0264 others(2): Show |
5 | HG01255.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-189_697-170del others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(15): Show |
T | 9 | a0001c0001t0002g0010 a0001c0001t0002g0020 a0001c0001t0006g0137 others(6): Show |
12 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.697-191_697-170del others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(17): Show |
T | 16 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0020 others(13): Show |
18 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.697-193_697-170del others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(21): Show |
T | 6 | a0001c0001t0001g0144 a0001c0001t0002g0114 a0001c0001t0002g0124 others(3): Show |
6 | HG00280.hp1 HG03490.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-197_697-170del others(28): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(23): Show |
T | 1 | a0001c0001t0004g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.697-199_697-170del others(30): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(25): Show |
T | 6 | a0001c0001t0001g0014 a0001c0001t0003g0019 a0001c0001t0004g0080 others(3): Show |
6 | HG01256.hp2 HG01346.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-201_697-170del others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(27): Show |
T | 20 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0081 others(17): Show |
22 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.697-203_697-170del others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(29): Show |
T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0005 |
3 | NA18995.hp2 NA19012.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.697-205_697-170del others(36): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(31): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697-207_697-170del others(38): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(33): Show |
T | 2 | a0001c0004t0006g0194 a0001c0004t0006g0195 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.697-209_697-170del others(40): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94465968 | TTATATAT others(35): Show |
T | 1 | a0007c0014t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.697-211_697-170del others(42): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | |||||||
| chr13:94466012 | ATAT | A | 3 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0006c0009t0002g0214 |
3 | HG03669.hp1 HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.697-216_697-214del others(3): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466012 | |||||||
| chr13:94466016 | A | C | 6 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(3): Show |
6 | HG02602.hp1 HG02683.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-217T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466016 | |||||||
| chr13:94466103 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.697-304A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466103 | |||||||
| chr13:94466352 | G | C | 29 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(26): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.696+206C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466352 | |||||||
| chr13:94466481 | T | C | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.696+77A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466481 | |||||||
| chr13:94466487 | C | T | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.696+71G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466487 | |||||||
| chr13:94466753 | A | G | 23 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(20): Show |
24 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.596-95T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466753 | |||||||
| chr13:94466755 | G | T | 1 | a0001c0001t0003g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596-97C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466755 | |||||||
| chr13:94466839 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.596-181T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466839 | |||||||
| chr13:94466938 | A | C | 1 | a0001c0001t0030g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.596-280T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466938 | |||||||
| chr13:94466959 | A | C | 1 | a0001c0001t0002g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596-301T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466959 | |||||||
| chr13:94466964 | T | C | 23 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(20): Show |
24 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.596-306A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466964 | |||||||
| chr13:94467000 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.596-342A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467000 | |||||||
| chr13:94467015 | G | T | 82 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(79): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.596-357C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467015 | |||||||
| chr13:94467173 | A | G | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.596-515T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467173 | |||||||
| chr13:94467355 | GT | G | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-698delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467355 | |||||||
| chr13:94467491 | G | C | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-833C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467491 | |||||||
| chr13:94467525 | A | G | 1 | a0001c0001t0006g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.596-867T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467525 | |||||||
| chr13:94467531 | G | A | 22 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(19): Show |
23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.596-873C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467531 | |||||||
| chr13:94467861 | C | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+885G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467861 | |||||||
| chr13:94467964 | A | C | 52 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0002g0114 others(49): Show |
62 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.595+782T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467964 | |||||||
| chr13:94467987 | T | C | 6 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+759A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467987 | |||||||
| chr13:94468070 | A | G | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.595+676T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468070 | |||||||
| chr13:94468190 | G | A | 6 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+556C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468190 | |||||||
| chr13:94468239 | T | C | 19 | a0001c0001t0006g0037 a0001c0001t0006g0038 a0001c0001t0006g0241 others(16): Show |
20 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.595+507A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468239 | |||||||
| chr13:94468409 | T | A | 52 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0002g0114 others(49): Show |
