Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6833 |
|---|---|
| ensemblid | ENSG00000006071.16 |
| hgncid | 59 |
| symbol | ABCC8 |
| name | ATP binding cassette subfamily C member 8 |
| refseq_nuc | NM_000352.6 |
| refseq_prot | NP_000343.2 |
| ensembl_nuc | ENST00000389817.8 |
| ensembl_prot | ENSP00000374467.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 17392885 |
| end | 17476845 |
| strand | - |
| ver | v1.2 |
| region | chr11:17392885-17476845 |
| region5000 | chr11:17387885-17481845 |
| regionname0 | ABCC8_chr11_17392885_17476845 |
| regionname5000 | ABCC8_chr11_17387885_17481845 |
| 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 | 0/0 | 1581 | 234 | 75 | 51 | 71 | 11 | 26 | 46 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002 | 1/0 | 1581 | 75 | 1 | 12 | 41 | 3 | 17 | 27 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003 | 0/1 | 1581 | 7 | 3 | 1 | 0 | 0 | 2 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004 | 0/0 | 1581 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0005 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0006 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0007 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0008 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0009 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0010 | 0/0 | 1247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0011 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0012 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0013 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0014 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0015 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| 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 | 4746 | 36 | 1 | 2 | 27 | 1 | 5 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0002 | 1/0 | 4746 | 24 | 0 | 3 | 18 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0003 | 0/0 | 4746 | 23 | 3 | 7 | 8 | 1 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0004 | 0/0 | 4746 | 18 | 5 | 5 | 4 | 2 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0005 | 0/0 | 4746 | 15 | 0 | 2 | 8 | 1 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0006 | 0/0 | 4746 | 13 | 5 | 4 | 4 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0007 | 0/0 | 4746 | 12 | 0 | 1 | 9 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0008 | 0/0 | 4746 | 11 | 3 | 4 | 0 | 0 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0009 | 0/0 | 4746 | 11 | 6 | 1 | 1 | 1 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0010 | 0/0 | 4746 | 11 | 4 | 6 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0011 | 0/0 | 4746 | 10 | 0 | 1 | 6 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0012 | 0/0 | 4746 | 9 | 0 | 0 | 3 | 3 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0013 | 0/0 | 4746 | 9 | 0 | 2 | 6 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0014 | 0/0 | 4746 | 8 | 6 | 2 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0015 | 0/0 | 4746 | 8 | 8 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0016 | 0/0 | 4746 | 6 | 0 | 2 | 1 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0017 | 0/0 | 4746 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0018 | 0/0 | 4746 | 6 | 1 | 1 | 4 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0019 | 0/0 | 4746 | 5 | 0 | 5 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0020 | 0/0 | 4746 | 5 | 1 | 3 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0021 | 0/0 | 4746 | 4 | 2 | 0 | 2 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0022 | 0/0 | 4746 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0023 | 0/0 | 4746 | 3 | 0 | 1 | 2 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0024 | 0/0 | 4746 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0025 | 0/0 | 4746 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0026 | 0/0 | 4746 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0027 | 0/0 | 4746 | 3 | 0 | 1 | 0 | 0 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0028 | 0/0 | 4746 | 2 | 0 | 0 | 1 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0029 | 0/0 | 4746 | 2 | 1 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0030 | 0/0 | 4746 | 2 | 0 | 0 | 0 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0031 | 0/0 | 4746 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0032 | 0/0 | 4746 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0033 | 0/0 | 4746 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0034 | 0/0 | 4746 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0035 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0036 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0037 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0038 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0039 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0040 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0041 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0042 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0043 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0044 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0045 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0046 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0047 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0048 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0049 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0050 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0051 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0052 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0053 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0054 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0055 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0056 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0057 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0058 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0059 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0060 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0061 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0062 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0063 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0064 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0065 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0066 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0067 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0068 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0069 | 0/1 | 4746 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0070 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0071 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0072 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0073 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0074 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0075 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0076 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0077 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0078 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0079 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0080 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| c0081 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| 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 | 1/1 | 176 | 318 | 74 | 62 | 120 | 14 | 46 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| t0002 | 0/0 | 176 | 9 | 8 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| t0003 | 0/0 | 176 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| t0004 | 0/0 | 176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| 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 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| 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 | 4746 | 36 | 1 | 2 | 27 | 1 | 5 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0003 | 0/0 | 4746 | 23 | 3 | 7 | 8 | 1 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0004 | 0/0 | 4746 | 18 | 5 | 5 | 4 | 2 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0006 | 0/0 | 4746 | 13 | 5 | 4 | 4 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0007 | 0/0 | 4746 | 12 | 0 | 1 | 9 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0008 | 0/0 | 4746 | 11 | 3 | 4 | 0 | 0 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0009 | 0/0 | 4746 | 11 | 6 | 1 | 1 | 1 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0010 | 0/0 | 4746 | 11 | 4 | 6 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0012 | 0/0 | 4746 | 9 | 0 | 0 | 3 | 3 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0013 | 0/0 | 4746 | 9 | 0 | 2 | 6 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0014 | 0/0 | 4746 | 8 | 6 | 2 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0015 | 0/0 | 4746 | 8 | 8 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0017 | 0/0 | 4746 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0019 | 0/0 | 4746 | 5 | 0 | 5 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0020 | 0/0 | 4746 | 5 | 1 | 3 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0021 | 0/0 | 4746 | 4 | 2 | 0 | 2 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0022 | 0/0 | 4746 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0023 | 0/0 | 4746 | 3 | 0 | 1 | 2 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0024 | 0/0 | 4746 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0025 | 0/0 | 4746 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0026 | 0/0 | 4746 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0028 | 0/0 | 4746 | 2 | 0 | 0 | 1 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0031 | 0/0 | 4746 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0033 | 0/0 | 4746 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0034 | 0/0 | 4746 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0035 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0043 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0046 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0049 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0051 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0053 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0058 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0059 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0061 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0062 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0065 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0068 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0070 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0071 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0073 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0075 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0076 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0077 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0079 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0080 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0081 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0002 | 1/0 | 4746 | 24 | 0 | 3 | 18 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0005 | 0/0 | 4746 | 15 | 0 | 2 | 8 | 1 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0011 | 0/0 | 4746 | 10 | 0 | 1 | 6 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0016 | 0/0 | 4746 | 6 | 0 | 2 | 1 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0018 | 0/0 | 4746 | 6 | 1 | 1 | 4 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0027 | 0/0 | 4746 | 3 | 0 | 1 | 0 | 0 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0030 | 0/0 | 4746 | 2 | 0 | 0 | 0 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0044 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0045 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0047 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0050 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0054 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0060 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0064 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0074 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0078 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0029 | 0/0 | 4746 | 2 | 1 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0032 | 0/0 | 4746 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0036 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0063 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0069 | 0/1 | 4746 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004c0038 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004c0040 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004c0041 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0005c0057 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0006c0056 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0007c0039 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0008c0055 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0009c0067 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0010c0066 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0011c0052 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0012c0072 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0013c0042 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0014c0048 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0015c0037 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4921 | 36 | 1 | 2 | 27 | 1 | 5 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0003t0001 | 0/0 | 4921 | 23 | 3 | 7 | 8 | 1 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0004t0001 | 0/0 | 4921 | 17 | 4 | 5 | 4 | 2 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0004t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0006t0001 | 0/0 | 4921 | 13 | 5 | 4 | 4 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0007t0001 | 0/0 | 4921 | 12 | 0 | 1 | 9 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0008t0001 | 0/0 | 4921 | 11 | 3 | 4 | 0 | 0 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0009t0001 | 0/0 | 4921 | 10 | 6 | 0 | 1 | 1 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0009t0003 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0010t0001 | 0/0 | 4921 | 10 | 3 | 6 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0010t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0012t0001 | 0/0 | 4921 | 9 | 0 | 0 | 3 | 3 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0013t0001 | 0/0 | 4921 | 9 | 0 | 2 | 6 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0014t0001 | 0/0 | 4921 | 6 | 5 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0014t0002 | 0/0 | 4921 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0015t0001 | 0/0 | 4921 | 8 | 8 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0017t0001 | 0/0 | 4921 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0019t0001 | 0/0 | 4921 | 5 | 0 | 5 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0020t0001 | 0/0 | 4921 | 5 | 1 | 3 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0021t0001 | 0/0 | 4921 | 3 | 1 | 0 | 2 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0021t0003 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0022t0001 | 0/0 | 4921 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0023t0001 | 0/0 | 4921 | 3 | 0 | 1 | 2 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0024t0001 | 0/0 | 4921 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0025t0001 | 0/0 | 4921 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0026t0001 | 0/0 | 4921 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0026t0004 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0028t0001 | 0/0 | 4921 | 2 | 0 | 0 | 1 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0031t0001 | 0/0 | 4921 | 2 | 0 | 2 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0033t0001 | 0/0 | 4921 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0034t0001 | 0/0 | 4921 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0035t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0043t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0046t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0049t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0051t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0053t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0058t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0059t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0061t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0062t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0065t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0068t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0070t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0071t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0073t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0075t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0076t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0077t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0079t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0080t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0001c0081t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0002t0001 | 1/0 | 4921 | 24 | 0 | 3 | 18 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0005t0001 | 0/0 | 4921 | 15 | 0 | 2 | 8 | 1 | 4 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0011t0001 | 0/0 | 4921 | 10 | 0 | 1 | 6 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0016t0001 | 0/0 | 4921 | 6 | 0 | 2 | 1 | 0 | 3 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0018t0001 | 0/0 | 4921 | 6 | 1 | 1 | 4 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0027t0001 | 0/0 | 4921 | 3 | 0 | 1 | 0 | 0 | 2 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0030t0001 | 0/0 | 4921 | 2 | 0 | 0 | 0 | 1 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0044t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0045t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0047t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0050t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0054t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0060t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0064t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0074t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0002c0078t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0029t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0029t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0032t0001 | 0/0 | 4921 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0036t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0063t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0003c0069t0001 | 0/1 | 4921 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004c0038t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004c0040t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0004c0041t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0005c0057t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0006c0056t0002 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0007c0039t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0008c0055t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0009c0067t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0010c0066t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0011c0052t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0012c0072t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0013c0042t0001 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0014c0048t0001 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| a0015c0037t0001 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | copy fasta | chr11 | 17387885 | 17481845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0004t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0007t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0008t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0009t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0010t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0012t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0013t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0014t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0015t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0017t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0017t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0017t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0017t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0017t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0019t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0019t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0019t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0019t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0019t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0020t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0020t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0020t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0020t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0021t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0021t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0021t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0021t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0022t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0022t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0022t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0022t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0023t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0023t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0023t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0024t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0024t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0024t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0025t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0025t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0025t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0026t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0026t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0026t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0028t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0028t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0031t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0031t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0033t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0034t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0034t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0035t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0043t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0046t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0049t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0051t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0053t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0058t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0059t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0061t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0062t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0065t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0068t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0070t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0071t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0073t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0075t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0076t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0077t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0079t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0080t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0001c0081t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0011t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0016t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0016t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0016t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0016t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0016t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0016t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0018t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0018t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0018t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0018t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0018t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0018t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0027t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0027t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0027t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0030t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0030t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0044t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0045t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0047t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0050t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0054t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0060t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0064t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0074t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0002c0078t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0029t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0029t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0032t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0032t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0036t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0063t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0003c0069t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0004c0038t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0004c0040t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0004c0041t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0005c0057t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0006c0056t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0007c0039t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0008c0055t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0009c0067t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0010c0066t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0011c0052t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0012c0072t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0013c0042t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0014c0048t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| a0015c0037t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0030 | t0001 | g0300 | EUR | GBR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00099 | hp2 | a0001 | c0010 | t0001 | g0191 | EUR | GBR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00140 | hp1 | a0002 | c0005 | t0001 | g0120 | EUR | GBR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00140 | hp2 | a0001 | c0009 | t0001 | g0268 | EUR | GBR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00408 | hp2 | a0002 | c0050 | t0001 | g0099 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00423 | hp1 | a0002 | c0018 | t0001 | g0196 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00558 | hp2 | a0002 | c0011 | t0001 | g0263 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00597 | hp1 | a0002 | c0060 | t0001 | g0209 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00609 | hp1 | a0001 | c0007 | t0001 | g0128 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00621 | hp1 | a0002 | c0018 | t0001 | g0197 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00621 | hp2 | a0001 | c0006 | t0001 | g0102 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00639 | hp1 | a0001 | c0077 | t0001 | g0313 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00639 | hp2 | a0001 | c0020 | t0001 | g0156 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00642 | hp1 | a0002 | c0018 | t0001 | g0193 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00673 | hp2 | a0001 | c0013 | t0001 | g0198 | EAS | CHS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00733 | hp1 | a0001 | c0010 | t0001 | g0136 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0323 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00735 | hp1 | a0001 | c0009 | t0003 | g0015 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00735 | hp2 | a0001 | c0046 | t0001 | g0166 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0256 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0257 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01070 | hp2 | a0001 | c0019 | t0001 | g0280 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01074 | hp1 | a0002 | c0016 | t0001 | g0306 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01074 | hp2 | a0001 | c0006 | t0001 | g0096 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01106 | hp1 | a0001 | c0049 | t0001 | g0141 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01106 | hp2 | a0001 | c0010 | t0001 | g0203 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0282 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01168 | hp2 | a0001 | c0006 | t0001 | g0083 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01169 | hp1 | a0002 | c0005 | t0001 | g0283 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0258 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01175 | hp1 | a0001 | c0006 | t0001 | g0097 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01175 | hp2 | a0002 | c0054 | t0001 | g0132 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01192 | hp1 | a0001 | c0010 | t0001 | g0135 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01192 | hp2 | a0002 | c0016 | t0001 | g0305 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01243 | hp1 | a0001 | c0010 | t0001 | g0142 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01243 | hp2 | a0001 | c0014 | t0001 | g0032 | AMR | PUR | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0130 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01255 | hp2 | a0001 | c0019 | t0001 | g0284 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01256 | hp1 | a0001 | c0008 | t0001 | g0308 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01256 | hp2 | a0001 | c0014 | t0002 | g0009 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01258 | hp1 | a0001 | c0019 | t0001 | g0121 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01258 | hp2 | a0001 | c0008 | t0001 | g0307 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01261 | hp1 | a0001 | c0010 | t0001 | g0192 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01261 | hp2 | a0001 | c0059 | t0001 | g0206 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01346 | hp1 | a0001 | c0010 | t0001 | g0204 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01346 | hp2 | a0001 | c0013 | t0001 | g0189 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01358 | hp1 | a0001 | c0008 | t0001 | g0140 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01358 | hp2 | a0001 | c0008 | t0001 | g0081 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01361 | hp1 | a0001 | c0033 | t0001 | g0001 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01433 | hp1 | a0001 | c0007 | t0001 | g0129 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01433 | hp2 | a0003 | c0032 | t0001 | g0194 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01496 | hp1 | a0001 | c0006 | t0001 | g0044 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0082 | EUR | IBS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01515 | hp2 | a0001 | c0012 | t0001 | g0210 | EUR | IBS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0218 | EUR | IBS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01516 | hp2 | a0001 | c0012 | t0001 | g0211 | EUR | IBS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01517 | hp1 | a0001 | c0012 | t0001 | g0212 | EUR | IBS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0266 | EUR | IBS | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01884 | hp1 | a0003 | c0029 | t0002 | g0011 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01884 | hp2 | a0001 | c0015 | t0001 | g0155 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01891 | hp1 | a0001 | c0008 | t0001 | g0041 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01891 | hp2 | a0001 | c0015 | t0001 | g0019 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0233 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01928 | hp2 | a0001 | c0013 | t0001 | g0314 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0261 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01934 | hp2 | a0001 | c0019 | t0001 | g0303 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01943 | hp1 | a0001 | c0031 | t0001 | g0244 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01943 | hp2 | a0002 | c0011 | t0001 | g0208 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01978 | hp1 | a0002 | c0005 | t0001 | g0110 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01978 | hp2 | a0001 | c0031 | t0001 | g0242 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02004 | hp1 | a0001 | c0023 | t0001 | g0205 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02004 | hp2 | a0002 | c0064 | t0001 | g0315 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02015 | hp1 | a0001 | c0007 | t0001 | g0163 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02027 | hp2 | a0001 | c0007 | t0001 | g0124 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02040 | hp1 | a0002 | c0011 | t0001 | g0217 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02040 | hp2 | a0001 | c0051 | t0001 | g0127 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02055 | hp2 | a0014 | c0048 | t0001 | g0169 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02056 | hp1 | a0001 | c0023 | t0001 | g0253 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02056 | hp2 | a0002 | c0011 | t0001 | g0062 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02071 | hp1 | a0001 | c0021 | t0001 | g0232 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02083 | hp1 | a0001 | c0023 | t0001 | g0031 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02083 | hp2 | a0001 | c0007 | t0001 | g0310 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02132 | hp1 | a0001 | c0007 | t0001 | g0119 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02132 | hp2 | a0002 | c0078 | t0001 | g0299 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02135 | hp1 | a0001 | c0007 | t0001 | g0125 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02145 | hp1 | a0001 | c0014 | t0001 | g0170 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02145 | hp2 | a0001 | c0010 | t0001 | g0298 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02148 | hp1 | a0001 | c0020 | t0001 | g0319 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02155 | hp1 | a0011 | c0052 | t0001 | g0281 | EAS | CDX | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02155 | hp2 | a0001 | c0013 | t0001 | g0069 | EAS | CDX | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0178 | EAS | CDX | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02257 | hp1 | a0001 | c0015 | t0001 | g0022 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02257 | hp2 | a0001 | c0034 | t0001 | g0177 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02258 | hp1 | a0001 | c0079 | t0001 | g0016 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02258 | hp2 | a0001 | c0035 | t0002 | g0013 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02280 | hp1 | a0001 | c0009 | t0001 | g0291 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02280 | hp2 | a0001 | c0065 | t0001 | g0288 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02293 | hp1 | a0001 | c0019 | t0001 | g0321 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0302 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02300 | hp2 | a0001 | c0062 | t0001 | g0260 | AMR | PEL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02451 | hp1 | a0001 | c0068 | t0001 | g0048 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02451 | hp2 | a0001 | c0061 | t0001 | g0311 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02523 | hp1 | a0001 | c0024 | t0001 | g0262 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02523 | hp2 | a0002 | c0005 | t0001 | g0161 | EAS | KHV | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02572 | hp1 | a0001 | c0010 | t0002 | g0005 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02572 | hp2 | a0001 | c0014 | t0001 | g0322 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02602 | hp1 | a0001 | c0008 | t0001 | g0157 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02602 | hp2 | a0001 | c0013 | t0001 | g0267 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02622 | hp1 | a0001 | c0009 | t0001 | g0002 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02622 | hp2 | a0003 | c0063 | t0001 | g0052 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02630 | hp1 | a0001 | c0009 | t0001 | g0002 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0091 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02698 | hp2 | a0002 | c0005 | t0001 | g0026 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02717 | hp1 | a0001 | c0026 | t0001 | g0035 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02717 | hp2 | a0001 | c0014 | t0001 | g0168 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0079 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02723 | hp2 | a0001 | c0070 | t0002 | g0008 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02735 | hp1 | a0003 | c0032 | t0001 | g0199 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02735 | hp2 | a0001 | c0058 | t0001 | g0046 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02738 | hp1 | a0002 | c0005 | t0001 | g0304 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02738 | hp2 | a0001 | c0053 | t0001 | g0158 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02809 | hp1 | a0001 | c0009 | t0001 | g0050 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02809 | hp2 | a0001 | c0017 | t0001 | g0179 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02818 | hp1 | a0001 | c0080 | t0001 | g0312 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02818 | hp2 | a0001 | c0075 | t0001 | g0033 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02886 | hp1 | a0009 | c0067 | t0001 | g0295 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02886 | hp2 | a0003 | c0036 | t0001 | g0045 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02896 | hp1 | a0001 | c0022 | t0001 | g0297 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02896 | hp2 | a0001 | c0020 | t0001 | g0043 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02922 | hp2 | a0001 | c0015 | t0001 | g0021 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02970 | hp1 | a0012 | c0072 | t0001 | g0053 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02970 | hp2 | a0001 | c0015 | t0001 | g0023 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02976 | hp1 | a0001 | c0017 | t0001 | g0051 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02976 | hp2 | a0001 | c0010 | t0001 | g0143 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03017 | hp1 | a0003 | c0029 | t0001 | g0325 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03017 | hp2 | a0002 | c0005 | t0001 | g0301 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03041 | hp1 | a0001 | c0015 | t0001 | g0020 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03041 | hp2 | a0001 | c0025 | t0001 | g0075 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03098 | hp1 | a0001 | c0022 | t0001 | g0072 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03098 | hp2 | a0001 | c0034 | t0001 | g0176 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03130 | hp1 | a0001 | c0021 | t0001 | g0138 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03130 | hp2 | a0001 | c0026 | t0004 | g0326 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03195 | hp1 | a0001 | c0010 | t0001 | g0049 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03195 | hp2 | a0001 | c0071 | t0001 | g0071 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03209 | hp1 | a0001 | c0008 | t0001 | g0042 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03209 | hp2 | a0001 | c0017 | t0001 | g0003 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03225 | hp1 | a0001 | c0022 | t0001 | g0294 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03225 | hp2 | a0001 | c0014 | t0001 | g0084 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03239 | hp1 | a0002 | c0011 | t0001 | g0243 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03239 | hp2 | a0001 | c0033 | t0001 | g0001 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03453 | hp1 | a0001 | c0017 | t0001 | g0186 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0296 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03490 | hp1 | a0001 | c0012 | t0001 | g0245 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03490 | hp2 | a0002 | c0027 | t0001 | g0029 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03491 | hp1 | a0001 | c0012 | t0001 | g0073 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03491 | hp2 | a0001 | c0008 | t0001 | g0039 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03492 | hp1 | a0002 | c0027 | t0001 | g0028 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03492 | hp2 | a0001 | c0008 | t0001 | g0040 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03516 | hp1 | a0001 | c0025 | t0001 | g0056 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03516 | hp2 | a0001 | c0021 | t0003 | g0014 | AFR | ESN | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03540 | hp1 | a0001 | c0015 | t0001 | g0018 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0144 | AFR | GWD | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03579 | hp1 | a0001 | c0009 | t0001 | g0289 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03579 | hp2 | a0001 | c0008 | t0001 | g0165 | AFR | MSL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03654 | hp1 | a0002 | c0016 | t0001 | g0037 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03669 | hp2 | a0002 | c0044 | t0001 | g0117 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03688 | hp1 | a0002 | c0016 | t0001 | g0098 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03688 | hp2 | a0001 | c0012 | t0001 | g0252 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0309 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03831 | hp1 | a0001 | c0009 | t0001 | g0251 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03834 | hp1 | a0001 | c0020 | t0001 | g0004 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03927 | hp1 | a0002 | c0011 | t0001 | g0213 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03927 | hp2 | a0002 | c0005 | t0001 | g0025 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03942 | hp1 | a0013 | c0042 | t0001 | g0123 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG03942 | hp2 | a0002 | c0030 | t0001 | g0184 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04115 | hp1 | a0002 | c0074 | t0001 | g0214 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04115 | hp2 | a0001 | c0008 | t0001 | g0047 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04184 | hp1 | a0002 | c0016 | t0001 | g0038 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0187 | SAS | BEB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0086 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0269 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0324 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04204 | hp2 | a0001 | c0009 | t0001 | g0201 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04228 | hp1 | a0002 | c0045 | t0001 | g0085 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG04228 | hp2 | a0001 | c0007 | t0001 | g0036 | SAS | STU | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18522 | hp1 | a0001 | c0017 | t0001 | g0003 | AFR | YRI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18522 | hp2 | a0001 | c0081 | t0001 | g0017 | AFR | YRI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18612 | hp2 | a0002 | c0005 | t0001 | g0122 | EAS | CHB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0090 | AFR | YRI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0293 | AFR | YRI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18940 | hp1 | a0001 | c0012 | t0001 | g0171 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18940 | hp2 | a0002 | c0005 | t0001 | g0134 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18941 | hp1 | a0005 | c0057 | t0001 | g0089 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18942 | hp2 | a0001 | c0024 | t0001 | g0153 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18946 | hp2 | a0004 | c0038 | t0001 | g0108 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18948 | hp1 | a0001 | c0007 | t0001 | g0131 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18948 | hp2 | a0001 | c0009 | t0001 | g0150 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18949 | hp1 | a0004 | c0041 | t0001 | g0145 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18949 | hp2 | a0001 | c0004 | t0001 | g0230 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18952 | hp2 | a0001 | c0021 | t0001 | g0221 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18959 | hp1 | a0002 | c0011 | t0001 | g0148 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18959 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18963 | hp1 | a0002 | c0016 | t0001 | g0276 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18964 | hp2 | a0001 | c0012 | t0001 | g0259 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18967 | hp1 | a0001 | c0007 | t0001 | g0116 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18967 | hp2 | a0002 | c0018 | t0001 | g0188 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18971 | hp2 | a0001 | c0006 | t0001 | g0080 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18983 | hp1 | a0007 | c0039 | t0001 | g0109 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18987 | hp1 | a0002 | c0018 | t0001 | g0190 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18987 | hp2 | a0010 | c0066 | t0001 | g0174 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18990 | hp2 | a0001 | c0013 | t0001 | g0152 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18993 | hp2 | a0001 | c0013 | t0001 | g0175 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18994 | hp1 | a0002 | c0011 | t0001 | g0149 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18995 | hp2 | a0002 | c0005 | t0001 | g0114 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19000 | hp1 | a0002 | c0005 | t0001 | g0277 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19005 | hp2 | a0002 | c0005 | t0001 | g0111 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19012 | hp1 | a0002 | c0005 | t0001 | g0133 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | LWK | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19030 | hp2 | a0001 | c0022 | t0001 | g0292 | AFR | LWK | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0012 | AFR | LWK | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19043 | hp2 | a0001 | c0017 | t0001 | g0070 | AFR | LWK | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19055 | hp1 | a0002 | c0047 | t0001 | g0112 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19056 | hp2 | a0001 | c0012 | t0001 | g0151 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19058 | hp1 | a0001 | c0013 | t0001 | g0064 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19060 | hp2 | a0002 | c0011 | t0001 | g0202 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19062 | hp1 | a0001 | c0007 | t0001 | g0126 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19065 | hp1 | a0001 | c0013 | t0001 | g0247 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19065 | hp2 | a0015 | c0037 | t0001 | g0104 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19067 | hp2 | a0001 | c0024 | t0001 | g0154 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19068 | hp2 | a0002 | c0005 | t0001 | g0279 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19080 | hp2 | a0004 | c0040 | t0001 | g0113 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19087 | hp2 | a0001 | c0028 | t0001 | g0159 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19088 | hp1 | a0001 | c0006 | t0001 | g0278 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19240 | hp1 | a0008 | c0055 | t0001 | g0078 | AFR | YRI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA19240 | hp2 | a0001 | c0025 | t0001 | g0054 | AFR | YRI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | ASW | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20129 | hp2 | a0001 | c0015 | t0001 | g0024 | AFR | ASW | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20752 | hp1 | a0001 | c0028 | t0001 | g0077 | EUR | TSI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0285 | EUR | TSI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20805 | hp1 | a0001 | c0007 | t0001 | g0139 | EUR | TSI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20905 | hp1 | a0002 | c0011 | t0001 | g0316 | SAS | GIH | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0087 | SAS | GIH | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01123 | hp1 | a0001 | c0020 | t0001 | g0004 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG01123 | hp2 | a0002 | c0027 | t0001 | g0027 | AMR | CLM | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02109 | hp1 | a0001 | c0014 | t0002 | g0006 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02109 | hp2 | a0001 | c0076 | t0002 | g0007 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02486 | hp1 | a0001 | c0009 | t0001 | g0290 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0103 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0092 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG02559 | hp2 | a0002 | c0018 | t0001 | g0200 | AFR | ACB | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG06807 | hp1 | a0006 | c0056 | t0002 | g0010 | AFR | USA | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| HG06807 | hp2 | a0001 | c0043 | t0001 | g0093 | AFR | USA | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA18955 | hp2 | a0001 | c0006 | t0001 | g0107 | EAS | JPT | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20300 | hp1 | a0001 | c0026 | t0001 | g0034 | AFR | USA | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA20300 | hp2 | a0001 | c0014 | t0001 | g0320 | AFR | USA | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0162 | AFR | LWK | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| NA21309 | hp2 | a0001 | c0073 | t0001 | g0055 | AFR | LWK | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0069 | t0001 | g0195 | REF | REF | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0147 | REF | REF | ABCC8_chr11_17387885_17481845 | ABCC8 | chr11 | 17387885 | 17481845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17393023
