| geneid | 368 |
|---|---|
| ensemblid | ENSG00000091262.17 |
| hgncid | 57 |
| symbol | ABCC6 |
| name | ATP binding cassette subfamily C member 6 |
| refseq_nuc | NM_001171.6 |
| refseq_prot | NP_001162.5 |
| ensembl_nuc | ENST00000205557.12 |
| ensembl_prot | ENSP00000205557.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 16149565 |
| end | 16223494 |
| strand | - |
| ver | v1.2 |
| region | chr16:16149565-16223494 |
| region5000 | chr16:16144565-16228494 |
| regionname0 | ABCC6_chr16_16149565_16223494 |
| regionname5000 | ABCC6_chr16_16144565_16228494 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1503 | 177 | 21 | 31 | 91 | 4 | 29 | 65 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002 | 0/0 | 1503 | 45 | 17 | 12 | 12 | 2 | 2 | 8 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003 | 0/0 | 1503 | 32 | 2 | 11 | 10 | 5 | 4 | 9 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004 | 0/0 | 1503 | 12 | 4 | 0 | 4 | 4 | 0 | 3 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005 | 0/0 | 1503 | 9 | 1 | 2 | 5 | 0 | 1 | 5 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0006 | 0/0 | 1503 | 7 | 0 | 3 | 4 | 0 | 0 | 4 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0007 | 0/0 | 1503 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0008 | 0/0 | 1503 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0009 | 0/0 | 1503 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010 | 0/0 | 1503 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0011 | 0/0 | 1503 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0012 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0013 | 0/0 | 1503 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0014 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0015 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0016 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0017 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0018 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0019 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0020 | 0/0 | 1503 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0021 | 0/0 | 198 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0022 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0023 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0024 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0025 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0026 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0027 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0028 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0029 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0030 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0031 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0032 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0033 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0034 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0035 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0036 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0037 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0038 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0039 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0040 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0041 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0042 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0043 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0044 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0045 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4512 | 92 | 9 | 20 | 43 | 1 | 19 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0002 | 0/0 | 4512 | 32 | 5 | 0 | 23 | 0 | 4 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0003 | 0/0 | 4512 | 27 | 14 | 4 | 7 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0004 | 0/0 | 4512 | 19 | 2 | 9 | 5 | 2 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0005 | 0/0 | 4512 | 19 | 1 | 5 | 6 | 4 | 3 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0006 | 0/0 | 4512 | 17 | 0 | 1 | 15 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0007 | 0/0 | 4512 | 10 | 0 | 4 | 4 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0008 | 0/0 | 4512 | 7 | 6 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0009 | 0/0 | 4512 | 7 | 0 | 3 | 4 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0010 | 0/0 | 4512 | 7 | 2 | 0 | 1 | 4 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0011 | 0/0 | 4512 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0012 | 0/0 | 4512 | 6 | 0 | 1 | 4 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0013 | 0/0 | 4512 | 5 | 0 | 4 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0014 | 0/0 | 4512 | 5 | 0 | 0 | 5 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0015 | 0/0 | 4512 | 4 | 1 | 3 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0016 | 0/0 | 4512 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0017 | 0/0 | 4512 | 4 | 1 | 0 | 3 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0018 | 0/0 | 4512 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0019 | 0/0 | 4512 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0020 | 0/0 | 4512 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0021 | 0/0 | 4512 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0022 | 0/0 | 4512 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0023 | 0/0 | 4512 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0024 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0025 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0026 | 0/0 | 4512 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0027 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0028 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0029 | 0/0 | 4512 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0030 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0031 | 0/0 | 4512 | 2 | 0 | 1 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0032 | 0/0 | 4512 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0033 | 0/0 | 4512 | 2 | 0 | 0 | 0 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0034 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0035 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0036 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0037 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0038 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0039 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0040 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0041 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0042 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0043 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0044 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0045 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0046 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0047 | 0/1 | 4512 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0048 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0049 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0050 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0051 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0052 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0053 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0054 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0055 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0056 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0057 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0058 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0059 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0060 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0061 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0062 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0063 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0064 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0065 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0066 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0067 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0068 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0069 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0070 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0071 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0072 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0073 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0074 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0075 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0076 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0077 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0078 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0079 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| c0080 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 629 | 313 | 80 | 63 | 125 | 16 | 29 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0002 | 0/1 | 629 | 22 | 0 | 3 | 8 | 2 | 8 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0003 | 0/0 | 629 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0004 | 0/0 | 629 | 4 | 0 | 2 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0005 | 0/0 | 630 | 3 | 0 | 1 | 1 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0006 | 0/0 | 629 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0007 | 0/0 | 629 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0008 | 0/0 | 629 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0009 | 0/0 | 629 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0010 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0011 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| t0012 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4512 | 92 | 9 | 20 | 43 | 1 | 19 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0002 | 0/0 | 4512 | 32 | 5 | 0 | 23 | 0 | 4 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0004 | 0/0 | 4512 | 19 | 2 | 9 | 5 | 2 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0006 | 0/0 | 4512 | 17 | 0 | 1 | 15 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0023 | 0/0 | 4512 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0026 | 0/0 | 4512 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0028 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0033 | 0/0 | 4512 | 2 | 0 | 0 | 0 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0043 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0047 | 0/1 | 4512 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0049 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0052 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0055 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0064 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0065 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0067 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0072 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0003 | 0/0 | 4512 | 27 | 14 | 4 | 7 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0013 | 0/0 | 4512 | 5 | 0 | 4 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0014 | 0/0 | 4512 | 5 | 0 | 0 | 5 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0022 | 0/0 | 4512 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0024 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0051 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0057 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0068 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0074 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0005 | 0/0 | 4512 | 19 | 1 | 5 | 6 | 4 | 3 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0007 | 0/0 | 4512 | 10 | 0 | 4 | 4 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0021 | 0/0 | 4512 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0071 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004c0010 | 0/0 | 4512 | 7 | 2 | 0 | 1 | 4 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004c0017 | 0/0 | 4512 | 4 | 1 | 0 | 3 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004c0078 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005c0012 | 0/0 | 4512 | 6 | 0 | 1 | 4 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005c0031 | 0/0 | 4512 | 2 | 0 | 1 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005c0048 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0006c0009 | 0/0 | 4512 | 7 | 0 | 3 | 4 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0007c0008 | 0/0 | 4512 | 7 | 6 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0008c0011 | 0/0 | 4512 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0009c0015 | 0/0 | 4512 | 4 | 1 | 3 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010c0029 | 0/0 | 4512 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010c0042 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010c0045 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0011c0016 | 0/0 | 4512 | 4 | 3 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0012c0025 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0012c0030 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0013c0020 | 0/0 | 4512 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0013c0050 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0014c0018 | 0/0 | 4512 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0015c0019 | 0/0 | 4512 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0016c0036 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0017c0034 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0018c0035 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0019c0027 | 0/0 | 4512 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0020c0032 | 0/0 | 4512 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0021c0079 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0022c0075 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0023c0076 | 0/0 | 4512 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0024c0077 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0025c0053 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0026c0056 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0027c0073 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0028c0044 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0029c0058 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0030c0046 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0031c0060 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0032c0059 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0033c0054 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0034c0063 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0035c0062 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0036c0066 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0037c0061 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0038c0069 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0039c0070 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0040c0041 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0041c0080 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0042c0039 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0043c0040 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0044c0038 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0045c0037 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5140 | 75 | 9 | 16 | 35 | 1 | 14 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0001t0002 | 0/0 | 5140 | 12 | 0 | 1 | 6 | 0 | 5 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0001t0004 | 0/0 | 5140 | 4 | 0 | 2 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0001t0005 | 0/0 | 5141 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0002t0001 | 0/0 | 5140 | 30 | 5 | 0 | 23 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0002t0002 | 0/0 | 5140 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0004t0001 | 0/0 | 5140 | 15 | 2 | 8 | 4 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0004t0002 | 0/0 | 5140 | 4 | 0 | 1 | 1 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0006t0001 | 0/0 | 5140 | 15 | 0 | 0 | 14 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0006t0002 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0006t0009 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0023t0001 | 0/0 | 5140 | 2 | 0 | 0 | 0 | 0 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0026t0001 | 0/0 | 5140 | 2 | 1 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0028t0001 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0033t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0033t0002 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0043t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0047t0002 | 0/1 | 5140 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0049t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0052t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0055t0012 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0064t0005 | 0/0 | 5141 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0065t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0067t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0001c0072t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0003t0001 | 0/0 | 5140 | 27 | 14 | 4 | 7 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0013t0001 | 0/0 | 5140 | 5 | 0 | 4 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0014t0001 | 0/0 | 5140 | 5 | 0 | 0 | 5 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0022t0001 | 0/0 | 5140 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0024t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0051t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0057t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0068t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0002c0074t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0005t0001 | 0/0 | 5140 | 17 | 1 | 5 | 5 | 4 | 2 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0005t0005 | 0/0 | 5141 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0005t0008 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0007t0001 | 0/0 | 5140 | 10 | 0 | 4 | 4 | 1 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0021t0001 | 0/0 | 5140 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0003c0071t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004c0010t0001 | 0/0 | 5140 | 7 | 2 | 0 | 1 | 4 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004c0017t0001 | 0/0 | 5140 | 4 | 1 | 0 | 3 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0004c0078t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005c0012t0001 | 0/0 | 5140 | 6 | 0 | 1 | 4 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005c0031t0001 | 0/0 | 5140 | 2 | 0 | 1 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0005c0048t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0006c0009t0001 | 0/0 | 5140 | 7 | 0 | 3 | 4 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0007c0008t0001 | 0/0 | 5140 | 7 | 6 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0008c0011t0003 | 0/0 | 5140 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0009c0015t0001 | 0/0 | 5140 | 4 | 1 | 3 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010c0029t0001 | 0/0 | 5140 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010c0042t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0010c0045t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0011c0016t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0011c0016t0006 | 0/0 | 5140 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0011c0016t0011 | 0/0 | 5141 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0012c0025t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0012c0030t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0013c0020t0001 | 0/0 | 5140 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0013c0050t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0014c0018t0001 | 0/0 | 5140 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0015c0019t0001 | 0/0 | 5140 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0016c0036t0001 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0017c0034t0001 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0018c0035t0001 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0019c0027t0007 | 0/0 | 5140 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0020c0032t0001 | 0/0 | 5140 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0021c0079t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0022c0075t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0023c0076t0001 | 0/0 | 5140 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0024c0077t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0025c0053t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0026c0056t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0027c0073t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0028c0044t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0029c0058t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0030c0046t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0031c0060t0010 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0032c0059t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0033c0054t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0034c0063t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0035c0062t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0036c0066t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0037c0061t0001 | 0/0 | 5153 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0038c0069t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0039c0070t0002 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0040c0041t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0041c0080t0001 | 0/0 | 5140 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0042c0039t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0043c0040t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0044c0038t0001 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| a0045c0037t0001 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | copy fasta | chr16 | 16144565 | 16228494 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0006t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0023t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0023t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0026t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0026t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0028t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0028t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0033t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0033t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0043t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0047t0002g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0049t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0052t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0055t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0064t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0065t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0067t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0001c0072t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0013t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0013t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0013t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0013t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0013t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0014t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0014t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0014t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0014t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0014t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0022t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0022t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0024t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0024t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0051t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0057t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0068t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0002c0074t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0005t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0007t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0021t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0021t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0003c0071t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0010t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0017t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0017t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0017t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0017t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0004c0078t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0012t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0012t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0012t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0012t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0012t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0031t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0031t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0005c0048t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0006c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0007c0008t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0008c0011t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0008c0011t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0008c0011t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0008c0011t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0008c0011t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0008c0011t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0009c0015t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0009c0015t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0009c0015t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0009c0015t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0010c0029t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0010c0029t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0010c0042t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0010c0045t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0011c0016t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0011c0016t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0011c0016t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0011c0016t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0012c0025t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0012c0025t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0012c0030t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0012c0030t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0013c0020t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0013c0020t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0013c0020t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0013c0050t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0014c0018t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0014c0018t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0014c0018t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0014c0018t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0015c0019t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0015c0019t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0015c0019t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0016c0036t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0016c0036t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0017c0034t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0018c0035t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0018c0035t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0019c0027t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0019c0027t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0020c0032t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0020c0032t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0021c0079t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0022c0075t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0023c0076t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0024c0077t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0025c0053t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0026c0056t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0027c0073t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0028c0044t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0029c0058t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0030c0046t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0031c0060t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0032c0059t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0033c0054t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0034c0063t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0035c0062t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0036c0066t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0037c0061t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0038c0069t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0039c0070t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0040c0041t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0041c0080t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0042c0039t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0043c0040t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0044c0038t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| a0045c0037t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0007 | t0001 | g0245 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00099 | hp2 | a0036 | c0066 | t0001 | g0052 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0150 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00140 | hp2 | a0003 | c0005 | t0001 | g0083 | EUR | GBR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0104 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00280 | hp2 | a0010 | c0042 | t0001 | g0099 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00323 | hp1 | a0004 | c0010 | t0001 | g0046 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00323 | hp2 | a0010 | c0045 | t0001 | g0107 | EUR | FIN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00408 | hp1 | a0040 | c0041 | t0001 | g0216 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00438 | hp1 | a0025 | c0053 | t0001 | g0153 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0320 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00544 | hp1 | a0001 | c0006 | t0001 | g0298 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0151 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0291 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00597 | hp1 | a0001 | c0006 | t0001 | g0329 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00639 | hp1 | a0005 | c0012 | t0001 | g0130 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00639 | hp2 | a0002 | c0068 | t0001 | g0097 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00642 | hp1 | a0022 | c0075 | t0001 | g0049 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0210 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00733 | hp1 | a0006 | c0009 | t0001 | g0044 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0220 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00735 | hp1 | a0001 | c0006 | t0002 | g0246 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00735 | hp2 | a0003 | c0007 | t0001 | g0211 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00741 | hp1 | a0002 | c0013 | t0001 | g0244 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0206 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01069 | hp1 | a0003 | c0007 | t0001 | g0110 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01069 | hp2 | a0010 | c0029 | t0001 | g0158 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0162 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01081 | hp1 | a0023 | c0076 | t0001 | g0047 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01099 | hp2 | a0009 | c0015 | t0001 | g0019 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01106 | hp2 | a0002 | c0057 | t0001 | g0255 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01109 | hp1 | a0007 | c0008 | t0001 | g0256 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0350 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01168 | hp1 | a0009 | c0015 | t0001 | g0018 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0217 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01175 | hp1 | a0010 | c0029 | t0001 | g0230 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0263 | AMR | PUR | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01255 | hp2 | a0003 | c0007 | t0001 | g0036 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01256 | hp1 | a0002 | c0013 | t0001 | g0241 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01257 | hp1 | a0009 | c0015 | t0001 | g0022 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01257 | hp2 | a0003 | c0021 | t0001 | g0011 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01258 | hp2 | a0003 | c0021 | t0001 | g0012 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01261 | hp2 | a0005 | c0031 | t0001 | g0349 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01346 | hp1 | a0006 | c0009 | t0001 | g0050 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0038 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01358 | hp1 | a0001 | c0004 | t0002 | g0218 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01361 | hp2 | a0002 | c0022 | t0001 | g0345 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01433 | hp2 | a0020 | c0032 | t0001 | g0051 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01496 | hp1 | a0002 | c0013 | t0001 | g0243 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01496 | hp2 | a0011 | c0016 | t0006 | g0271 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01515 | hp1 | a0003 | c0005 | t0001 | g0029 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01515 | hp2 | a0004 | c0010 | t0001 | g0045 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01516 | hp1 | a0004 | c0010 | t0001 | g0042 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01516 | hp2 | a0002 | c0022 | t0001 | g0095 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01517 | hp1 | a0003 | c0005 | t0001 | g0028 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01517 | hp2 | a0004 | c0010 | t0001 | g0043 | EUR | IBS | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0186 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01928 | hp2 | a0013 | c0050 | t0001 | g0040 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0141 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01975 | hp1 | a0002 | c0013 | t0001 | g0253 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0155 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0224 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01978 | hp2 | a0003 | c0007 | t0001 | g0221 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0225 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01981 | hp2 | a0003 | c0005 | t0001 | g0309 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01993 | hp1 | a0002 | c0051 | t0001 | g0353 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0034 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02004 | hp2 | a0003 | c0005 | t0001 | g0134 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02040 | hp2 | a0003 | c0005 | t0001 | g0318 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02055 | hp1 | a0005 | c0048 | t0001 | g0063 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0333 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0208 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02071 | hp1 | a0004 | c0010 | t0001 | g0342 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02074 | hp1 | a0001 | c0006 | t0001 | g0330 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02132 | hp1 | a0001 | c0006 | t0001 | g0189 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02132 | hp2 | a0001 | c0028 | t0001 | g0279 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02135 | hp2 | a0001 | c0006 | t0001 | g0278 | EAS | KHV | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02145 | hp1 | a0007 | c0008 | t0001 | g0264 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02145 | hp2 | a0011 | c0016 | t0011 | g0301 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02165 | hp1 | a0001 | c0006 | t0001 | g0297 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02165 | hp2 | a0001 | c0006 | t0009 | g0285 | EAS | CDX | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0175 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02258 | hp1 | a0014 | c0018 | t0001 | g0252 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02258 | hp2 | a0018 | c0035 | t0001 | g0078 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02273 | hp2 | a0003 | c0005 | t0001 | g0307 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02280 | hp1 | a0008 | c0011 | t0003 | g0091 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02280 | hp2 | a0042 | c0039 | t0001 | g0032 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0037 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02293 | hp2 | a0003 | c0005 | t0001 | g0319 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02300 | hp1 | a0003 | c0005 | t0001 | g0177 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02300 | hp2 | a0006 | c0009 | t0001 | g0048 | AMR | PEL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02451 | hp1 | a0015 | c0019 | t0001 | g0124 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02451 | hp2 | a0027 | c0073 | t0001 | g0016 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0267 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02572 | hp2 | a0001 | c0065 | t0001 | g0312 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02615 | hp1 | a0003 | c0005 | t0001 | g0260 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02615 | hp2 | a0007 | c0008 | t0001 | g0259 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0168 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02622 | hp2 | a0008 | c0011 | t0003 | g0061 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02630 | hp1 | a0007 | c0008 | t0001 | g0053 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0065 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02647 | hp2 | a0002 | c0024 | t0001 | g0154 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02698 | hp1 | a0003 | c0005 | t0001 | g0228 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02717 | hp2 | a0038 | c0069 | t0001 | g0015 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02723 | hp2 | a0030 | c0046 | t0001 | g0304 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0332 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02809 | hp2 | a0008 | c0011 | t0003 | g0060 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02818 | hp1 | a0008 | c0011 | t0003 | g0062 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02886 | hp1 | a0029 | c0058 | t0001 | g0164 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02886 | hp2 | a0007 | c0008 | t0001 | g0262 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02895 | hp1 | a0012 | c0025 | t0001 | g0007 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0167 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02897 | hp1 | a0013 | c0020 | t0001 | g0057 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02897 | hp2 | a0012 | c0025 | t0001 | g0008 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02922 | hp1 | a0008 | c0011 | t0003 | g0058 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02922 | hp2 | a0014 | c0018 | t0001 | g0251 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02965 | hp1 | a0014 | c0018 | t0001 | g0250 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0074 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02970 | hp1 | a0004 | c0078 | t0001 | g0199 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02970 | hp2 | a0008 | c0011 | t0003 | g0059 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0261 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02976 | hp2 | a0002 | c0074 | t0001 | g0185 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03098 | hp1 | a0009 | c0015 | t0001 | g0327 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0123 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03130 | hp2 | a0015 | c0019 | t0001 | g0125 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0306 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03139 | hp2 | a0011 | c0016 | t0001 | g0275 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03195 | hp1 | a0004 | c0010 | t0001 | g0073 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03195 | hp2 | a0001 | c0055 | t0012 | g0163 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03209 | hp2 | a0044 | c0038 | t0001 | g0033 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03225 | hp2 | a0007 | c0008 | t0001 | g0265 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03239 | hp1 | a0003 | c0007 | t0001 | g0111 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03239 | hp2 | a0020 | c0032 | t0001 | g0149 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03453 | hp1 | a0002 | c0024 | t0001 | g0152 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03453 | hp2 | a0013 | c0020 | t0001 | g0055 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03486 | hp1 | a0026 | c0056 | t0001 | g0041 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03490 | hp1 | a0001 | c0023 | t0001 | g0066 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03490 | hp2 | a0001 | c0004 | t0002 | g0219 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03492 | hp1 | a0001 | c0023 | t0001 | g0100 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03516 | hp1 | a0015 | c0019 | t0001 | g0122 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0257 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03540 | hp2 | a0031 | c0060 | t0010 | g0240 | AFR | GWD | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03579 | hp1 | a0004 | c0010 | t0001 | g0075 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03579 | hp2 | a0001 | c0072 | t0001 | g0356 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03688 | hp1 | a0002 | c0013 | t0001 | g0266 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03688 | hp2 | a0005 | c0012 | t0001 | g0027 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03704 | hp2 | a0003 | c0005 | t0001 | g0196 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0084 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03834 | hp1 | a0001 | c0006 | t0001 | g0296 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03834 | hp2 | a0001 | c0043 | t0001 | g0236 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03927 | hp1 | a0003 | c0005 | t0005 | g0213 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG04204 | hp2 | a0001 | c0033 | t0001 | g0070 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18522 | hp1 | a0007 | c0008 | t0001 | g0258 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0187 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0316 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | CHB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18906 | hp1 | a0012 | c0030 | t0001 | g0113 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18906 | hp2 | a0032 | c0059 | t0001 | g0009 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18939 | hp2 | a0005 | c0012 | t0001 | g0138 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18941 | hp2 | a0001 | c0006 | t0001 | g0300 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18942 | hp1 | a0004 | c0017 | t0001 | g0192 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18943 | hp2 | a0017 | c0034 | t0001 | g0001 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18944 | hp1 | a0016 | c0036 | t0001 | g0344 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18949 | hp1 | a0003 | c0007 | t0001 | g0105 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18952 | hp1 | a0001 | c0006 | t0001 | g0286 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18952 | hp2 | a0001 | c0006 | t0001 | g0292 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18953 | hp1 | a0003 | c0005 | t0001 | g0314 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18953 | hp2 | a0001 | c0004 | t0002 | g0106 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18962 | hp1 | a0019 | c0027 | t0007 | g0294 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18964 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18964 | hp2 | a0005 | c0012 | t0001 | g0139 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18968 | hp2 | a0003 | c0007 | t0001 | g0103 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18969 | hp2 | a0001 | c0026 | t0001 | g0096 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18971 | hp1 | a0003 | c0007 | t0001 | g0098 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18977 | hp1 | a0035 | c0062 | t0001 | g0315 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18977 | hp2 | a0001 | c0064 | t0005 | g0324 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18978 | hp1 | a0006 | c0009 | t0001 | g0120 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18979 | hp1 | a0002 | c0014 | t0001 | g0288 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0109 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18981 | hp2 | a0006 | c0009 | t0001 | g0119 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18983 | hp1 | a0004 | c0017 | t0001 | g0254 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0212 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18985 | hp2 | a0002 | c0014 | t0001 | g0328 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18986 | hp2 | a0003 | c0005 | t0001 | g0282 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18987 | hp2 | a0001 | c0028 | t0001 | g0295 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18990 | hp2 | a0002 | c0014 | t0001 | g0289 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18993 | hp2 | a0003 | c0005 | t0001 | g0321 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18995 | hp2 | a0005 | c0012 | t0001 | g0178 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19000 | hp2 | a0021 | c0079 | t0001 | g0238 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19002 | hp2 | a0019 | c0027 | t0007 | g0293 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19003 | hp1 | a0001 | c0006 | t0001 | g0277 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19005 | hp1 | a0002 | c0014 | t0001 | g0284 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19007 | hp1 | a0006 | c0009 | t0001 | g0118 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19007 | hp2 | a0045 | c0037 | t0001 | g0355 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0145 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19011 | hp1 | a0003 | c0005 | t0008 | g0317 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19011 | hp2 | a0002 | c0014 | t0001 | g0331 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19030 | hp2 | a0011 | c0016 | t0006 | g0280 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19043 | hp1 | a0043 | c0040 | t0001 | g0031 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19043 | hp2 | a0001 | c0049 | t0001 | g0352 | AFR | LWK | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19056 | hp1 | a0001 | c0006 | t0001 | g0276 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19060 | hp1 | a0003 | c0005 | t0001 | g0157 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19060 | hp2 | a0001 | c0006 | t0001 | g0290 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19065 | hp1 | a0016 | c0036 | t0001 | g0343 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19065 | hp2 | a0001 | c0006 | t0001 | g0299 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19066 | hp1 | a0003 | c0007 | t0001 | g0102 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19066 | hp2 | a0004 | c0017 | t0001 | g0214 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19070 | hp2 | a0005 | c0012 | t0001 | g0121 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19074 | hp2 | a0039 | c0070 | t0002 | g0067 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19077 | hp1 | a0001 | c0052 | t0001 | g0283 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19077 | hp2 | a0037 | c0061 | t0001 | g0129 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19079 | hp2 | a0006 | c0009 | t0001 | g0116 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19084 | hp1 | a0017 | c0034 | t0001 | g0001 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19084 | hp2 | a0034 | c0063 | t0001 | g0170 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19087 | hp2 | a0005 | c0031 | t0001 | g0132 | EAS | JPT | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19240 | hp1 | a0004 | c0017 | t0001 | g0076 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA19240 | hp2 | a0028 | c0044 | t0001 | g0302 | AFR | YRI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20129 | hp1 | a0013 | c0020 | t0001 | g0056 | AFR | ASW | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20129 | hp2 | a0003 | c0071 | t0001 | g0035 | AFR | ASW | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20752 | hp1 | a0003 | c0005 | t0001 | g0176 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20752 | hp2 | a0001 | c0033 | t0002 | g0195 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0133 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20905 | hp2 | a0041 | c0080 | t0001 | g0090 | SAS | GIH | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG01123 | hp2 | a0001 | c0067 | t0001 | g0351 | AMR | CLM | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02109 | hp2 | a0012 | c0030 | t0001 | g0274 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02559 | hp1 | a0033 | c0054 | t0001 | g0072 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0232 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG03471 | hp2 | a0024 | c0077 | t0001 | g0198 | AFR | MSL | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG06807 | hp1 | a0014 | c0018 | t0001 | g0249 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| HG06807 | hp2 | a0001 | c0026 | t0001 | g0272 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20300 | hp1 | a0018 | c0035 | t0001 | g0077 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | USA | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0047 | t0002 | g0101 | REF | REF | ABCC6_chr16_16144565_16228494 | ABCC6 | chr16 | 16144565 | 16228494 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16154767
|
G | A | 1 | a0034 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.4069C>T | p.Arg1357Trp | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/31 | 4129/5140 | 4069/4512 | 1357/1503 | chr16 | 16154767 | ||
| chr16:16154934
|
C | T | 1 | a0018 | 2 | HG02258.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.3980G>A | p.Gly1327Glu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/31 | 4040/5140 | 3980/4512 | 1327/1503 | chr16 | 16154934 | ||
| chr16:16155007
|
C | T | 1 | a0035 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.3907G>A | p.Ala1303Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/31 | 3967/5140 | 3907/4512 | 1303/1503 | chr16 | 16155007 | ||
| chr16:16157674
|
C | T | 6 | a0008a0011a0015others(3): Show | 16 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
missense_variant | MODERATE | c.3871G>A | p.Ala1291Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/31 | 3931/5140 | 3871/4512 | 1291/1503 | chr16 | 16157674 | ||
| chr16:16157742
|
C | T | 6 | a0003a0005a0010others(3): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
missense_variant | MODERATE | c.3803G>A | p.Arg1268Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/31 | 3863/5140 | 3803/4512 | 1268/1503 | chr16 | 16157742 | ||
| chr16:16161509
|
T | G | 1 | a0029 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.3562A>C | p.Thr1188Pro | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/31 | 3622/5140 | 3562/4512 | 1188/1503 | chr16 | 16161509 | ||
| chr16:16165640
|
G | T | 2 | a0022a0028 | 2 | HG00642.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.3289C>A | p.Leu1097Ile | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/31 | 3349/5140 | 3289/4512 | 1097/1503 | chr16 | 16165640 | ||
| chr16:16165739
|
G | A | 2 | a0020a0036 | 3 | HG00099.hp2 HG01433.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.3190C>T | p.Arg1064Trp | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/31 | 3250/5140 | 3190/4512 | 1064/1503 | chr16 | 16165739 | ||
| chr16:16165865
|
G | C | 1 | a0026 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.3064C>G | p.Gln1022Glu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/31 | 3124/5140 | 3064/4512 | 1022/1503 | chr16 | 16165865 | ||
| chr16:16169805
|
G | T | 1 | a0010 | 4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
missense_variant | MODERATE | c.2836C>A | p.Leu946Ile | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2896/5140 | 2836/4512 | 946/1503 | chr16 | 16169805 | ||
| chr16:16173364
|
C | G | 2 | a0012a0030 | 5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.2707G>C | p.Glu903Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2767/5140 | 2707/4512 | 903/1503 | chr16 | 16173364 | ||
| chr16:16173375
|
C | T | 1 | a0033 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.2696G>A | p.Arg899His | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2756/5140 | 2696/4512 | 899/1503 | chr16 | 16173375 | ||
| chr16:16173376
|
G | A | 1 | a0015 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2695C>T | p.Arg899Cys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2755/5140 | 2695/4512 | 899/1503 | chr16 | 16173376 | ||
| chr16:16177500
|
T | C | 41 | a0001a0002a0003others(38): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.2542A>G | p.Met848Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2602/5140 | 2542/4512 | 848/1503 | chr16 | 16177500 | ||
| chr16:16177618
|
A | AATCCGTG others(6): Show |
1 | a0037 | 1 | NA19077.hp2 | frameshift_variant | HIGH | c.2416-5_2423dupCCCA others(9): Show |
p.Leu809fs | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2483/5140 | 2423/4512 | 808/1503 | chr16 | 16177618 | ||
| chr16:16182435
|
T | C | 4 | a0022a0028a0031others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.2224A>G | p.Ile742Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2284/5140 | 2224/4512 | 742/1503 | chr16 | 16182435 | ||
| chr16:16182488
|
C | T | 2 | a0031a0032 | 2 | HG03540.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2171G>A | p.Arg724Lys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2231/5140 | 2171/4512 | 724/1503 | chr16 | 16182488 | ||
| chr16:16182519
|
C | T | 1 | a0023 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2140G>A | p.Gly714Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2200/5140 | 2140/4512 | 714/1503 | chr16 | 16182519 | ||
| chr16:16182911
|
G | T | 1 | a0030 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1963C>A | p.Gln655Lys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 16/31 | 2023/5140 | 1963/4512 | 655/1503 | chr16 | 16182911 | ||
| chr16:16185006
|
G | T | 11 | a0002a0003a0006others(8): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
missense_variant | MODERATE | c.1896C>A | p.His632Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/31 | 1956/5140 | 1896/4512 | 632/1503 | chr16 | 16185006 | ||
| chr16:16187150
|
A | G | 14 | a0002a0003a0006others(11): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
missense_variant | MODERATE | c.1841T>C | p.Val614Ala | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/31 | 1901/5140 | 1841/4512 | 614/1503 | chr16 | 16187150 | ||
| chr16:16190229
|
C | A | 1 | a0038 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1570G>T | p.Ala524Ser | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/31 | 1630/5140 | 1570/4512 | 524/1503 | chr16 | 16190229 | ||
| chr16:16198076
|
T | C | 1 | a0039 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.1283A>G | p.Asn428Ser | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1343/5140 | 1283/4512 | 428/1503 | chr16 | 16198076 | ||
| chr16:16198116
|
C | T | 1 | a0025 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1243G>A | p.Val415Met | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1303/5140 | 1243/4512 | 415/1503 | chr16 | 16198116 | ||
| chr16:16203453
|
T | C | 1 | a0018 | 2 | HG02258.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.955A>G | p.Ile319Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/31 | 1015/5140 | 955/4512 | 319/1503 | chr16 | 16203453 | ||
| chr16:16208729
|
T | C | 7 | a0004a0006a0017others(4): Show | 26 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(23): Show |
missense_variant&splice_region_variant | MODERATE | c.793A>G | p.Arg265Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/31 | 853/5140 | 793/4512 | 265/1503 | chr16 | 16208729 | ||
| chr16:16212240
|
A | G | 1 | a0040 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.607T>C | p.Cys203Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/31 | 667/5140 | 607/4512 | 203/1503 | chr16 | 16212240 | ||
| chr16:16214329
|
G | A | 1 | a0021 | 1 | NA19000.hp2 | stop_gained | HIGH | c.595C>T | p.Gln199* | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/31 | 655/5140 | 595/4512 | 199/1503 | chr16 | 16214329 | ||
| chr16:16214364
|
G | A | 1 | a0041 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.560C>T | p.Ala187Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/31 | 620/5140 | 560/4512 | 187/1503 | chr16 | 16214364 | ||
| chr16:16214437
|
C | T | 3 | a0042a0043a0044 | 3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.487G>A | p.Asp163Asn | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/31 | 547/5140 | 487/4512 | 163/1503 | chr16 | 16214437 | ||
| chr16:16219555
|
G | A | 1 | a0014 | 4 | HG02258.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.473C>T | p.Ala158Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/31 | 533/5140 | 473/4512 | 158/1503 | chr16 | 16219555 | ||
| chr16:16219655
|
C | T | 1 | a0045 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.373G>A | p.Glu125Lys | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/31 | 433/5140 | 373/4512 | 125/1503 | chr16 | 16219655 | ||
| chr16:16221759
|
C | A | 1 | a0016 | 2 | NA18944.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.109G>T | p.Val37Phe | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/31 | 169/5140 | 109/4512 | 37/1503 | chr16 | 16221759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16154660
|
C | T | 1 | a0001c0049 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4176G>A | p.Gln1392Gln | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/31 | 4236/5140 | 4176/4512 | 1392/1503 | chr16 | 16154660 | ||
| chr16:16155011
|
G | A | 1 | a0001c0064 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.3903C>T | p.Thr1301Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/31 | 3963/5140 | 3903/4512 | 1301/1503 | chr16 | 16155011 | ||
| chr16:16157693
|
G | A | 1 | a0001c0055 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3852C>T | p.Gly1284Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/31 | 3912/5140 | 3852/4512 | 1284/1503 | chr16 | 16157693 | ||
| chr16:16163040
|
G | A | 2 | a0001c0065a0004c0078 | 2 | HG02572.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.3459C>T | p.Arg1153Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/31 | 3519/5140 | 3459/4512 | 1153/1503 | chr16 | 16163040 | ||
| chr16:16169737
|
C | T | 1 | a0001c0047 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.2904G>A | p.Leu968Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2964/5140 | 2904/4512 | 968/1503 | chr16 | 16169737 | ||
| chr16:16169806
|
G | A | 15 | a0001c0002a0001c0026a0001c0028others(12): Show | 59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
synonymous_variant | LOW | c.2835C>T | p.Pro945Pro | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2895/5140 | 2835/4512 | 945/1503 | chr16 | 16169806 | ||
| chr16:16169806
|
G | C | 1 | a0001c0067 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.2835C>G | p.Pro945Pro | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/31 | 2895/5140 | 2835/4512 | 945/1503 | chr16 | 16169806 | ||
| chr16:16173290
|
G | A | 1 | a0015c0019 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.2781C>T | p.Tyr927Tyr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/31 | 2841/5140 | 2781/4512 | 927/1503 | chr16 | 16173290 | ||
| chr16:16177468
|
T | A | 1 | a0001c0052 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.2574A>T | p.Gly858Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2634/5140 | 2574/4512 | 858/1503 | chr16 | 16177468 | ||
| chr16:16177552
|
G | A | 12 | a0002c0003a0002c0014a0002c0022others(9): Show | 53 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
synonymous_variant | LOW | c.2490C>T | p.Ala830Ala | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/31 | 2550/5140 | 2490/4512 | 830/1503 | chr16 | 16177552 | ||
| chr16:16178813
|
T | C | 77 | a0001c0001a0001c0002a0001c0004others(74): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
synonymous_variant | LOW | c.2400A>G | p.Gly800Gly | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/31 | 2460/5140 | 2400/4512 | 800/1503 | chr16 | 16178813 | ||
| chr16:16182484
|
T | A | 4 | a0022c0075a0028c0044a0031c0060others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
synonymous_variant | LOW | c.2175A>T | p.Val725Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2235/5140 | 2175/4512 | 725/1503 | chr16 | 16182484 | ||
| chr16:16182574
|
G | A | 1 | a0040c0041 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.2085C>T | p.Tyr695Tyr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/31 | 2145/5140 | 2085/4512 | 695/1503 | chr16 | 16182574 | ||
| chr16:16185012
|
G | C | 25 | a0002c0003a0002c0013a0002c0014others(22): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
synonymous_variant | LOW | c.1890C>G | p.Thr630Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/31 | 1950/5140 | 1890/4512 | 630/1503 | chr16 | 16185012 | ||
| chr16:16187176
|
G | A | 1 | a0002c0068 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1815C>T | p.Leu605Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/31 | 1875/5140 | 1815/4512 | 605/1503 | chr16 | 16187176 | ||
| chr16:16192917
|
C | T | 4 | a0001c0055a0013c0020a0033c0054others(1): Show | 6 | HG02559.hp1 HG02897.hp1 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.1344G>A | p.Leu448Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/31 | 1404/5140 | 1344/4512 | 448/1503 | chr16 | 16192917 | ||
| chr16:16198114
|
C | T | 22 | a0001c0004a0001c0023a0001c0026others(19): Show | 69 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
synonymous_variant | LOW | c.1245G>A | p.Val415Val | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1305/5140 | 1245/4512 | 415/1503 | chr16 | 16198114 | ||
| chr16:16198126
|
A | G | 28 | a0001c0004a0001c0006a0001c0023others(25): Show | 97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
synonymous_variant | LOW | c.1233T>C | p.Asn411Asn | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1293/5140 | 1233/4512 | 411/1503 | chr16 | 16198126 | ||
| chr16:16198144
|
C | T | 1 | a0001c0043 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1215G>A | p.Ala405Ala | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/31 | 1275/5140 | 1215/4512 | 405/1503 | chr16 | 16198144 | ||
| chr16:16202100
|
T | C | 5 | a0001c0033a0001c0072a0002c0074others(2): Show | 6 | HG02451.hp2 HG02976.hp2 HG03579.hp2 others(3): Show |
synonymous_variant | LOW | c.1077A>G | p.Ser359Ser | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/31 | 1137/5140 | 1077/4512 | 359/1503 | chr16 | 16202100 | ||
| chr16:16203415
|
C | A | 1 | a0013c0020 | 3 | HG02897.hp1 HG03453.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.993G>T | p.Leu331Leu | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/31 | 1053/5140 | 993/4512 | 331/1503 | chr16 | 16203415 | ||
| chr16:16212202
|
C | T | 3 | a0001c0023a0002c0022a0010c0042 | 5 | HG00280.hp2 HG01361.hp2 HG01516.hp2 others(2): Show |
synonymous_variant | LOW | c.645G>A | p.Thr215Thr | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/31 | 705/5140 | 645/4512 | 215/1503 | chr16 | 16212202 | ||
| chr16:16221678
|
G | T | 1 | a0003c0021 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.190C>A | p.Arg64Arg | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/31 | 250/5140 | 190/4512 | 64/1503 | chr16 | 16221678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16149668
|
T | TG | 4 | a0001c0001t0005a0001c0064t0005a0003c0005t0005others(1): Show | 4 | HG00741.hp2 HG02145.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*464dupC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 464 | chr16 | 16149668 | |||||
| chr16:16149675
|
C | G | 2 | a0001c0055t0012a0031c0060t0010 | 2 | HG03195.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 458 | chr16 | 16149675 | |||||
| chr16:16149685
|
G | A | 2 | a0011c0016t0006a0011c0016t0011 | 3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*448C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 448 | chr16 | 16149685 | |||||
| chr16:16149880
|
C | T | 1 | a0008c0011t0003 | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*253G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 253 | chr16 | 16149880 | |||||
| chr16:16149926
|
C | T | 1 | a0001c0006t0009 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 207 | chr16 | 16149926 | |||||
| chr16:16149981
|
T | C | 1 | a0001c0055t0012 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 152 | chr16 | 16149981 | |||||
| chr16:16150033
|
C | T | 1 | a0003c0005t0008 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 100 | chr16 | 16150033 | |||||
| chr16:16150095
|
C | T | 1 | a0001c0001t0004 | 4 | HG01928.hp1 HG01975.hp2 NA18968.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 38 | chr16 | 16150095 | |||||
| chr16:16150108
|
C | A | 1 | a0019c0027t0007 | 2 | NA18962.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 25 | chr16 | 16150108 | |||||
| chr16:16150116
|
C | T | 7 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(4): Show | 22 | HG00735.hp1 HG01261.hp1 HG01358.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 31/31 | 17 | chr16 | 16150116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16150272
|
T | C | 79 | a0001c0001t0001g0086a0001c0001t0001g0201a0001c0001t0001g0202others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.4404-31A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150272 | ||||||
| chr16:16150317
|
T | C | 59 | a0001c0001t0001g0126a0001c0001t0001g0239a0001c0001t0001g0273others(56): Show | 59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4404-76A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150317 | ||||||
| chr16:16150418
|
C | G | 1 | a0001c0002t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4403+160G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150418 | ||||||
| chr16:16150519
|
G | A | 1 | a0031c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4403+59C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 30/30 | chr16 | 16150519 | ||||||
| chr16:16150780
|
C | T | 1 | a0013c0050t0001g0040 | 1 | HG01928.hp2 | splice_region_variant&intron_variant | LOW | c.4209-8G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150780 | ||||||
| chr16:16150802
|
C | T | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4209-30G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150802 | ||||||
| chr16:16150806
|
C | T | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4209-34G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150806 | ||||||
| chr16:16150816
|
C | T | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4209-44G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16150816 | ||||||
| chr16:16151139
|
G | A | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4209-367C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151139 | ||||||
| chr16:16151222
|
C | T | 1 | a0004c0017t0001g0192 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4209-450G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151222 | ||||||
| chr16:16151243
|
G | A | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4209-471C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151243 | ||||||
| chr16:16151248
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4209-476C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151248 | ||||||
| chr16:16151267
|
G | C | 55 | a0001c0001t0001g0183a0001c0001t0001g0339a0001c0002t0001g0014others(52): Show | 55 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.4209-495C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151267 | ||||||
| chr16:16151268
|
G | A | 8 | a0001c0001t0001g0239a0002c0013t0001g0241a0002c0013t0001g0243others(5): Show | 8 | HG00741.hp1 HG01256.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.4209-496C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151268 | ||||||
| chr16:16151396
|
A | G | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4209-624T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151396 | ||||||
| chr16:16151412
|
G | A | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4209-640C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151412 | ||||||
| chr16:16151491
|
T | C | 1 | a0004c0017t0001g0254 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4209-719A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151491 | ||||||
| chr16:16151492
|
G | C | 346 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.4209-720C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151492 | ||||||
| chr16:16151519
|
A | T | 1 | a0003c0007t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4209-747T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151519 | ||||||
| chr16:16151551
|
G | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0082others(23): Show | 26 | HG00597.hp1 HG00639.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.4209-779C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151551 | ||||||
| chr16:16151603
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4209-831A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151603 | ||||||
| chr16:16151845
|
G | T | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4209-1073C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151845 | ||||||
| chr16:16151866
|
G | A | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4209-1094C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151866 | ||||||
| chr16:16151872
|
G | A | 48 | a0001c0004t0001g0263a0003c0005t0001g0028a0003c0005t0001g0029others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.4209-1100C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151872 | ||||||
| chr16:16151914
|
G | A | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4209-1142C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151914 | ||||||
| chr16:16151921
|
G | A | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4209-1149C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151921 | ||||||
| chr16:16151975
|
G | A | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4209-1203C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16151975 | ||||||
| chr16:16152053
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(113): Show | 116 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.4209-1281C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152053 | ||||||
| chr16:16152116
|
C | T | 1 | a0039c0070t0002g0067 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4209-1344G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152116 | ||||||
| chr16:16152132
|
CA | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(146): Show | 149 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.4209-1361delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152132 | ||||||
| chr16:16152192
|
C | CA | 91 | a0001c0001t0001g0126a0001c0001t0001g0239a0001c0001t0001g0339others(88): Show | 91 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.4209-1421dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAA | 64 | a0001c0001t0001g0183a0001c0001t0002g0088a0001c0002t0001g0014others(61): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.4209-1422_4209-142 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAAA | 29 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0030others(26): Show | 29 | HG00323.hp1 HG00735.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.4209-1423_4209-142 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAAAAA | 25 | a0001c0001t0001g0017a0001c0001t0001g0127a0001c0001t0001g0142others(22): Show | 25 | HG00597.hp1 HG00639.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4209-1425_4209-142 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAAAAAA | 12 | a0001c0001t0001g0020a0001c0001t0001g0089a0001c0001t0001g0108others(9): Show | 12 | HG01106.hp2 HG01358.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.4209-1426_4209-142 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAAAAAAA | 78 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0079others(75): Show | 78 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.4209-1427_4209-142 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAAAAAAA others(1): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0136others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.4209-1428_4209-142 others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0135 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4209-1430_4209-142 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152192
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4209-1430_4209-142 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152192 | ||||||
| chr16:16152222
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.4209-1450T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152222 | ||||||
| chr16:16152307
|
T | G | 50 | a0001c0002t0001g0014a0001c0004t0001g0263a0003c0005t0001g0028others(47): Show | 51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.4209-1535A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152307 | ||||||
| chr16:16152333
|
A | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.4209-1561T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152333 | ||||||
| chr16:16152453
|
A | G | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4209-1681T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152453 | ||||||
| chr16:16152722
|
C | T | 4 | a0001c0001t0002g0203a0011c0016t0006g0271a0011c0016t0006g0280others(1): Show | 4 | HG01496.hp2 HG02145.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.4208+1906G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152722 | ||||||
| chr16:16152724
|
G | A | 1 | a0004c0017t0001g0214 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4208+1904C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152724 | ||||||
| chr16:16152730
|
G | A | 1 | a0001c0001t0004g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4208+1898C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152730 | ||||||
| chr16:16152733
|
G | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4208+1895C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152733 | ||||||
| chr16:16152906
|
G | GT | 149 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.4208+1721dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152906 | ||||||
| chr16:16152927
|
T | C | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+1701A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16152927 | ||||||
| chr16:16153036
|
C | G | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+1592G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153036 | ||||||
| chr16:16153089
|
G | A | 2 | a0001c0001t0001g0326a0001c0001t0001g0338 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4208+1539C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153089 | ||||||
| chr16:16153175
|
G | A | 5 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0172others(2): Show | 5 | HG03491.hp1 HG03492.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.4208+1453C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153175 | ||||||
| chr16:16153240
|
T | G | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4208+1388A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153240 | ||||||
| chr16:16153255
|
A | T | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4208+1373T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153255 | ||||||
| chr16:16153439
|
A | G | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+1189T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153439 | ||||||
| chr16:16153463
|
C | T | 1 | a0001c0004t0001g0263 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4208+1165G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153463 | ||||||
| chr16:16153493
|
C | CA | 34 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0082others(31): Show | 34 | HG00597.hp1 HG00639.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.4208+1134dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153493 | ||||||
| chr16:16153520
|
G | A | 2 | a0009c0015t0001g0327a0026c0056t0001g0041 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4208+1108C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153520 | ||||||
| chr16:16153614
|
A | T | 53 | a0001c0001t0001g0183a0001c0001t0001g0339a0001c0006t0009g0285others(50): Show | 53 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.4208+1014T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153614 | ||||||
| chr16:16153722
|
G | A | 1 | a0031c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4208+906C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153722 | ||||||
| chr16:16153914
|
GA | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.4208+713delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153914 | ||||||
| chr16:16153969
|
C | G | 1 | a0031c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4208+659G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153969 | ||||||
| chr16:16153996
|
A | C | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4208+632T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16153996 | ||||||
| chr16:16154088