62 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.595+337A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468409 | |||||||
| chr13:94468425 | T | C | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+321A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468425 | |||||||
| chr13:94468452 | C | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+294G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468452 | |||||||
| chr13:94468493 | G | A | 1 | a0001c0001t0008g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.595+253C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468493 | |||||||
| chr13:94468597 | GTA | G | 6 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+147_595+148del others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468597 | |||||||
| chr13:94469180 | C | T | 1 | a0001c0001t0004g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-135G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469180 | |||||||
| chr13:94469234 | G | A | 29 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(26): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.296-189C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469234 | |||||||
| chr13:94469369 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0022g0155 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.296-324T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469369 | |||||||
| chr13:94469388 | T | C | 22 | a0001c0001t0005g0035 a0001c0001t0005g0257 a0001c0001t0005g0258 others(19): Show |
23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.296-343A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469388 | |||||||
| chr13:94469544 | T | A | 7 | a0001c0001t0009g0034 a0001c0001t0009g0246 a0001c0001t0009g0252 others(4): Show |
8 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-499A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469544 | |||||||
| chr13:94469625 | G | A | 8 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(5): Show |
9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-580C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469625 | |||||||
| chr13:94469692 | C | T | 22 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(19): Show |
24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-647G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469692 | |||||||
| chr13:94469741 | G | C | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.296-696C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469741 | |||||||
| chr13:94469803 | G | A | 2 | a0001c0001t0009g0034 a0001c0001t0009g0246 |
3 | HG02280.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.296-758C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469803 | |||||||
| chr13:94470416 | G | A | 1 | a0004c0013t0001g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.296-1371C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470416 | |||||||
| chr13:94470662 | T | G | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-1617A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470662 | |||||||
| chr13:94470677 | C | T | 1 | a0007c0014t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.296-1632G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470677 | |||||||
| chr13:94470733 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.296-1688A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470733 | |||||||
| chr13:94470911 | G | T | 8 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(5): Show |
9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-1866C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470911 | |||||||
| chr13:94470936 | C | T | 30 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(27): Show |
39 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.296-1891G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470936 | |||||||
| chr13:94470972 | A | G | 22 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(19): Show |
24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-1927T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470972 | |||||||
| chr13:94471132 | GAAAGGAA others(16): Show |
G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.296-2110_296-2088d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471132 | |||||||
| chr13:94471227 | T | C | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2182A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471227 | |||||||
| chr13:94471259 | G | A | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.296-2214C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471259 | |||||||
| chr13:94471296 | T | C | 1 | a0001c0001t0013g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.296-2251A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471296 | |||||||
| chr13:94471392 | T | C | 18 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(15): Show |
19 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.296-2347A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471392 | |||||||
| chr13:94471413 | C | T | 22 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(19): Show |
24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-2368G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471413 | |||||||
| chr13:94471548 | A | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2503T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471548 | |||||||
| chr13:94471663 | C | T | 37 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.296-2618G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471663 | |||||||
| chr13:94472259 | A | G | 3 | a0001c0001t0003g0095 a0001c0001t0003g0097 a0001c0001t0023g0186 |
3 | NA18970.hp1 NA19064.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.296-3214T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472259 | |||||||
| chr13:94472513 | CATACATA others(7): Show |
C | 1 | a0001c0012t0002g0224 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.296-3482_296-3469d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472513 | |||||||
| chr13:94472517 | C | T | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-3472G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472517 | CATACATA others(1): Show |
C | 3 | a0001c0001t0005g0271 a0001c0001t0005g0272 a0001c0001t0005g0273 |
3 | HG01884.hp2 HG02145.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.296-3480_296-3473d others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472517 | CATACATA others(3): Show |
C | 3 | a0001c0001t0002g0127 a0001c0001t0005g0035 a0001c0001t0034g0262 |
4 | HG02055.hp2 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3482_296-3473d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472517 | CATACATA others(5): Show |
C | 3 | a0001c0001t0005g0263 a0001c0001t0005g0265 a0001c0001t0026g0128 |
3 | HG00140.hp2 HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.296-3484_296-3473d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472517 | CATACATA others(7): Show |
C | 1 | a0001c0001t0005g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.296-3486_296-3473d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472517 | CATACATA others(11): Show |
C | 1 | a0001c0001t0018g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-3490_296-3473d others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472517 | CATACATA others(25): Show |