|
C | T | 1 | a0003 | 7 | HG01433.hp2 HG01884.hp1 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.4714G>A | p.Val1572Ile | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 39/39 | 4783/4921 | 4714/4746 | 1572/1581 | chr11 | 17393023 | ||
| chr11:17396930
|
C | A | 12 | a0001a0003a0004others(9): Show | 253 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(250): Show |
missense_variant | MODERATE | c.4105G>T | p.Ala1369Ser | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/39 | 4174/4921 | 4105/4746 | 1369/1581 | chr11 | 17396930 | ||
| chr11:17397205
|
C | T | 1 | a0011 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.3976G>A | p.Glu1326Lys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 32/39 | 4045/4921 | 3976/4746 | 1326/1581 | chr11 | 17397205 | ||
| chr11:17398350
|
C | A | 1 | a0010 | 1 | NA18987.hp2 | stop_gained | HIGH | c.3742G>T | p.Glu1248* | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 30/39 | 3811/4921 | 3742/4746 | 1248/1581 | chr11 | 17398350 | ||
| chr11:17414512
|
C | T | 1 | a0009 | 1 | HG02886.hp1 | missense_variant&splice_region_variant | MODERATE | c.2390G>A | p.Arg797Gln | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/39 | 2459/4921 | 2390/4746 | 797/1581 | chr11 | 17414512 | ||
| chr11:17414608
|
T | A | 1 | a0012 | 1 | HG02970.hp1 | missense_variant&splice_region_variant | MODERATE | c.2294A>T | p.Lys765Met | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/39 | 2363/4921 | 2294/4746 | 765/1581 | chr11 | 17414608 | ||
| chr11:17428606
|
C | T | 1 | a0013 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1882G>A | p.Glu628Lys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 13/39 | 1951/4921 | 1882/4746 | 628/1581 | chr11 | 17428606 | ||
| chr11:17428614
|
G | A | 1 | a0014 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1874C>T | p.Ala625Val | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 13/39 | 1943/4921 | 1874/4746 | 625/1581 | chr11 | 17428614 | ||
| chr11:17428630
|
G | A | 1 | a0008 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1858C>T | p.Arg620Cys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 13/39 | 1927/4921 | 1858/4746 | 620/1581 | chr11 | 17428630 | ||
| chr11:17430953
|
C | T | 2 | a0004a0007 | 4 | NA18946.hp2 NA18949.hp1 NA18983.hp1 others(1): Show |
missense_variant | MODERATE | c.1678G>A | p.Val560Met | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/39 | 1747/4921 | 1678/4746 | 560/1581 | chr11 | 17430953 | ||
| chr11:17442795
|
G | A | 1 | a0006 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1555C>T | p.Arg519Cys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/39 | 1624/4921 | 1555/4746 | 519/1581 | chr11 | 17442795 | ||
| chr11:17442840
|
G | A | 1 | a0005 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.1510C>T | p.Arg504Cys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/39 | 1579/4921 | 1510/4746 | 504/1581 | chr11 | 17442840 | ||
| chr11:17460616
|
A | T | 1 | a0015 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.883T>A | p.Phe295Ile | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/39 | 952/4921 | 883/4746 | 295/1581 | chr11 | 17460616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17393009
|
G | A | 4 | a0001c0035a0001c0071a0001c0076others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.4728C>T | p.Phe1576Phe | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 39/39 | 4797/4921 | 4728/4746 | 1576/1581 | chr11 | 17393009 | ||
| chr11:17393081
|
C | T | 1 | a0001c0046 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.4656G>A | p.Lys1552Lys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 39/39 | 4725/4921 | 4656/4746 | 1552/1581 | chr11 | 17393081 | ||
| chr11:17394269
|
G | T | 2 | a0001c0061a0001c0077 | 2 | HG00639.hp1 HG02451.hp2 |
synonymous_variant | LOW | c.4542C>A | p.Ala1514Ala | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 37/39 | 4611/4921 | 4542/4746 | 1514/1581 | chr11 | 17394269 | ||
| chr11:17395910
|
G | C | 1 | a0002c0064 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.4140C>G | p.Thr1380Thr | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 34/39 | 4209/4921 | 4140/4746 | 1380/1581 | chr11 | 17395910 | ||
| chr11:17396919
|
C | T | 1 | a0001c0051 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.4116G>A | p.Gln1372Gln | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/39 | 4185/4921 | 4116/4746 | 1372/1581 | chr11 | 17396919 | ||
| chr11:17397732
|
C | T | 39 | a0001c0004a0001c0006a0001c0008others(36): Show | 132 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(129): Show |
synonymous_variant | LOW | c.3819G>A | p.Arg1273Arg | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 31/39 | 3888/4921 | 3819/4746 | 1273/1581 | chr11 | 17397732 | ||
| chr11:17402699
|
G | A | 4 | a0001c0019a0001c0031a0001c0059others(1): Show | 9 | HG01070.hp2 HG01255.hp2 HG01258.hp1 others(6): Show |
synonymous_variant | LOW | c.3612C>T | p.Ala1204Ala | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/39 | 3681/4921 | 3612/4746 | 1204/1581 | chr11 | 17402699 | ||
| chr11:17404634
|
G | A | 1 | a0001c0053 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.3435C>T | p.Ser1145Ser | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/39 | 3504/4921 | 3435/4746 | 1145/1581 | chr11 | 17404634 | ||
| chr11:17407011
|
C | T | 1 | a0002c0060 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.3039G>A | p.Ser1013Ser | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 25/39 | 3108/4921 | 3039/4746 | 1013/1581 | chr11 | 17407011 | ||
| chr11:17407050
|
G | A | 1 | a0002c0047 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.3000C>T | p.Cys1000Cys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 25/39 | 3069/4921 | 3000/4746 | 1000/1581 | chr11 | 17407050 | ||
| chr11:17407092
|
C | T | 3 | a0001c0065a0001c0068a0001c0081 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.2958G>A | p.Ser986Ser | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 25/39 | 3027/4921 | 2958/4746 | 986/1581 | chr11 | 17407092 | ||
| chr11:17410600
|
G | A | 1 | a0001c0070 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2610C>T | p.Ala870Ala | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/39 | 2679/4921 | 2610/4746 | 870/1581 | chr11 | 17410600 | ||
| chr11:17412684
|
G | A | 2 | a0001c0071a0008c0055 | 2 | HG03195.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.2538C>T | p.His846His | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/39 | 2607/4921 | 2538/4746 | 846/1581 | chr11 | 17412684 | ||
| chr11:17412737
|
G | A | 13 | a0001c0014a0001c0015a0001c0017others(10): Show | 43 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
synonymous_variant | LOW | c.2485C>T | p.Leu829Leu | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/39 | 2554/4921 | 2485/4746 | 829/1581 | chr11 | 17412737 | ||
| chr11:17415318
|
G | A | 1 | a0002c0054 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.2277C>T | p.Thr759Thr | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/39 | 2346/4921 | 2277/4746 | 759/1581 | chr11 | 17415318 | ||
| chr11:17427096
|
G | A | 1 | a0004c0041 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.2175C>T | p.Ala725Ala | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/39 | 2244/4921 | 2175/4746 | 725/1581 | chr11 | 17427096 | ||
| chr11:17428382
|
C | T | 25 | a0001c0007a0001c0009a0001c0012others(22): Show | 74 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(71): Show |
synonymous_variant | LOW | c.1947G>A | p.Lys649Lys | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 14/39 | 2016/4921 | 1947/4746 | 649/1581 | chr11 | 17428382 | ||
| chr11:17428403
|
G | C | 2 | a0001c0079a0001c0080 | 2 | HG02258.hp1 HG02818.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1926C>G | p.Pro642Pro | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 14/39 | 1995/4921 | 1926/4746 | 642/1581 | chr11 | 17428403 | ||
| chr11:17430864
|
C | T | 1 | a0002c0064 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.1767G>A | p.Pro589Pro | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/39 | 1836/4921 | 1767/4746 | 589/1581 | chr11 | 17430864 | ||
| chr11:17430945
|
G | A | 45 | a0001c0007a0001c0008a0001c0009others(42): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(137): Show |
synonymous_variant | LOW | c.1686C>T | p.His562His | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/39 | 1755/4921 | 1686/4746 | 562/1581 | chr11 | 17430945 | ||
| chr11:17442778
|
C | T | 2 | a0001c0026a0001c0075 | 4 | HG02717.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.1572G>A | p.Thr524Thr | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/39 | 1641/4921 | 1572/4746 | 524/1581 | chr11 | 17442778 | ||
| chr11:17453137
|
G | A | 3 | a0001c0025a0001c0073a0012c0072 | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
synonymous_variant | LOW | c.1158C>T | p.Asn386Asn | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/39 | 1227/4921 | 1158/4746 | 386/1581 | chr11 | 17453137 | ||
| chr11:17460554
|
G | A | 1 | a0001c0081 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.945C>T | p.Ala315Ala | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/39 | 1014/4921 | 945/4746 | 315/1581 | chr11 | 17460554 | ||
| chr11:17461670
|
G | A | 1 | a0002c0074 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.735C>T | p.Ile245Ile | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/39 | 804/4921 | 735/4746 | 245/1581 | chr11 | 17461670 | ||
| chr11:17463594
|
C | T | 2 | a0001c0035a0003c0036 | 2 | HG02258.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.423G>A | p.Val141Val | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/39 | 492/4921 | 423/4746 | 141/1581 | chr11 | 17463594 | ||
| chr11:17470183
|
G | A | 13 | a0001c0015a0001c0026a0001c0033others(10): Show | 26 | HG00639.hp1 HG01123.hp2 HG01361.hp1 others(23): Show |
synonymous_variant | LOW | c.330C>T | p.Ala110Ala | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/39 | 399/4921 | 330/4746 | 110/1581 | chr11 | 17470183 | ||
| chr11:17474969
|
A | G | 35 | a0001c0003a0001c0006a0001c0007others(32): Show | 126 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(123): Show |
synonymous_variant | LOW | c.207T>C | p.Pro69Pro | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/39 | 276/4921 | 207/4746 | 69/1581 | chr11 | 17474969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17476795
|
T | C | 3 | a0001c0009t0003a0001c0021t0003a0001c0026t0004 | 3 | HG00735.hp1 HG03130.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-19A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/39 | 19 | chr11 | 17476795 | |||||
| chr11:17476825
|
C | G | 10 | a0001c0004t0002a0001c0009t0003a0001c0010t0002others(7): Show | 11 | HG00735.hp1 HG01256.hp2 HG01884.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-49G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/39 | 49 | chr11 | 17476825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17393168
|
T | C | 125 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.4609-40A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 38/38 | chr11 | 17393168 | ||||||
| chr11:17393210
|
C | T | 29 | a0001c0001t0001g0173a0001c0001t0001g0219a0001c0001t0001g0241others(26): Show | 31 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.4609-82G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 38/38 | chr11 | 17393210 | ||||||
| chr11:17393230
|
AG | A | 90 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(87): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.4609-103delC | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 38/38 | chr11 | 17393230 | ||||||
| chr11:17393396
|
A | G | 1 | a0001c0007t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4609-268T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 38/38 | chr11 | 17393396 | ||||||
| chr11:17393596
|
A | C | 59 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.4608+101T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 38/38 | chr11 | 17393596 | ||||||
| chr11:17393643
|
C | G | 250 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(247): Show | 254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.4608+54G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 38/38 | chr11 | 17393643 | ||||||
| chr11:17394075
|
C | T | 2 | a0001c0061t0001g0311a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.4545+191G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 37/38 | chr11 | 17394075 | ||||||
| chr11:17394107
|
C | G | 1 | a0001c0010t0002g0005 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4545+159G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 37/38 | chr11 | 17394107 | ||||||
| chr11:17394465
|
G | A | 2 | a0002c0002t0001g0236a0002c0005t0001g0161 | 2 | HG02523.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.4412-66C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 36/38 | chr11 | 17394465 | ||||||
| chr11:17394537
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4412-138C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 36/38 | chr11 | 17394537 | ||||||
| chr11:17394550
|
G | A | 3 | a0001c0001t0001g0317a0001c0013t0001g0189a0001c0033t0001g0001 | 4 | HG01346.hp2 HG01361.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.4412-151C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 36/38 | chr11 | 17394550 | ||||||
| chr11:17394578
|
G | A | 18 | a0001c0004t0001g0270a0001c0006t0001g0096a0001c0006t0001g0097others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.4412-179C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 36/38 | chr11 | 17394578 | ||||||
| chr11:17394835
|
C | T | 5 | a0001c0010t0002g0005a0001c0035t0002g0013a0001c0071t0001g0071others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.4411+337G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 36/38 | chr11 | 17394835 | ||||||
| chr11:17394860
|
G | T | 1 | a0001c0049t0001g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4411+312C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 36/38 | chr11 | 17394860 | ||||||
| chr11:17395331
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4308-56G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 35/38 | chr11 | 17395331 | ||||||
| chr11:17395787
|
G | A | 2 | a0001c0073t0001g0055a0001c0080t0001g0312 | 2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4198+65C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 34/38 | chr11 | 17395787 | ||||||
| chr11:17395790
|
C | T | 18 | a0001c0004t0001g0270a0001c0006t0001g0096a0001c0006t0001g0097others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.4198+62G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 34/38 | chr11 | 17395790 | ||||||
| chr11:17395834
|
G | A | 2 | a0001c0034t0001g0176a0001c0034t0001g0177 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4198+18C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 34/38 | chr11 | 17395834 | ||||||
| chr11:17395949
|
G | A | 18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG01070.hp1 HG01433.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.4120-19C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17395949 | ||||||
| chr11:17395957
|
A | G | 134 | a0001c0004t0001g0144a0001c0004t0001g0178a0001c0004t0001g0187others(131): Show | 136 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.4120-27T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17395957 | ||||||
| chr11:17396074
|
A | T | 1 | a0001c0020t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4120-144T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396074 | ||||||
| chr11:17396362
|
C | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0275 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.4120-432G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396362 | ||||||
| chr11:17396476
|
A | G | 16 | a0001c0004t0001g0270a0001c0006t0001g0096a0001c0006t0001g0097others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.4119+440T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396476 | ||||||
| chr11:17396534
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4119+382G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396534 | ||||||
| chr11:17396558
|
G | A | 3 | a0002c0002t0001g0183a0002c0005t0001g0279a0002c0011t0001g0263 | 3 | HG00558.hp2 NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.4119+358C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396558 | ||||||
| chr11:17396652
|
G | A | 1 | a0001c0009t0001g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4119+264C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396652 | ||||||
| chr11:17396662
|
G | C | 15 | a0002c0002t0001g0067a0002c0002t0001g0239a0002c0002t0001g0240others(12): Show | 15 | HG00423.hp2 HG01074.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.4119+254C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396662 | ||||||
| chr11:17396758
|
G | A | 1 | a0001c0008t0001g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4119+158C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396758 | ||||||
| chr11:17396823
|
C | A | 71 | a0001c0004t0001g0178a0001c0004t0001g0187a0001c0004t0001g0218others(68): Show | 71 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.4119+93G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396823 | ||||||
| chr11:17396898
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4119+18A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396898 | ||||||
| chr11:17396901
|
G | A | 1 | a0002c0011t0001g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4119+15C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 33/38 | chr11 | 17396901 | ||||||
| chr11:17397056
|
G | A | 1 | a0001c0053t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3989-10C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 32/38 | chr11 | 17397056 | ||||||
| chr11:17397108
|
C | A | 1 | a0001c0003t0001g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3989-62G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 32/38 | chr11 | 17397108 | ||||||
| chr11:17397131
|
G | T | 1 | a0002c0018t0001g0190 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3988+62C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 32/38 | chr11 | 17397131 | ||||||
| chr11:17397351
|
G | A | 1 | a0001c0021t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3868-38C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 31/38 | chr11 | 17397351 | ||||||
| chr11:17397527
|
G | A | 17 | a0001c0004t0001g0270a0001c0006t0001g0096a0001c0006t0001g0097others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.3867+157C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 31/38 | chr11 | 17397527 | ||||||
| chr11:17397552
|
C | T | 1 | a0001c0020t0001g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3867+132G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 31/38 | chr11 | 17397552 | ||||||
| chr11:17397825
|
C | T | 1 | a0002c0011t0001g0202 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3754-28G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 30/38 | chr11 | 17397825 | ||||||
| chr11:17397953
|
G | A | 98 | a0001c0004t0001g0178a0001c0004t0001g0187a0001c0004t0001g0218others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.3754-156C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 30/38 | chr11 | 17397953 | ||||||
| chr11:17397983
|
C | T | 2 | a0001c0034t0001g0176a0001c0034t0001g0177 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3754-186G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 30/38 | chr11 | 17397983 | ||||||
| chr11:17398040
|
T | A | 2 | a0001c0061t0001g0311a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3754-243A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 30/38 | chr11 | 17398040 | ||||||
| chr11:17398070
|
G | T | 17 | a0001c0004t0001g0270a0001c0006t0001g0096a0001c0006t0001g0097others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.3753+269C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 30/38 | chr11 | 17398070 | ||||||
| chr11:17398549
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3651-108T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17398549 | ||||||
| chr11:17398596
|
A | G | 2 | a0001c0013t0001g0064a0001c0013t0001g0247 | 2 | NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.3651-155T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17398596 | ||||||
| chr11:17398670
|
T | C | 58 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3651-229A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17398670 | ||||||
| chr11:17398790
|
A | G | 2 | a0001c0061t0001g0311a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3651-349T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17398790 | ||||||
| chr11:17398990
|
C | T | 86 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(83): Show | 88 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.3651-549G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17398990 | ||||||
| chr11:17398997
|
G | A | 58 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3651-556C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17398997 | ||||||
| chr11:17399006
|
C | G | 29 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0079others(26): Show | 31 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.3651-565G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399006 | ||||||
| chr11:17399031
|