|
T | C | 2 | a0009c0015t0001g0327a0026c0056t0001g0041 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4208+540A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154088 | ||||||
| chr16:16154263
|
CA | C | 7 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(4): Show | 7 | HG00639.hp2 HG01496.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.4208+364delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154263 | ||||||
| chr16:16154369
|
C | T | 2 | a0010c0042t0001g0099a0010c0045t0001g0107 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.4208+259G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154369 | ||||||
| chr16:16154371
|
A | G | 1 | a0007c0008t0001g0258 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4208+257T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 29/30 | chr16 | 16154371 | ||||||
| chr16:16154823
|
C | T | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4042-29G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/30 | chr16 | 16154823 | ||||||
| chr16:16154824
|
G | A | 52 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(49): Show | 52 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.4042-30C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 28/30 | chr16 | 16154824 | ||||||
| chr16:16155038
|
G | A | 1 | a0001c0002t0001g0287 | 1 | NA18939.hp1 | splice_region_variant&intron_variant | LOW | c.3883-7C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155038 | ||||||
| chr16:16155148
|
T | G | 2 | a0012c0030t0001g0113a0012c0030t0001g0274 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3883-117A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155148 | ||||||
| chr16:16155333
|
C | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.3883-302G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155333 | ||||||
| chr16:16155361
|
CATCT | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(89): Show | 92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3883-334_3883-331d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155361 | ||||||
| chr16:16155373
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3883-342G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155373 | ||||||
| chr16:16155411
|
GCCAT | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.3883-384_3883-381d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155411 | ||||||
| chr16:16155687
|
C | T | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3883-656G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155687 | ||||||
| chr16:16155807
|
A | C | 1 | a0001c0002t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3883-776T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155807 | ||||||
| chr16:16155904
|
C | CTTTA | 95 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.3883-877_3883-874d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155904 | ||||||
| chr16:16155904
|
CTTTA | C | 3 | a0004c0010t0001g0073a0018c0035t0001g0077a0018c0035t0001g0078 | 3 | HG02258.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3883-877_3883-874d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155904 | ||||||
| chr16:16155980
|
A | G | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3883-949T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16155980 | ||||||
| chr16:16156136
|
A | T | 4 | a0010c0029t0001g0158a0010c0029t0001g0230a0010c0042t0001g0099others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.3883-1105T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156136 | ||||||
| chr16:16156402
|
C | A | 1 | a0001c0001t0001g0337 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3882+1261G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156402 | ||||||
| chr16:16156437
|
C | T | 3 | a0001c0002t0001g0054a0001c0002t0001g0093a0001c0002t0001g0310 | 3 | NA18990.hp1 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.3882+1226G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156437 | ||||||
| chr16:16156462
|
G | A | 1 | a0038c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3882+1201C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156462 | ||||||
| chr16:16156499
|
C | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0079a0001c0001t0001g0143others(16): Show | 19 | HG00642.hp2 HG00741.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.3882+1164G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156499 | ||||||
| chr16:16156620
|
G | C | 1 | a0003c0005t0001g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3882+1043C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156620 | ||||||
| chr16:16156639
|
C | T | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3882+1024G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156639 | ||||||
| chr16:16156741
|
C | G | 208 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.3882+922G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156741 | ||||||
| chr16:16156935
|
T | A | 2 | a0001c0001t0002g0094a0001c0001t0002g0311 | 2 | NA18959.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3882+728A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156935 | ||||||
| chr16:16156942
|
C | CA | 123 | a0001c0001t0001g0086a0001c0001t0001g0183a0001c0001t0001g0201others(120): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.3882+720dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | ||||||
| chr16:16156942
|
C | CAA | 39 | a0001c0001t0001g0126a0001c0002t0001g0024a0001c0002t0001g0025others(36): Show | 39 | HG00408.hp1 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.3882+719_3882+720d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | ||||||
| chr16:16156942
|
C | CAAA | 14 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0085others(11): Show | 14 | HG00597.hp2 HG00673.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.3882+718_3882+720d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | ||||||
| chr16:16156942
|
CA | C | 38 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0082others(35): Show | 38 | HG00438.hp1 HG00735.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.3882+720delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | ||||||
| chr16:16156942
|
CAA | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(75): Show | 78 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3882+719_3882+720d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16156942 | ||||||
| chr16:16157003
|
C | G | 3 | a0001c0001t0001g0270a0001c0006t0001g0189a0001c0006t0001g0298 | 3 | HG00544.hp1 HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.3882+660G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157003 | ||||||
| chr16:16157043
|
C | T | 1 | a0003c0007t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3882+620G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157043 | ||||||
| chr16:16157402
|
G | A | 24 | a0001c0001t0001g0082a0001c0001t0002g0030a0001c0001t0002g0087others(21): Show | 24 | HG00735.hp1 HG01074.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.3882+261C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157402 | ||||||
| chr16:16157547
|
A | G | 1 | a0003c0007t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3882+116T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157547 | ||||||
| chr16:16157578
|
G | A | 344 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.3882+85C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157578 | ||||||
| chr16:16157600
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3882+63G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157600 | ||||||
| chr16:16157615
|
C | T | 2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3882+48G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 27/30 | chr16 | 16157615 | ||||||
| chr16:16158042
|
T | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0135others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.3736-233A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158042 | ||||||
| chr16:16158109
|
T | C | 1 | a0004c0078t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3736-300A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158109 | ||||||
| chr16:16158143
|
T | G | 31 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(28): Show | 31 | HG00323.hp1 HG00735.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.3736-334A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158143 | ||||||
| chr16:16158229
|
T | A | 16 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(13): Show | 16 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3736-420A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158229 | ||||||
| chr16:16158311
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.3736-502C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158311 | ||||||
| chr16:16158330
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3736-521T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158330 | ||||||
| chr16:16158367
|
C | T | 80 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0108others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.3736-558G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158367 | ||||||
| chr16:16158441
|
G | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(87): Show | 90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3736-632C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158441 | ||||||
| chr16:16158455
|
A | ATCCC | 74 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3736-647_3736-646i others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158455 | ||||||
| chr16:16158455
|
A | C | 17 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(14): Show | 17 | HG00558.hp2 HG00673.hp1 HG03831.hp1 others(14): Show |
intron_variant | MODIFIER | c.3736-646T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158455 | ||||||
| chr16:16158491
|
T | C | 1 | a0004c0078t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3736-682A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158491 | ||||||
| chr16:16158525
|
C | A | 48 | a0003c0005t0001g0028a0003c0005t0001g0029a0003c0005t0001g0083others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.3736-716G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158525 | ||||||
| chr16:16158630
|
C | T | 2 | a0011c0016t0006g0280a0011c0016t0011g0301 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3736-821G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158630 | ||||||
| chr16:16158676
|
T | C | 6 | a0009c0015t0001g0327a0013c0020t0001g0055a0013c0020t0001g0056others(3): Show | 6 | HG02897.hp1 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3735+806A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158676 | ||||||
| chr16:16158839
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.3735+643A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158839 | ||||||
| chr16:16158900
|
G | A | 6 | a0009c0015t0001g0327a0013c0020t0001g0055a0013c0020t0001g0056others(3): Show | 6 | HG02897.hp1 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3735+582C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16158900 | ||||||
| chr16:16159181
|
T | C | 7 | a0001c0004t0001g0065a0001c0004t0001g0263a0002c0057t0001g0255others(4): Show | 7 | HG01106.hp2 HG01175.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3735+301A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159181 | ||||||
| chr16:16159229
|
C | T | 2 | a0001c0002t0001g0231a0001c0004t0001g0212 | 2 | NA18962.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3735+253G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159229 | ||||||
| chr16:16159364
|
G | C | 1 | a0001c0004t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3735+118C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159364 | ||||||
| chr16:16159382
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3735+100C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159382 | ||||||
| chr16:16159382
|
G | C | 1 | a0001c0001t0002g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3735+100C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159382 | ||||||
| chr16:16159426
|
GC | G | 342 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3735+55delG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159426 | ||||||
| chr16:16159435
|
C | G | 8 | a0009c0015t0001g0327a0013c0020t0001g0055a0013c0020t0001g0056others(5): Show | 8 | HG00642.hp1 HG02897.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.3735+47G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159435 | ||||||
| chr16:16159455
|
A | AC | 6 | a0001c0001t0001g0188a0001c0002t0001g0354a0001c0004t0001g0034others(3): Show | 6 | HG00597.hp2 HG01993.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3735+26dupG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 26/30 | chr16 | 16159455 | ||||||
| chr16:16159587
|
G | A | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.3634-4C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159587 | ||||||
| chr16:16159713
|
C | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(87): Show | 90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3634-130G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159713 | ||||||
| chr16:16159778
|
C | T | 1 | a0002c0003t0001g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3634-195G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159778 | ||||||
| chr16:16159835
|
C | T | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3634-252G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159835 | ||||||
| chr16:16159939
|
G | A | 2 | a0001c0001t0001g0180a0001c0004t0001g0104 | 2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.3634-356C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16159939 | ||||||
| chr16:16160059
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3634-476A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160059 | ||||||
| chr16:16160300
|
C | T | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-717G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160300 | ||||||
| chr16:16160316
|
G | T | 1 | a0014c0018t0001g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3634-733C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160316 | ||||||
| chr16:16160618
|
C | T | 1 | a0005c0012t0001g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3633+820G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160618 | ||||||
| chr16:16160628
|
C | CA | 54 | a0001c0001t0001g0126a0001c0001t0001g0239a0001c0001t0001g0305others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.3633+809dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
C | CAA | 72 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0188others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.3633+808_3633+809d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
C | CAAA | 38 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0001t0001g0169others(35): Show | 38 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.3633+807_3633+809d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
C | CAAAA | 20 | a0001c0001t0001g0020a0001c0001t0001g0127a0001c0001t0001g0142others(17): Show | 20 | HG00597.hp1 HG01981.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.3633+806_3633+809d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
C | CAAAAA | 7 | a0011c0016t0006g0271a0011c0016t0006g0280a0012c0030t0001g0113others(4): Show | 7 | HG01496.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3633+805_3633+809d others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
CA | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0135others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3633+809delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
CAA | C | 46 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.3633+808_3633+809d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
CAAAAA | C | 19 | a0001c0001t0001g0339a0001c0026t0001g0272a0002c0003t0001g0013others(16): Show | 19 | HG01346.hp1 HG01516.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3633+805_3633+809d others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160628
|
CAAAAAA | C | 28 | a0001c0001t0001g0183a0001c0006t0009g0285a0002c0003t0001g0002others(25): Show | 28 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.3633+804_3633+809d others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160628 | ||||||
| chr16:16160641
|
A | C | 1 | a0007c0008t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3633+797T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160641 | ||||||
| chr16:16160644
|
A | G | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3633+794T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160644 | ||||||
| chr16:16160769
|
C | T | 50 | a0001c0002t0001g0014a0003c0005t0001g0028a0003c0005t0001g0029others(47): Show | 51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.3633+669G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160769 | ||||||
| chr16:16160830
|
C | T | 12 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(9): Show | 12 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3633+608G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160830 | ||||||
| chr16:16160909
|
A | G | 57 | a0001c0001t0001g0086a0001c0001t0001g0201a0001c0001t0001g0202others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.3633+529T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16160909 | ||||||
| chr16:16161054
|
G | A | 1 | a0001c0006t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3633+384C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161054 | ||||||
| chr16:16161058
|
T | C | 2 | a0001c0001t0001g0313a0001c0001t0001g0337 | 2 | NA18949.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.3633+380A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161058 | ||||||
| chr16:16161236
|
ACAAGGAA others(11): Show |
A | 6 | a0001c0001t0001g0069a0001c0001t0001g0179a0001c0001t0001g0193others(3): Show | 6 | HG00140.hp1 HG01123.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3633+184_3633+201d others(20): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161236 | ||||||
| chr16:16161338
|
T | G | 346 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.3633+100A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161338 | ||||||
| chr16:16161339
|
T | G | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3633+99A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161339 | ||||||
| chr16:16161348
|
C | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(87): Show | 90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3633+90G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161348 | ||||||
| chr16:16161383
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(87): Show | 90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3633+55C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 25/30 | chr16 | 16161383 | ||||||
| chr16:16161567
|
G | A | 4 | a0010c0029t0001g0158a0010c0029t0001g0230a0010c0042t0001g0099others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3507-3C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161567 | ||||||
| chr16:16161580
|
A | G | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0108others(29): Show | 32 | HG00597.hp1 HG00639.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3507-16T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161580 | ||||||
| chr16:16161583
|
G | A | 1 | a0002c0074t0001g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3507-19C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161583 | ||||||
| chr16:16161594
|
G | T | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3507-30C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161594 | ||||||
| chr16:16161726
|
C | T | 1 | a0001c0004t0001g0162 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3507-162G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161726 | ||||||
| chr16:16161771
|
G | A | 1 | a0001c0002t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3507-207C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161771 | ||||||
| chr16:16161982
|
T | C | 7 | a0002c0013t0001g0241a0002c0013t0001g0243a0002c0013t0001g0244others(4): Show | 7 | HG00741.hp1 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3507-418A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16161982 | ||||||
| chr16:16162293
|
T | C | 2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3506+700A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162293 | ||||||
| chr16:16162478
|
G | A | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3506+515C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162478 | ||||||
| chr16:16162562
|
C | T | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3506+431G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162562 | ||||||
| chr16:16162752
|
G | C | 3 | a0005c0048t0001g0063a0031c0060t0010g0240a0032c0059t0001g0009 | 3 | HG02055.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3506+241C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162752 | ||||||
| chr16:16162821
|
C | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(26): Show | 29 | HG00597.hp1 HG00639.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.3506+172G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162821 | ||||||
| chr16:16162852
|
T | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3506+141A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162852 | ||||||
| chr16:16162879
|
C | T | 1 | a0001c0002t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3506+114G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162879 | ||||||
| chr16:16162910
|
T | A | 2 | a0020c0032t0001g0051a0036c0066t0001g0052 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3506+83A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162910 | ||||||
| chr16:16162910
|
T | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(245): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.3506+83A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 24/30 | chr16 | 16162910 | ||||||
| chr16:16163297
|
G | C | 2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3307-105C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163297 | ||||||
| chr16:16163412
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3307-220G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163412 | ||||||
| chr16:16163416
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3307-224A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163416 | ||||||
| chr16:16163443
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0200others(1): Show | 4 | HG02135.hp1 HG02155.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3307-251G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163443 | ||||||
| chr16:16163553
|
C | A | 93 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(90): Show | 94 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.3307-361G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163553 | ||||||
| chr16:16163581
|
T | C | 3 | a0001c0001t0001g0313a0001c0001t0001g0335a0001c0001t0001g0337 | 3 | NA18949.hp2 NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3307-389A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163581 | ||||||
| chr16:16163615
|
G | A | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3307-423C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163615 | ||||||
| chr16:16163664
|
G | T | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3307-472C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16163664 | ||||||
| chr16:16164089
|
A | G | 62 | a0001c0001t0001g0126a0001c0001t0001g0183a0001c0002t0001g0010others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3307-897T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164089 | ||||||
| chr16:16164092
|
G | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3307-900C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164092 | ||||||
| chr16:16164127
|
G | A | 1 | a0001c0002t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3307-935C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164127 | ||||||
| chr16:16164138
|
A | G | 2 | a0001c0006t0001g0300a0016c0036t0001g0343 | 2 | NA18941.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3307-946T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164138 | ||||||
| chr16:16164182
|
C | T | 2 | a0003c0005t0001g0228a0003c0007t0001g0245 | 2 | HG00099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3307-990G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164182 | ||||||
| chr16:16164188
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3307-996G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164188 | ||||||
| chr16:16164316
|
G | A | 59 | a0001c0001t0001g0233a0001c0001t0001g0239a0001c0001t0001g0305others(56): Show | 60 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.3307-1124C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164316 | ||||||
| chr16:16164336
|
C | T | 5 | a0012c0025t0001g0007a0012c0025t0001g0008a0012c0030t0001g0113others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3307-1144G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164336 | ||||||
| chr16:16164391
|
G | T | 2 | a0012c0030t0001g0113a0012c0030t0001g0274 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3307-1199C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164391 | ||||||
| chr16:16164973
|
T | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.3306+650A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16164973 | ||||||
| chr16:16165034
|
C | G | 2 | a0009c0015t0001g0327a0026c0056t0001g0041 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3306+589G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165034 | ||||||
| chr16:16165092
|
G | A | 3 | a0004c0010t0001g0073a0018c0035t0001g0077a0018c0035t0001g0078 | 3 | HG02258.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3306+531C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165092 | ||||||
| chr16:16165092
|
G | C | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3306+531C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165092 | ||||||
| chr16:16165124
|
G | T | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3306+499C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165124 | ||||||
| chr16:16165133
|
G | A | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3306+490C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165133 | ||||||
| chr16:16165363
|
A | G | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3306+260T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165363 | ||||||
| chr16:16165432
|
A | T | 2 | a0001c0001t0001g0340a0003c0005t0005g0213 | 2 | HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3306+191T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165432 | ||||||
| chr16:16165597
|
C | T | 1 | a0005c0012t0001g0178 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3306+26G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 23/30 | chr16 | 16165597 | ||||||
| chr16:16166001
|
G | A | 1 | a0002c0003t0001g0306 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2996-68C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166001 | ||||||
| chr16:16166008
|
T | TCTC | 3 | a0001c0006t0001g0276a0001c0006t0001g0290a0001c0006t0001g0292 | 3 | NA18952.hp2 NA19056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2996-78_2996-76dup others(3): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166008 | ||||||
| chr16:16166162
|
C | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2996-229G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166162 | ||||||
| chr16:16166340
|
C | T | 2 | a0001c0001t0001g0326a0001c0001t0001g0338 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2996-407G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166340 | ||||||
| chr16:16166454
|
C | CTAGAGGA others(3): Show |
2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2996-522_2996-521i others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166454 | ||||||
| chr16:16166485
|
C | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2996-552G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166485 | ||||||
| chr16:16166570
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2996-637G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166570 | ||||||
| chr16:16166586
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2996-653T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166586 | ||||||
| chr16:16166593
|
C | T | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2996-660G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166593 | ||||||
| chr16:16166657
|
A | G | 1 | a0001c0001t0001g0020 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2996-724T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166657 | ||||||
| chr16:16166697
|
C | T | 1 | a0043c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2996-764G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166697 | ||||||
| chr16:16166792
|
G | C | 6 | a0001c0055t0012g0163a0005c0048t0001g0063a0022c0075t0001g0049others(3): Show | 6 | HG00642.hp1 HG02055.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-859C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166792 | ||||||
| chr16:16166792
|
G | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.2996-859C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166792 | ||||||
| chr16:16166796
|
C | T | 61 | a0001c0001t0001g0239a0001c0001t0001g0339a0002c0003t0001g0002others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.2996-863G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166796 | ||||||
| chr16:16166902
|
A | AAAAC | 246 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.2996-973_2996-970d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166902 | ||||||
| chr16:16166902
|
A | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2996-969T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166902 | ||||||
| chr16:16166961
|
C | A | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2996-1028G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16166961 | ||||||
| chr16:16167146
|
C | T | 242 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2996-1213G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167146 | ||||||
| chr16:16167276
|
A | G | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2996-1343T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167276 | ||||||
| chr16:16167286
|
C | T | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2996-1353G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167286 | ||||||
| chr16:16167313
|
G | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2996-1380C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167313 | ||||||
| chr16:16167366
|
C | G | 1 | a0002c0051t0001g0353 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2996-1433G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167366 | ||||||
| chr16:16167394
|
C | T | 69 | a0001c0001t0001g0233a0001c0001t0001g0239a0001c0001t0001g0305others(66): Show | 70 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2996-1461G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167394 | ||||||
| chr16:16167553
|
C | T | 246 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.2996-1620G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167553 | ||||||
| chr16:16167560
|
C | G | 1 | a0001c0004t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2996-1627G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167560 | ||||||
| chr16:16167573
|
G | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2996-1640C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167573 | ||||||
| chr16:16167758
|
C | T | 246 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.2996-1825G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167758 | ||||||
| chr16:16167784
|
T | G | 1 | a0001c0006t0001g0298 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2996-1851A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167784 | ||||||
| chr16:16167816
|
C | A | 1 | a0004c0017t0001g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2995+1830G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167816 | ||||||
| chr16:16167829
|
C | T | 2 | a0004c0017t0001g0214a0004c0017t0001g0254 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2995+1817G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167829 | ||||||
| chr16:16167830
|
C | T | 2 | a0004c0017t0001g0214a0004c0017t0001g0254 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2995+1816G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16167830 | ||||||
| chr16:16168068
|
T | G | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+1578A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168068 | ||||||
| chr16:16168087
|
C | T | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2995+1559G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168087 | ||||||
| chr16:16168088
|
G | A | 2 | a0001c0001t0001g0234a0001c0033t0001g0070 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2995+1558C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168088 | ||||||
| chr16:16168111
|
C | T | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2995+1535G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168111 | ||||||
| chr16:16168169
|
C | A | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+1477G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168169 | ||||||
| chr16:16168206
|
G | GCCAGGCC others(79): Show |
1 | a0001c0072t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2995+1439_2995+144 others(90): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168206 | ||||||
| chr16:16168212
|
C | A | 1 | a0001c0004t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2995+1434G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168212 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(165): Show |
6 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(3): Show | 6 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(251): Show |
2 | a0009c0015t0001g0327a0026c0056t0001g0041 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(251): Show |
57 | a0001c0001t0001g0239a0001c0001t0001g0339a0002c0003t0001g0002others(54): Show | 58 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(79): Show |
45 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(90): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(251): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2995+1427_2995+142 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(165): Show |
81 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(78): Show | 81 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168218
|
G | GTGGTGGC others(165): Show |
18 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(15): Show | 18 | HG00558.hp2 HG00673.hp1 HG03831.hp1 others(15): Show |
intron_variant | MODIFIER | c.2995+1427_2995+142 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168218 | ||||||
| chr16:16168243
|
A | ACACTTTG others(251): Show |
1 | a0003c0007t0001g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2995+1402_2995+140 others(262): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168243 | ||||||
| chr16:16168243
|
A | ACACTTTG others(165): Show |
45 | a0002c0013t0001g0241a0002c0013t0001g0243a0002c0013t0001g0244others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2995+1402_2995+140 others(176): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168243 | ||||||
| chr16:16168317
|
C | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(202): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2995+1329G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168317 | ||||||
| chr16:16168353
|
G | A | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+1293C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168353 | ||||||
| chr16:16168434
|
C | T | 59 | a0001c0001t0001g0239a0001c0001t0001g0339a0002c0003t0001g0002others(56): Show | 60 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2995+1212G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168434 | ||||||
| chr16:16168485
|
A | T | 1 | a0004c0010t0001g0342 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2995+1161T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168485 | ||||||
| chr16:16168513
|
G | A | 1 | a0006c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2995+1133C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168513 | ||||||
| chr16:16168663
|
G | C | 104 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(101): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.2995+983C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168663 | ||||||
| chr16:16168666
|
G | T | 104 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(101): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.2995+980C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168666 | ||||||
| chr16:16168674
|
A | T | 1 | a0002c0014t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2995+972T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168674 | ||||||
| chr16:16168715
|
G | A | 80 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2995+931C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168715 | ||||||
| chr16:16168719
|
A | T | 80 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2995+927T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168719 | ||||||
| chr16:16168810
|
G | A | 80 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2995+836C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168810 | ||||||
| chr16:16168847
|
G | C | 4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+799C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168847 | ||||||
| chr16:16168878
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0201 | 2 | HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2995+768G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168878 | ||||||
| chr16:16168952
|
T | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0005 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2995+694A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16168952 | ||||||
| chr16:16169006
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2995+640G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169006 | ||||||
| chr16:16169023
|
G | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(25): Show | 28 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.2995+623C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169023 | ||||||
| chr16:16169035
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2995+611C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169035 | ||||||
| chr16:16169046
|
C | A | 261 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(258): Show | 262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2995+600G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169046 | ||||||
| chr16:16169127
|
T | C | 34 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(31): Show | 35 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2995+519A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169127 | ||||||
| chr16:16169221
|
G | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2995+425C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169221 | ||||||
| chr16:16169293
|
G | C | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2995+353C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169293 | ||||||
| chr16:16169403
|