C | 1 | a0001c0001t0002g0225 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.296-3504_296-3473d others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | |||||||
| chr13:94472521 | C | T | 111 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0212 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.296-3476G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472521 | CAT | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
5 | HG00621.hp1 HG01255.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3478_296-3477d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472521 | CATATAT | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0152 a0001c0001t0005g0268 others(1): Show |
4 | HG00558.hp2 HG01358.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3482_296-3477d others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472521 | CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0064 a0001c0001t0003g0068 a0001c0001t0003g0166 |
3 | HG01069.hp2 HG03710.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.296-3486_296-3477d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472521 | CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0170 |
2 | NA19030.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.296-3488_296-3477d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472521 | CATATATA others(15): Show |
C | 2 | a0001c0001t0006g0091 a0001c0001t0007g0185 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.296-3498_296-3477d others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472521 | CATATATA others(17): Show |
C | 1 | a0001c0001t0007g0094 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-3500_296-3477d others(26): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | |||||||
| chr13:94472523 | T | C | 1 | a0001c0004t0006g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.296-3478A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472523 | |||||||
| chr13:94472525 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.296-3480A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472525 | |||||||
| chr13:94472532 | ATATATAT others(36): Show |
A | 4 | a0001c0003t0004g0105 a0001c0003t0004g0197 a0001c0003t0004g0198 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-3530_296-3488d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472532 | |||||||
| chr13:94472532 | ATATATAT others(37): Show |
A | 1 | a0001c0001t0004g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.296-3531_296-3488d others(46): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472532 | |||||||
| chr13:94472533 | TATATATA others(28): Show |
T | 1 | a0001c0001t0005g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.296-3523_296-3489d others(37): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472533 | |||||||
| chr13:94472534 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0005g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.296-3524_296-3490d others(37): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | |||||||
| chr13:94472534 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.296-3528_296-3490d others(41): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | |||||||
| chr13:94472534 | ATATATAT others(34): Show |
A | 1 | a0001c0001t0004g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.296-3530_296-3490d others(43): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | |||||||
| chr13:94472534 | ATATATAT others(35): Show |
A | 1 | a0001c0001t0004g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-3531_296-3490d others(44): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | |||||||
| chr13:94472534 | ATATATAT others(36): Show |
A | 1 | a0001c0001t0004g0183 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.296-3532_296-3490d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | |||||||
| chr13:94472534 | ATATATAT others(37): Show |
A | 15 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(12): Show |
16 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.296-3533_296-3490d others(46): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | |||||||
| chr13:94472536 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.296-3525_296-3492d others(36): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472536 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.296-3527_296-3492d others(38): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472536 | ATATATAT others(30): Show |
A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0221 others(13): Show |
22 | HG00438.hp1 HG00544.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.296-3528_296-3492d others(39): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472536 | ATATATAT others(33): Show |
A | 4 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0136 others(1): Show |
5 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3531_296-3492d others(42): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472536 | ATATATAT others(34): Show |
A | 2 | a0001c0001t0008g0040 a0001c0001t0008g0041 |
2 | HG01981.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.296-3532_296-3492d others(43): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472536 | ATATATAT others(36): Show |
A | 5 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3534_296-3492d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472536 | ATATATAT others(37): Show |
A | 1 | a0001c0001t0004g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.296-3535_296-3492d others(46): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | |||||||
| chr13:94472538 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0002g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.296-3526_296-3494d others(35): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | |||||||
| chr13:94472538 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.296-3529_296-3494d others(38): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | |||||||
| chr13:94472538 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.296-3530_296-3494d others(39): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | |||||||
| chr13:94472538 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0008g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.296-3532_296-3494d others(41): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | |||||||
| chr13:94472538 | ATATATAT others(36): Show |
A | 1 | a0001c0001t0015g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.296-3536_296-3494d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | |||||||
| chr13:94472540 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0003g0007 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.296-3526_296-3496d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472540 | |||||||
| chr13:94472540 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0002g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.296-3528_296-3496d others(35): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472540 | |||||||
| chr13:94472542 | ATATATAT others(23): Show |
A | 3 | a0001c0001t0003g0187 a0001c0001t0006g0180 a0001c0001t0012g0098 |
3 | HG02615.hp2 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.296-3527_296-3498d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | |||||||