G | A | 1 | a0002c0018t0001g0188 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3651-590C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399031 | ||||||
| chr11:17399039
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0275 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3651-598G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399039 | ||||||
| chr11:17399040
|
G | A | 18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG01070.hp1 HG01433.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.3651-599C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399040 | ||||||
| chr11:17399066
|
C | T | 2 | a0001c0061t0001g0311a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3651-625G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399066 | ||||||
| chr11:17399077
|
T | C | 1 | a0001c0004t0001g0270 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3651-636A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399077 | ||||||
| chr11:17399091
|
G | A | 58 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3651-650C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399091 | ||||||
| chr11:17399179
|
G | A | 1 | a0001c0010t0002g0005 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3651-738C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399179 | ||||||
| chr11:17399186
|
T | G | 58 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3651-745A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399186 | ||||||
| chr11:17399275
|
C | CA | 32 | a0001c0003t0001g0087a0001c0003t0001g0088a0001c0003t0001g0164others(29): Show | 32 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.3651-835dupT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399275
|
CA | C | 34 | a0001c0001t0001g0061a0001c0001t0001g0172a0001c0004t0001g0187others(31): Show | 34 | HG00621.hp2 HG00738.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.3651-835delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399275
|
CAA | C | 33 | a0001c0004t0001g0178a0001c0004t0001g0218a0001c0004t0001g0223others(30): Show | 33 | HG00733.hp1 HG00741.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.3651-836_3651-835d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399275
|
CAAA | C | 6 | a0001c0008t0001g0157a0001c0014t0001g0168a0001c0014t0001g0322others(3): Show | 6 | HG02572.hp2 HG02602.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3651-837_3651-835d others(5): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399275
|
CAAAAAAA others(3): Show |
C | 17 | a0001c0001t0001g0215a0001c0001t0001g0254a0001c0001t0001g0255others(14): Show | 17 | HG00673.hp1 HG00733.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.3651-844_3651-835d others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399275
|
CAAAAAAA others(4): Show |
C | 70 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(67): Show | 72 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.3651-845_3651-835d others(13): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399275
|
CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001g0231 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3651-846_3651-835d others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399275 | ||||||
| chr11:17399293
|
A | AAC | 18 | a0001c0004t0001g0296a0001c0006t0001g0079a0001c0009t0001g0002others(15): Show | 20 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.3651-853_3651-852i others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399293 | ||||||
| chr11:17399293
|
A | AC | 12 | a0001c0004t0001g0144a0001c0006t0001g0091a0001c0008t0001g0041others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3651-853_3651-852i others(3): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399293 | ||||||
| chr11:17399297
|
A | AAAC | 11 | a0001c0006t0001g0097a0001c0009t0001g0289a0001c0019t0001g0121others(8): Show | 11 | HG01070.hp2 HG01175.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.3651-857_3651-856i others(5): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399297 | ||||||
| chr11:17399297
|
A | AAC | 9 | a0001c0004t0002g0012a0001c0006t0001g0096a0001c0009t0001g0268others(6): Show | 9 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.3651-857_3651-856i others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399297 | ||||||
| chr11:17399297
|
A | AC | 5 | a0001c0004t0001g0270a0001c0035t0002g0013a0001c0071t0001g0071others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3651-857_3651-856i others(3): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399297 | ||||||
| chr11:17399297
|
A | C | 33 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0079others(30): Show | 35 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.3651-856T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399297 | ||||||
| chr11:17399298
|
A | C | 2 | a0001c0073t0001g0055a0001c0080t0001g0312 | 2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3651-857T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399298 | ||||||
| chr11:17399301
|
A | C | 59 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.3651-860T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399301 | ||||||
| chr11:17399546
|
G | A | 58 | a0001c0004t0001g0144a0001c0004t0001g0270a0001c0004t0001g0296others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3651-1105C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399546 | ||||||
| chr11:17399645
|
A | G | 4 | a0001c0035t0002g0013a0001c0071t0001g0071a0001c0076t0002g0007others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3651-1204T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399645 | ||||||
| chr11:17399684
|
C | T | 1 | a0001c0003t0001g0100 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3651-1243G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399684 | ||||||
| chr11:17399819
|
G | T | 32 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0079others(29): Show | 34 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.3651-1378C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399819 | ||||||
| chr11:17399885
|
C | T | 7 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0047others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.3651-1444G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399885 | ||||||
| chr11:17399886
|
G | A | 2 | a0001c0007t0001g0119a0001c0007t0001g0163 | 2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.3651-1445C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399886 | ||||||
| chr11:17399926
|
G | A | 129 | a0001c0004t0001g0144a0001c0004t0001g0178a0001c0004t0001g0187others(126): Show | 131 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.3651-1485C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399926 | ||||||
| chr11:17399975
|
G | A | 1 | a0001c0046t0001g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3651-1534C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17399975 | ||||||
| chr11:17400027
|
G | T | 1 | a0002c0005t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3651-1586C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400027 | ||||||
| chr11:17400046
|
G | A | 1 | a0001c0021t0001g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3651-1605C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400046 | ||||||
| chr11:17400073
|
G | C | 19 | a0001c0004t0001g0270a0001c0004t0002g0012a0001c0006t0001g0096others(16): Show | 19 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.3651-1632C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400073 | ||||||
| chr11:17400167
|
G | T | 149 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(146): Show | 151 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(148): Show |
intron_variant | MODIFIER | c.3651-1726C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400167 | ||||||
| chr11:17400243
|
G | A | 92 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(89): Show | 94 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3651-1802C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400243 | ||||||
| chr11:17400257
|
C | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3651-1816G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400257 | ||||||
| chr11:17400304
|
C | A | 1 | a0001c0007t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3651-1863G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400304 | ||||||
| chr11:17400313
|
A | G | 240 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(237): Show | 244 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.3651-1872T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400313 | ||||||
| chr11:17400339
|
T | C | 254 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(251): Show | 258 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.3651-1898A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400339 | ||||||
| chr11:17400552
|
T | C | 148 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(145): Show | 150 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(147): Show |
intron_variant | MODIFIER | c.3650+2109A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400552 | ||||||
| chr11:17400613
|
C | G | 1 | a0001c0022t0001g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3650+2048G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400613 | ||||||
| chr11:17400697
|
G | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0275 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3650+1964C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400697 | ||||||
| chr11:17400721
|
C | T | 1 | a0001c0073t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3650+1940G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400721 | ||||||
| chr11:17400731
|
G | A | 1 | a0001c0014t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3650+1930C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400731 | ||||||
| chr11:17400850
|
C | T | 19 | a0001c0004t0001g0270a0001c0004t0002g0012a0001c0006t0001g0096others(16): Show | 19 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.3650+1811G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400850 | ||||||
| chr11:17400872
|
A | G | 148 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(145): Show | 150 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(147): Show |
intron_variant | MODIFIER | c.3650+1789T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400872 | ||||||
| chr11:17400885
|
A | G | 9 | a0001c0019t0001g0121a0001c0019t0001g0280a0001c0019t0001g0284others(6): Show | 9 | HG01070.hp2 HG01255.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3650+1776T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400885 | ||||||
| chr11:17400974
|
C | A | 1 | a0001c0010t0002g0005 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3650+1687G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17400974 | ||||||
| chr11:17401072
|
T | C | 157 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 159 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(156): Show |
intron_variant | MODIFIER | c.3650+1589A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401072 | ||||||
| chr11:17401162
|
A | G | 4 | a0001c0035t0002g0013a0001c0071t0001g0071a0001c0076t0002g0007others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3650+1499T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401162 | ||||||
| chr11:17401388
|
C | T | 1 | a0001c0021t0001g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3650+1273G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401388 | ||||||
| chr11:17401408
|
C | A | 92 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(89): Show | 94 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3650+1253G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401408 | ||||||
| chr11:17401515
|
G | C | 16 | a0001c0004t0001g0296a0001c0006t0001g0079a0001c0009t0001g0002others(13): Show | 18 | HG00735.hp1 HG01243.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3650+1146C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401515 | ||||||
| chr11:17401526
|
T | C | 3 | a0001c0035t0002g0013a0001c0071t0001g0071a0008c0055t0001g0078 | 3 | HG02258.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3650+1135A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401526 | ||||||
| chr11:17401615
|
C | T | 2 | a0002c0016t0001g0305a0002c0016t0001g0306 | 2 | HG01074.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.3650+1046G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401615 | ||||||
| chr11:17401847
|
C | CA | 32 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0079others(29): Show | 34 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.3650+813dupT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401847 | ||||||
| chr11:17401860
|
GT | G | 96 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(93): Show | 98 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.3650+800delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17401860 | ||||||
| chr11:17402088
|
C | T | 52 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(49): Show | 54 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.3650+573G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17402088 | ||||||
| chr11:17402186
|
G | T | 1 | a0001c0003t0001g0130 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3650+475C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17402186 | ||||||
| chr11:17402195
|
C | T | 20 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(17): Show | 20 | HG00639.hp1 HG01070.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.3650+466G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17402195 | ||||||
| chr11:17402279
|
T | G | 17 | a0001c0004t0001g0270a0001c0006t0001g0096a0001c0006t0001g0097others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.3650+382A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17402279 | ||||||
| chr11:17402373
|
G | T | 1 | a0001c0003t0001g0309 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3650+288C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 29/38 | chr11 | 17402373 | ||||||
| chr11:17402848
|
G | A | 52 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(49): Show | 54 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.3558-95C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17402848 | ||||||
| chr11:17402986
|
A | T | 32 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0079others(29): Show | 34 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.3558-233T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17402986 | ||||||
| chr11:17403148
|
A | G | 1 | a0001c0013t0001g0175 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3558-395T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17403148 | ||||||
| chr11:17403164
|
C | T | 96 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0076others(93): Show | 98 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.3558-411G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17403164 | ||||||
| chr11:17403272
|
A | G | 1 | a0007c0039t0001g0109 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3558-519T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17403272 | ||||||
| chr11:17403379
|
A | T | 2 | a0002c0005t0001g0120a0002c0011t0001g0213 | 2 | HG00140.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3558-626T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17403379 | ||||||
| chr11:17403441
|
C | T | 53 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(50): Show | 55 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.3558-688G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17403441 | ||||||
| chr11:17403904
|
T | C | 9 | a0001c0024t0001g0153a0001c0061t0001g0311a0001c0075t0001g0033others(6): Show | 9 | HG00642.hp1 HG01433.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3557+608A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17403904 | ||||||
| chr11:17404104
|
G | A | 28 | a0001c0004t0001g0293a0001c0006t0001g0044a0001c0006t0001g0092others(25): Show | 28 | HG01243.hp2 HG01256.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.3557+408C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404104 | ||||||
| chr11:17404149
|
G | T | 41 | a0001c0004t0001g0293a0001c0006t0001g0044a0001c0006t0001g0079others(38): Show | 41 | HG01106.hp1 HG01243.hp2 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.3557+363C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404149 | ||||||
| chr11:17404195
|
A | G | 1 | a0002c0030t0001g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3557+317T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404195 | ||||||
| chr11:17404250
|
T | C | 4 | a0001c0001t0001g0235a0001c0013t0001g0064a0001c0013t0001g0247others(1): Show | 4 | HG02040.hp2 NA18975.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.3557+262A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404250 | ||||||
| chr11:17404390
|
GTTTT | G | 49 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(46): Show | 49 | HG01243.hp1 HG01261.hp2 HG01516.hp1 others(46): Show |
intron_variant | MODIFIER | c.3557+118_3557+121d others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404390 | ||||||
| chr11:17404441
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3557+71C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404441 | ||||||
| chr11:17404489
|
C | A | 1 | a0001c0020t0001g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3557+23G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 28/38 | chr11 | 17404489 | ||||||
| chr11:17404738
|
G | A | 1 | a0001c0010t0001g0192 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3400-69C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17404738 | ||||||
| chr11:17404823
|
G | A | 2 | a0002c0002t0001g0216a0002c0002t0001g0222 | 2 | NA19056.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.3400-154C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17404823 | ||||||
| chr11:17404964
|
G | T | 5 | a0001c0010t0001g0298a0001c0015t0001g0020a0001c0025t0001g0054others(2): Show | 5 | HG02145.hp2 HG03041.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3400-295C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17404964 | ||||||
| chr11:17405084
|
G | A | 1 | a0001c0012t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3399+410C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17405084 | ||||||
| chr11:17405336
|
C | G | 1 | a0002c0005t0001g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3399+158G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17405336 | ||||||
| chr11:17405465
|
G | A | 1 | a0001c0010t0001g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3399+29C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17405465 | ||||||
| chr11:17405481
|
C | T | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3399+13G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 27/38 | chr11 | 17405481 | ||||||
| chr11:17405789
|
G | C | 248 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(245): Show | 251 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.3330-226C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17405789 | ||||||
| chr11:17405816
|
C | T | 102 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(99): Show | 104 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.3330-253G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17405816 | ||||||
| chr11:17405876
|
C | A | 1 | a0002c0005t0001g0026 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3330-313G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17405876 | ||||||
| chr11:17405922
|
G | A | 1 | a0001c0020t0001g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3330-359C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17405922 | ||||||
| chr11:17406010
|
T | C | 141 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0173others(138): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.3330-447A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406010 | ||||||
| chr11:17406124
|
T | G | 1 | a0002c0011t0001g0217 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3329+498A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406124 | ||||||
| chr11:17406135
|
A | G | 1 | a0001c0007t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3329+487T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406135 | ||||||
| chr11:17406262
|
G | A | 1 | a0001c0007t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3329+360C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406262 | ||||||
| chr11:17406275
|
T | C | 248 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(245): Show | 251 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.3329+347A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406275 | ||||||
| chr11:17406315
|
G | A | 101 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(98): Show | 103 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.3329+307C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406315 | ||||||
| chr11:17406354
|
C | G | 99 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(96): Show | 101 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.3329+268G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406354 | ||||||
| chr11:17406438
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3329+184G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 26/38 | chr11 | 17406438 | ||||||
| chr11:17407234
|
G | A | 1 | a0001c0025t0001g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2921-105C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 24/38 | chr11 | 17407234 | ||||||
| chr11:17407275
|
C | T | 1 | a0002c0002t0001g0222 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2920+79G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 24/38 | chr11 | 17407275 | ||||||
| chr11:17407617
|
G | C | 1 | a0001c0017t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2821-164C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17407617 | ||||||
| chr11:17407760
|
C | T | 3 | a0001c0006t0001g0096a0001c0006t0001g0097a0002c0011t0001g0243 | 3 | HG01074.hp2 HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2821-307G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17407760 | ||||||
| chr11:17407811
|
G | A | 171 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(168): Show | 173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.2821-358C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17407811 | ||||||
| chr11:17408187
|
C | T | 2 | a0001c0004t0002g0012a0001c0061t0001g0311 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2820+205G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17408187 | ||||||
| chr11:17408270
|
C | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2820+122G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17408270 | ||||||
| chr11:17408281
|
C | A | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2820+111G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17408281 | ||||||
| chr11:17408291
|
C | T | 1 | a0002c0005t0001g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2820+101G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17408291 | ||||||
| chr11:17408325
|
G | A | 40 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(37): Show | 41 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2820+67C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17408325 | ||||||
| chr11:17408375
|
T | C | 203 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(200): Show | 205 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2820+17A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 23/38 | chr11 | 17408375 | ||||||
| chr11:17408769
|
G | T | 31 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 32 | HG00558.hp1 HG00639.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.2695-252C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17408769 | ||||||
| chr11:17408834
|
C | T | 1 | a0002c0005t0001g0111 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2695-317G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17408834 | ||||||
| chr11:17408839
|
T | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.2695-322A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17408839 | ||||||
| chr11:17408952
|
C | CT | 145 | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0076others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2695-436dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17408952 | ||||||