G | A | 1 | a0006c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2995+243C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169403 | ||||||
| chr16:16169478
|
G | C | 1 | a0002c0013t0001g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2995+168C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169478 | ||||||
| chr16:16169495
|
C | T | 5 | a0003c0005t0001g0134a0003c0005t0001g0177a0003c0005t0001g0307others(2): Show | 5 | HG01981.hp2 HG02004.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.2995+151G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169495 | ||||||
| chr16:16169504
|
G | A | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2995+142C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 22/30 | chr16 | 16169504 | ||||||
| chr16:16169980
|
T | C | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-127A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16169980 | ||||||
| chr16:16170006
|
G | A | 1 | a0006c0009t0001g0120 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2788-153C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170006 | ||||||
| chr16:16170007
|
A | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-154T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170007 | ||||||
| chr16:16170094
|
T | TTTTC | 4 | a0001c0001t0001g0179a0015c0019t0001g0122a0022c0075t0001g0049others(1): Show | 4 | HG00642.hp1 HG01433.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2788-242_2788-241i others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170094 | ||||||
| chr16:16170095
|
T | TTTC | 340 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2788-243_2788-242i others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170095 | ||||||
| chr16:16170096
|
T | TTC | 4 | a0001c0001t0001g0207a0001c0001t0001g0268a0002c0003t0001g0074others(1): Show | 4 | HG00438.hp1 HG01168.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2788-244_2788-243i others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170096 | ||||||
| chr16:16170098
|
G | T | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-245C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170098 | ||||||
| chr16:16170160
|
G | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(29): Show | 32 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.2788-307C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170160 | ||||||
| chr16:16170241
|
T | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-388A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170241 | ||||||
| chr16:16170292
|
A | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-439T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170292 | ||||||
| chr16:16170337
|
T | C | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-484A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170337 | ||||||
| chr16:16170419
|
C | T | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2788-566G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170419 | ||||||
| chr16:16170559
|
A | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-706T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170559 | ||||||
| chr16:16170758
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2788-905T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170758 | ||||||
| chr16:16170875
|
C | T | 1 | a0003c0005t0001g0282 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2788-1022G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170875 | ||||||
| chr16:16170876
|
A | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-1023T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170876 | ||||||
| chr16:16170906
|
T | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2788-1053A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170906 | ||||||
| chr16:16170906
|
T | C | 353 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2788-1053A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170906 | ||||||
| chr16:16170936
|
AAAAAAGA others(3): Show |
A | 1 | a0033c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2788-1093_2788-108 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170936 | ||||||
| chr16:16170938
|
AAAAG | A | 66 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0064others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2788-1089_2788-108 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170938 | ||||||
| chr16:16170939
|
AAAG | A | 62 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0079others(59): Show | 62 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2788-1089_2788-108 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170939 | ||||||
| chr16:16170939
|
AAAGAAAG | A | 14 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0054others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2788-1093_2788-108 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170939 | ||||||
| chr16:16170940
|
AAG | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0172others(77): Show | 81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2788-1089_2788-108 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170940 | ||||||
| chr16:16170940
|
AAGAAAG | A | 78 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0025others(75): Show | 78 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2788-1093_2788-108 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170940 | ||||||
| chr16:16170941
|
AG | A | 28 | a0001c0001t0001g0171a0001c0001t0001g0183a0001c0001t0001g0202others(25): Show | 28 | HG00438.hp2 HG00558.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2788-1089delC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170941 | ||||||
| chr16:16170941
|
AGAAAG | A | 11 | a0001c0002t0001g0026a0001c0002t0001g0085a0001c0002t0001g0332others(8): Show | 11 | HG00673.hp2 HG01496.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2788-1093_2788-108 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170941 | ||||||
| chr16:16170942
|
G | A | 4 | a0001c0001t0001g0200a0008c0011t0003g0059a0031c0060t0010g0240others(1): Show | 4 | HG02970.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2788-1089C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170942 | ||||||
| chr16:16170946
|
G | A | 187 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(184): Show | 187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.2788-1093C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16170946 | ||||||
| chr16:16171121
|
C | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(240): Show | 243 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.2788-1268G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171121 | ||||||
| chr16:16171124
|
G | A | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-1271C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171124 | ||||||
| chr16:16171196
|
G | T | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2788-1343C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171196 | ||||||
| chr16:16171223
|
A | AT | 17 | a0001c0001t0001g0235a0001c0001t0001g0247a0001c0001t0001g0248others(14): Show | 17 | HG00408.hp2 HG00544.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2788-1371dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171223 | ||||||
| chr16:16171375
|
C | T | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2788-1522G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171375 | ||||||
| chr16:16171455
|
G | A | 1 | a0003c0007t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2788-1602C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171455 | ||||||
| chr16:16171557
|
A | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(29): Show | 32 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.2788-1704T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171557 | ||||||
| chr16:16171654
|
G | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(28): Show | 31 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.2787+1630C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171654 | ||||||
| chr16:16171704
|
C | A | 151 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(148): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2787+1580G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171704 | ||||||
| chr16:16171705
|
G | A | 1 | a0030c0046t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2787+1579C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171705 | ||||||
| chr16:16171908
|
T | C | 3 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2787+1376A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171908 | ||||||
| chr16:16171923
|
G | A | 1 | a0001c0002t0001g0156 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2787+1361C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | ||||||
| chr16:16171923
|
G | GA | 350 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(347): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2787+1360_2787+136 others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | ||||||
| chr16:16171923
|
G | GATGGATA others(15): Show |
3 | a0005c0048t0001g0063a0022c0075t0001g0049a0028c0044t0001g0302 | 3 | HG00642.hp1 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2787+1360_2787+136 others(26): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | ||||||
| chr16:16171923
|
G | GATGGATA others(94): Show |
2 | a0001c0006t0001g0329a0021c0079t0001g0238 | 2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2787+1360_2787+136 others(105): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171923 | ||||||
| chr16:16171934
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2787+1350C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171934 | ||||||
| chr16:16171963
|
G | GGTGGGTG others(14): Show |
5 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0055t0012g0163others(2): Show | 5 | HG00544.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2787+1320_2787+132 others(25): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171963 | ||||||
| chr16:16171965
|
T | C | 3 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2787+1319A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171965 | ||||||
| chr16:16171983
|
A | G | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1301T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171983 | ||||||
| chr16:16171989
|
A | G | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1295T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16171989 | ||||||
| chr16:16172004
|
G | A | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1280C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172004 | ||||||
| chr16:16172005
|
G | A | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1279C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172005 | ||||||
| chr16:16172007
|
A | T | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1277T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172007 | ||||||
| chr16:16172010
|
G | A | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1274C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172010 | ||||||
| chr16:16172026
|
A | G | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1258T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172026 | ||||||
| chr16:16172028
|
T | A | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1256A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172028 | ||||||
| chr16:16172029
|
A | G | 53 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(50): Show | 53 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2787+1255T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172029 | ||||||
| chr16:16172039
|
C | G | 53 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(50): Show | 53 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2787+1245G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172039 | ||||||
| chr16:16172047
|
A | AGTAG | 52 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(35): Show |
1 | a0001c0002t0001g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2787+1236_2787+123 others(46): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(481): Show |
3 | a0004c0010t0001g0042a0004c0010t0001g0043a0004c0010t0001g0046 | 3 | HG00323.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(492): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(502): Show |
3 | a0001c0001t0001g0086a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01106.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(513): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(523): Show |
30 | a0001c0001t0002g0030a0001c0001t0002g0087a0001c0001t0002g0088others(27): Show | 30 | HG00733.hp2 HG00735.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(534): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(330): Show |
3 | a0013c0020t0001g0055a0013c0020t0001g0056a0013c0020t0001g0057 | 3 | HG02897.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(341): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(523): Show |
2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2787+1236_2787+123 others(534): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
A | AGTGGGAT others(523): Show |
1 | a0004c0010t0001g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2787+1236_2787+123 others(534): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172047
|
AGTGGGAT others(14): Show |
A | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1216_2787+123 others(25): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172047 | ||||||
| chr16:16172050
|
G | GGGATGGA others(418): Show |
1 | a0001c0004t0001g0217 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2787+1233_2787+123 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172050 | ||||||
| chr16:16172056
|
G | C | 53 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(50): Show | 53 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2787+1228C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172056 | ||||||
| chr16:16172057
|
A | ATAAATGA others(825): Show |
1 | a0001c0006t0001g0290 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(836): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | ATAAATGA others(498): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | NA18951.hp1 NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2787+1226_2787+122 others(509): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | ATAAATGA others(498): Show |
1 | a0001c0004t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(509): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | ATAAATGA others(498): Show |
7 | a0001c0001t0001g0064a0001c0001t0001g0188a0001c0001t0001g0190others(4): Show | 7 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1226_2787+122 others(509): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | ATAAATGA others(140): Show |
1 | a0002c0003t0001g0150 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(151): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | ATAAATGA others(56): Show |
1 | a0044c0038t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(67): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | ATAAATGA others(35): Show |
1 | a0003c0007t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2787+1226_2787+122 others(46): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172057
|
A | C | 1 | a0002c0014t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2787+1227T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172057 | ||||||
| chr16:16172064
|
A | AGTGGGTG others(695): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0235 | 2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2787+1219_2787+122 others(706): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172064 | ||||||
| chr16:16172064
|
AGTGG | A | 54 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(51): Show | 54 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2787+1216_2787+121 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172064 | ||||||
| chr16:16172065
|
G | A | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1219C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172065 | ||||||
| chr16:16172068
|
G | GGTGGGAT others(611): Show |
4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787+1215_2787+121 others(622): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172068 | ||||||
| chr16:16172068
|
G | GGTGGGAT others(140): Show |
43 | a0002c0013t0001g0241a0002c0013t0001g0243a0002c0013t0001g0244others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.2787+1215_2787+121 others(151): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172068 | ||||||
| chr16:16172068
|
G | GGTGGGAT others(1065): Show |
1 | a0003c0007t0001g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2787+1215_2787+121 others(1076): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172068 | ||||||
| chr16:16172077
|
G | C | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1207C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172077 | ||||||
| chr16:16172078
|
A | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(183): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.2787+1206T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172078 | ||||||
| chr16:16172085
|
A | G | 53 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(50): Show | 53 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2787+1199T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172085 | ||||||
| chr16:16172089
|
G | A | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1195C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172089 | ||||||
| chr16:16172099
|
C | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(183): Show | 187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.2787+1185G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172099 | ||||||
| chr16:16172106
|
A | AATGGGTG others(35): Show |
175 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(172): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2787+1177_2787+117 others(46): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172106 | ||||||
| chr16:16172106
|
A | G | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1178T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172106 | ||||||
| chr16:16172107
|
G | A | 8 | a0001c0001t0001g0082a0001c0002t0001g0014a0004c0017t0001g0076others(5): Show | 8 | HG01074.hp1 HG01109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2787+1177C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172107 | ||||||
| chr16:16172110
|
G | GGTGGGAT others(10): Show |
1 | a0001c0001t0001g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2787+1173_2787+117 others(21): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172110 | ||||||
| chr16:16172119
|
G | C | 7 | a0001c0002t0001g0014a0004c0017t0001g0076a0007c0008t0001g0256others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1165C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172119 | ||||||
| chr16:16172126
|
G | GAGGGGGT others(427): Show |
1 | a0003c0007t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2787+1157_2787+115 others(438): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172126 | ||||||
| chr16:16172127
|
A | G | 1 | a0001c0006t0001g0290 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2787+1157T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172127 | ||||||
| chr16:16172128
|
A | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(239): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2787+1156T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172128 | ||||||
| chr16:16172131
|
G | A | 7 | a0001c0002t0001g0014a0004c0017t0001g0076a0007c0008t0001g0256others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1153C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172131 | ||||||
| chr16:16172132
|
A | G | 353 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2787+1152T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172132 | ||||||
| chr16:16172140
|
C | G | 66 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(63): Show | 66 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2787+1144G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172140 | ||||||
| chr16:16172141
|
A | C | 54 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(51): Show | 54 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2787+1143T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172141 | ||||||
| chr16:16172148
|
A | G | 3 | a0001c0002t0001g0014a0001c0006t0001g0290a0004c0017t0001g0076 | 3 | NA19060.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1136T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172148 | ||||||
| chr16:16172152
|
A | AGTGGGAT others(56): Show |
5 | a0007c0008t0001g0256a0007c0008t0001g0262a0007c0008t0001g0264others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1131_2787+113 others(67): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172152 | ||||||
| chr16:16172152
|
A | G | 61 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(58): Show | 61 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2787+1132T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172152 | ||||||
| chr16:16172169
|
G | A | 3 | a0001c0002t0001g0014a0001c0006t0001g0290a0004c0017t0001g0076 | 3 | NA19060.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1115C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172169 | ||||||
| chr16:16172176
|
G | GGGATGGA others(250): Show |
1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+1107_2787+110 others(261): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | ||||||
| chr16:16172176
|
G | GGGATGGA others(594): Show |
2 | a0001c0001t0001g0313a0001c0001t0001g0337 | 2 | NA18949.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2787+1107_2787+110 others(605): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | ||||||
| chr16:16172176
|
G | GGGATGGA others(250): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0340 | 3 | HG01123.hp1 HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2787+1107_2787+110 others(261): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | ||||||
| chr16:16172176
|
G | GGGATGGA others(443): Show |
1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2787+1107_2787+110 others(454): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172176 | ||||||
| chr16:16172182
|
G | C | 2 | a0001c0002t0001g0014a0004c0017t0001g0076 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1102C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172182 | ||||||
| chr16:16172183
|
A | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0235a0001c0004t0001g0217others(3): Show | 6 | HG00408.hp2 HG01169.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787+1101T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172183 | ||||||
| chr16:16172190
|
A | G | 55 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(52): Show | 55 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.2787+1094T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172190 | ||||||
| chr16:16172199
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0188a0001c0001t0001g0190others(5): Show | 8 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2787+1085C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172199 | ||||||
| chr16:16172199
|
G | GATGGATA others(452): Show |
1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2787+1084_2787+108 others(463): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172199 | ||||||
| chr16:16172203
|
C | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(232): Show | 236 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.2787+1081G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172203 | ||||||
| chr16:16172204
|
A | ATAAATGA others(418): Show |
2 | a0008c0011t0003g0061a0008c0011t0003g0062 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(678): Show |
1 | a0001c0001t0001g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(689): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(680): Show |
1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(691): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(657): Show |
1 | a0001c0001t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(668): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(464): Show |
1 | a0001c0001t0001g0183 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(475): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(678): Show |
19 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(16): Show | 19 | HG00423.hp1 HG00544.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(689): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(678): Show |
1 | a0001c0006t0001g0292 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(689): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(699): Show |
7 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG00558.hp2 HG00673.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(710): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(783): Show |
1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(794): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(376): Show |
3 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(387): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(439): Show |
1 | a0038c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(450): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(334): Show |
59 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(345): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(355): Show |
1 | a0001c0001t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(366): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(624): Show |
1 | a0002c0074t0001g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(635): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(414): Show |
2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(425): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(582): Show |
5 | a0002c0003t0001g0013a0002c0003t0001g0123a0002c0003t0001g0175others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(519): Show |
2 | a0002c0003t0001g0167a0029c0058t0001g0164 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(530): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(582): Show |
2 | a0002c0003t0001g0257a0002c0024t0001g0154 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(561): Show |
1 | a0002c0014t0001g0289 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(582): Show |
16 | a0002c0003t0001g0002a0002c0003t0001g0074a0002c0003t0001g0084others(13): Show | 16 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(561): Show |
1 | a0002c0022t0001g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(561): Show |
1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(393): Show |
4 | a0012c0025t0001g0007a0012c0025t0001g0008a0012c0030t0001g0274others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(404): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(582): Show |
3 | a0002c0003t0001g0080a0002c0003t0001g0081a0002c0014t0001g0288 | 3 | NA18947.hp1 NA18979.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(393): Show |
9 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0172others(6): Show | 9 | HG00597.hp1 HG01106.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.2787+1079_2787+108 others(404): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(351): Show |
1 | a0001c0001t0001g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(362): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(411): Show |
1 | a0026c0056t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(422): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | ATAAATGA others(712): Show |
1 | a0002c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2787+1079_2787+108 others(723): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172204
|
A | C | 2 | a0001c0004t0001g0217a0001c0006t0001g0290 | 2 | HG01169.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2787+1080T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172204 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(418): Show |
2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(439): Show |
3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(450): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(418): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(429): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(561): Show |
1 | a0002c0003t0001g0306 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(393): Show |
1 | a0002c0003t0001g0145 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(404): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(414): Show |
6 | a0002c0014t0001g0331a0006c0009t0001g0116a0006c0009t0001g0118others(3): Show | 7 | NA18943.hp2 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(425): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(582): Show |
1 | a0002c0003t0001g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(582): Show |
2 | a0002c0003t0001g0225a0002c0003t0001g0350 | 2 | HG01109.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(593): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(561): Show |
2 | a0002c0003t0001g0141a0002c0003t0001g0224 | 2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2787+1072_2787+107 others(572): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | AGTGGGTG others(603): Show |
1 | a0013c0050t0001g0040 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2787+1072_2787+107 others(614): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172211
|
A | G | 2 | a0001c0002t0001g0014a0004c0017t0001g0076 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+1073T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172211 | ||||||
| chr16:16172212
|
G | A | 1 | a0043c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2787+1072C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172212 | ||||||
| chr16:16172215
|
A | AGTGGGAT others(497): Show |
4 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787+1068_2787+106 others(508): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172215 | ||||||
| chr16:16172215
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(284): Show | 288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.2787+1069T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172215 | ||||||
| chr16:16172225
|
A | C | 8 | a0001c0001t0001g0191a0001c0001t0001g0235a0001c0004t0001g0217others(5): Show | 8 | HG00408.hp2 HG01169.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2787+1059T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172225 | ||||||
| chr16:16172232
|
G | A | 56 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(53): Show | 56 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2787+1052C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172232 | ||||||
| chr16:16172233
|
G | A | 1 | a0043c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2787+1051C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172233 | ||||||
| chr16:16172246
|
A | C | 5 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0313others(2): Show | 5 | HG01123.hp1 HG01358.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+1038T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172246 | ||||||
| chr16:16172253
|
G | A | 121 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0194others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.2787+1031C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172253 | ||||||
| chr16:16172259
|
T | A | 1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+1025A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172259 | ||||||
| chr16:16172260
|
G | T | 1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+1024C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172260 | ||||||
| chr16:16172262
|
G | A | 48 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0172others(45): Show | 48 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2787+1022C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172262 | ||||||
| chr16:16172267
|
A | C | 51 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(48): Show | 51 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.2787+1017T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172267 | ||||||
| chr16:16172274
|
A | G | 6 | a0001c0001t0001g0191a0001c0001t0001g0235a0002c0024t0001g0152others(3): Show | 6 | HG00408.hp2 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787+1010T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172274 | ||||||
| chr16:16172283
|
G | A | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+1001C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172283 | ||||||
| chr16:16172283
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2787+1001C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172283 | ||||||
| chr16:16172287
|
C | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(234): Show | 238 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2787+997G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172287 | ||||||
| chr16:16172288
|
A | C | 5 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0313others(2): Show | 5 | HG01123.hp1 HG01358.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+996T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172288 | ||||||
| chr16:16172288
|
ATAAATGA others(125): Show |
A | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+864_2787+995d others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172288 | ||||||
| chr16:16172295
|
A | G | 12 | a0001c0001t0001g0247a0002c0003t0001g0145a0002c0014t0001g0331others(9): Show | 13 | HG02451.hp2 HG02809.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.2787+989T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172295 | ||||||
| chr16:16172299
|
A | G | 346 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.2787+985T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172299 | ||||||
| chr16:16172308
|
G | C | 108 | a0001c0001t0001g0082a0001c0002t0001g0010a0001c0002t0001g0023others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2787+976C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172308 | ||||||
| chr16:16172309
|
A | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2787+975T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172309 | ||||||
| chr16:16172315
|
G | GA | 108 | a0001c0001t0001g0082a0001c0002t0001g0010a0001c0002t0001g0023others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2787+968_2787+969i others(3): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172315 | ||||||
| chr16:16172316
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(12): Show | 15 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2787+968C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172316 | ||||||
| chr16:16172316
|
GGTATGA | G | 84 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.2787+962_2787+967d others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172316 | ||||||
| chr16:16172318
|
T | TGGGATGG others(558): Show |
1 | a0001c0001t0001g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(567): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(527): Show |
1 | a0001c0002t0001g0156 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(536): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(730): Show |
2 | a0003c0005t0001g0028a0003c0005t0001g0029 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(739): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(428): Show |
40 | a0002c0013t0001g0241a0002c0013t0001g0243a0002c0013t0001g0244others(37): Show | 40 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(437): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(449): Show |
1 | a0003c0005t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(458): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(428): Show |
1 | a0003c0007t0001g0098 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(437): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(491): Show |
5 | a0007c0008t0001g0256a0007c0008t0001g0262a0007c0008t0001g0264others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(500): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(512): Show |
1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(521): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(533): Show |
2 | a0001c0026t0001g0272a0033c0054t0001g0072 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(542): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(659): Show |
1 | a0002c0003t0001g0150 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(668): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(424): Show |
1 | a0003c0007t0001g0245 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(433): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(428): Show |
1 | a0003c0005t0001g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(437): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(575): Show |
1 | a0044c0038t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(584): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(491): Show |
1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(500): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(531): Show |
1 | a0001c0002t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(540): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(906): Show |
1 | a0001c0002t0001g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(915): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(467): Show |
1 | a0001c0002t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(476): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(488): Show |
43 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(40): Show | 43 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(497): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(467): Show |
1 | a0005c0012t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(476): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGATGG others(509): Show |
2 | a0001c0002t0001g0068a0001c0002t0001g0332 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(518): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(8): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(9): Show | 12 | HG01175.hp2 HG02040.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(29): Show |
1 | a0034c0063t0001g0170 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(555): Show |
1 | a0007c0008t0001g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(564): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(576): Show |
2 | a0007c0008t0001g0053a0007c0008t0001g0258 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(585): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(594): Show |
1 | a0043c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(603): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(492): Show |
2 | a0001c0002t0001g0014a0004c0017t0001g0076 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(501): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(29): Show |
2 | a0001c0001t0001g0313a0001c0001t0001g0337 | 2 | NA18949.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(71): Show |
1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(80): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(218): Show |
3 | a0013c0020t0001g0055a0013c0020t0001g0056a0013c0020t0001g0057 | 3 | HG02897.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(227): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(134): Show |