| chr13:94472542 | ATATATAT others(24): Show |
A | 16 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(13): Show |
23 | HG00597.hp2 HG00621.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.296-3528_296-3498d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | |||||||
| chr13:94472542 | ATATATAT others(25): Show |
A | 2 | a0001c0001t0003g0006 a0001c0001t0003g0233 |
2 | HG01168.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3498d others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | |||||||
| chr13:94472542 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0020g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.296-3530_296-3498d others(35): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | |||||||
| chr13:94472542 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0008g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.296-3534_296-3498d others(39): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | |||||||
| chr13:94472544 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0006g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.296-3524_296-3500d others(27): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | |||||||
| chr13:94472544 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0003g0173 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.296-3528_296-3500d others(31): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | |||||||
| chr13:94472544 | ATATATAT others(23): Show |
A | 2 | a0001c0001t0003g0174 a0001c0001t0003g0178 |
2 | HG04199.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3500d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | |||||||
| chr13:94472544 | ATATATAT others(24): Show |
A | 5 | a0001c0001t0003g0095 a0001c0001t0006g0096 a0001c0001t0014g0104 others(2): Show |
5 | HG03490.hp1 HG03492.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3530_296-3500d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | |||||||
| chr13:94472544 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0006g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.296-3531_296-3500d others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | |||||||
| chr13:94472546 | ATATATAT others(16): Show |
A | 5 | a0001c0001t0007g0092 a0001c0001t0007g0093 a0001c0001t0007g0184 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3524_296-3502d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472546 | |||||||
| chr13:94472546 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0003g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.296-3531_296-3502d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472546 | |||||||
| chr13:94472546 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0023g0186 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.296-3532_296-3502d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472546 | |||||||
| chr13:94472548 | ATATATAT others(16): Show |
A | 1 | a0001c0004t0006g0194 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.296-3526_296-3504d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472548 | |||||||
| chr13:94472548 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0006g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-3529_296-3504d others(28): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472548 | |||||||
| chr13:94472548 | ATATATAT others(27): Show |
A | 2 | a0001c0001t0010g0236 a0001c0001t0010g0237 |
2 | HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.296-3537_296-3504d others(36): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472548 | |||||||
| chr13:94472550 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0157 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.296-3525_296-3506d others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472550 | |||||||
| chr13:94472550 | ATATATAT others(14): Show |
A | 1 | a0001c0004t0006g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.296-3526_296-3506d others(23): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472550 | |||||||
| chr13:94472551 | TATATATA others(8): Show |
T | 1 | a0001c0001t0005g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.296-3521_296-3507d others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472551 | |||||||
| chr13:94472551 | TATATATA others(10): Show |
T | 1 | a0001c0001t0002g0229 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.296-3523_296-3507d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472551 | |||||||
| chr13:94472552 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0008 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.296-3527_296-3508d others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472552 | |||||||
| chr13:94472552 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0045 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.296-3528_296-3508d others(23): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472552 | |||||||
| chr13:94472552 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.296-3529_296-3508d others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472552 | |||||||
| chr13:94472553 | TATATATA others(6): Show |
T | 1 | a0001c0001t0005g0259 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.296-3521_296-3509d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472553 | |||||||
| chr13:94472553 | TATATATA others(8): Show |
T | 1 | a0001c0001t0002g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.296-3523_296-3509d others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472553 | |||||||
| chr13:94472554 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0002 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.296-3526_296-3510d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472554 | |||||||
| chr13:94472554 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0008 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.296-3528_296-3510d others(21): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472554 | |||||||
| chr13:94472554 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0145 |
2 | HG01993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.296-3529_296-3510d others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472554 | |||||||
| chr13:94472555 | TATATATA others(4): Show |
T | 2 | a0001c0001t0035g0270 a0003c0005t0016g0253 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.296-3521_296-3511d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472555 | |||||||
| chr13:94472556 | ATATATAT others(6): Show |
A | 3 | a0001c0001t0002g0002 a0001c0001t0002g0132 a0001c0001t0005g0275 |
3 | HG00099.hp2 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.296-3524_296-3512d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0006g0038 a0001c0001t0017g0169 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-3525_296-3512d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(10): Show |
A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0149 a0001c0001t0002g0119 others(3): Show |
6 | HG01261.hp1 HG03139.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-3528_296-3512d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(11): Show |
A | 3 | a0001c0001t0002g0118 a0001c0001t0002g0134 a0001c0001t0002g0232 |