| chr11:17408952
|
CT | C | 7 | a0001c0003t0001g0167a0001c0009t0001g0201a0001c0014t0002g0009others(4): Show | 7 | HG00099.hp1 HG01070.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2695-436delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17408952 | ||||||
| chr11:17409101
|
C | T | 206 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(203): Show | 208 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.2695-584G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409101 | ||||||
| chr11:17409119
|
AT | A | 191 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2695-603delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409119 | ||||||
| chr11:17409119
|
ATT | A | 11 | a0001c0003t0001g0282a0001c0004t0001g0258a0001c0004t0001g0261others(8): Show | 11 | HG01074.hp1 HG01168.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.2695-604_2695-603d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409119 | ||||||
| chr11:17409141
|
A | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2695-624T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409141 | ||||||
| chr11:17409176
|
C | T | 3 | a0001c0080t0001g0312a0002c0016t0001g0305a0002c0016t0001g0306 | 3 | HG01074.hp1 HG01192.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2695-659G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409176 | ||||||
| chr11:17409326
|
C | A | 2 | a0001c0006t0001g0096a0001c0006t0001g0097 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2695-809G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409326 | ||||||
| chr11:17409350
|
G | A | 171 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(168): Show | 173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.2695-833C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409350 | ||||||
| chr11:17409386
|
A | G | 249 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(246): Show | 252 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.2695-869T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409386 | ||||||
| chr11:17409584
|
A | G | 2 | a0001c0004t0001g0293a0001c0008t0001g0165 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2694+932T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409584 | ||||||
| chr11:17409663
|
A | G | 249 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(246): Show | 252 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.2694+853T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409663 | ||||||
| chr11:17409814
|
G | A | 40 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(37): Show | 41 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2694+702C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409814 | ||||||
| chr11:17409999
|
G | C | 1 | a0001c0014t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2694+517C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17409999 | ||||||
| chr11:17410043
|
C | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2694+473G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17410043 | ||||||
| chr11:17410121
|
A | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2694+395T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17410121 | ||||||
| chr11:17410134
|
A | G | 1 | a0001c0007t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2694+382T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17410134 | ||||||
| chr11:17410270
|
C | T | 4 | a0001c0012t0001g0210a0001c0012t0001g0211a0001c0012t0001g0212others(1): Show | 4 | HG01515.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.2694+246G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17410270 | ||||||
| chr11:17410308
|
G | A | 1 | a0001c0076t0002g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2694+208C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 22/38 | chr11 | 17410308 | ||||||
| chr11:17410902
|
C | T | 1 | a0001c0017t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2557-249G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17410902 | ||||||
| chr11:17411040
|
C | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2557-387G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411040 | ||||||
| chr11:17411041
|
G | A | 1 | a0002c0005t0001g0277 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2557-388C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411041 | ||||||
| chr11:17411240
|
C | T | 28 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0044others(25): Show | 28 | HG00735.hp1 HG01243.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.2557-587G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411240 | ||||||
| chr11:17411347
|
C | T | 7 | a0001c0010t0001g0298a0001c0025t0001g0054a0001c0025t0001g0056others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2557-694G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411347 | ||||||
| chr11:17411541
|
A | C | 42 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(39): Show | 43 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2557-888T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411541 | ||||||
| chr11:17411681
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2556+985A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411681 | ||||||
| chr11:17411744
|
G | T | 42 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(39): Show | 43 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2556+922C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411744 | ||||||
| chr11:17411888
|
G | A | 1 | a0001c0007t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2556+778C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411888 | ||||||
| chr11:17411891
|
C | CT | 57 | a0001c0001t0001g0226a0001c0001t0001g0249a0001c0001t0001g0254others(54): Show | 59 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2556+774dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411891 | ||||||
| chr11:17411891
|
CT | C | 10 | a0001c0001t0001g0068a0001c0001t0001g0180a0001c0001t0001g0224others(7): Show | 10 | HG00639.hp1 HG01516.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2556+774delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411891 | ||||||
| chr11:17411891
|
CTT | C | 8 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0298others(5): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2556+773_2556+774d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411891 | ||||||
| chr11:17411985
|
C | T | 1 | a0002c0060t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2556+681G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17411985 | ||||||
| chr11:17412017
|
G | C | 245 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2556+649C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412017 | ||||||
| chr11:17412068
|
A | AT | 3 | a0001c0001t0001g0181a0001c0003t0001g0101a0002c0047t0001g0112 | 3 | HG02071.hp2 NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.2556+597dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412068 | ||||||
| chr11:17412084
|
G | C | 42 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(39): Show | 43 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2556+582C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412084 | ||||||
| chr11:17412143
|
C | T | 7 | a0001c0010t0001g0298a0001c0025t0001g0054a0001c0025t0001g0056others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2556+523G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412143 | ||||||
| chr11:17412190
|
C | T | 42 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(39): Show | 43 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2556+476G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412190 | ||||||
| chr11:17412200
|
T | A | 2 | a0002c0027t0001g0028a0002c0027t0001g0029 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2556+466A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412200 | ||||||
| chr11:17412315
|
A | G | 138 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(135): Show | 139 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2556+351T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412315 | ||||||
| chr11:17412328
|
T | C | 2 | a0001c0003t0001g0095a0002c0011t0001g0263 | 2 | HG00558.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.2556+338A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412328 | ||||||
| chr11:17412473
|
TG | T | 133 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0173others(130): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.2556+192delC | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412473 | ||||||
| chr11:17412587
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2556+79C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412587 | ||||||
| chr11:17412636
|
G | A | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2556+30C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412636 | ||||||
| chr11:17412644
|
C | T | 2 | a0001c0071t0001g0071a0008c0055t0001g0078 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2556+22G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 21/38 | chr11 | 17412644 | ||||||
| chr11:17412777
|
C | T | 1 | a0001c0061t0001g0311 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2476-31G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 20/38 | chr11 | 17412777 | ||||||
| chr11:17412820
|
T | A | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2476-74A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 20/38 | chr11 | 17412820 | ||||||
| chr11:17413056
|
C | T | 244 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2476-310G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 20/38 | chr11 | 17413056 | ||||||
| chr11:17413097
|
G | A | 2 | a0001c0004t0001g0293a0001c0008t0001g0165 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2475+297C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 20/38 | chr11 | 17413097 | ||||||
| chr11:17413135
|
G | A | 2 | a0001c0007t0001g0129a0001c0009t0001g0268 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2475+259C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 20/38 | chr11 | 17413135 | ||||||
| chr11:17413248
|
A | G | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2475+146T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 20/38 | chr11 | 17413248 | ||||||
| chr11:17413546
|
G | A | 3 | a0002c0002t0001g0065a0002c0002t0001g0264a0002c0002t0001g0271 | 3 | NA18945.hp2 NA19080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2391-68C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17413546 | ||||||
| chr11:17413618
|
C | A | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2391-140G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17413618 | ||||||
| chr11:17413667
|
G | A | 138 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(135): Show | 139 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2391-189C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17413667 | ||||||
| chr11:17413955
|
T | C | 7 | a0001c0010t0001g0298a0001c0025t0001g0054a0001c0025t0001g0056others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2391-477A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17413955 | ||||||
| chr11:17414144
|
T | C | 3 | a0001c0004t0001g0218a0001c0004t0001g0250a0001c0004t0001g0266 | 3 | HG01516.hp1 HG01517.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2390+368A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414144 | ||||||
| chr11:17414235
|
G | A | 1 | a0006c0056t0002g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2390+277C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414235 | ||||||
| chr11:17414293
|
A | G | 293 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2390+219T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414293 | ||||||
| chr11:17414305
|
TCCCCTAT others(13): Show |
T | 1 | a0003c0036t0001g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2390+187_2390+206d others(22): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414305 | ||||||
| chr11:17414331
|
A | G | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2390+181T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414331 | ||||||
| chr11:17414389
|
G | A | 243 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2390+123C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414389 | ||||||
| chr11:17414419
|
G | A | 243 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2390+93C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414419 | ||||||
| chr11:17414495
|
C | G | 2 | a0001c0003t0001g0094a0002c0005t0001g0111 | 2 | NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2390+17G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 19/38 | chr11 | 17414495 | ||||||
| chr11:17414644
|
A | G | 106 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2292-34T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17414644 | ||||||
| chr11:17414646
|
G | A | 86 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2292-36C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17414646 | ||||||
| chr11:17414724
|
G | A | 42 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(39): Show | 43 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2292-114C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17414724 | ||||||
| chr11:17414759
|
C | A | 1 | a0001c0049t0001g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2292-149G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17414759 | ||||||
| chr11:17414910
|
C | T | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2292-300G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17414910 | ||||||
| chr11:17415004
|
C | CT | 30 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0044others(27): Show | 30 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2291+299dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17415004 | ||||||
| chr11:17415004
|
CT | C | 11 | a0001c0001t0001g0226a0001c0004t0001g0258a0001c0013t0001g0064others(8): Show | 11 | HG01070.hp2 HG01169.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2291+299delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17415004 | ||||||
| chr11:17415021
|
A | T | 54 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(51): Show | 55 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2291+283T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17415021 | ||||||
| chr11:17415065
|
G | GAAGAAAA | 317 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(314): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.2291+232_2291+238d others(9): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17415065 | ||||||
| chr11:17415099
|
G | A | 2 | a0002c0027t0001g0028a0002c0027t0001g0029 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2291+205C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17415099 | ||||||
| chr11:17415103
|
T | C | 1 | a0001c0017t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2291+201A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 18/38 | chr11 | 17415103 | ||||||
| chr11:17415389
|
A | G | 293 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2256-50T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17415389 | ||||||
| chr11:17415404
|
C | T | 64 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(61): Show | 66 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2256-65G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17415404 | ||||||
| chr11:17415806
|
G | C | 2 | a0001c0013t0001g0198a0002c0060t0001g0209 | 2 | HG00597.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.2256-467C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17415806 | ||||||
| chr11:17415977
|
T | A | 2 | a0001c0014t0001g0320a0001c0014t0001g0322 | 2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2256-638A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17415977 | ||||||
| chr11:17416160
|
G | A | 1 | a0001c0080t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2255+770C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416160 | ||||||
| chr11:17416237
|
G | T | 1 | a0001c0043t0001g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2255+693C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416237 | ||||||
| chr11:17416238
|
T | C | 135 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2255+692A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416238 | ||||||
| chr11:17416279
|
T | C | 86 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2255+651A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416279 | ||||||
| chr11:17416374
|
C | T | 1 | a0002c0044t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2255+556G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416374 | ||||||
| chr11:17416526
|
T | C | 23 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0044others(20): Show | 23 | HG01243.hp1 HG01496.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2255+404A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416526 | ||||||
| chr11:17416595
|
T | G | 4 | a0001c0010t0001g0298a0001c0025t0001g0054a0001c0025t0001g0056others(1): Show | 4 | HG02145.hp2 HG03516.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2255+335A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416595 | ||||||
| chr11:17416763
|
A | G | 1 | a0002c0011t0001g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2255+167T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 17/38 | chr11 | 17416763 | ||||||
| chr11:17417177
|
T | C | 3 | a0001c0003t0001g0086a0002c0005t0001g0025a0002c0005t0001g0026 | 3 | HG02698.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2223-215A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417177 | ||||||
| chr11:17417186
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2223-224C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417186 | ||||||
| chr11:17417322
|
G | A | 1 | a0002c0002t0001g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2223-360C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417322 | ||||||
| chr11:17417343
|
A | C | 138 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.2223-381T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417343 | ||||||
| chr11:17417615
|
G | A | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2223-653C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417615 | ||||||
| chr11:17417896
|
C | T | 134 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(131): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2223-934G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417896 | ||||||
| chr11:17417927
|
T | A | 1 | a0001c0020t0001g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2223-965A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17417927 | ||||||
| chr11:17418043
|
C | T | 44 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(41): Show | 45 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.2223-1081G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17418043 | ||||||
| chr11:17418108
|
C | T | 134 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(131): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2223-1146G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17418108 | ||||||
| chr11:17418114
|
G | A | 134 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(131): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2223-1152C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17418114 | ||||||
| chr11:17418682
|
A | G | 157 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2223-1720T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17418682 | ||||||
| chr11:17418926
|
A | G | 293 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2223-1964T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17418926 | ||||||
| chr11:17419120
|
C | T | 1 | a0001c0003t0001g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2223-2158G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419120 | ||||||
| chr11:17419233
|
G | C | 134 | a0001c0001t0001g0274a0001c0003t0001g0087a0001c0003t0001g0302others(131): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2223-2271C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419233 | ||||||
| chr11:17419321
|
C | T | 7 | a0001c0012t0001g0171a0001c0012t0001g0259a0001c0023t0001g0205others(4): Show | 7 | HG01261.hp2 HG01943.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2223-2359G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419321 | ||||||
| chr11:17419443
|
G | C | 134 | a0001c0001t0001g0274a0001c0003t0001g0087a0001c0003t0001g0302others(131): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2223-2481C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419443 | ||||||
| chr11:17419681
|
A | G | 47 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(44): Show | 48 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2223-2719T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419681 | ||||||
| chr11:17419838
|
C | T | 129 | a0001c0001t0001g0274a0001c0003t0001g0087a0001c0003t0001g0302others(126): Show | 132 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2223-2876G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419838 | ||||||
| chr11:17419861
|
T | C | 2 | a0001c0024t0001g0153a0001c0024t0001g0154 | 2 | NA18942.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2223-2899A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17419861 | ||||||
| chr11:17420079
|
C | G | 1 | a0001c0003t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2223-3117G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420079 | ||||||
| chr11:17420113
|
A | C | 1 | a0001c0025t0001g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2223-3151T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420113 | ||||||
| chr11:17420146
|
A | G | 3 | a0002c0002t0001g0065a0002c0002t0001g0264a0002c0002t0001g0271 | 3 | NA18945.hp2 NA19080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2223-3184T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420146 | ||||||
| chr11:17420172
|
C | T | 1 | a0001c0061t0001g0311 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2223-3210G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420172 | ||||||
| chr11:17420250
|
C | G | 2 | a0001c0070t0002g0008a0001c0080t0001g0312 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2223-3288G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420250 | ||||||
| chr11:17420281
|
G | A | 134 | a0001c0001t0001g0274a0001c0003t0001g0087a0001c0003t0001g0302others(131): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2223-3319C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420281 | ||||||
| chr11:17420375
|
A | G | 87 | a0001c0001t0001g0274a0001c0003t0001g0087a0001c0003t0001g0302others(84): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2223-3413T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420375 | ||||||
| chr11:17420467
|
C | A | 1 | a0001c0014t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2223-3505G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420467 | ||||||
| chr11:17420604
|
C | A | 1 | a0001c0014t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2223-3642G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420604 | ||||||
| chr11:17420720
|
G | T | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2223-3758C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420720 | ||||||
| chr11:17420868
|
T | A | 1 | a0003c0069t0001g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2223-3906A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420868 | ||||||
| chr11:17420913
|
T | A | 38 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0204others(35): Show | 39 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.2223-3951A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17420913 | ||||||
| chr11:17421004
|
G | C | 2 | a0001c0070t0002g0008a0001c0080t0001g0312 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2223-4042C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421004 | ||||||
| chr11:17421019
|
C | T | 4 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(1): Show | 4 | HG00735.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2223-4057G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421019 | ||||||
| chr11:17421034
|
C | T | 11 | a0001c0014t0001g0032a0001c0014t0001g0084a0001c0014t0001g0168others(8): Show | 11 | HG01243.hp2 HG01256.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2223-4072G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421034 | ||||||