5 | a0002c0014t0001g0331a0006c0009t0001g0118a0006c0009t0001g0119others(2): Show | 6 | NA18943.hp2 NA18978.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(143): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(155): Show |
1 | a0002c0003t0001g0145 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(164): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(176): Show |
1 | a0006c0009t0001g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(185): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(8): Show |
41 | a0001c0001t0001g0003a0001c0001t0001g0191a0001c0001t0001g0229others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(50): Show |
1 | a0001c0001t0001g0335 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(29): Show |
70 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(67): Show | 70 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(218): Show |
1 | a0001c0004t0001g0217 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(227): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(50): Show |
8 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(134): Show |
1 | a0008c0011t0003g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2787+965_2787+966i others(143): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(50): Show |
2 | a0008c0011t0003g0061a0008c0011t0003g0062 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(29): Show |
1 | a0031c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(38): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172318
|
T | TGGGTGGG others(50): Show |
1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2787+965_2787+966i others(59): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172318 | ||||||
| chr16:16172322
|
A | AGTGGGTG others(35): Show |
43 | a0001c0002t0001g0010a0001c0002t0001g0023a0001c0002t0001g0025others(40): Show | 43 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2787+961_2787+962i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172322 | ||||||
| chr16:16172322
|
A | G | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(29): Show | 32 | HG00639.hp2 HG01175.hp2 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.2787+962T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172322 | ||||||
| chr16:16172336
|
C | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0128others(183): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.2787+948G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172336 | ||||||
| chr16:16172336
|
C | CTAAATGA others(35): Show |
1 | a0001c0002t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2787+947_2787+948i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172336 | ||||||
| chr16:16172343
|
G | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(206): Show | 209 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2787+941C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172343 | ||||||
| chr16:16172343
|
G | AGTGGGTG others(35): Show |
1 | a0005c0012t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2787+941_2787+942i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172343 | ||||||
| chr16:16172357
|
C | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.2787+927G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172357 | ||||||
| chr16:16172364
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0169others(52): Show | 55 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2787+920T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172364 | ||||||
| chr16:16172366
|
T | C | 18 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(15): Show | 18 | HG00558.hp2 HG00673.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.2787+918A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172366 | ||||||
| chr16:16172378
|
C | A | 110 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2787+906G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172378 | ||||||
| chr16:16172378
|
C | CTAAATGA others(14): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2787+905_2787+906i others(23): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172378 | ||||||
| chr16:16172384
|
G | GAGTGGGT others(123): Show |
1 | a0001c0004t0002g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2787+899_2787+900i others(132): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172384 | ||||||
| chr16:16172385
|
A | GGTGGGTG others(35): Show |
64 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2787+899_2787+900i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172385 | ||||||
| chr16:16172385
|
A | GGTGGGTG others(35): Show |
19 | a0001c0001t0001g0086a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01106.hp1 HG01261.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2787+899_2787+900i others(44): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172385 | ||||||
| chr16:16172387
|
T | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0191a0001c0001t0001g0229others(16): Show | 19 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.2787+897A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172387 | ||||||
| chr16:16172399
|
C | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(115): Show | 118 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2787+885G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172399 | ||||||
| chr16:16172399
|
C | CTAAATGA others(14): Show |
112 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0172others(109): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.2787+884_2787+885i others(23): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172399 | ||||||
| chr16:16172406
|
A | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0340 | 3 | HG01123.hp1 HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2787+878T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172406 | ||||||
| chr16:16172411
|
G | GTGGGATG others(114): Show |
3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2787+872_2787+873i others(123): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172411 | ||||||
| chr16:16172420
|
C | A | 113 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2787+864G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172420 | ||||||
| chr16:16172420
|
C | CTAAATGA others(14): Show |
46 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0191others(43): Show | 46 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.2787+843_2787+863d others(23): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172420 | ||||||
| chr16:16172440
|
G | C | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+844C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172440 | ||||||
| chr16:16172451
|
G | T | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+833C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172451 | ||||||
| chr16:16172452
|
GGTGGGAT | G | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+825_2787+831d others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172452 | ||||||
| chr16:16172494
|
G | A | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787+790C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172494 | ||||||
| chr16:16172582
|
G | T | 4 | a0002c0003t0001g0168a0002c0003t0001g0186a0002c0003t0001g0187others(1): Show | 4 | HG01884.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787+702C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172582 | ||||||
| chr16:16172719
|
A | G | 1 | a0023c0076t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2787+565T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172719 | ||||||
| chr16:16172741
|
G | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2787+543C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172741 | ||||||
| chr16:16172911
|
A | C | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2787+373T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172911 | ||||||
| chr16:16172915
|
G | A | 59 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(56): Show | 59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2787+369C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172915 | ||||||
| chr16:16172961
|
T | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2787+323A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172961 | ||||||
| chr16:16172974
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2787+310G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172974 | ||||||
| chr16:16172983
|
A | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2787+301T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16172983 | ||||||
| chr16:16173065
|
A | T | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2787+219T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173065 | ||||||
| chr16:16173173
|
G | A | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2787+111C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173173 | ||||||
| chr16:16173180
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2787+104T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173180 | ||||||
| chr16:16173185
|
A | G | 2 | a0001c0001t0002g0161a0039c0070t0002g0067 | 2 | NA18943.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2787+99T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173185 | ||||||
| chr16:16173222
|
A | G | 348 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2787+62T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 21/30 | chr16 | 16173222 | ||||||
| chr16:16173541
|
A | G | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2667-137T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173541 | ||||||
| chr16:16173583
|
T | C | 1 | a0044c0038t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2667-179A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173583 | ||||||
| chr16:16173625
|
C | T | 1 | a0001c0004t0002g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2667-221G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173625 | ||||||
| chr16:16173692
|
T | TTTTC | 137 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(134): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2667-292_2667-289d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173692 | ||||||
| chr16:16173696
|
C | CT | 8 | a0001c0002t0001g0112a0001c0002t0001g0148a0001c0002t0001g0156others(5): Show | 8 | HG01928.hp2 HG02300.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2667-293dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173696 | ||||||
| chr16:16173696
|
C | CTTTCT | 12 | a0001c0001t0001g0127a0001c0001t0001g0165a0001c0001t0001g0179others(9): Show | 12 | HG01433.hp1 HG01433.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2667-293_2667-292i others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173696 | ||||||
| chr16:16173697
|
T | TTTC | 8 | a0001c0001t0001g0079a0001c0001t0001g0128a0001c0001t0001g0229others(5): Show | 8 | HG00099.hp2 HG01081.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2667-294_2667-293i others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173697 | ||||||
| chr16:16173807
|
G | A | 1 | a0001c0006t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2667-403C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173807 | ||||||
| chr16:16173921
|
A | T | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2667-517T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173921 | ||||||
| chr16:16173928
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2667-524T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173928 | ||||||
| chr16:16173980
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2667-576C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16173980 | ||||||
| chr16:16174111
|
A | G | 98 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0074others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.2667-707T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174111 | ||||||
| chr16:16174177
|
G | A | 1 | a0002c0024t0001g0154 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2667-773C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174177 | ||||||
| chr16:16174266
|
CAACCGTT others(7): Show |
C | 1 | a0001c0001t0001g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2667-876_2667-863d others(16): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174266 | ||||||
| chr16:16174271
|
G | A | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2667-867C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174271 | ||||||
| chr16:16174373
|
A | G | 98 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0074others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.2667-969T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174373 | ||||||
| chr16:16174438
|
G | A | 3 | a0001c0001t0001g0336a0001c0004t0001g0109a0025c0053t0001g0153 | 3 | HG00438.hp1 HG02056.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2667-1034C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174438 | ||||||
| chr16:16174496
|
C | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0069others(148): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2667-1092G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174496 | ||||||
| chr16:16174671
|
C | T | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2666+1240G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174671 | ||||||
| chr16:16174742
|
G | A | 1 | a0003c0005t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2666+1169C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174742 | ||||||
| chr16:16174759
|
A | ACCC | 3 | a0008c0011t0003g0058a0008c0011t0003g0060a0011c0016t0006g0271 | 3 | HG01496.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCC | 9 | a0001c0001t0002g0092a0001c0001t0002g0094a0001c0004t0002g0106others(6): Show | 9 | HG02280.hp1 HG02572.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC | 9 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0227others(6): Show | 9 | HG01256.hp2 HG02451.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(1): Show |
18 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0126others(15): Show | 18 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(2): Show |
24 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0191others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(13): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(3): Show |
27 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0142others(24): Show | 27 | HG00099.hp2 HG00408.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(4): Show |
8 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0234others(5): Show | 8 | HG00673.hp1 HG02273.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(5): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0303others(3): Show | 6 | HG02135.hp1 HG02135.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(16): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(6): Show |
5 | a0001c0001t0001g0179a0001c0001t0001g0338a0001c0001t0001g0340others(2): Show | 5 | HG00558.hp2 HG01433.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(7): Show |
2 | a0001c0001t0001g0269a0001c0001t0001g0308 | 2 | HG03831.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(18): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCCC others(8): Show |
1 | a0001c0001t0001g0335 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2666+1151_2666+115 others(19): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCGC others(1): Show |
5 | a0001c0001t0001g0233a0001c0001t0001g0305a0002c0068t0001g0097others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2666+1151_2666+115 others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCCGC others(4): Show |
1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2666+1151_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | ACCCCGCC others(4): Show |
1 | a0001c0001t0001g0334 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2666+1151_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174759
|
A | C | 1 | a0004c0010t0001g0342 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2666+1152T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174759 | ||||||
| chr16:16174760
|
A | ACCCCCC | 25 | a0001c0002t0001g0014a0001c0002t0001g0023a0001c0002t0001g0024others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2666+1145_2666+115 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | ||||||
| chr16:16174760
|
A | ACCCCCCC | 14 | a0001c0002t0001g0010a0001c0002t0001g0085a0001c0002t0001g0093others(11): Show | 14 | HG00639.hp1 HG00673.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2666+1144_2666+115 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | ||||||
| chr16:16174760
|
A | ACCCCCCC others(4): Show |
1 | a0001c0001t0001g0159 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2666+1150_2666+115 others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | ||||||
| chr16:16174760
|
A | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(152): Show | 155 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2666+1151T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | ||||||
| chr16:16174760
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0002g0094a0001c0004t0002g0106 | 3 | HG02738.hp1 NA18953.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2666+1151T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174760 | ||||||
| chr16:16174761
|
C | CCCG | 29 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(26): Show | 29 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2666+1149_2666+115 others(7): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174761 | ||||||
| chr16:16174933
|
T | A | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2666+978A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174933 | ||||||
| chr16:16174934
|
T | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.2666+977A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16174934 | ||||||
| chr16:16175011
|
G | A | 45 | a0002c0013t0001g0241a0002c0013t0001g0243a0002c0013t0001g0244others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2666+900C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175011 | ||||||
| chr16:16175069
|
A | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(210): Show | 213 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.2666+842T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175069 | ||||||
| chr16:16175261
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2666+650T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175261 | ||||||
| chr16:16175395
|
C | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.2666+516G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175395 | ||||||
| chr16:16175412
|
G | A | 52 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(49): Show | 52 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2666+499C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175412 | ||||||
| chr16:16175566
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2666+345T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175566 | ||||||
| chr16:16175575
|
A | T | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2666+336T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175575 | ||||||
| chr16:16175713
|
A | G | 316 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2666+198T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175713 | ||||||
| chr16:16175767
|
A | C | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2666+144T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175767 | ||||||
| chr16:16175771
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2666+140G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175771 | ||||||
| chr16:16175776
|
TG | T | 310 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2666+134delC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175776 | ||||||
| chr16:16175896
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2666+15G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 20/30 | chr16 | 16175896 | ||||||
| chr16:16176077
|
C | A | 1 | a0001c0002t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2591-91G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176077 | ||||||
| chr16:16176105
|
G | A | 55 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(52): Show | 55 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2591-119C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176105 | ||||||
| chr16:16176189
|
A | G | 60 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(57): Show | 60 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2591-203T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176189 | ||||||
| chr16:16176219
|
T | G | 2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2591-233A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176219 | ||||||
| chr16:16176274
|
C | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.2591-288G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176274 | ||||||
| chr16:16176317
|
T | C | 309 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(306): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2591-331A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176317 | ||||||
| chr16:16176318
|
T | C | 1 | a0001c0052t0001g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2591-332A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176318 | ||||||
| chr16:16176331
|
TCTCACCT others(3): Show |
T | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2591-355_2591-346d others(12): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176331 | ||||||
| chr16:16176368
|
A | C | 1 | a0001c0002t0001g0117 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2591-382T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176368 | ||||||
| chr16:16176548
|
C | T | 4 | a0010c0029t0001g0158a0010c0029t0001g0230a0010c0042t0001g0099others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.2591-562G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176548 | ||||||
| chr16:16176582
|
C | T | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2591-596G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176582 | ||||||
| chr16:16176583
|
A | C | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2591-597T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176583 | ||||||
| chr16:16176584
|
C | A | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2591-598G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176584 | ||||||
| chr16:16176688
|
A | T | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2591-702T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176688 | ||||||
| chr16:16176794
|
T | G | 3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2590+658A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176794 | ||||||
| chr16:16176852
|
A | G | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2590+600T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176852 | ||||||
| chr16:16176982
|
A | C | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2590+470T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176982 | ||||||
| chr16:16176993
|
C | T | 342 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2590+459G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16176993 | ||||||
| chr16:16177020
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2590+432A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177020 | ||||||
| chr16:16177047
|
C | T | 54 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2590+405G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177047 | ||||||
| chr16:16177165
|
T | A | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2590+287A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177165 | ||||||
| chr16:16177230
|
A | AT | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2590+221dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177230 | ||||||
| chr16:16177281
|
G | A | 1 | a0038c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2590+171C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177281 | ||||||
| chr16:16177407
|
G | A | 2 | a0001c0004t0001g0109a0025c0053t0001g0153 | 2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2590+45C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 19/30 | chr16 | 16177407 | ||||||
| chr16:16177745
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2416-119G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177745 | ||||||
| chr16:16177760
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0165others(3): Show | 6 | NA18941.hp2 NA18947.hp2 NA19064.hp1 others(3): Show |
intron_variant | MODIFIER | c.2416-134G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177760 | ||||||
| chr16:16177771
|
C | T | 342 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2416-145G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177771 | ||||||
| chr16:16177815
|
C | A | 1 | a0001c0004t0002g0133 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2416-189G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177815 | ||||||
| chr16:16177848
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2416-222G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177848 | ||||||
| chr16:16177891
|
C | T | 57 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(54): Show | 57 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2416-265G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177891 | ||||||
| chr16:16177972
|
A | G | 1 | a0001c0002t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2416-346T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16177972 | ||||||
| chr16:16178129
|
C | T | 1 | a0001c0004t0001g0217 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2416-503G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178129 | ||||||
| chr16:16178141
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2416-515G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178141 | ||||||
| chr16:16178219
|
C | T | 1 | a0003c0007t0001g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2415+579G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178219 | ||||||
| chr16:16178220
|
G | A | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2415+578C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178220 | ||||||
| chr16:16178258
|
C | T | 1 | a0038c0069t0001g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2415+540G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178258 | ||||||
| chr16:16178326
|
C | CA | 55 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(52): Show | 55 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2415+471dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178326 | ||||||
| chr16:16178406
|
T | C | 2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2415+392A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178406 | ||||||
| chr16:16178451
|
C | T | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2415+347G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178451 | ||||||
| chr16:16178621
|
T | C | 2 | a0001c0065t0001g0312a0004c0078t0001g0199 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2415+177A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178621 | ||||||
| chr16:16178651
|
G | A | 101 | a0001c0026t0001g0272a0001c0055t0012g0163a0002c0003t0001g0002others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.2415+147C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178651 | ||||||
| chr16:16178707
|
G | C | 2 | a0012c0030t0001g0113a0012c0030t0001g0274 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2415+91C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 18/30 | chr16 | 16178707 | ||||||
| chr16:16179061
|
G | C | 1 | a0040c0041t0001g0216 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2248-96C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179061 | ||||||
| chr16:16179180
|
C | T | 5 | a0012c0025t0001g0007a0012c0025t0001g0008a0012c0030t0001g0113others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2248-215G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179180 | ||||||
| chr16:16179340
|
G | T | 89 | a0001c0026t0001g0272a0001c0055t0012g0163a0002c0003t0001g0002others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2248-375C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179340 | ||||||
| chr16:16179517
|
C | T | 269 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2248-552G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179517 | ||||||
| chr16:16179563
|
G | A | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2248-598C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179563 | ||||||
| chr16:16179595
|
G | A | 1 | a0003c0005t0001g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2248-630C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179595 | ||||||
| chr16:16179793
|
G | A | 3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2248-828C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179793 | ||||||
| chr16:16179834
|
G | A | 156 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(153): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2248-869C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179834 | ||||||
| chr16:16179939
|
A | G | 1 | a0001c0002t0001g0287 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2248-974T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16179939 | ||||||
| chr16:16180349
|
C | G | 160 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2248-1384G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180349 | ||||||
| chr16:16180475
|
C | T | 1 | a0033c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2248-1510G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180475 | ||||||
| chr16:16180829
|
C | T | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+1583G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180829 | ||||||
| chr16:16180838
|
G | A | 3 | a0001c0004t0002g0133a0031c0060t0010g0240a0032c0059t0001g0009 | 3 | HG03540.hp2 NA18906.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2247+1574C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180838 | ||||||
| chr16:16180905
|
C | T | 2 | a0001c0002t0001g0068a0001c0002t0001g0332 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2247+1507G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180905 | ||||||
| chr16:16180958
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2247+1454T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16180958 | ||||||
| chr16:16181012
|
A | C | 1 | a0005c0048t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2247+1400T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181012 | ||||||
| chr16:16181286
|
T | C | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+1126A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181286 | ||||||
| chr16:16181344
|
GA | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(109): Show | 112 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2247+1067delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181344 | ||||||
| chr16:16181344
|
GAA | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0160a0001c0001t0001g0188others(10): Show | 13 | HG00642.hp2 HG00673.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2247+1066_2247+106 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181344 | ||||||
| chr16:16181344
|
GAAAAAAA | G | 37 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0202others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.2247+1061_2247+106 others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181344 | ||||||
| chr16:16181356
|
A | G | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2247+1056T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181356 | ||||||
| chr16:16181357
|
A | G | 154 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2247+1055T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181357 | ||||||
| chr16:16181358
|
A | G | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2247+1054T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181358 | ||||||
| chr16:16181363
|
AAAAAAG | A | 154 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2247+1043_2247+104 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181363 | ||||||
| chr16:16181367
|
A | G | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2247+1045T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181367 | ||||||
| chr16:16181403
|
C | T | 4 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+1009G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181403 | ||||||
| chr16:16181413
|
G | A | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2247+999C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181413 | ||||||
| chr16:16181488
|
G | A | 102 | a0001c0026t0001g0272a0001c0055t0012g0163a0002c0003t0001g0002others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2247+924C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181488 | ||||||
| chr16:16181609
|
G | A | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+803C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181609 | ||||||
| chr16:16181638
|
C | A | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2247+774G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181638 | ||||||
| chr16:16181641
|
G | A | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+771C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181641 | ||||||
| chr16:16181662
|
G | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2247+750C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181662 | ||||||
| chr16:16181671
|
T | G | 1 | a0003c0007t0001g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2247+741A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181671 | ||||||
| chr16:16181767
|
TACTAAAA | T | 5 | a0012c0025t0001g0007a0012c0025t0001g0008a0012c0030t0001g0113others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2247+638_2247+644d others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181767 | ||||||
| chr16:16181855
|
C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2247+557G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16181855 | ||||||
| chr16:16182023
|
G | A | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+389C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182023 | ||||||
| chr16:16182123
|
G | A | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247+289C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182123 | ||||||
| chr16:16182172
|
C | G | 2 | a0001c0001t0002g0203a0001c0006t0002g0246 | 2 | HG00735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2247+240G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182172 | ||||||
| chr16:16182262
|
C | T | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+150G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182262 | ||||||
| chr16:16182294
|
C | T | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2247+118G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182294 | ||||||
| chr16:16182353
|
A | G | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2247+59T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182353 | ||||||
| chr16:16182354
|
C | A | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2247+58G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 17/30 | chr16 | 16182354 | ||||||
| chr16:16182691
|
G | A | 3 | a0001c0002t0001g0166a0001c0002t0001g0174a0043c0040t0001g0031 | 3 | HG01884.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2071-103C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 16/30 | chr16 | 16182691 | ||||||
| chr16:16183107
|
C | T | 57 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(54): Show | 57 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1944-177G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183107 | ||||||
| chr16:16183133
|
C | T | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1944-203G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183133 | ||||||
| chr16:16183307
|
C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1944-377G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183307 | ||||||
| chr16:16183343
|
C | T | 5 | a0005c0048t0001g0063a0022c0075t0001g0049a0028c0044t0001g0302others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-413G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183343 | ||||||
| chr16:16183384
|
C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1944-454G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183384 | ||||||
| chr16:16183385
|
G | C | 5 | a0005c0048t0001g0063a0022c0075t0001g0049a0028c0044t0001g0302others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-455C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183385 | ||||||
| chr16:16183415
|
A | G | 5 | a0005c0048t0001g0063a0022c0075t0001g0049a0028c0044t0001g0302others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-485T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183415 | ||||||
| chr16:16183432
|
C | A | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1944-502G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183432 | ||||||
| chr16:16183477
|
G | A | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944-547C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183477 | ||||||
| chr16:16183535
|
G | C | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1944-605C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183535 | ||||||
| chr16:16183563
|
G | C | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1944-633C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183563 | ||||||
| chr16:16183593
|
G | A | 5 | a0012c0025t0001g0007a0012c0025t0001g0008a0012c0030t0001g0113others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1944-663C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183593 | ||||||
| chr16:16183755
|
C | T | 5 | a0005c0048t0001g0063a0022c0075t0001g0049a0028c0044t0001g0302others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-825G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183755 | ||||||
| chr16:16183804
|
G | A | 5 | a0005c0048t0001g0063a0022c0075t0001g0049a0028c0044t0001g0302others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944-874C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183804 | ||||||
| chr16:16183826
|
C | T | 26 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(23): Show | 26 | HG00597.hp1 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1944-896G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183826 | ||||||
| chr16:16183828
|
G | A | 39 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0201others(36): Show | 39 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1944-898C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183828 | ||||||
| chr16:16183996
|
T | G | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+963A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183996 | ||||||
| chr16:16183998
|
G | T | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+961C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16183998 | ||||||
| chr16:16184037
|
A | G | 1 | a0033c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1943+922T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184037 | ||||||
| chr16:16184081
|
C | G | 3 | a0005c0048t0001g0063a0031c0060t0010g0240a0032c0059t0001g0009 | 3 | HG02055.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1943+878G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184081 | ||||||
| chr16:16184174
|
G | A | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1943+785C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184174 | ||||||
| chr16:16184179