3 | HG02559.hp2 HG02809.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3512d others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0002g0002 a0001c0001t0002g0109 a0001c0001t0002g0206 |
3 | HG01109.hp1 HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.296-3530_296-3512d others(21): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0008 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.296-3534_296-3512d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0010g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.296-3540_296-3512d others(31): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472556 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0010g0235 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.296-3541_296-3512d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | |||||||
| chr13:94472557 | TATATATA others(4): Show |
T | 3 | a0001c0001t0005g0264 a0001c0001t0005g0274 a0001c0001t0006g0037 |
3 | HG01891.hp2 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.296-3523_296-3513d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472557 | |||||||
| chr13:94472558 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0107 |
2 | HG00438.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.296-3525_296-3514d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | |||||||
| chr13:94472558 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0003g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-3526_296-3514d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | |||||||
| chr13:94472558 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.296-3527_296-3514d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | |||||||
| chr13:94472558 | ATATATAT others(8): Show |
A | 4 | a0001c0001t0001g0217 a0001c0001t0002g0020 a0001c0001t0002g0112 others(1): Show |
4 | HG01123.hp1 HG02451.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3528_296-3514d others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | |||||||
| chr13:94472558 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0219 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.296-3530_296-3514d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | |||||||
| chr13:94472558 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.296-3532_296-3514d others(21): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | |||||||
| chr13:94472559 | TATATATA others(2): Show |
T | 6 | a0001c0001t0001g0013 a0001c0001t0003g0015 a0001c0001t0003g0025 others(3): Show |
7 | HG01071.hp2 HG01099.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-3523_296-3515d others(11): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472559 | |||||||
| chr13:94472560 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0005 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.296-3525_296-3516d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | |||||||
| chr13:94472560 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0124 |
2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.296-3526_296-3516d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | |||||||
| chr13:94472560 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0059 a0001c0001t0002g0120 |
2 | HG01257.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.296-3527_296-3516d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | |||||||
| chr13:94472560 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0002g0220 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.296-3528_296-3516d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | |||||||
| chr13:94472560 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0115 a0006c0009t0002g0214 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.296-3529_296-3516d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | |||||||
| chr13:94472561 | TATATATA | T | 3 | a0001c0001t0001g0001 a0001c0001t0005g0258 a0001c0001t0005g0260 |
3 | HG01109.hp2 HG01358.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.296-3523_296-3517d others(9): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472561 | |||||||
| chr13:94472562 | A | T | 2 | a0001c0001t0007g0171 a0001c0001t0007g0172 |
2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.296-3517T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | |||||||
| chr13:94472562 | ATATATAT others(3): Show |
A | 4 | a0001c0001t0002g0002 a0001c0001t0003g0027 a0001c0001t0013g0048 others(1): Show |
4 | HG00280.hp1 NA18963.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3527_296-3518d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | |||||||
| chr13:94472562 | ATATATAT others(4): Show |
A | 5 | a0001c0001t0001g0044 a0001c0001t0002g0002 a0001c0001t0002g0010 others(2): Show |
5 | HG00099.hp1 HG01255.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3528_296-3518d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | |||||||
| chr13:94472562 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0216 |
2 | HG02293.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3518d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | |||||||
| chr13:94472564 | A | T | 3 | a0001c0001t0007g0171 a0001c0001t0007g0172 a0001c0001t0029g0242 |
3 | HG01192.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-3519T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | |||||||
| chr13:94472564 | ATATATTT others(2): Show |
A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0074 others(5): Show |
8 | HG00673.hp1 HG00741.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-3528_296-3520d others(11): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | |||||||
| chr13:94472564 | ATATATTT others(3): Show |
A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0215 |
3 | HG01516.hp1 HG01517.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3520d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | |||||||
| chr13:94472564 | ATATATTT others(4): Show |
A | 3 | a0001c0001t0001g0163 a0001c0001t0002g0010 a0001c0001t0002g0223 |
3 | HG00733.hp2 HG03239.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.296-3530_296-3520d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | |||||||
| chr13:94472564 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.296-3531_296-3520d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | |||||||
| chr13:94472566 | A | T | 5 | a0001c0001t0007g0028 a0001c0001t0007g0171 a0001c0001t0007g0172 others(2): Show |
5 | HG01192.hp1 HG01243.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3521T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | |||||||
| chr13:94472566 | ATATTTT | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0056 others(3): Show |
7 | HG03688.hp1 NA18747.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-3527_296-3522d others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | |||||||
| chr13:94472566 | ATATTTTT others(4): Show |
A | 1 | a0001c0001t0033g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.296-3532_296-3522d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | |||||||
| chr13:94472566 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.296-3533_296-3522d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | |||||||
| chr13:94472567 | TA | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0006g0243 others(1): Show |