| chr11:17421054
|
T | G | 5 | a0001c0003t0001g0094a0001c0007t0001g0116a0001c0007t0001g0125others(2): Show | 5 | HG02083.hp2 HG02135.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2223-4092A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421054 | ||||||
| chr11:17421111
|
T | C | 38 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0204others(35): Show | 39 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.2223-4149A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421111 | ||||||
| chr11:17421198
|
T | G | 79 | a0001c0001t0001g0274a0001c0003t0001g0087a0001c0003t0001g0302others(76): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2223-4236A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421198 | ||||||
| chr11:17421324
|
A | G | 4 | a0001c0007t0001g0119a0001c0007t0001g0124a0001c0007t0001g0163others(1): Show | 4 | HG02015.hp1 HG02027.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-4362T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421324 | ||||||
| chr11:17421373
|
G | A | 2 | a0001c0006t0001g0096a0001c0006t0001g0097 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2223-4411C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421373 | ||||||
| chr11:17421801
|
G | A | 5 | a0002c0018t0001g0193a0002c0018t0001g0200a0002c0054t0001g0132others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2223-4839C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17421801 | ||||||
| chr11:17422011
|
G | A | 5 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0065t0001g0288others(2): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2222+5038C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422011 | ||||||
| chr11:17422040
|
G | A | 39 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0204others(36): Show | 40 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2222+5009C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422040 | ||||||
| chr11:17422091
|
C | G | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2222+4958G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422091 | ||||||
| chr11:17422255
|
G | A | 1 | a0001c0012t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2222+4794C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422255 | ||||||
| chr11:17422286
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2222+4763T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422286 | ||||||
| chr11:17422477
|
A | G | 52 | a0001c0004t0001g0293a0001c0010t0001g0135a0001c0010t0001g0136others(49): Show | 53 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2222+4572T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422477 | ||||||
| chr11:17422587
|
T | C | 257 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(254): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2222+4462A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17422587 | ||||||
| chr11:17423037
|
A | G | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2222+4012T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423037 | ||||||
| chr11:17423043
|
C | T | 39 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0204others(36): Show | 40 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2222+4006G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423043 | ||||||
| chr11:17423070
|
C | T | 1 | a0001c0004t0001g0230 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2222+3979G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423070 | ||||||
| chr11:17423105
|
T | G | 157 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2222+3944A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423105 | ||||||
| chr11:17423311
|
C | T | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2222+3738G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423311 | ||||||
| chr11:17423332
|
G | C | 1 | a0002c0002t0001g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2222+3717C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423332 | ||||||
| chr11:17423356
|
C | CA | 103 | a0001c0001t0001g0224a0001c0003t0001g0086a0001c0003t0001g0087others(100): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.2222+3692dupT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423356 | ||||||
| chr11:17423356
|
C | CAA | 7 | a0001c0006t0001g0092a0001c0006t0001g0103a0001c0009t0001g0150others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.2222+3691_2222+369 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423356 | ||||||
| chr11:17423356
|
C | CAAA | 11 | a0001c0004t0001g0293a0001c0006t0001g0107a0001c0010t0001g0298others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2222+3690_2222+369 others(7): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423356 | ||||||
| chr11:17423356
|
C | CAAAA | 10 | a0001c0003t0001g0094a0001c0013t0001g0267a0001c0014t0002g0009others(7): Show | 10 | HG01256.hp2 HG02257.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2222+3689_2222+369 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423356 | ||||||
| chr11:17423356
|
C | CAAAAA | 102 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2222+3688_2222+369 others(9): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423356 | ||||||
| chr11:17423356
|
C | CAAAAAA | 30 | a0001c0001t0001g0181a0001c0003t0001g0082a0001c0003t0001g0088others(27): Show | 31 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2222+3687_2222+369 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423356 | ||||||
| chr11:17423479
|
C | T | 105 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2222+3570G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423479 | ||||||
| chr11:17423592
|
A | G | 158 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2222+3457T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423592 | ||||||
| chr11:17423964
|
T | G | 1 | a0001c0004t0001g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2222+3085A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17423964 | ||||||
| chr11:17424028
|
G | A | 13 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0014t0002g0006others(10): Show | 13 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2222+3021C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424028 | ||||||
| chr11:17424149
|
T | C | 156 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2222+2900A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424149 | ||||||
| chr11:17424167
|
G | T | 1 | a0001c0012t0001g0259 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2222+2882C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424167 | ||||||
| chr11:17424198
|
C | A | 96 | a0001c0003t0001g0087a0001c0004t0001g0144a0001c0004t0001g0296others(93): Show | 98 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.2222+2851G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424198 | ||||||
| chr11:17424210
|
A | G | 156 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2222+2839T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424210 | ||||||
| chr11:17424226
|
A | ATCT | 156 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2222+2822_2222+282 others(7): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424226 | ||||||
| chr11:17424391
|
T | C | 102 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2222+2658A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424391 | ||||||
| chr11:17424441
|
A | G | 1 | a0002c0011t0001g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2222+2608T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424441 | ||||||
| chr11:17424443
|
G | T | 6 | a0001c0004t0001g0293a0001c0014t0002g0006a0001c0022t0001g0292others(3): Show | 6 | HG02109.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2222+2606C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424443 | ||||||
| chr11:17424474
|
T | C | 161 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2222+2575A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424474 | ||||||
| chr11:17424593
|
G | A | 11 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0014t0002g0006others(8): Show | 11 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2222+2456C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424593 | ||||||
| chr11:17424881
|
C | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG00558.hp1 NA18941.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.2222+2168G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424881 | ||||||
| chr11:17424911
|
T | A | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2222+2138A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424911 | ||||||
| chr11:17424943
|
T | C | 1 | a0002c0002t0001g0318 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2222+2106A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17424943 | ||||||
| chr11:17425100
|
C | T | 2 | a0001c0010t0001g0191a0001c0010t0001g0192 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2222+1949G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425100 | ||||||
| chr11:17425101
|
A | G | 2 | a0002c0027t0001g0028a0002c0027t0001g0029 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2222+1948T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425101 | ||||||
| chr11:17425254
|
CA | C | 3 | a0001c0007t0001g0139a0001c0009t0001g0201a0001c0049t0001g0141 | 3 | HG01106.hp1 HG04204.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2222+1794delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425254 | ||||||
| chr11:17425294
|
G | A | 1 | a0001c0053t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2222+1755C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425294 | ||||||
| chr11:17425336
|
G | T | 1 | a0001c0073t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2222+1713C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425336 | ||||||
| chr11:17425389
|
T | C | 13 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0014t0002g0006others(10): Show | 13 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2222+1660A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425389 | ||||||
| chr11:17425415
|
T | A | 41 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(38): Show | 42 | HG00558.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2222+1634A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425415 | ||||||
| chr11:17425462
|
T | C | 1 | a0002c0002t0001g0237 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2222+1587A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425462 | ||||||
| chr11:17425474
|
G | A | 2 | a0001c0028t0001g0077a0002c0030t0001g0300 | 2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2222+1575C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425474 | ||||||
| chr11:17425501
|
C | A | 2 | a0001c0001t0001g0224a0001c0004t0001g0223 | 2 | NA18986.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2222+1548G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425501 | ||||||
| chr11:17425560
|
A | C | 118 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2222+1489T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425560 | ||||||
| chr11:17425893
|
T | C | 22 | a0001c0004t0001g0144a0001c0004t0001g0296a0001c0006t0001g0044others(19): Show | 22 | HG01243.hp1 HG01496.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2222+1156A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425893 | ||||||
| chr11:17425916
|
A | G | 1 | a0001c0003t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2222+1133T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425916 | ||||||
| chr11:17425931
|
T | C | 122 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2222+1118A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17425931 | ||||||
| chr11:17426218
|
G | A | 1 | a0002c0074t0001g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2222+831C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17426218 | ||||||
| chr11:17426766
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2222+283A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17426766 | ||||||
| chr11:17427012
|
T | C | 1 | a0001c0017t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2222+37A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 16/38 | chr11 | 17427012 | ||||||
| chr11:17427157
|
G | A | 105 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0137others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
splice_region_variant&intron_variant | LOW | c.2117-3C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427157 | ||||||
| chr11:17427415
|
C | T | 13 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0014t0002g0006others(10): Show | 13 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2117-261G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427415 | ||||||
| chr11:17427455
|
A | G | 258 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2117-301T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427455 | ||||||
| chr11:17427572
|
T | C | 3 | a0001c0003t0001g0160a0001c0003t0001g0162a0001c0003t0001g0309 | 3 | HG00738.hp1 HG03704.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2116+295A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427572 | ||||||
| chr11:17427593
|
A | G | 1 | a0002c0016t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2116+274T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427593 | ||||||
| chr11:17427640
|
T | C | 1 | a0001c0012t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2116+227A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427640 | ||||||
| chr11:17427722
|
C | A | 3 | a0001c0001t0001g0180a0001c0035t0002g0013a0003c0036t0001g0045 | 3 | HG02258.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2116+145G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 15/38 | chr11 | 17427722 | ||||||
| chr11:17427970
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2041-28C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 14/38 | chr11 | 17427970 | ||||||
| chr11:17428901
|
A | G | 1 | a0001c0034t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1818-231T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17428901 | ||||||
| chr11:17428906
|
G | C | 1 | a0001c0004t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1818-236C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17428906 | ||||||
| chr11:17429444
|
G | C | 100 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(97): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1818-774C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429444 | ||||||
| chr11:17429473
|
G | A | 2 | a0001c0003t0001g0101a0002c0047t0001g0112 | 2 | NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1818-803C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429473 | ||||||
| chr11:17429535
|
C | A | 15 | a0001c0004t0001g0296a0001c0006t0001g0044a0001c0006t0001g0079others(12): Show | 15 | HG01496.hp1 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1818-865G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429535 | ||||||
| chr11:17429595
|
T | C | 5 | a0001c0003t0001g0105a0001c0003t0001g0323a0001c0003t0001g0324others(2): Show | 5 | HG00733.hp2 HG00741.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818-925A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429595 | ||||||
| chr11:17429658
|
A | C | 1 | a0002c0002t0001g0240 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1818-988T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429658 | ||||||
| chr11:17429738
|
G | A | 1 | a0001c0004t0001g0223 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1818-1068C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429738 | ||||||
| chr11:17429739
|
A | G | 1 | a0001c0004t0001g0223 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1818-1069T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429739 | ||||||
| chr11:17429880
|
C | A | 36 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(33): Show | 37 | HG00558.hp1 HG00639.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1817+934G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429880 | ||||||
| chr11:17429916
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0246a0001c0001t0001g0248 | 3 | HG02165.hp1 HG03831.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1817+898G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429916 | ||||||
| chr11:17429987
|
C | T | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1817+827G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17429987 | ||||||
| chr11:17430099
|
G | A | 5 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1817+715C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430099 | ||||||
| chr11:17430372
|
G | A | 1 | a0003c0029t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1817+442C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430372 | ||||||
| chr11:17430438
|
A | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1817+376T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430438 | ||||||
| chr11:17430458
|
C | A | 69 | a0001c0003t0001g0088a0001c0004t0001g0256a0001c0004t0001g0257others(66): Show | 70 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1817+356G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430458 | ||||||
| chr11:17430472
|
T | G | 15 | a0001c0004t0001g0293a0001c0009t0003g0015a0001c0014t0002g0006others(12): Show | 15 | HG00735.hp1 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1817+342A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430472 | ||||||
| chr11:17430478
|
T | A | 18 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0201others(15): Show | 19 | HG01106.hp1 HG01358.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1817+336A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430478 | ||||||
| chr11:17430547
|
G | T | 38 | a0001c0001t0001g0254a0001c0007t0001g0036a0001c0007t0001g0116others(35): Show | 39 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1817+267C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430547 | ||||||
| chr11:17430547
|
GT | G | 11 | a0001c0004t0002g0012a0001c0015t0001g0018a0001c0015t0001g0019others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1817+266delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 12/38 | chr11 | 17430547 | ||||||
| chr11:17430990
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1672-31A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17430990 | ||||||
| chr11:17431033
|
C | T | 47 | a0001c0007t0001g0036a0001c0007t0001g0116a0001c0007t0001g0119others(44): Show | 48 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1672-74G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431033 | ||||||
| chr11:17431056
|
T | G | 22 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0047others(19): Show | 23 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1672-97A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431056 | ||||||
| chr11:17431318
|
G | A | 7 | a0001c0033t0001g0001a0001c0058t0001g0046a0002c0027t0001g0027others(4): Show | 8 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1672-359C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431318 | ||||||
| chr11:17431592
|
G | A | 10 | a0001c0006t0001g0044a0001c0006t0001g0079a0001c0006t0001g0090others(7): Show | 10 | HG01496.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1671+612C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431592 | ||||||
| chr11:17431616
|
C | G | 1 | a0001c0010t0001g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1671+588G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431616 | ||||||
| chr11:17431647
|
A | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1671+557T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431647 | ||||||
| chr11:17431748
|
C | T | 1 | a0001c0003t0001g0087 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1671+456G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431748 | ||||||
| chr11:17431800
|
G | A | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1671+404C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431800 | ||||||
| chr11:17431896
|
C | T | 34 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(31): Show | 34 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1671+308G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17431896 | ||||||
| chr11:17432027
|
C | T | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1671+177G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17432027 | ||||||
| chr11:17432115
|
T | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1671+89A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 11/38 | chr11 | 17432115 | ||||||
| chr11:17432680
|
A | G | 7 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1631-436T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17432680 | ||||||
| chr11:17432716
|
A | T | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-472T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17432716 | ||||||
| chr11:17432770
|
C | T | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-526G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17432770 | ||||||
| chr11:17433057
|
C | A | 1 | a0001c0003t0001g0095 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1631-813G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433057 | ||||||
| chr11:17433077
|
C | T | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1631-833G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433077 | ||||||
| chr11:17433583
|
T | C | 1 | a0001c0024t0001g0153 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1631-1339A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433583 | ||||||
| chr11:17433676
|
G | C | 1 | a0001c0022t0001g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1631-1432C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433676 | ||||||
| chr11:17433697
|
C | T | 3 | a0001c0070t0002g0008a0002c0002t0001g0239a0002c0002t0001g0318 | 3 | HG00423.hp2 HG02723.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1631-1453G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433697 | ||||||
| chr11:17433824
|
G | A | 93 | a0001c0004t0001g0144a0001c0004t0001g0293a0001c0004t0001g0296others(90): Show | 96 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1631-1580C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433824 | ||||||
| chr11:17433868
|
A | C | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-1624T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433868 | ||||||
| chr11:17433930
|
T | C | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-1686A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17433930 | ||||||
| chr11:17434195
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1631-1951G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434195 | ||||||
| chr11:17434364
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1631-2120T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434364 | ||||||
| chr11:17434374
|
A | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-2130T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434374 | ||||||
| chr11:17434663
|
C | A | 1 | a0001c0004t0002g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1631-2419G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434663 | ||||||
| chr11:17434671
|
G | A | 30 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0207others(27): Show | 30 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1631-2427C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434671 | ||||||
| chr11:17434982
|
C | CGT | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1631-2739_1631-273 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434982 | ||||||
| chr11:17434982
|
CGCGTGT | C | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1631-2744_1631-273 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434982 | ||||||
| chr11:17434984
|
C | CGCGCGTG others(3): Show |
1 | a0001c0003t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1631-2741_1631-274 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGCGTG others(5): Show |
1 | a0001c0003t0001g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1631-2741_1631-274 others(16): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGCGTG others(9): Show |