|
A | T | 2 | a0001c0023t0001g0066a0001c0023t0001g0100 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1943+780T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184179 | ||||||
| chr16:16184191
|
T | C | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+768A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184191 | ||||||
| chr16:16184192
|
C | T | 1 | a0001c0001t0004g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1943+767G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184192 | ||||||
| chr16:16184193
|
C | T | 156 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(153): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1943+766G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184193 | ||||||
| chr16:16184198
|
C | CA | 13 | a0001c0001t0001g0064a0001c0001t0001g0171a0001c0001t0001g0273others(10): Show | 13 | HG01175.hp2 HG02055.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1943+760dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | ||||||
| chr16:16184198
|
CA | C | 129 | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0172others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1943+760delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | ||||||
| chr16:16184198
|
CAA | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(144): Show | 147 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1943+759_1943+760d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | ||||||
| chr16:16184198
|
CAAA | C | 9 | a0001c0001t0004g0155a0001c0002t0001g0231a0001c0026t0001g0272others(6): Show | 9 | HG00642.hp1 HG01099.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1943+758_1943+760d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | ||||||
| chr16:16184198
|
CAAAAAAA others(4): Show |
C | 1 | a0042c0039t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1943+750_1943+760d others(13): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184198 | ||||||
| chr16:16184270
|
T | C | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1943+689A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184270 | ||||||
| chr16:16184291
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1943+668C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184291 | ||||||
| chr16:16184368
|
C | A | 4 | a0022c0075t0001g0049a0028c0044t0001g0302a0031c0060t0010g0240others(1): Show | 4 | HG00642.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1943+591G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184368 | ||||||
| chr16:16184424
|
C | T | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1943+535G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184424 | ||||||
| chr16:16184446
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1943+513T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184446 | ||||||
| chr16:16184459
|
G | C | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1943+500C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184459 | ||||||
| chr16:16184482
|
C | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0049t0001g0352 | 3 | HG02109.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1943+477G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184482 | ||||||
| chr16:16184494
|
T | G | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1943+465A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184494 | ||||||
| chr16:16184589
|
C | T | 100 | a0001c0001t0001g0089a0002c0003t0001g0002a0002c0003t0001g0013others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1943+370G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184589 | ||||||
| chr16:16184742
|
G | A | 1 | a0001c0047t0002g0101 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1943+217C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184742 | ||||||
| chr16:16184754
|
T | C | 1 | a0005c0012t0001g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1943+205A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184754 | ||||||
| chr16:16184808
|
G | C | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1943+151C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184808 | ||||||
| chr16:16184817
|
C | T | 1 | a0001c0002t0001g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1943+142G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184817 | ||||||
| chr16:16184838
|
A | T | 99 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0074others(96): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1943+121T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184838 | ||||||
| chr16:16184868
|
C | A | 1 | a0003c0005t0001g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1943+91G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184868 | ||||||
| chr16:16184949
|
C | G | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1943+10G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 15/30 | chr16 | 16184949 | ||||||
| chr16:16185091
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1868-57G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185091 | ||||||
| chr16:16185118
|
G | T | 1 | a0001c0001t0001g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1868-84C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185118 | ||||||
| chr16:16185118
|
GC | G | 155 | a0001c0001t0001g0341a0001c0002t0001g0010a0001c0002t0001g0014others(152): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1868-85delG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185118 | ||||||
| chr16:16185124
|
C | A | 33 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(30): Show | 33 | HG00597.hp1 HG00642.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1868-90G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185124 | ||||||
| chr16:16185124
|
C | G | 5 | a0002c0024t0001g0152a0013c0020t0001g0055a0013c0020t0001g0056others(2): Show | 5 | HG02897.hp1 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1868-90G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185124 | ||||||
| chr16:16185125
|
C | G | 1 | a0001c0049t0001g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1868-91G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185125 | ||||||
| chr16:16185191
|
G | C | 153 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(150): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1868-157C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185191 | ||||||
| chr16:16185222
|
C | T | 153 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(150): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1868-188G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185222 | ||||||
| chr16:16185225
|
G | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1868-191C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185225 | ||||||
| chr16:16185426
|
G | A | 151 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0023others(148): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1868-392C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185426 | ||||||
| chr16:16185470
|
C | A | 1 | a0001c0006t0001g0277 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1868-436G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185470 | ||||||
| chr16:16185626
|
A | T | 1 | a0003c0005t0005g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1868-592T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185626 | ||||||
| chr16:16185728
|
T | A | 35 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0089others(32): Show | 35 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1868-694A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185728 | ||||||
| chr16:16185776
|
CTG | C | 57 | a0002c0003t0001g0123a0002c0003t0001g0150a0002c0003t0001g0257others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.1868-744_1868-743d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185776 | ||||||
| chr16:16185784
|
C | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1868-750G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185784 | ||||||
| chr16:16185949
|
G | A | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1868-915C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16185949 | ||||||
| chr16:16186122
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(25): Show | 28 | HG00597.hp1 HG01496.hp2 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.1867+1002A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186122 | ||||||
| chr16:16186245
|
C | T | 3 | a0012c0025t0001g0007a0012c0025t0001g0008a0030c0046t0001g0304 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1867+879G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186245 | ||||||
| chr16:16186346
|
T | G | 1 | a0037c0061t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1867+778A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186346 | ||||||
| chr16:16186548
|
C | T | 101 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0074others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1867+576G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186548 | ||||||
| chr16:16186790
|
G | A | 1 | a0004c0010t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1867+334C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186790 | ||||||
| chr16:16186919
|
G | C | 34 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0089others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1867+205C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16186919 | ||||||
| chr16:16187032
|
C | T | 101 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0074others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1867+92G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187032 | ||||||
| chr16:16187038
|
A | G | 100 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0074others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1867+86T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187038 | ||||||
| chr16:16187064
|
T | A | 3 | a0001c0004t0001g0034a0001c0004t0001g0038a0001c0067t0001g0351 | 3 | HG01123.hp2 HG01346.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1867+60A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187064 | ||||||
| chr16:16187064
|
T | C | 336 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(333): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1867+60A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 14/30 | chr16 | 16187064 | ||||||
| chr16:16187247
|
A | T | 1 | a0003c0005t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1780-36T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187247 | ||||||
| chr16:16187297
|
C | A | 105 | a0001c0004t0002g0106a0002c0003t0001g0002a0002c0003t0001g0013others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1780-86G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187297 | ||||||
| chr16:16187330
|
G | A | 6 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0060others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1780-119C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187330 | ||||||
| chr16:16187434
|
C | T | 1 | a0003c0005t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1780-223G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187434 | ||||||
| chr16:16187704
|
G | T | 3 | a0004c0010t0001g0073a0018c0035t0001g0077a0018c0035t0001g0078 | 3 | HG02258.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1780-493C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187704 | ||||||
| chr16:16187781
|
G | C | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1780-570C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187781 | ||||||
| chr16:16187819
|
T | A | 2 | a0001c0006t0001g0277a0001c0006t0001g0299 | 2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1780-608A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187819 | ||||||
| chr16:16187904
|
AAAT | A | 49 | a0001c0001t0004g0071a0001c0004t0001g0109a0001c0004t0002g0106others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1780-696_1780-694d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187904 | ||||||
| chr16:16187904
|
AAATT | A | 4 | a0022c0075t0001g0049a0027c0073t0001g0016a0028c0044t0001g0302others(1): Show | 4 | HG00642.hp1 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-697_1780-694d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187904 | ||||||
| chr16:16187907
|
T | A | 3 | a0002c0013t0001g0241a0003c0007t0001g0098a0031c0060t0010g0240 | 3 | HG01256.hp1 HG03540.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1780-696A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187907 | ||||||
| chr16:16187907
|
T | TTAAA | 4 | a0001c0001t0001g0235a0001c0001t0001g0326a0001c0001t0001g0339others(1): Show | 4 | HG00408.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-700_1780-697d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187907 | ||||||
| chr16:16187907
|
TTAAA | T | 176 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1780-700_1780-697d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187907 | ||||||
| chr16:16187908
|
T | A | 16 | a0001c0001t0001g0108a0001c0001t0001g0169a0001c0001t0001g0171others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1780-697A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187908 | ||||||
| chr16:16187912
|
T | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(60): Show | 64 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1780-701A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187912 | ||||||
| chr16:16187950
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1780-739C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187950 | ||||||
| chr16:16187953
|
C | T | 188 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(185): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1780-742G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187953 | ||||||
| chr16:16187957
|
C | T | 3 | a0027c0073t0001g0016a0031c0060t0010g0240a0032c0059t0001g0009 | 3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1780-746G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187957 | ||||||
| chr16:16187974
|
G | A | 51 | a0001c0001t0004g0071a0001c0004t0001g0109a0001c0004t0002g0106others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-763C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16187974 | ||||||
| chr16:16188082
|
CAATA | C | 3 | a0011c0016t0006g0271a0011c0016t0006g0280a0011c0016t0011g0301 | 3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1779+745_1779+748d others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188082 | ||||||
| chr16:16188173
|
G | A | 3 | a0027c0073t0001g0016a0031c0060t0010g0240a0032c0059t0001g0009 | 3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1779+658C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188173 | ||||||
| chr16:16188225
|
C | CA | 122 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1779+605dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188225 | ||||||
| chr16:16188225
|
C | CAA | 10 | a0001c0001t0001g0188a0001c0002t0001g0112a0002c0014t0001g0288others(7): Show | 10 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1779+604_1779+605d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188225 | ||||||
| chr16:16188225
|
C | CAAA | 8 | a0001c0001t0001g0273a0001c0001t0001g0341a0001c0004t0001g0065others(5): Show | 8 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1779+603_1779+605d others(5): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188225 | ||||||
| chr16:16188279
|
C | A | 1 | a0013c0050t0001g0040 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1779+552G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188279 | ||||||
| chr16:16188449
|
C | T | 1 | a0006c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1779+382G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188449 | ||||||
| chr16:16188450
|
G | A | 50 | a0001c0004t0001g0109a0001c0004t0001g0210a0001c0004t0002g0106others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1779+381C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188450 | ||||||
| chr16:16188667
|
G | A | 9 | a0001c0001t0001g0273a0001c0001t0001g0341a0001c0004t0001g0065others(6): Show | 9 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1779+164C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188667 | ||||||
| chr16:16188686
|
C | T | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779+145G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188686 | ||||||
| chr16:16188721
|
C | T | 2 | a0001c0001t0002g0242a0001c0033t0002g0195 | 2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1779+110G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188721 | ||||||
| chr16:16188742
|
C | T | 2 | a0003c0005t0001g0028a0003c0005t0001g0029 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1779+89G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188742 | ||||||
| chr16:16188793
|
C | T | 1 | a0002c0024t0001g0154 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1779+38G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 13/30 | chr16 | 16188793 | ||||||
| chr16:16188984
|
G | A | 2 | a0001c0055t0012g0163a0038c0069t0001g0015 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1636-10C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16188984 | ||||||
| chr16:16189086
|
G | A | 12 | a0001c0001t0001g0233a0001c0001t0001g0305a0001c0055t0012g0163others(9): Show | 12 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1636-112C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189086 | ||||||
| chr16:16189101
|
C | T | 1 | a0001c0072t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1636-127G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189101 | ||||||
| chr16:16189185
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1636-211A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189185 | ||||||
| chr16:16189214
|
C | T | 54 | a0001c0001t0001g0144a0001c0002t0001g0112a0001c0002t0001g0166others(51): Show | 55 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1636-240G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189214 | ||||||
| chr16:16189419
|
C | CT | 8 | a0001c0001t0001g0184a0001c0001t0001g0308a0001c0001t0001g0335others(5): Show | 8 | HG01928.hp2 HG02970.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636-446dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189419 | ||||||
| chr16:16189419
|
CTT | C | 73 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1636-447_1636-446d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189419 | ||||||
| chr16:16189456
|
C | T | 3 | a0027c0073t0001g0016a0031c0060t0010g0240a0032c0059t0001g0009 | 3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1636-482G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189456 | ||||||
| chr16:16189552
|
G | C | 1 | a0002c0003t0001g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1636-578C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189552 | ||||||
| chr16:16189720
|
C | G | 2 | a0001c0004t0001g0006a0011c0016t0001g0275 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1635+444G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189720 | ||||||
| chr16:16189754
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1635+410C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189754 | ||||||
| chr16:16189822
|
G | A | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1635+342C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189822 | ||||||
| chr16:16189910
|
C | A | 3 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1635+254G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189910 | ||||||
| chr16:16189955
|
C | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0305 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1635+209G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16189955 | ||||||
| chr16:16190034
|
C | A | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1635+130G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190034 | ||||||
| chr16:16190035
|
A | C | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1635+129T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190035 | ||||||
| chr16:16190036
|
G | A | 1 | a0001c0028t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1635+128C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190036 | ||||||
| chr16:16190085
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1635+79C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190085 | ||||||
| chr16:16190116
|
G | A | 100 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1635+48C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 12/30 | chr16 | 16190116 | ||||||
| chr16:16190408
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0039others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1432-41A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190408 | ||||||
| chr16:16190415
|
C | T | 336 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(333): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1432-48G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190415 | ||||||
| chr16:16190503
|
C | T | 2 | a0020c0032t0001g0051a0036c0066t0001g0052 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1432-136G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190503 | ||||||
| chr16:16190552
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1432-185C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190552 | ||||||
| chr16:16190573
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1432-206A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190573 | ||||||
| chr16:16190582
|
T | C | 356 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1432-215A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190582 | ||||||
| chr16:16190668
|
T | C | 5 | a0022c0075t0001g0049a0027c0073t0001g0016a0028c0044t0001g0302others(2): Show | 5 | HG00642.hp1 HG02451.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432-301A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190668 | ||||||
| chr16:16190669
|
G | A | 49 | a0001c0001t0001g0303a0001c0004t0001g0109a0001c0004t0001g0162others(46): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1432-302C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190669 | ||||||
| chr16:16190685
|
C | CT | 8 | a0001c0001t0002g0204a0001c0001t0004g0181a0001c0002t0001g0023others(5): Show | 8 | HG01496.hp1 HG03688.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432-319dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190685 | ||||||
| chr16:16190706
|
A | C | 1 | a0003c0007t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1432-339T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190706 | ||||||
| chr16:16190720
|
G | A | 1 | a0001c0002t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1432-353C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190720 | ||||||
| chr16:16190940
|
G | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(14): Show | 17 | HG00597.hp1 HG02040.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1432-573C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190940 | ||||||
| chr16:16190952
|
C | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1432-585G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190952 | ||||||
| chr16:16190971
|
G | A | 3 | a0001c0001t0001g0188a0001c0049t0001g0352a0011c0016t0001g0275 | 3 | HG03139.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1432-604C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16190971 | ||||||
| chr16:16191011
|
G | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0039others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1432-644C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191011 | ||||||
| chr16:16191067
|
C | T | 340 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1432-700G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191067 | ||||||
| chr16:16191083
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1432-716C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191083 | ||||||
| chr16:16191085
|
CG | C | 347 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1432-719delC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191085 | ||||||
| chr16:16191139
|
C | T | 80 | a0001c0001t0001g0144a0001c0001t0001g0303a0001c0002t0001g0112others(77): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1432-772G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191139 | ||||||
| chr16:16191202
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1432-835C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191202 | ||||||
| chr16:16191208
|
T | C | 1 | a0039c0070t0002g0067 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1432-841A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191208 | ||||||
| chr16:16191236
|
T | C | 242 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(239): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1432-869A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191236 | ||||||
| chr16:16191241
|
G | A | 1 | a0033c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432-874C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191241 | ||||||
| chr16:16191265
|
G | A | 3 | a0011c0016t0006g0271a0011c0016t0006g0280a0011c0016t0011g0301 | 3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1432-898C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191265 | ||||||
| chr16:16191288
|
G | A | 240 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0064others(237): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1432-921C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191288 | ||||||
| chr16:16191620
|
T | C | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1431+1210A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191620 | ||||||
| chr16:16191642
|
CCTTTT | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(258): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1431+1183_1431+118 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191642 | ||||||
| chr16:16191703
|
G | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(258): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1431+1127C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191703 | ||||||
| chr16:16191795
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(257): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1431+1035G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191795 | ||||||
| chr16:16191895
|
G | C | 2 | a0001c0001t0002g0204a0001c0002t0001g0093 | 2 | NA18987.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1431+935C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191895 | ||||||
| chr16:16191911
|
G | A | 12 | a0001c0001t0001g0273a0001c0001t0001g0341a0001c0004t0001g0065others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1431+919C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191911 | ||||||
| chr16:16191966
|
G | A | 1 | a0001c0002t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1431+864C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191966 | ||||||
| chr16:16191990
|
G | T | 128 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1431+840C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16191990 | ||||||
| chr16:16192105
|
G | A | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1431+725C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192105 | ||||||
| chr16:16192111
|
A | G | 1 | a0001c0004t0002g0219 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1431+719T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192111 | ||||||
| chr16:16192231
|
G | A | 1 | a0007c0008t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1431+599C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192231 | ||||||
| chr16:16192258
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1431+572T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192258 | ||||||
| chr16:16192373
|
G | C | 1 | a0030c0046t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1431+457C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192373 | ||||||
| chr16:16192444
|
G | A | 1 | a0031c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1431+386C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192444 | ||||||
| chr16:16192505
|
C | T | 353 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1431+325G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192505 | ||||||
| chr16:16192515
|
A | G | 3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1431+315T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192515 | ||||||
| chr16:16192577
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1431+253C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192577 | ||||||
| chr16:16192662
|
G | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1431+168C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192662 | ||||||
| chr16:16192704
|
C | T | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1431+126G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192704 | ||||||
| chr16:16192710
|
A | G | 1 | a0001c0001t0002g0204 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1431+120T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192710 | ||||||
| chr16:16192729
|
C | T | 62 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1431+101G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192729 | ||||||
| chr16:16192743
|
C | T | 1 | a0014c0018t0001g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1431+87G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192743 | ||||||
| chr16:16192757
|
G | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(262): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1431+73C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192757 | ||||||
| chr16:16192807
|
C | T | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1431+23G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 11/30 | chr16 | 16192807 | ||||||
| chr16:16193049
|
T | A | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1339-127A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193049 | ||||||
| chr16:16193057
|
C | T | 2 | a0031c0060t0010g0240a0032c0059t0001g0009 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1339-135G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193057 | ||||||
| chr16:16193096
|
C | T | 1 | a0003c0005t0001g0321 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1339-174G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193096 | ||||||
| chr16:16193154
|
C | T | 1 | a0018c0035t0001g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1339-232G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193154 | ||||||
| chr16:16193227
|
C | T | 82 | a0001c0001t0001g0144a0001c0001t0001g0303a0001c0002t0001g0112others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1339-305G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193227 | ||||||
| chr16:16193250
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1339-328T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193250 | ||||||
| chr16:16193504
|
A | G | 3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1339-582T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193504 | ||||||
| chr16:16193524
|
G | C | 3 | a0011c0016t0006g0271a0011c0016t0006g0280a0011c0016t0011g0301 | 3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1339-602C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193524 | ||||||
| chr16:16193527
|
A | G | 3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1339-605T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193527 | ||||||
| chr16:16193552
|
A | G | 1 | a0006c0009t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1339-630T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193552 | ||||||
| chr16:16193568
|
G | T | 35 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0089others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1339-646C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193568 | ||||||
| chr16:16193646
|
G | A | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1339-724C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193646 | ||||||
| chr16:16193680
|
C | T | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1339-758G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193680 | ||||||
| chr16:16193690
|
G | C | 3 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0091 | 3 | HG02280.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1339-768C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193690 | ||||||
| chr16:16193756
|
G | T | 2 | a0005c0048t0001g0063a0038c0069t0001g0015 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1339-834C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193756 | ||||||
| chr16:16193762
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-840T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193762 | ||||||
| chr16:16193782
|
C | T | 3 | a0001c0001t0001g0159a0010c0029t0001g0158a0010c0029t0001g0230 | 3 | HG01069.hp2 HG01175.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1339-860G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16193782 | ||||||
| chr16:16194015
|
G | A | 1 | a0003c0005t0001g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1339-1093C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194015 | ||||||
| chr16:16194136
|
T | A | 2 | a0001c0001t0002g0094a0001c0001t0002g0311 | 2 | NA18959.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1339-1214A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194136 | ||||||
| chr16:16194188
|
C | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1266G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194188 | ||||||
| chr16:16194338
|
A | C | 6 | a0001c0055t0012g0163a0013c0020t0001g0055a0013c0020t0001g0056others(3): Show | 6 | HG02559.hp1 HG02897.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339-1416T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194338 | ||||||
| chr16:16194397
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1339-1475C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194397 | ||||||
| chr16:16194397
|
G | T | 81 | a0001c0001t0001g0144a0001c0001t0001g0303a0001c0002t0001g0112others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1339-1475C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194397 | ||||||
| chr16:16194499
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(276): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1339-1577C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194499 | ||||||
| chr16:16194518
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1596C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194518 | ||||||
| chr16:16194528
|
G | A | 1 | a0001c0002t0001g0287 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1339-1606C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194528 | ||||||
| chr16:16194535
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1339-1613C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194535 | ||||||
| chr16:16194696
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1774C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194696 | ||||||
| chr16:16194764
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 128 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1339-1842G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194764 | ||||||
| chr16:16194797
|
G | T | 1 | a0043c0040t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1339-1875C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194797 | ||||||
| chr16:16194809
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1339-1887A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194809 | ||||||
| chr16:16194830
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1339-1908T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194830 | ||||||
| chr16:16194889
|
A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1339-1967T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194889 | ||||||
| chr16:16194899
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-1977G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194899 | ||||||
| chr16:16194953
|
T | TACAGGTT others(6): Show |
1 | a0001c0004t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1339-2044_1339-203 others(17): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194953 | ||||||
| chr16:16194993
|
T | C | 6 | a0001c0055t0012g0163a0013c0020t0001g0055a0013c0020t0001g0056others(3): Show | 6 | HG02559.hp1 HG02897.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339-2071A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16194993 | ||||||
| chr16:16195035
|
G | A | 1 | a0002c0003t0001g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1339-2113C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195035 | ||||||
| chr16:16195047
|
C | G | 1 | a0005c0031t0001g0349 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1339-2125G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195047 | ||||||
| chr16:16195147
|
A | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-2225T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195147 | ||||||
| chr16:16195200
|
A | G | 1 | a0031c0060t0010g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1339-2278T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195200 | ||||||
| chr16:16195234
|
G | A | 2 | a0022c0075t0001g0049a0028c0044t0001g0302 | 2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1339-2312C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195234 | ||||||
| chr16:16195242
|
A | T | 41 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1339-2320T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195242 | ||||||
| chr16:16195269
|
G | A | 2 | a0003c0021t0001g0011a0003c0021t0001g0012 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1339-2347C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195269 | ||||||
| chr16:16195269
|
G | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-2347C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195269 | ||||||
| chr16:16195282
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1339-2360T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195282 | ||||||
| chr16:16195303
|
A | AT | 41 | a0001c0001t0001g0069a0001c0001t0001g0184a0001c0001t0001g0201others(38): Show | 41 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1339-2382dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | ||||||
| chr16:16195303
|
AT | A | 49 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0064others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1339-2382delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | ||||||
| chr16:16195303
|
ATT | A | 7 | a0001c0001t0001g0165a0001c0001t0001g0182a0001c0001t0002g0087others(4): Show | 7 | HG02071.hp2 NA18906.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339-2383_1339-238 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | ||||||
| chr16:16195303
|
ATTTTT | A | 8 | a0001c0001t0001g0191a0001c0001t0001g0335a0001c0001t0004g0223others(5): Show | 8 | HG01928.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1339-2386_1339-238 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | ||||||
| chr16:16195303
|
ATTTTTT | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0108others(114): Show | 117 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1339-2387_1339-238 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195303 | ||||||
| chr16:16195405
|
C | T | 32 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0108others(29): Show | 32 | HG00597.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1339-2483G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195405 | ||||||