4 | HG01928.hp2 HG01975.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-3523delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472567 | |||||||
| chr13:94472568 | A | T | 26 | a0001c0001t0001g0051 a0001c0001t0001g0064 a0001c0001t0001g0065 others(23): Show |
28 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.296-3523T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | |||||||
| chr13:94472568 | ATT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(5): Show |
8 | HG01496.hp1 HG03942.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-3525_296-3524d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | |||||||
| chr13:94472568 | ATTT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0060 others(3): Show |
7 | HG00544.hp1 HG00609.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-3526_296-3524d others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | |||||||
| chr13:94472568 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0026 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.296-3533_296-3524d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | |||||||
| chr13:94472570 | T | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0002g0127 others(4): Show |
7 | HG00140.hp2 HG01175.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-3525A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472570 | |||||||
| chr13:94472572 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0144 a0001c0001t0001g0150 others(1): Show |
4 | HG01496.hp1 NA18959.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-3527A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472572 | |||||||
| chr13:94472573 | T | A | 2 | a0001c0001t0003g0073 a0009c0006t0001g0036 |
2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.296-3528A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472573 | |||||||
| chr13:94472574 | T | A | 1 | a0001c0001t0031g0057 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.296-3529A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472574 | |||||||
| chr13:94472575 | T | A | 1 | a0001c0001t0003g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.296-3530A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472575 | |||||||
| chr13:94472601 | C | G | 1 | a0001c0001t0006g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.296-3556G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472601 | |||||||
| chr13:94472642 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0006g0091 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-3597G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472642 | |||||||
| chr13:94472660 | C | T | 29 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(26): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.296-3615G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472660 | |||||||
| chr13:94472676 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0212 others(3): Show |
7 | HG02074.hp2 HG02080.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-3631C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472676 | |||||||
| chr13:94472724 | G | C | 2 | a0001c0001t0006g0037 a0001c0001t0006g0038 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-3679C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472724 | |||||||
| chr13:94472725 | G | A | 8 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(5): Show |
9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-3680C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472725 | |||||||
| chr13:94472750 | T | G | 43 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(40): Show |
52 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.296-3705A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472750 | |||||||
| chr13:94472835 | G | A | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3790C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472835 | |||||||
| chr13:94473004 | C | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3959G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473004 | |||||||
| chr13:94473006 | T | A | 1 | a0001c0001t0006g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-3961A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473006 | |||||||
| chr13:94473033 | A | T | 1 | a0001c0001t0023g0186 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.296-3988T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473033 | |||||||
| chr13:94473155 | T | C | 2 | a0001c0001t0011g0201 a0001c0001t0011g0202 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.296-4110A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473155 | |||||||
| chr13:94473223 | G | A | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.296-4178C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473223 | |||||||
| chr13:94473265 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.296-4220T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473265 | |||||||
| chr13:94473520 | G | A | 1 | a0001c0001t0011g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.296-4475C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473520 | |||||||
| chr13:94473627 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.296-4582G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473627 | |||||||
| chr13:94473691 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.296-4646A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473691 | |||||||
| chr13:94473773 | T | G | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4728A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473773 | |||||||
| chr13:94473777 | G | C | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4732C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473777 | |||||||
| chr13:94473781 | T | G | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4736A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473781 | |||||||
| chr13:94473782 | A | C | 1 | a0001c0001t0003g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.296-4737T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473782 | |||||||
| chr13:94473782 | A | G | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4737T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473782 | |||||||
| chr13:94474016 | T | C | 1 | a0001c0001t0010g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.295+4945A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474016 | |||||||
| chr13:94474099 | T | C | 85 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(82): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.295+4862A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474099 | |||||||
| chr13:94474115 | G | A | 2 | a0001c0001t0014g0104 a0001c0001t0014g0193 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.295+4846C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474115 | |||||||
| chr13:94474258 | GA | G | 109 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(106): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.295+4702delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474258 | |||||||
| chr13:94474297 | C | A | 30 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(27): Show |
39 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.295+4664G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474297 | |||||||