1 | a0013c0042t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1631-2741_1631-274 others(20): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGTGT | 9 | a0001c0003t0001g0030a0001c0003t0001g0118a0001c0006t0001g0044others(6): Show | 9 | HG01496.hp1 HG02135.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1631-2741_1631-274 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGTGTG others(1): Show |
8 | a0001c0006t0001g0092a0001c0014t0002g0006a0001c0023t0001g0031others(5): Show | 8 | HG00597.hp1 HG02083.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1631-2741_1631-274 others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGTGTG others(3): Show |
44 | a0001c0001t0001g0076a0001c0003t0001g0087a0001c0003t0001g0094others(41): Show | 44 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1631-2741_1631-274 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGTGTG others(5): Show |
7 | a0001c0001t0001g0173a0001c0003t0001g0082a0001c0003t0001g0086others(4): Show | 7 | HG00140.hp1 HG01168.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1631-2741_1631-274 others(16): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGTGTG others(7): Show |
2 | a0001c0008t0001g0165a0002c0045t0001g0085 | 2 | HG03579.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1631-2741_1631-274 others(18): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGCGTGTG others(9): Show |
1 | a0001c0003t0001g0130 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1631-2741_1631-274 others(20): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGT | 65 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(62): Show | 65 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1631-2742_1631-274 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGTGT | 7 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0224others(4): Show | 7 | HG01358.hp1 HG01934.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.1631-2744_1631-274 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGTGTGT | 17 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0047others(14): Show | 18 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1631-2746_1631-274 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGTGTGTG others(1): Show |
16 | a0001c0007t0001g0036a0001c0008t0001g0081a0001c0009t0001g0289others(13): Show | 17 | HG01358.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1631-2748_1631-274 others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGTGTGTG others(3): Show |
1 | a0001c0053t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1631-2750_1631-274 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | CGTGTGTG others(7): Show |
2 | a0001c0013t0001g0064a0001c0013t0001g0247 | 2 | NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1631-2754_1631-274 others(18): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
C | T | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1631-2740G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
CGT | C | 44 | a0001c0001t0001g0235a0001c0004t0001g0144a0001c0004t0001g0266others(41): Show | 44 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1631-2742_1631-274 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434984
|
CGTGT | C | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 8 | HG01123.hp2 HG01361.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1631-2744_1631-274 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434984 | ||||||
| chr11:17434986
|
T | C | 4 | a0001c0001t0001g0181a0001c0003t0001g0302a0002c0002t0001g0063others(1): Show | 4 | HG02071.hp2 HG02300.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631-2742A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434986 | ||||||
| chr11:17434988
|
T | C | 5 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(2): Show | 5 | HG01891.hp1 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1631-2744A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434988 | ||||||
| chr11:17434990
|
T | C | 3 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042 | 3 | HG01891.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1631-2746A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434990 | ||||||
| chr11:17434994
|
T | TGTGC | 8 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(5): Show | 8 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1631-2751_1631-275 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17434994 | ||||||
| chr11:17435018
|
T | TGTGTGTG others(4): Show |
3 | a0001c0001t0001g0181a0001c0003t0001g0302a0002c0002t0001g0063 | 3 | HG02071.hp2 HG02300.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1631-2775_1631-277 others(15): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435018 | ||||||
| chr11:17435018
|
T | TGTGTGTG others(6): Show |
1 | a0002c0044t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1631-2775_1631-277 others(17): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435018 | ||||||
| chr11:17435047
|
A | G | 1 | a0001c0076t0002g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1631-2803T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435047 | ||||||
| chr11:17435341
|
G | A | 30 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0207others(27): Show | 30 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1631-3097C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435341 | ||||||
| chr11:17435492
|
C | G | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1631-3248G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435492 | ||||||
| chr11:17435696
|
G | GGACA | 7 | a0001c0014t0002g0009a0001c0017t0001g0003a0001c0017t0001g0051others(4): Show | 8 | HG01256.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1631-3456_1631-345 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435696 | ||||||
| chr11:17435714
|
C | T | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1631-3470G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435714 | ||||||
| chr11:17435799
|
A | G | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1631-3555T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435799 | ||||||
| chr11:17435893
|
C | G | 9 | a0001c0014t0002g0009a0001c0017t0001g0003a0001c0017t0001g0051others(6): Show | 10 | HG01256.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1631-3649G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435893 | ||||||
| chr11:17435946
|
C | T | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1631-3702G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17435946 | ||||||
| chr11:17436063
|
T | C | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1631-3819A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436063 | ||||||
| chr11:17436150
|
C | T | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1631-3906G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436150 | ||||||
| chr11:17436151
|
A | G | 1 | a0001c0004t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1631-3907T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436151 | ||||||
| chr11:17436205
|
G | A | 1 | a0001c0007t0001g0310 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1631-3961C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436205 | ||||||
| chr11:17436230
|
G | A | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1631-3986C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436230 | ||||||
| chr11:17436589
|
T | C | 36 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(33): Show | 36 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1631-4345A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436589 | ||||||
| chr11:17436752
|
G | A | 36 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(33): Show | 36 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1631-4508C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436752 | ||||||
| chr11:17436786
|
C | A | 1 | a0001c0001t0001g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1631-4542G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436786 | ||||||
| chr11:17436992
|
G | C | 1 | a0001c0019t0001g0284 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1631-4748C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17436992 | ||||||
| chr11:17437050
|
C | T | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1631-4806G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437050 | ||||||
| chr11:17437053
|
T | G | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1631-4809A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437053 | ||||||
| chr11:17437056
|
A | C | 1 | a0001c0006t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1631-4812T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437056 | ||||||
| chr11:17437091
|
C | CA | 34 | a0001c0003t0001g0082a0001c0003t0001g0094a0001c0003t0001g0095others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1631-4848dupT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437091
|
C | CAA | 55 | a0001c0001t0001g0173a0001c0003t0001g0030a0001c0003t0001g0087others(52): Show | 55 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1631-4849_1631-484 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437091
|
C | CAAA | 12 | a0001c0001t0001g0076a0001c0003t0001g0088a0001c0003t0001g0100others(9): Show | 12 | HG00673.hp1 HG00735.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1631-4850_1631-484 others(7): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437091
|
CA | C | 129 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(126): Show | 130 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1631-4848delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437091
|
CAA | C | 15 | a0001c0001t0001g0057a0001c0010t0001g0298a0001c0012t0001g0210others(12): Show | 15 | HG01256.hp2 HG01515.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1631-4849_1631-484 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437091
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0022t0001g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1631-4860_1631-484 others(17): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437091
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-4861_1631-484 others(18): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437091 | ||||||
| chr11:17437125
|
T | C | 1 | a0002c0005t0001g0111 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1631-4881A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437125 | ||||||
| chr11:17437183
|
A | G | 77 | a0001c0004t0001g0144a0001c0007t0001g0036a0001c0007t0001g0139others(74): Show | 79 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1631-4939T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437183 | ||||||
| chr11:17437197
|
T | TG | 52 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0150others(49): Show | 53 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1631-4954dupC | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437197 | ||||||
| chr11:17437270
|
A | C | 1 | a0001c0068t0001g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1631-5026T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437270 | ||||||
| chr11:17437322
|
T | C | 19 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(16): Show | 21 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1631-5078A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437322 | ||||||
| chr11:17437399
|
CAGAAGTT others(9): Show |
C | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(7): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1631-5171_1631-515 others(20): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437399 | ||||||
| chr11:17437537
|
G | C | 1 | a0008c0055t0001g0078 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1630+5183C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437537 | ||||||
| chr11:17437560
|
G | A | 60 | a0001c0003t0001g0302a0001c0007t0001g0036a0001c0008t0001g0039others(57): Show | 62 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1630+5160C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437560 | ||||||
| chr11:17437571
|
A | T | 99 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(96): Show | 99 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.1630+5149T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437571 | ||||||
| chr11:17437623
|
T | C | 1 | a0001c0007t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1630+5097A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437623 | ||||||
| chr11:17437642
|
C | A | 3 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014 | 3 | HG00735.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1630+5078G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437642 | ||||||
| chr11:17437695
|
T | C | 4 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0201others(1): Show | 4 | HG01106.hp1 HG01358.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630+5025A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437695 | ||||||
| chr11:17437802
|
T | A | 22 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(19): Show | 22 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1630+4918A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437802 | ||||||
| chr11:17437911
|
C | A | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(7): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1630+4809G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437911 | ||||||
| chr11:17437988
|
C | A | 2 | a0001c0013t0001g0189a0003c0069t0001g0195 | 2 | HG01346.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1630+4732G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17437988 | ||||||
| chr11:17438056
|
C | T | 2 | a0002c0002t0001g0238a0002c0047t0001g0112 | 2 | HG02080.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1630+4664G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438056 | ||||||
| chr11:17438096
|
A | G | 141 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0001t0001g0181others(138): Show | 143 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1630+4624T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438096 | ||||||
| chr11:17438177
|
T | C | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(7): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1630+4543A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438177 | ||||||
| chr11:17438251
|
G | A | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1630+4469C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438251 | ||||||
| chr11:17438304
|
C | T | 16 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(13): Show | 17 | HG01123.hp2 HG01243.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.1630+4416G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438304 | ||||||
| chr11:17438382
|
G | GCACA | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+4337_1630+433 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438382 | ||||||
| chr11:17438384
|
T | C | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+4336A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438384 | ||||||
| chr11:17438412
|
C | G | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630+4308G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438412 | ||||||
| chr11:17438537
|
T | A | 112 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(109): Show | 113 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1630+4183A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438537 | ||||||
| chr11:17438631
|
T | G | 4 | a0001c0014t0002g0009a0001c0017t0001g0179a0001c0017t0001g0186others(1): Show | 4 | HG01256.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630+4089A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438631 | ||||||
| chr11:17438634
|
A | G | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+4086T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438634 | ||||||
| chr11:17438732
|
A | G | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+3988T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438732 | ||||||
| chr11:17438747
|
G | A | 1 | a0001c0014t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1630+3973C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438747 | ||||||
| chr11:17438755
|
T | C | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+3965A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438755 | ||||||
| chr11:17438816
|
G | A | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630+3904C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438816 | ||||||
| chr11:17438849
|
T | A | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1630+3871A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17438849 | ||||||
| chr11:17439115
|
T | C | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(7): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1630+3605A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439115 | ||||||
| chr11:17439158
|
A | G | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630+3562T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439158 | ||||||
| chr11:17439165
|
C | T | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+3555G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439165 | ||||||
| chr11:17439181
|
AATTCTGG others(55): Show |
A | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630+3477_1630+353 others(66): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439181 | ||||||
| chr11:17439311
|
C | A | 2 | a0002c0027t0001g0028a0002c0027t0001g0029 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1630+3409G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439311 | ||||||
| chr11:17439352
|
T | C | 138 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(135): Show | 140 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.1630+3368A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439352 | ||||||
| chr11:17439353
|
G | A | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1630+3367C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439353 | ||||||
| chr11:17439359
|
G | A | 9 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0201others(6): Show | 9 | HG01106.hp1 HG01358.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1630+3361C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439359 | ||||||
| chr11:17439364
|
T | C | 1 | a0001c0009t0001g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1630+3356A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439364 | ||||||
| chr11:17439443
|
T | C | 19 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0201others(16): Show | 19 | HG00735.hp1 HG01106.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1630+3277A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439443 | ||||||
| chr11:17439473
|
C | A | 12 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(9): Show | 13 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1630+3247G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439473 | ||||||
| chr11:17439538
|
C | T | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1630+3182G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439538 | ||||||
| chr11:17439720
|
C | T | 3 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014 | 3 | HG00735.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1630+3000G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439720 | ||||||
| chr11:17439782
|
C | A | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1630+2938G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439782 | ||||||
| chr11:17439782
|
C | G | 137 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(134): Show | 139 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(136): Show |
intron_variant | MODIFIER | c.1630+2938G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439782 | ||||||
| chr11:17439783
|
G | A | 1 | a0001c0012t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1630+2937C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439783 | ||||||
| chr11:17439908
|
T | TTCTGGGG others(2): Show |
6 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(3): Show | 6 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630+2803_1630+281 others(13): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439908 | ||||||
| chr11:17439930
|
T | G | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1630+2790A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439930 | ||||||
| chr11:17439996
|
T | C | 104 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(101): Show | 104 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.1630+2724A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17439996 | ||||||
| chr11:17440082
|
C | T | 2 | a0001c0017t0001g0070a0001c0022t0001g0072 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1630+2638G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440082 | ||||||
| chr11:17440116
|
A | G | 19 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(16): Show | 21 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1630+2604T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440116 | ||||||
| chr11:17440169
|
G | A | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630+2551C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440169 | ||||||
| chr11:17440184
|
C | T | 2 | a0001c0070t0002g0008a0001c0077t0001g0313 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1630+2536G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440184 | ||||||
| chr11:17440199
|
G | C | 16 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(13): Show | 17 | HG01123.hp2 HG01243.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.1630+2521C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440199 | ||||||
| chr11:17440581
|
C | A | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1630+2139G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440581 | ||||||
| chr11:17440630
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1630+2090A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440630 | ||||||
| chr11:17440673
|
A | G | 200 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(197): Show | 204 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1630+2047T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440673 | ||||||
| chr11:17440677
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1630+2043A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440677 | ||||||
| chr11:17440688
|
C | T | 7 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630+2032G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440688 | ||||||
| chr11:17440700
|
T | C | 5 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(2): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630+2020A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440700 | ||||||
| chr11:17440757
|
A | C | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+1963T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17440757 | ||||||
| chr11:17441113
|
G | A | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630+1607C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441113 | ||||||
| chr11:17441158
|
C | A | 1 | a0002c0018t0001g0188 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1630+1562G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441158 | ||||||
| chr11:17441165
|
A | AT | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630+1554dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441165 | ||||||
| chr11:17441180
|
G | A | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 141 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.1630+1540C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441180 | ||||||
| chr11:17441305
|
G | T | 1 | a0001c0031t0001g0242 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1630+1415C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441305 | ||||||
| chr11:17441311
|
T | C | 53 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0002others(50): Show | 55 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1630+1409A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441311 | ||||||
| chr11:17441419
|
C | T | 1 | a0001c0051t0001g0127 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1630+1301G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441419 | ||||||
| chr11:17441473
|
T | C | 2 | a0001c0017t0001g0070a0001c0022t0001g0072 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1630+1247A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441473 | ||||||
| chr11:17441631
|