| chr16:16195422
|
C | T | 1 | a0001c0033t0001g0070 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1339-2500G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195422 | ||||||
| chr16:16195496
|
A | G | 5 | a0001c0004t0001g0065a0014c0018t0001g0249a0014c0018t0001g0250others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+2525T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195496 | ||||||
| chr16:16195559
|
G | T | 1 | a0033c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1338+2462C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195559 | ||||||
| chr16:16195675
|
T | C | 125 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1338+2346A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195675 | ||||||
| chr16:16195839
|
T | C | 125 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1338+2182A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195839 | ||||||
| chr16:16195887
|
T | C | 1 | a0020c0032t0001g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1338+2134A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195887 | ||||||
| chr16:16195988
|
T | C | 1 | a0033c0054t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1338+2033A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16195988 | ||||||
| chr16:16196073
|
T | C | 136 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(133): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1338+1948A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196073 | ||||||
| chr16:16196083
|
G | A | 62 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1338+1938C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196083 | ||||||
| chr16:16196155
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0142 | 2 | HG02135.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1338+1866T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196155 | ||||||
| chr16:16196158
|
C | T | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1338+1863G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196158 | ||||||
| chr16:16196209
|
C | CA | 84 | a0001c0001t0001g0205a0001c0001t0001g0303a0001c0002t0001g0112others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1338+1811dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | ||||||
| chr16:16196209
|
C | CAA | 87 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0069others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1338+1810_1338+181 others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | ||||||
| chr16:16196209
|
C | CAAAA | 60 | a0001c0001t0001g0126a0001c0001t0001g0144a0001c0001t0001g0172others(57): Show | 60 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1338+1808_1338+181 others(8): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | ||||||
| chr16:16196209
|
C | CAAAAA | 35 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0108others(32): Show | 35 | HG00597.hp1 HG00673.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.1338+1807_1338+181 others(9): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | ||||||
| chr16:16196209
|
C | CAAAAAA | 41 | a0001c0001t0001g0003a0001c0001t0001g0135a0001c0001t0001g0136others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1338+1806_1338+181 others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | ||||||
| chr16:16196209
|
CA | C | 9 | a0004c0010t0001g0073a0004c0010t0001g0075a0011c0016t0006g0271others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338+1811delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196209 | ||||||
| chr16:16196234
|
A | T | 2 | a0004c0010t0001g0042a0004c0010t0001g0043 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1338+1787T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196234 | ||||||
| chr16:16196245
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1338+1776G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196245 | ||||||
| chr16:16196330
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(139): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1338+1691T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196330 | ||||||
| chr16:16196385
|
A | G | 55 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1338+1636T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196385 | ||||||
| chr16:16196473
|
G | A | 43 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1338+1548C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196473 | ||||||
| chr16:16196484
|
C | G | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1338+1537G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196484 | ||||||
| chr16:16196486
|
C | T | 55 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0086others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1338+1535G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196486 | ||||||
| chr16:16196489
|
C | T | 3 | a0011c0016t0006g0271a0011c0016t0006g0280a0011c0016t0011g0301 | 3 | HG01496.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1338+1532G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196489 | ||||||
| chr16:16196520
|
C | T | 242 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1338+1501G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196520 | ||||||
| chr16:16196638
|
A | G | 285 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1338+1383T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196638 | ||||||
| chr16:16196678
|
G | A | 13 | a0001c0001t0001g0235a0001c0001t0001g0247a0001c0001t0001g0313others(10): Show | 13 | HG00408.hp2 HG00544.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1338+1343C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196678 | ||||||
| chr16:16196679
|
A | G | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1338+1342T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196679 | ||||||
| chr16:16196801
|
A | G | 1 | a0013c0020t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1338+1220T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196801 | ||||||
| chr16:16196938
|
C | T | 1 | a0006c0009t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1338+1083G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16196938 | ||||||
| chr16:16197011
|
A | T | 252 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(249): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1338+1010T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197011 | ||||||
| chr16:16197012
|
A | T | 1 | a0003c0005t0001g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1338+1009T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197012 | ||||||
| chr16:16197030
|
C | T | 1 | a0002c0057t0001g0255 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1338+991G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197030 | ||||||
| chr16:16197242
|
A | G | 103 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(100): Show | 103 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1338+779T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197242 | ||||||
| chr16:16197334
|
G | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(10): Show | 13 | HG02040.hp1 HG02056.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1338+687C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197334 | ||||||
| chr16:16197387
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1338+634T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197387 | ||||||
| chr16:16197443
|
G | A | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1338+578C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197443 | ||||||
| chr16:16197563
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0069others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1338+458C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197563 | ||||||
| chr16:16197658
|
C | T | 1 | a0002c0013t0001g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1338+363G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197658 | ||||||
| chr16:16197721
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1338+300C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197721 | ||||||
| chr16:16197770
|
G | A | 201 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1338+251C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197770 | ||||||
| chr16:16197861
|
C | T | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+160G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197861 | ||||||
| chr16:16197942
|
G | A | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+79C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197942 | ||||||
| chr16:16197959
|
G | C | 65 | a0001c0001t0001g0064a0001c0001t0001g0079a0001c0001t0001g0082others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1338+62C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16197959 | ||||||
| chr16:16198001
|
G | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1338+20C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16198001 | ||||||
| chr16:16198014
|
G | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
splice_region_variant&intron_variant | LOW | c.1338+7C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 10/30 | chr16 | 16198014 | ||||||
| chr16:16198211
|
A | C | 1 | a0001c0001t0001g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1177-29T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198211 | ||||||
| chr16:16198223
|
C | T | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1177-41G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198223 | ||||||
| chr16:16198271
|
C | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1177-89G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198271 | ||||||
| chr16:16198276
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1177-94T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198276 | ||||||
| chr16:16198343
|
G | C | 2 | a0001c0001t0002g0161a0039c0070t0002g0067 | 2 | NA18943.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1177-161C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198343 | ||||||
| chr16:16198466
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1177-284C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198466 | ||||||
| chr16:16198486
|
A | G | 1 | a0001c0002t0001g0137 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1177-304T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198486 | ||||||
| chr16:16198633
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-451C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198633 | ||||||
| chr16:16198659
|
C | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-477G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198659 | ||||||
| chr16:16198661
|
C | T | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1177-479G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198661 | ||||||
| chr16:16198721
|
C | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-539G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198721 | ||||||
| chr16:16198721
|
C | G | 1 | a0028c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1177-539G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198721 | ||||||
| chr16:16198721
|
C | T | 1 | a0004c0017t0001g0192 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1177-539G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198721 | ||||||
| chr16:16198733
|
T | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(116): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1177-551A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198733 | ||||||
| chr16:16198736
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-554T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198736 | ||||||
| chr16:16198739
|
A | T | 1 | a0003c0007t0001g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1177-557T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198739 | ||||||
| chr16:16198747
|
A | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG00673.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1177-565T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198747 | ||||||
| chr16:16198850
|
T | C | 356 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1177-668A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198850 | ||||||
| chr16:16198851
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(48): Show | 51 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1177-669C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198851 | ||||||
| chr16:16198909
|
G | T | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1177-727C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198909 | ||||||
| chr16:16198962
|
C | G | 1 | a0004c0017t0001g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1177-780G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198962 | ||||||
| chr16:16198999
|
G | GAA | 58 | a0001c0001t0001g0188a0001c0002t0001g0025a0001c0002t0001g0026others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1177-818_1177-817i others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198999 | ||||||
| chr16:16198999
|
G | GAC | 54 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(51): Show | 54 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1177-818_1177-817i others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16198999 | ||||||
| chr16:16199000
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1177-818C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199000 | ||||||
| chr16:16199000
|
G | GA | 171 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(168): Show | 171 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1177-819dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199000 | ||||||
| chr16:16199013
|
A | T | 1 | a0001c0004t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1177-831T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199013 | ||||||
| chr16:16199037
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1177-855C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199037 | ||||||
| chr16:16199048
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-866A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199048 | ||||||
| chr16:16199055
|
C | A | 1 | a0001c0001t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1177-873G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199055 | ||||||
| chr16:16199125
|
G | A | 1 | a0002c0003t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1177-943C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199125 | ||||||
| chr16:16199281
|
G | GA | 5 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0239others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-1100dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199281 | ||||||
| chr16:16199298
|
C | T | 1 | a0001c0002t0001g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1177-1116G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199298 | ||||||
| chr16:16199299
|
G | T | 3 | a0015c0019t0001g0122a0015c0019t0001g0124a0015c0019t0001g0125 | 3 | HG02451.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1177-1117C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199299 | ||||||
| chr16:16199333
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1151A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199333 | ||||||
| chr16:16199350
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1168A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199350 | ||||||
| chr16:16199401
|
T | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1219A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199401 | ||||||
| chr16:16199431
|
G | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1249C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199431 | ||||||
| chr16:16199459
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1277A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199459 | ||||||
| chr16:16199560
|
A | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1177-1378T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199560 | ||||||
| chr16:16199567
|
C | T | 1 | a0001c0002t0001g0156 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1177-1385G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199567 | ||||||
| chr16:16199592
|
T | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1410A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199592 | ||||||
| chr16:16199623
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1441A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199623 | ||||||
| chr16:16199659
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1477A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199659 | ||||||
| chr16:16199735
|
C | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1553G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199735 | ||||||
| chr16:16199948
|
A | T | 1 | a0001c0004t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1177-1766T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199948 | ||||||
| chr16:16199958
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1776A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199958 | ||||||
| chr16:16199982
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1800A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199982 | ||||||
| chr16:16199983
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177-1801C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16199983 | ||||||
| chr16:16200099
|
A | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1176+1902T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200099 | ||||||
| chr16:16200124
|
G | C | 3 | a0001c0004t0001g0263a0001c0072t0001g0356a0002c0024t0001g0152 | 3 | HG01175.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1176+1877C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200124 | ||||||
| chr16:16200159
|
C | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339others(1): Show | 4 | HG02559.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+1842G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200159 | ||||||
| chr16:16200169
|
T | C | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1176+1832A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200169 | ||||||
| chr16:16200216
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1176+1785C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200216 | ||||||
| chr16:16200253
|
A | G | 1 | a0001c0004t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1176+1748T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200253 | ||||||
| chr16:16200286
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1176+1715C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200286 | ||||||
| chr16:16200297
|
C | G | 1 | a0003c0005t0001g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1176+1704G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200297 | ||||||
| chr16:16200299
|
C | T | 2 | a0001c0002t0001g0222a0001c0002t0001g0354 | 2 | HG00597.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1176+1702G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200299 | ||||||
| chr16:16200360
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1641G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200360 | ||||||
| chr16:16200387
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1614G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200387 | ||||||
| chr16:16200429
|
G | GA | 23 | a0001c0001t0001g0089a0001c0001t0001g0108a0001c0001t0001g0184others(20): Show | 23 | HG00323.hp2 HG00438.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1176+1571dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200429 | ||||||
| chr16:16200429
|
GA | G | 13 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339others(10): Show | 13 | HG01069.hp1 HG01515.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1176+1571delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200429 | ||||||
| chr16:16200473
|
T | C | 1 | a0001c0004t0001g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1176+1528A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200473 | ||||||
| chr16:16200511
|
T | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1490A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200511 | ||||||
| chr16:16200537
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1464C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200537 | ||||||
| chr16:16200552
|
G | A | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+1449C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200552 | ||||||
| chr16:16200608
|
T | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0064others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1176+1393A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200608 | ||||||
| chr16:16200644
|
T | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1176+1357A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200644 | ||||||
| chr16:16200662
|
A | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1176+1339T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200662 | ||||||
| chr16:16200684
|
G | A | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+1317C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200684 | ||||||
| chr16:16200704
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1297G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200704 | ||||||
| chr16:16200763
|
A | G | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1176+1238T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200763 | ||||||
| chr16:16200764
|
C | T | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+1237G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200764 | ||||||
| chr16:16200829
|
C | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1172G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200829 | ||||||
| chr16:16200853
|
A | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1148T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200853 | ||||||
| chr16:16200858
|
C | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0127others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1176+1143G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200858 | ||||||
| chr16:16200858
|
C | T | 1 | a0017c0034t0001g0001 | 2 | NA18943.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1176+1143G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200858 | ||||||
| chr16:16200885
|
G | A | 7 | a0001c0001t0001g0273a0001c0001t0001g0341a0001c0002t0001g0014others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1176+1116C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16200885 | ||||||
| chr16:16201027
|
C | T | 1 | a0028c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1176+974G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201027 | ||||||
| chr16:16201060
|
G | A | 1 | a0001c0001t0002g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1176+941C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201060 | ||||||
| chr16:16201210
|
G | A | 1 | a0012c0030t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1176+791C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201210 | ||||||
| chr16:16201758
|
G | A | 123 | a0001c0001t0001g0039a0001c0001t0001g0064a0001c0001t0001g0069others(120): Show | 123 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1176+243C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 9/30 | chr16 | 16201758 | ||||||
| chr16:16202258
|
ATGTGGAG others(26): Show |
A | 1 | a0001c0001t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.999-113_999-81delC others(32): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202258 | ||||||
| chr16:16202435
|
T | C | 5 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0172others(2): Show | 5 | HG03491.hp1 HG03492.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-257A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202435 | ||||||
| chr16:16202447
|
G | C | 1 | a0001c0006t0001g0189 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.999-269C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202447 | ||||||
| chr16:16202509
|
C | T | 2 | a0001c0006t0001g0329a0004c0017t0001g0076 | 2 | HG00597.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.999-331G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202509 | ||||||
| chr16:16202568
|
A | AC | 176 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(173): Show | 177 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.999-391_999-390ins others(1): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202568 | ||||||
| chr16:16202573
|
G | T | 1 | a0003c0005t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.999-395C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202573 | ||||||
| chr16:16202603
|
C | T | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.999-425G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202603 | ||||||
| chr16:16202631
|
G | A | 154 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(151): Show | 155 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.999-453C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202631 | ||||||
| chr16:16202930
|
C | T | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.998+480G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16202930 | ||||||
| chr16:16203101
|
C | T | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.998+309G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203101 | ||||||
| chr16:16203114
|
C | T | 1 | a0002c0003t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.998+296G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203114 | ||||||
| chr16:16203212
|
T | C | 1 | a0001c0049t0001g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.998+198A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203212 | ||||||
| chr16:16203311
|
C | T | 63 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0086others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.998+99G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 8/30 | chr16 | 16203311 | ||||||
| chr16:16203938
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.795-325T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16203938 | ||||||
| chr16:16204095
|
C | T | 1 | a0025c0053t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.795-482G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204095 | ||||||
| chr16:16204132
|
C | T | 1 | a0002c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.795-519G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204132 | ||||||
| chr16:16204347
|
C | T | 1 | a0009c0015t0001g0327 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.795-734G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204347 | ||||||
| chr16:16204352
|
G | A | 67 | a0001c0001t0001g0273a0001c0001t0001g0281a0001c0001t0001g0303others(64): Show | 67 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.795-739C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204352 | ||||||
| chr16:16204366
|
T | C | 1 | a0002c0024t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.795-753A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204366 | ||||||
| chr16:16204391
|
T | A | 1 | a0001c0004t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.795-778A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204391 | ||||||
| chr16:16204398
|
A | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339others(1): Show | 4 | HG02559.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-785T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204398 | ||||||
| chr16:16204431
|
G | T | 51 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0086others(48): Show | 52 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.795-818C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204431 | ||||||
| chr16:16204434
|
A | T | 3 | a0008c0011t0003g0058a0008c0011t0003g0059a0008c0011t0003g0091 | 3 | HG02280.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.795-821T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204434 | ||||||
| chr16:16204703
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.795-1090C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204703 | ||||||
| chr16:16204723
|
C | T | 1 | a0001c0002t0001g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.795-1110G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204723 | ||||||
| chr16:16204837
|
C | CT | 61 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0086others(58): Show | 62 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.795-1225dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204837 | ||||||
| chr16:16204865
|
C | T | 4 | a0014c0018t0001g0249a0014c0018t0001g0250a0014c0018t0001g0251others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-1252G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204865 | ||||||
| chr16:16204896
|
A | G | 2 | a0001c0001t0001g0273a0012c0030t0001g0274 | 2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-1283T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16204896 | ||||||
| chr16:16205009
|
T | C | 1 | a0001c0067t0001g0351 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.795-1396A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205009 | ||||||
| chr16:16205062
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1449G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205062 | ||||||
| chr16:16205085
|
C | T | 7 | a0001c0004t0001g0162a0001c0004t0001g0217a0001c0004t0001g0220others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-1472G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205085 | ||||||
| chr16:16205118
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.795-1505C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205118 | ||||||
| chr16:16205131
|
C | T | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.795-1518G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205131 | ||||||
| chr16:16205174
|
C | T | 4 | a0002c0024t0001g0154a0015c0019t0001g0122a0015c0019t0001g0124others(1): Show | 4 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-1561G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205174 | ||||||
| chr16:16205291
|
T | C | 6 | a0001c0001t0001g0200a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | HG02074.hp2 NA18612.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.795-1678A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205291 | ||||||
| chr16:16205376
|
A | T | 1 | a0021c0079t0001g0238 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.795-1763T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205376 | ||||||
| chr16:16205444
|
G | GA | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1832dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205444 | ||||||
| chr16:16205474
|
AC | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1862delG | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205474 | ||||||
| chr16:16205747
|
A | G | 1 | a0001c0006t0001g0299 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.795-2134T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205747 | ||||||
| chr16:16205751
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-2138C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205751 | ||||||
| chr16:16205898
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(24): Show | 27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.795-2285A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205898 | ||||||
| chr16:16205905
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(24): Show | 27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.795-2292T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16205905 | ||||||
| chr16:16206092
|
C | T | 1 | a0028c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.795-2479G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206092 | ||||||
| chr16:16206347
|
G | A | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+2381C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206347 | ||||||
| chr16:16206395
|
C | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(13): Show | 16 | HG00733.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.794+2333G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206395 | ||||||
| chr16:16206466
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+2262G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206466 | ||||||
| chr16:16206499
|
T | C | 1 | a0001c0055t0012g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.794+2229A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206499 | ||||||
| chr16:16206500
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+2228C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206500 | ||||||
| chr16:16206503
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.794+2225G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206503 | ||||||
| chr16:16206609
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.794+2119C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206609 | ||||||
| chr16:16206625
|
G | A | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.794+2103C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206625 | ||||||
| chr16:16206884
|
C | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(24): Show | 27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.794+1844G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16206884 | ||||||
| chr16:16207101
|
C | T | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.794+1627G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207101 | ||||||
| chr16:16207233
|
T | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0009c0015t0001g0327 | 3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.794+1495A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207233 | ||||||
| chr16:16207375
|
T | C | 11 | a0001c0001t0001g0064a0001c0004t0001g0065a0005c0048t0001g0063others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+1353A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207375 | ||||||
| chr16:16207411
|
G | A | 1 | a0025c0053t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.794+1317C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207411 | ||||||
| chr16:16207618
|
C | T | 1 | a0004c0010t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.794+1110G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207618 | ||||||
| chr16:16207673
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(24): Show | 27 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.794+1055T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207673 | ||||||
| chr16:16207901
|
T | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+827A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16207901 | ||||||
| chr16:16208056
|
T | C | 1 | a0002c0074t0001g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.794+672A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208056 | ||||||
| chr16:16208183
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.794+545G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208183 | ||||||
| chr16:16208192
|
C | T | 1 | a0001c0006t0001g0296 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.794+536G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208192 | ||||||
| chr16:16208229
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.794+499T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208229 | ||||||
| chr16:16208296
|
C | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG01074.hp2 HG01099.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.794+432G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208296 | ||||||
| chr16:16208297
|
G | A | 3 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.794+431C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208297 | ||||||
| chr16:16208342
|
TTTTTTG | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(7): Show | 10 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.794+380_794+385del others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208342 | ||||||
| chr16:16208379
|
G | GT | 8 | a0001c0001t0001g0165a0001c0001t0001g0247a0001c0001t0001g0346others(5): Show | 8 | HG01256.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.794+348dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208379 | ||||||
| chr16:16208379
|
GT | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+348delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208379 | ||||||
| chr16:16208408
|
T | C | 2 | a0001c0001t0001g0325a0001c0064t0005g0324 | 2 | NA18977.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.794+320A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208408 | ||||||
| chr16:16208447
|
A | G | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+281T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208447 | ||||||
| chr16:16208546
|
C | G | 11 | a0001c0001t0001g0064a0001c0004t0001g0065a0005c0048t0001g0063others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+182G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208546 | ||||||
| chr16:16208547
|
T | C | 11 | a0001c0001t0001g0064a0001c0004t0001g0065a0005c0048t0001g0063others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+181A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208547 | ||||||
| chr16:16208574
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+154T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208574 | ||||||
| chr16:16208615
|
G | A | 1 | a0003c0005t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794+113C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208615 | ||||||
| chr16:16208618
|
T | A | 1 | a0001c0043t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.794+110A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208618 | ||||||
| chr16:16208652
|
G | A | 4 | a0002c0024t0001g0154a0015c0019t0001g0122a0015c0019t0001g0124others(1): Show | 4 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+76C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 7/30 | chr16 | 16208652 | ||||||
| chr16:16208862
|
G | A | 2 | a0002c0003t0001g0186a0002c0003t0001g0187 | 2 | HG01884.hp2 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.663-3C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16208862 | ||||||
| chr16:16208960
|
T | C | 1 | a0002c0003t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.663-101A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16208960 | ||||||
| chr16:16208965
|
G | C | 1 | a0002c0003t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.663-106C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16208965 | ||||||
| chr16:16209097
|
T | C | 1 | a0001c0001t0004g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.663-238A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209097 | ||||||
| chr16:16209544
|
G | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(7): Show | 10 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.663-685C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209544 | ||||||
| chr16:16209557
|
A | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-698T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209557 | ||||||
| chr16:16209591
|
CT | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-733delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209591 | ||||||
| chr16:16209602
|
T | A | 1 | a0003c0007t0001g0110 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.663-743A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209602 | ||||||
| chr16:16209621
|