| chr13:94474308 | T | C | 3 | a0001c0001t0006g0039 a0001c0001t0006g0141 a0001c0001t0030g0140 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+4653A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474308 | |||||||
| chr13:94474309 | C | G | 1 | a0001c0001t0004g0196 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.295+4652G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474309 | |||||||
| chr13:94474406 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.295+4555T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474406 | |||||||
| chr13:94474413 | A | C | 3 | a0001c0001t0006g0039 a0001c0001t0006g0141 a0001c0001t0030g0140 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+4548T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474413 | |||||||
| chr13:94474562 | G | A | 7 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 others(4): Show |
7 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+4399C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474562 | |||||||
| chr13:94474588 | C | T | 1 | a0001c0001t0011g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.295+4373G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474588 | |||||||
| chr13:94474594 | T | C | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+4367A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474594 | |||||||
| chr13:94474693 | G | A | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+4268C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474693 | |||||||
| chr13:94474702 | C | T | 41 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0079 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.295+4259G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474702 | |||||||
| chr13:94474848 | G | A | 1 | a0001c0001t0020g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+4113C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474848 | |||||||
| chr13:94474892 | G | A | 1 | a0001c0001t0019g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.295+4069C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474892 | |||||||
| chr13:94475015 | G | A | 3 | a0001c0001t0006g0039 a0001c0001t0006g0141 a0001c0001t0030g0140 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+3946C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475015 | |||||||
| chr13:94475021 | G | A | 1 | a0001c0001t0006g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.295+3940C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475021 | |||||||
| chr13:94475049 | C | A | 2 | a0001c0004t0006g0194 a0001c0004t0006g0195 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.295+3912G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475049 | |||||||
| chr13:94475184 | C | T | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+3777G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475184 | |||||||
| chr13:94475213 | T | A | 6 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+3748A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475213 | |||||||
| chr13:94475251 | A | C | 1 | a0004c0013t0001g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.295+3710T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475251 | |||||||
| chr13:94475256 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.295+3705G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475256 | |||||||
| chr13:94475282 | C | T | 40 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(37): Show |
49 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.295+3679G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475282 | |||||||
| chr13:94475294 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.295+3667T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475294 | |||||||
| chr13:94475375 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.295+3586C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475375 | |||||||
| chr13:94475377 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.295+3584C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475377 | |||||||
| chr13:94475503 | G | A | 1 | a0001c0001t0008g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295+3458C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475503 | |||||||
| chr13:94475978 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.295+2983C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475978 | |||||||
| chr13:94475981 | G | T | 1 | a0001c0001t0002g0132 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.295+2980C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475981 | |||||||
| chr13:94476093 | T | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0106 |
3 | HG00140.hp1 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.295+2868A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476093 | |||||||
| chr13:94476108 | C | T | 80 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(77): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.295+2853G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476108 | |||||||
| chr13:94476120 | A | G | 5 | a0002c0002t0006g0238 a0002c0002t0006g0239 a0002c0002t0006g0247 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+2841T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476120 | |||||||
| chr13:94476180 | C | CT | 17 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0142 others(14): Show |
18 | HG01346.hp2 HG01884.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.295+2780dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | |||||||
| chr13:94476180 | C | CTT | 6 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(3): Show |
7 | HG01981.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+2779_295+2780d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | |||||||
| chr13:94476180 | CT | C | 62 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0067 others(59): Show |
72 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.295+2780delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | |||||||
| chr13:94476180 | CTT | C | 52 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0217 others(49): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.295+2779_295+2780d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | |||||||
| chr13:94476180 | CTTT | C | 9 | a0001c0001t0002g0112 a0001c0001t0002g0132 a0001c0001t0002g0133 others(6): Show |
9 | HG00099.hp2 HG01123.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2778_295+2780d others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | |||||||
| chr13:94476180 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+2769_295+2780d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | |||||||
| chr13:94476212 | G | T | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+2749C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476212 | |||||||
| chr13:94476274 | C | G | 108 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(105): Show |
122 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.295+2687G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476274 | |||||||
| chr13:94476289 | A | G | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+2672T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476289 | |||||||
| chr13:94476303 | T | G | 3 | a0001c0001t0011g0108 a0001c0001t0011g0201 a0001c0001t0011g0202 |