T | G | 15 | a0001c0001t0001g0064a0001c0004t0001g0065a0005c0048t0001g0063others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.663-762A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209621 | ||||||
| chr16:16209644
|
C | A | 7 | a0001c0006t0001g0278a0001c0006t0001g0296a0001c0006t0001g0297others(4): Show | 7 | HG00544.hp1 HG02074.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.663-785G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209644 | ||||||
| chr16:16209664
|
T | C | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.663-805A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209664 | ||||||
| chr16:16209706
|
C | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-847G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209706 | ||||||
| chr16:16209706
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.663-847G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209706 | ||||||
| chr16:16209713
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.663-854G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209713 | ||||||
| chr16:16209799
|
C | T | 3 | a0042c0039t0001g0032a0043c0040t0001g0031a0044c0038t0001g0033 | 3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.663-940G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209799 | ||||||
| chr16:16209804
|
C | T | 1 | a0001c0006t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.663-945G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209804 | ||||||
| chr16:16209820
|
T | A | 1 | a0001c0002t0001g0156 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.663-961A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209820 | ||||||
| chr16:16209927
|
C | T | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.663-1068G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16209927 | ||||||
| chr16:16210119
|
C | G | 1 | a0003c0007t0001g0098 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.663-1260G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210119 | ||||||
| chr16:16210267
|
A | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-1408T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210267 | ||||||
| chr16:16210340
|
TTGGTCAG others(2): Show |
T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.663-1490_663-1482d others(11): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210340 | ||||||
| chr16:16210467
|
C | T | 3 | a0042c0039t0001g0032a0043c0040t0001g0031a0044c0038t0001g0033 | 3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.663-1608G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210467 | ||||||
| chr16:16210528
|
A | G | 1 | a0003c0005t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.662+1657T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210528 | ||||||
| chr16:16210534
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1651C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210534 | ||||||
| chr16:16210557
|
A | G | 1 | a0030c0046t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.662+1628T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210557 | ||||||
| chr16:16210736
|
C | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.662+1449G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210736 | ||||||
| chr16:16210753
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1432A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210753 | ||||||
| chr16:16210864
|
G | T | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.662+1321C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210864 | ||||||
| chr16:16210904
|
G | T | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662+1281C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210904 | ||||||
| chr16:16210909
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.662+1276G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210909 | ||||||
| chr16:16210910
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1275C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210910 | ||||||
| chr16:16210984
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1201C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16210984 | ||||||
| chr16:16211085
|
A | T | 1 | a0012c0030t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662+1100T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211085 | ||||||
| chr16:16211095
|
C | CA | 73 | a0001c0001t0001g0069a0001c0001t0001g0159a0001c0001t0001g0160others(70): Show | 73 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.662+1089dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211095 | ||||||
| chr16:16211095
|
CAA | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+1088_662+1089d others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211095 | ||||||
| chr16:16211164
|
A | G | 1 | a0001c0004t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.662+1021T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211164 | ||||||
| chr16:16211200
|
C | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+985G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211200 | ||||||
| chr16:16211241
|
A | C | 1 | a0001c0006t0009g0285 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.662+944T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211241 | ||||||
| chr16:16211354
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.662+831A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211354 | ||||||
| chr16:16211388
|
C | T | 1 | a0005c0031t0001g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.662+797G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211388 | ||||||
| chr16:16211473
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+712G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211473 | ||||||
| chr16:16211498
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+687T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211498 | ||||||
| chr16:16211782
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+403T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211782 | ||||||
| chr16:16211880
|
A | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+305T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211880 | ||||||
| chr16:16211887
|
G | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+298C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211887 | ||||||
| chr16:16211939
|
G | A | 1 | a0007c0008t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.662+246C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211939 | ||||||
| chr16:16211975
|
G | A | 4 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339others(1): Show | 4 | HG02559.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+210C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16211975 | ||||||
| chr16:16212067
|
G | A | 1 | a0001c0006t0001g0189 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.662+118C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212067 | ||||||
| chr16:16212071
|
A | G | 156 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(153): Show | 157 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.662+114T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212071 | ||||||
| chr16:16212150
|
G | T | 1 | a0002c0014t0001g0284 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.662+35C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212150 | ||||||
| chr16:16212173
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.662+12C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 6/30 | chr16 | 16212173 | ||||||
| chr16:16212288
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-42C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212288 | ||||||
| chr16:16212328
|
A | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0009c0015t0001g0327 | 3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.601-82T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212328 | ||||||
| chr16:16212335
|
G | T | 57 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0086others(54): Show | 58 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.601-89C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212335 | ||||||
| chr16:16212340
|
G | A | 1 | a0014c0018t0001g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.601-94C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212340 | ||||||
| chr16:16212366
|
C | T | 1 | a0014c0018t0001g0249 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.601-120G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212366 | ||||||
| chr16:16212457
|
C | T | 6 | a0001c0001t0001g0200a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | HG02074.hp2 NA18612.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-211G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212457 | ||||||
| chr16:16212518
|
C | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-272G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212518 | ||||||
| chr16:16212590
|
A | G | 15 | a0001c0001t0001g0064a0001c0004t0001g0065a0005c0048t0001g0063others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-344T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212590 | ||||||
| chr16:16212615
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.601-369C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212615 | ||||||
| chr16:16212706
|
G | A | 3 | a0003c0005t0001g0028a0003c0005t0001g0029a0005c0012t0001g0027 | 3 | HG01515.hp1 HG01517.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.601-460C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212706 | ||||||
| chr16:16212754
|
A | C | 5 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339others(2): Show | 5 | HG02559.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-508T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212754 | ||||||
| chr16:16212899
|
G | A | 1 | a0001c0002t0001g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.601-653C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16212899 | ||||||
| chr16:16213082
|
A | AT | 9 | a0001c0001t0001g0247a0001c0002t0001g0131a0002c0003t0001g0013others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-837dupA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213082 | ||||||
| chr16:16213082
|
A | ATT | 55 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0086others(52): Show | 56 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.601-838_601-837dup others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213082 | ||||||
| chr16:16213082
|
AT | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(11): Show | 14 | HG01074.hp2 HG01257.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-837delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213082 | ||||||
| chr16:16213096
|
T | C | 1 | a0002c0022t0001g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.601-850A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213096 | ||||||
| chr16:16213141
|
A | G | 1 | a0007c0008t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601-895T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213141 | ||||||
| chr16:16213188
|
A | C | 1 | a0001c0002t0001g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601-942T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213188 | ||||||
| chr16:16213201
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.601-955A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213201 | ||||||
| chr16:16213476
|
C | G | 1 | a0001c0004t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.600+848G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213476 | ||||||
| chr16:16213558
|
CT | C | 328 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.600+765delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213558 | ||||||
| chr16:16213558
|
CTT | C | 9 | a0001c0001t0001g0190a0001c0006t0001g0300a0003c0005t0001g0282others(6): Show | 9 | HG02040.hp1 HG02559.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+764_600+765del others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213558 | ||||||
| chr16:16213589
|
C | A | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+735G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213589 | ||||||
| chr16:16213603
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+721G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213603 | ||||||
| chr16:16213607
|
C | A | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.600+717G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213607 | ||||||
| chr16:16213686
|
G | A | 1 | a0028c0044t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.600+638C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213686 | ||||||
| chr16:16213933
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.600+391G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16213933 | ||||||
| chr16:16214103
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.600+221C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214103 | ||||||
| chr16:16214143
|
G | A | 1 | a0001c0001t0001g0348 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.600+181C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214143 | ||||||
| chr16:16214210
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+114C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214210 | ||||||
| chr16:16214259
|
G | C | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+65C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 5/30 | chr16 | 16214259 | ||||||
| chr16:16214488
|
A | T | 1 | a0002c0068t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.475-39T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214488 | ||||||
| chr16:16214494
|
G | A | 56 | a0001c0001t0001g0281a0001c0001t0001g0303a0001c0001t0001g0308others(53): Show | 56 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.475-45C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214494 | ||||||
| chr16:16214778
|
T | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-329A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214778 | ||||||
| chr16:16214818
|
C | T | 51 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0086others(48): Show | 52 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.475-369G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214818 | ||||||
| chr16:16214950
|
A | G | 2 | a0001c0002t0001g0117a0006c0009t0001g0116 | 2 | NA18951.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.475-501T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16214950 | ||||||
| chr16:16215098
|
C | T | 1 | a0002c0003t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475-649G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215098 | ||||||
| chr16:16215137
|
T | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.475-688A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215137 | ||||||
| chr16:16215438
|
G | GGT | 36 | a0001c0001t0001g0003a0001c0001t0002g0092a0001c0001t0002g0094others(33): Show | 37 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.475-991_475-990dup others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | ||||||
| chr16:16215438
|
G | GGTGT | 8 | a0001c0001t0002g0204a0001c0002t0001g0014a0003c0005t0005g0213others(5): Show | 8 | HG00733.hp1 HG02559.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-993_475-990dup others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | ||||||
| chr16:16215438
|
GGT | G | 153 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0064others(150): Show | 153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.475-991_475-990del others(2): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | ||||||
| chr16:16215438
|
GGTGT | G | 32 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0191others(29): Show | 32 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.475-993_475-990del others(4): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | ||||||
| chr16:16215438
|
GGTGTGT | G | 6 | a0001c0004t0001g0263a0001c0049t0001g0352a0001c0067t0001g0351others(3): Show | 6 | HG01123.hp2 HG01175.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-995_475-990del others(6): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | ||||||
| chr16:16215438
|
GGTGTGTG others(3): Show |
G | 1 | a0002c0014t0001g0331 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.475-999_475-990del others(10): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215438 | ||||||
| chr16:16215444
|
T | G | 2 | a0001c0006t0001g0299a0001c0006t0001g0300 | 2 | NA18941.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.475-995A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215444 | ||||||
| chr16:16215478
|
CT | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(23): Show | 26 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.475-1030delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215478 | ||||||
| chr16:16215549
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-1100G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215549 | ||||||
| chr16:16215590
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-1141A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215590 | ||||||
| chr16:16215910
|
T | C | 1 | a0002c0003t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.475-1461A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215910 | ||||||
| chr16:16215950
|
C | T | 4 | a0013c0020t0001g0055a0013c0020t0001g0056a0013c0020t0001g0057others(1): Show | 4 | HG02559.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1501G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16215950 | ||||||
| chr16:16216069
|
G | A | 1 | a0001c0004t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.475-1620C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216069 | ||||||
| chr16:16216076
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0115 | 2 | NA18963.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.475-1627G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216076 | ||||||
| chr16:16216260
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.475-1811A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216260 | ||||||
| chr16:16216270
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-1821G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216270 | ||||||
| chr16:16216339
|
C | T | 1 | a0002c0022t0001g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.475-1890G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216339 | ||||||
| chr16:16216437
|
G | T | 71 | a0001c0001t0001g0273a0001c0001t0001g0281a0001c0001t0001g0303others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.475-1988C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216437 | ||||||
| chr16:16216504
|
A | G | 4 | a0013c0020t0001g0055a0013c0020t0001g0056a0013c0020t0001g0057others(1): Show | 4 | HG02559.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2055T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216504 | ||||||
| chr16:16216638
|
C | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-2189G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216638 | ||||||
| chr16:16216810
|
A | C | 2 | a0002c0003t0001g0013a0012c0030t0001g0113 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.475-2361T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16216810 | ||||||
| chr16:16217045
|
A | G | 3 | a0001c0002t0001g0112a0004c0010t0001g0042a0004c0010t0001g0043 | 3 | HG01516.hp1 HG01517.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.474+2509T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217045 | ||||||
| chr16:16217144
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2410A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217144 | ||||||
| chr16:16217188
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2366C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217188 | ||||||
| chr16:16217409
|
C | T | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.474+2145G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217409 | ||||||
| chr16:16217438
|
A | G | 1 | a0001c0052t0001g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.474+2116T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217438 | ||||||
| chr16:16217438
|
A | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2116T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217438 | ||||||
| chr16:16217459
|
C | T | 42 | a0001c0001t0001g0039a0001c0001t0001g0108a0001c0001t0002g0242others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+2095G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217459 | ||||||
| chr16:16217489
|
C | G | 3 | a0042c0039t0001g0032a0043c0040t0001g0031a0044c0038t0001g0033 | 3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.474+2065G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217489 | ||||||
| chr16:16217566
|
G | A | 3 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.474+1988C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217566 | ||||||
| chr16:16217609
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1945C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217609 | ||||||
| chr16:16217721
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1833A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217721 | ||||||
| chr16:16217807
|
C | T | 1 | a0042c0039t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.474+1747G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217807 | ||||||
| chr16:16217854
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0005g0206 | 3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.474+1700G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217854 | ||||||
| chr16:16217946
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0002g0092others(1): Show | 4 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1608A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16217946 | ||||||
| chr16:16218014
|
C | CG | 3 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0005g0206 | 3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.474+1539dupC | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218014 | ||||||
| chr16:16218065
|
G | T | 1 | a0001c0002t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.474+1489C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218065 | ||||||
| chr16:16218274
|
G | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(7): Show | 10 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+1280C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218274 | ||||||
| chr16:16218367
|
G | A | 4 | a0001c0001t0002g0094a0001c0001t0002g0204a0001c0002t0001g0093others(1): Show | 4 | NA18987.hp1 NA18990.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1187C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218367 | ||||||
| chr16:16218383
|
A | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+1171T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218383 | ||||||
| chr16:16218422
|
C | T | 123 | a0001c0001t0001g0064a0001c0001t0001g0079a0001c0001t0001g0082others(120): Show | 123 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.474+1132G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218422 | ||||||
| chr16:16218491
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+1063C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218491 | ||||||
| chr16:16218613
|
C | T | 1 | a0001c0001t0004g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.474+941G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218613 | ||||||
| chr16:16218650
|
T | C | 6 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0239others(3): Show | 6 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+904A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218650 | ||||||
| chr16:16218668
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.474+886A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218668 | ||||||
| chr16:16218729
|
C | G | 26 | a0001c0002t0001g0287a0001c0006t0001g0276a0001c0006t0001g0277others(23): Show | 26 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.474+825G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218729 | ||||||
| chr16:16218730
|
G | A | 1 | a0003c0005t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.474+824C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218730 | ||||||
| chr16:16218767
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+787C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218767 | ||||||
| chr16:16218824
|
C | G | 1 | a0001c0033t0001g0070 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.474+730G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218824 | ||||||
| chr16:16218838
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+716C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218838 | ||||||
| chr16:16218861
|
TTTTAGTA others(28): Show |
T | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+658_474+692del others(35): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218861 | ||||||
| chr16:16218872
|
ATTTAGTA others(6): Show |
A | 1 | a0001c0002t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.474+669_474+681del others(13): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16218872 | ||||||
| chr16:16219059
|
C | CA | 83 | a0001c0001t0001g0003a0001c0001t0001g0200a0001c0001t0001g0201others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.474+494dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | ||||||
| chr16:16219059
|
CA | C | 30 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0268others(27): Show | 30 | HG01256.hp2 HG01257.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.474+494delT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | ||||||
| chr16:16219059
|
CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+481_474+494del others(14): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | ||||||
| chr16:16219059
|
CAAAAAAA others(8): Show |
C | 1 | a0027c0073t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474+480_474+494del others(15): Show |
ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219059 | ||||||
| chr16:16219066
|
A | C | 1 | a0011c0016t0001g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.474+488T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219066 | ||||||
| chr16:16219107
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+447C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219107 | ||||||
| chr16:16219179
|
C | A | 2 | a0011c0016t0006g0271a0031c0060t0010g0240 | 2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.474+375G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219179 | ||||||
| chr16:16219253
|
G | A | 6 | a0001c0001t0002g0242a0001c0006t0002g0246a0002c0013t0001g0241others(3): Show | 6 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+301C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219253 | ||||||
| chr16:16219314
|
T | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+240A>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219314 | ||||||
| chr16:16219339
|
C | G | 2 | a0001c0002t0001g0054a0045c0037t0001g0355 | 2 | NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.474+215G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219339 | ||||||
| chr16:16219360
|
T | G | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+194A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219360 | ||||||
| chr16:16219454
|
A | G | 1 | a0007c0008t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474+100T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219454 | ||||||
| chr16:16219495
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | NA18947.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.474+59C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219495 | ||||||
| chr16:16219511
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.474+43C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219511 | ||||||
| chr16:16219541
|
C | T | 2 | a0020c0032t0001g0051a0036c0066t0001g0052 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.474+13G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 4/30 | chr16 | 16219541 | ||||||
| chr16:16219688
|
C | T | 9 | a0004c0010t0001g0042a0004c0010t0001g0043a0004c0010t0001g0045others(6): Show | 9 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.346-6G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 3/30 | chr16 | 16219688 | ||||||
| chr16:16219796
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+26C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 3/30 | chr16 | 16219796 | ||||||
| chr16:16219810
|
A | G | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.345+12T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 3/30 | chr16 | 16219810 | ||||||
| chr16:16220010
|
C | T | 4 | a0001c0001t0001g0273a0012c0030t0001g0274a0026c0056t0001g0041others(1): Show | 4 | HG02109.hp2 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-63G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220010 | ||||||
| chr16:16220084
|
C | A | 4 | a0002c0013t0001g0253a0002c0057t0001g0255a0004c0017t0001g0254others(1): Show | 4 | HG01106.hp2 HG01975.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-137G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220084 | ||||||
| chr16:16220087
|
C | T | 9 | a0001c0001t0001g0039a0001c0004t0001g0034a0001c0004t0001g0037others(6): Show | 9 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-140G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220087 | ||||||
| chr16:16220183
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-236C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220183 | ||||||
| chr16:16220234
|
G | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-287C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220234 | ||||||
| chr16:16220234
|
G | T | 344 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.220-287C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220234 | ||||||
| chr16:16220238
|
G | A | 1 | a0002c0013t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.220-291C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220238 | ||||||
| chr16:16220314
|
C | T | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-367G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220314 | ||||||
| chr16:16220330
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-383C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220330 | ||||||
| chr16:16220433
|
C | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-486G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220433 | ||||||
| chr16:16220460
|
G | A | 1 | a0002c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.220-513C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220460 | ||||||
| chr16:16220467
|
G | T | 3 | a0042c0039t0001g0032a0043c0040t0001g0031a0044c0038t0001g0033 | 3 | HG02280.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.220-520C>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220467 | ||||||
| chr16:16220550
|
A | G | 1 | a0002c0003t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220-603T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220550 | ||||||
| chr16:16220608
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-661C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220608 | ||||||
| chr16:16220608
|
G | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02074.hp2 NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.220-661C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220608 | ||||||
| chr16:16220631
|
T | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-684A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220631 | ||||||
| chr16:16220660
|
C | T | 2 | a0001c0002t0001g0014a0038c0069t0001g0015 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.220-713G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220660 | ||||||
| chr16:16220711
|
C | T | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.220-764G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220711 | ||||||
| chr16:16220737
|
A | G | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.220-790T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220737 | ||||||
| chr16:16220897
|
C | CA | 11 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.219+751dupT | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220897 | ||||||
| chr16:16220903
|
A | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+746T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220903 | ||||||
| chr16:16220908
|
A | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+741T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220908 | ||||||
| chr16:16220992
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.219+657G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16220992 | ||||||
| chr16:16221037
|
C | T | 3 | a0003c0005t0001g0028a0003c0005t0001g0029a0005c0012t0001g0027 | 3 | HG01515.hp1 HG01517.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.219+612G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221037 | ||||||
| chr16:16221038
|
G | A | 1 | a0001c0026t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.219+611C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221038 | ||||||
| chr16:16221087
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+562C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221087 | ||||||
| chr16:16221324
|
T | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+325A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221324 | ||||||
| chr16:16221327
|
A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.219+322T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221327 | ||||||
| chr16:16221353
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+296A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221353 | ||||||
| chr16:16221475
|
C | A | 70 | a0001c0001t0001g0273a0001c0001t0001g0281a0001c0001t0001g0303others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.219+174G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221475 | ||||||
| chr16:16221489
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+160C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221489 | ||||||
| chr16:16221503
|
C | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | HG00544.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.219+146G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221503 | ||||||
| chr16:16221550
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+99G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221550 | ||||||
| chr16:16221571
|
A | G | 1 | a0002c0003t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.219+78T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221571 | ||||||
| chr16:16221600
|
G | C | 1 | a0004c0010t0001g0342 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.219+49C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221600 | ||||||
| chr16:16221609
|
G | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+40C>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221609 | ||||||
| chr16:16221611
|
A | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.219+38T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 2/30 | chr16 | 16221611 | ||||||
| chr16:16221895
|
A | G | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-64T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221895 | ||||||
| chr16:16221924
|
A | G | 1 | a0001c0002t0001g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.37-93T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221924 | ||||||
| chr16:16221942
|
A | G | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-111T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221942 | ||||||
| chr16:16221948
|
T | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-117A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16221948 | ||||||
| chr16:16222072
|
C | G | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-241G>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222072 | ||||||
| chr16:16222117
|
A | T | 1 | a0032c0059t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37-286T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222117 | ||||||
| chr16:16222236
|
C | T | 2 | a0012c0025t0001g0007a0012c0025t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.37-405G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222236 | ||||||
| chr16:16222251
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-420C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222251 | ||||||
| chr16:16222254
|
G | A | 1 | a0002c0022t0001g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.37-423C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222254 | ||||||
| chr16:16222260
|
C | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-429G>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222260 | ||||||
| chr16:16222364
|
G | A | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-533C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222364 | ||||||
| chr16:16222370
|
AT | A | 6 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348others(3): Show | 6 | HG01109.hp2 HG01123.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-540delA | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222370 | ||||||
| chr16:16222450
|
C | T | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-619G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222450 | ||||||
| chr16:16222495
|
G | A | 1 | a0001c0049t0001g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.37-664C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222495 | ||||||
| chr16:16222513
|
G | A | 1 | a0002c0051t0001g0353 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.37-682C>T | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222513 | ||||||
| chr16:16222529
|
A | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-698T>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222529 | ||||||
| chr16:16222610
|
T | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.37-779A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222610 | ||||||
| chr16:16222809
|
C | T | 2 | a0001c0004t0001g0006a0045c0037t0001g0355 | 2 | HG02717.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.36+590G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222809 | ||||||
| chr16:16222855
|
T | C | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.36+544A>G | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222855 | ||||||
| chr16:16222866
|
A | T | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.36+533T>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222866 | ||||||
| chr16:16222904
|
T | G | 2 | a0001c0002t0001g0354a0045c0037t0001g0355 | 2 | HG00597.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.36+495A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16222904 | ||||||
| chr16:16223163
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0005a0045c0037t0001g0355 | 3 | HG02602.hp1 HG04204.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.36+236T>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223163 | ||||||
| chr16:16223173
|
C | T | 1 | a0045c0037t0001g0355 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.36+226G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223173 | ||||||
| chr16:16223224
|
T | G | 2 | a0001c0072t0001g0356a0045c0037t0001g0355 | 2 | HG03579.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.36+175A>C | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223224 | ||||||
| chr16:16223283
|
C | T | 2 | a0001c0001t0001g0003a0002c0003t0001g0002 | 2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.36+116G>A | ABCC6 | ENSG00000091262.17 | transcript | ENST00000205557.12 | protein_coding | 1/30 | chr16 | 16223283 |