3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.295+2658A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476303 | |||||||
| chr13:94476469 | C | CT | 30 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0168 others(27): Show |
32 | HG00438.hp2 HG01192.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.295+2491dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476469 | |||||||
| chr13:94476469 | CT | C | 64 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0131 others(61): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.295+2491delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476469 | |||||||
| chr13:94476514 | T | C | 76 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(73): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.295+2447A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476514 | |||||||
| chr13:94476537 | G | A | 1 | a0001c0001t0004g0204 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.295+2424C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476537 | |||||||
| chr13:94476624 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.295+2337G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476624 | |||||||
| chr13:94476756 | G | T | 21 | a0001c0001t0006g0241 a0001c0001t0006g0243 a0001c0001t0006g0249 others(18): Show |
23 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+2205C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476756 | |||||||
| chr13:94476831 | G | A | 1 | a0001c0001t0028g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+2130C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476831 | |||||||
| chr13:94476880 | G | A | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+2081C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476880 | |||||||
| chr13:94476899 | C | A | 84 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(81): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.295+2062G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476899 | |||||||
| chr13:94477084 | C | G | 1 | a0001c0001t0003g0173 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.295+1877G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477084 | |||||||
| chr13:94477107 | A | T | 4 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(1): Show |
4 | HG02683.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+1854T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477107 | |||||||
| chr13:94477108 | T | C | 3 | a0001c0001t0006g0037 a0001c0001t0006g0038 a0001c0001t0019g0251 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295+1853A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477108 | |||||||
| chr13:94477156 | T | C | 207 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0074 others(204): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.295+1805A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477156 | |||||||
| chr13:94477157 | G | A | 4 | a0001c0001t0007g0028 a0001c0001t0007g0076 a0001c0001t0007g0171 others(1): Show |
5 | HG01192.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1804C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477157 | |||||||
| chr13:94477181 | T | C | 111 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(108): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.295+1780A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477181 | |||||||
| chr13:94477418 | G | A | 8 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(5): Show |
9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+1543C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477418 | |||||||
| chr13:94477517 | T | C | 1 | a0001c0003t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295+1444A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477517 | |||||||
| chr13:94477660 | T | TA | 112 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0212 others(109): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.295+1300dupT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477660 | |||||||
| chr13:94477660 | T | TAA | 84 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0003g0006 others(81): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.295+1299_295+1300d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477660 | |||||||
| chr13:94477785 | TGAGAA | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | NA18968.hp2 NA18974.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1171_295+1175d others(7): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477785 | |||||||
| chr13:94477857 | A | G | 3 | a0001c0001t0006g0039 a0001c0001t0006g0141 a0001c0001t0030g0140 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+1104T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477857 | |||||||
| chr13:94477961 | G | A | 7 | a0001c0001t0009g0034 a0001c0001t0009g0246 a0001c0001t0009g0252 others(4): Show |
8 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+1000C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477961 | |||||||
| chr13:94478041 | G | A | 63 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0212 others(60): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.295+920C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478041 | |||||||
| chr13:94478151 | C | T | 8 | a0001c0001t0006g0137 a0001c0001t0008g0012 a0001c0001t0008g0040 others(5): Show |
9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+810G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478151 | |||||||
| chr13:94478157 | G | C | 1 | a0001c0001t0002g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.295+804C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478157 | |||||||
| chr13:94478157 | G | GC | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(135): Show |
169 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.295+803dupG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478157 | |||||||
| chr13:94478165 | C | G | 1 | a0001c0001t0002g0011 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.295+796G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478165 | |||||||
| chr13:94478206 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.295+755C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478206 | |||||||
| chr13:94478311 | G | A | 4 | a0001c0001t0010g0234 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+650C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478311 | |||||||
| chr13:94478638 | C | T | 3 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0007t0005g0256 |
3 | HG01346.hp2 HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.295+323G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478638 | |||||||
| chr13:94478671 | C | A | 20 | a0001c0001t0006g0037 a0001c0001t0006g0038 a0001c0001t0006g0241 others(17): Show |
21 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.295+290G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478671 | |||||||
| chr13:94478743 | C | T | 1 | a0001c0001t0006g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.295+218G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478743 | |||||||
| chr13:94478828 | C | T | 2 | a0001c0001t0006g0037 a0001c0001t0006g0038 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.295+133G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478828 |