G | A | 2 | a0001c0006t0001g0096a0001c0006t0001g0097 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1630+1089C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441631 | ||||||
| chr11:17441641
|
T | C | 2 | a0001c0017t0001g0070a0001c0022t0001g0072 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1630+1079A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441641 | ||||||
| chr11:17441646
|
T | C | 1 | a0002c0011t0001g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1630+1074A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441646 | ||||||
| chr11:17441662
|
C | T | 75 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(72): Show | 75 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1630+1058G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441662 | ||||||
| chr11:17441794
|
C | A | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1630+926G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441794 | ||||||
| chr11:17441852
|
C | T | 2 | a0001c0014t0001g0320a0001c0014t0001g0322 | 2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1630+868G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441852 | ||||||
| chr11:17441855
|
G | T | 2 | a0001c0003t0001g0101a0001c0006t0001g0102 | 2 | HG00621.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1630+865C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441855 | ||||||
| chr11:17441891
|
C | T | 1 | a0001c0049t0001g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1630+829G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441891 | ||||||
| chr11:17441917
|
T | C | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630+803A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17441917 | ||||||
| chr11:17442087
|
GA | G | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630+632delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17442087 | ||||||
| chr11:17442300
|
T | A | 1 | a0001c0034t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1630+420A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17442300 | ||||||
| chr11:17442569
|
C | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1630+151G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 10/38 | chr11 | 17442569 | ||||||
| chr11:17442956
|
A | G | 1 | a0001c0019t0001g0303 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1468-74T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 9/38 | chr11 | 17442956 | ||||||
| chr11:17442987
|
T | C | 131 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(128): Show | 134 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.1468-105A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 9/38 | chr11 | 17442987 | ||||||
| chr11:17443459
|
G | A | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1333-147C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17443459 | ||||||
| chr11:17443640
|
C | T | 17 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(14): Show | 19 | HG01256.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1333-328G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17443640 | ||||||
| chr11:17443645
|
C | A | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-333G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17443645 | ||||||
| chr11:17444021
|
A | AAGAGAGA others(1): Show |
7 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1333-717_1333-710d others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444021 | ||||||
| chr11:17444140
|
G | T | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333-828C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444140 | ||||||
| chr11:17444177
|
A | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1333-865T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444177 | ||||||
| chr11:17444195
|
T | G | 1 | a0001c0014t0001g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1333-883A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444195 | ||||||
| chr11:17444344
|
C | T | 5 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(2): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-1032G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444344 | ||||||
| chr11:17444363
|
G | C | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1333-1051C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444363 | ||||||
| chr11:17444433
|
A | G | 1 | a0001c0006t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1333-1121T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444433 | ||||||
| chr11:17444498
|
A | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(118): Show | 123 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1333-1186T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444498 | ||||||
| chr11:17444499
|
G | A | 7 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1333-1187C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444499 | ||||||
| chr11:17444577
|
T | C | 17 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(14): Show | 19 | HG01256.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1333-1265A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444577 | ||||||
| chr11:17444721
|
A | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(118): Show | 123 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1333-1409T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444721 | ||||||
| chr11:17444865
|
G | A | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333-1553C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444865 | ||||||
| chr11:17444969
|
A | G | 29 | a0001c0009t0001g0150a0001c0010t0001g0135a0001c0010t0001g0136others(26): Show | 29 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1333-1657T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444969 | ||||||
| chr11:17444976
|
A | G | 97 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(94): Show | 97 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.1333-1664T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17444976 | ||||||
| chr11:17445011
|
G | A | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1333-1699C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445011 | ||||||
| chr11:17445158
|
A | T | 1 | a0001c0013t0001g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1333-1846T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445158 | ||||||
| chr11:17445305
|
C | T | 7 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1333-1993G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445305 | ||||||
| chr11:17445441
|
T | G | 122 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(119): Show | 124 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1333-2129A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445441 | ||||||
| chr11:17445506
|
T | G | 121 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(118): Show | 123 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1333-2194A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445506 | ||||||
| chr11:17445628
|
T | A | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1333-2316A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445628 | ||||||
| chr11:17445656
|
T | C | 132 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(129): Show | 135 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.1333-2344A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445656 | ||||||
| chr11:17445678
|
T | C | 6 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(3): Show | 6 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-2366A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445678 | ||||||
| chr11:17445790
|
T | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(118): Show | 123 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1333-2478A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445790 | ||||||
| chr11:17445890
|
C | T | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-2578G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445890 | ||||||
| chr11:17445966
|
C | CT | 102 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(99): Show | 103 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.1332+2549dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445966 | ||||||
| chr11:17445966
|
CT | C | 20 | a0001c0001t0001g0287a0001c0004t0001g0218a0001c0007t0001g0163others(17): Show | 21 | HG01123.hp2 HG01256.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1332+2549delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17445966 | ||||||
| chr11:17446115
|
G | A | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(7): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1332+2401C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446115 | ||||||
| chr11:17446185
|
C | T | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1332+2331G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446185 | ||||||
| chr11:17446186
|
G | A | 1 | a0001c0004t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1332+2330C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446186 | ||||||
| chr11:17446224
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1332+2292G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446224 | ||||||
| chr11:17446247
|
C | G | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1332+2269G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446247 | ||||||
| chr11:17446298
|
A | C | 2 | a0002c0005t0001g0301a0002c0005t0001g0304 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1332+2218T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446298 | ||||||
| chr11:17446444
|
CA | C | 15 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(12): Show | 17 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.1332+2071delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446444 | ||||||
| chr11:17446475
|
C | G | 24 | a0001c0004t0001g0293a0001c0009t0001g0002a0001c0009t0001g0050others(21): Show | 26 | HG00639.hp1 HG01256.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1332+2041G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446475 | ||||||
| chr11:17446570
|
C | T | 24 | a0001c0004t0001g0293a0001c0009t0001g0002a0001c0009t0001g0050others(21): Show | 26 | HG00639.hp1 HG01256.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1332+1946G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446570 | ||||||
| chr11:17446601
|
G | C | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1332+1915C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446601 | ||||||
| chr11:17446741
|
A | G | 1 | a0001c0022t0001g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1332+1775T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446741 | ||||||
| chr11:17446770
|
T | C | 170 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(167): Show | 174 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(171): Show |
intron_variant | MODIFIER | c.1332+1746A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446770 | ||||||
| chr11:17446883
|
G | A | 1 | a0002c0016t0001g0276 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1332+1633C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446883 | ||||||
| chr11:17446946
|
A | C | 115 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(112): Show | 117 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1332+1570T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446946 | ||||||
| chr11:17446997
|
G | T | 1 | a0002c0060t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1332+1519C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17446997 | ||||||
| chr11:17447006
|
C | A | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1332+1510G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447006 | ||||||
| chr11:17447065
|
G | T | 170 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(167): Show | 174 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(171): Show |
intron_variant | MODIFIER | c.1332+1451C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447065 | ||||||
| chr11:17447351
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1332+1165A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447351 | ||||||
| chr11:17447423
|
C | T | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+1093G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447423 | ||||||
| chr11:17447558
|
T | C | 91 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(88): Show | 91 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1332+958A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447558 | ||||||
| chr11:17447559
|
G | A | 1 | a0001c0006t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1332+957C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447559 | ||||||
| chr11:17447639
|
G | A | 1 | a0001c0015t0001g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1332+877C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447639 | ||||||
| chr11:17447919
|
T | C | 105 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(102): Show | 106 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.1332+597A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447919 | ||||||
| chr11:17447924
|
T | C | 1 | a0001c0023t0001g0205 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1332+592A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447924 | ||||||
| chr11:17447954
|
A | T | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+562T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447954 | ||||||
| chr11:17447980
|
A | G | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(7): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1332+536T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17447980 | ||||||
| chr11:17448098
|
C | T | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1332+418G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17448098 | ||||||
| chr11:17448111
|
C | T | 1 | a0001c0053t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1332+405G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17448111 | ||||||
| chr11:17448207
|
C | T | 14 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(11): Show | 15 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1332+309G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17448207 | ||||||
| chr11:17448304
|
G | A | 2 | a0001c0033t0001g0001a0002c0027t0001g0027 | 3 | HG01123.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1332+212C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17448304 | ||||||
| chr11:17448488
|
C | T | 18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1332+28G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 8/38 | chr11 | 17448488 | ||||||
| chr11:17448720
|
A | G | 1 | a0001c0010t0001g0203 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1177-49T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17448720 | ||||||
| chr11:17448833
|
G | A | 1 | a0002c0074t0001g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1177-162C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17448833 | ||||||
| chr11:17448839
|
T | C | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177-168A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17448839 | ||||||
| chr11:17449009
|
C | T | 4 | a0001c0026t0001g0034a0001c0026t0001g0035a0001c0026t0004g0326others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177-338G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449009 | ||||||
| chr11:17449036
|
C | T | 7 | a0001c0014t0002g0009a0001c0017t0001g0003a0001c0017t0001g0051others(4): Show | 8 | HG01256.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-365G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449036 | ||||||
| chr11:17449037
|
A | G | 142 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(139): Show | 145 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(142): Show |
intron_variant | MODIFIER | c.1177-366T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449037 | ||||||
| chr11:17449073
|
C | T | 2 | a0001c0004t0001g0218a0001c0004t0001g0266 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1177-402G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449073 | ||||||
| chr11:17449076
|
G | A | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1177-405C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449076 | ||||||
| chr11:17449190
|
T | A | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1177-519A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449190 | ||||||
| chr11:17449253
|
C | T | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177-582G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449253 | ||||||
| chr11:17449385
|
G | A | 2 | a0001c0010t0001g0142a0001c0010t0001g0143 | 2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1177-714C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449385 | ||||||
| chr11:17449428
|
T | A | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1177-757A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449428 | ||||||
| chr11:17449460
|
C | G | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1177-789G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449460 | ||||||
| chr11:17449479
|
C | T | 1 | a0002c0005t0001g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1177-808G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449479 | ||||||
| chr11:17449551
|
C | T | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1177-880G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449551 | ||||||
| chr11:17449652
|
T | C | 1 | a0002c0018t0001g0188 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1177-981A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449652 | ||||||
| chr11:17449654
|
C | T | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177-983G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449654 | ||||||
| chr11:17449729
|
C | T | 16 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(13): Show | 18 | HG01256.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1177-1058G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449729 | ||||||
| chr11:17449824
|
T | C | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1177-1153A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17449824 | ||||||
| chr11:17450029
|
T | C | 1 | a0001c0012t0001g0259 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1177-1358A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450029 | ||||||
| chr11:17450140
|
C | G | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1177-1469G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450140 | ||||||
| chr11:17450153
|
A | G | 4 | a0001c0013t0001g0198a0002c0018t0001g0190a0002c0018t0001g0196others(1): Show | 4 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177-1482T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450153 | ||||||
| chr11:17450214
|
G | GT | 11 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(8): Show | 11 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1177-1544dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450214 | ||||||
| chr11:17450244
|
TTTTCTTT others(11): Show |
T | 9 | a0001c0003t0001g0105a0001c0003t0001g0167a0001c0008t0001g0157others(6): Show | 9 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1177-1591_1177-157 others(22): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450244 | ||||||
| chr11:17450244
|
TTTTCTTT others(15): Show |
T | 7 | a0001c0003t0001g0087a0001c0006t0001g0092a0001c0020t0001g0319others(4): Show | 7 | HG00423.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-1595_1177-157 others(26): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450244 | ||||||
| chr11:17450244
|
TTTTCTTT others(23): Show |
T | 1 | a0001c0014t0002g0009 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1177-1603_1177-157 others(34): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450244 | ||||||
| chr11:17450244
|
TTTTCTTT others(27): Show |
T | 2 | a0002c0027t0001g0028a0002c0027t0001g0029 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1177-1607_1177-157 others(38): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450244 | ||||||
| chr11:17450246
|
TTCTTTCT others(7): Show |
T | 32 | a0001c0003t0001g0100a0001c0003t0001g0302a0001c0004t0001g0178others(29): Show | 33 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1177-1589_1177-157 others(18): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450246 | ||||||
| chr11:17450249
|
T | C | 1 | a0005c0057t0001g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1177-1578A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450249 | ||||||
| chr11:17450250
|
T | C | 1 | a0001c0010t0002g0005 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1177-1579A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450250 | ||||||
| chr11:17450250
|
TTCTTTCT others(3): Show |
T | 49 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0181others(46): Show | 50 | HG00621.hp2 HG00673.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1177-1589_1177-158 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450250 | ||||||
| chr11:17450254
|
TTCTTTC | T | 46 | a0001c0001t0001g0254a0001c0003t0001g0088a0001c0003t0001g0094others(43): Show | 48 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.1177-1589_1177-158 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450254 | ||||||
| chr11:17450258
|
TTC | T | 35 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0001t0001g0185others(32): Show | 35 | HG00140.hp1 HG00733.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.1177-1589_1177-158 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450258 | ||||||
| chr11:17450260
|
C | CTCTT | 4 | a0001c0007t0001g0119a0001c0007t0001g0129a0001c0007t0001g0163others(1): Show | 4 | HG01433.hp1 HG02015.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177-1593_1177-159 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
C | CTCTTCTT others(4): Show |
1 | a0002c0002t0001g0231 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1177-1590_1177-158 others(15): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
C | CTT | 30 | a0001c0003t0001g0086a0001c0003t0001g0095a0001c0003t0001g0101others(27): Show | 30 | HG00609.hp1 HG00639.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1177-1590_1177-158 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
C | CTTTCTT | 3 | a0001c0015t0001g0022a0001c0019t0001g0321a0001c0020t0001g0043 | 3 | HG02257.hp1 HG02293.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1177-1590_1177-158 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
C | CTTTCTTT others(3): Show |
1 | a0001c0008t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1177-1590_1177-158 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
CTCTT | C | 26 | a0001c0001t0001g0207a0001c0001t0001g0219a0001c0001t0001g0241others(23): Show | 26 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1177-1593_1177-159 others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
CTCTTTCT others(1): Show |
C | 13 | a0001c0001t0001g0074a0001c0001t0001g0235a0001c0001t0001g0249others(10): Show | 13 | HG00738.hp2 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1177-1597_1177-159 others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
CTCTTTCT others(5): Show |
C | 10 | a0001c0001t0001g0229a0001c0001t0001g0234a0001c0001t0001g0275others(7): Show | 10 | HG00741.hp2 HG03688.hp2 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177-1601_1177-159 others(16): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450260
|
CTCTTTCT others(9): Show |
C | 1 | a0015c0037t0001g0104 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1177-1605_1177-159 others(20): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450260 | ||||||
| chr11:17450277
|
T | C | 1 | a0002c0064t0001g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1177-1606A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450277 | ||||||
| chr11:17450316
|
T | C | 3 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014 | 3 | HG00735.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1177-1645A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450316 | ||||||
| chr11:17450318
|
CTT | C | 6 | a0001c0003t0001g0106a0001c0080t0001g0312a0002c0002t0001g0063others(3): Show | 6 | HG02818.hp1 NA18612.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177-1649_1177-164 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450318 | ||||||
| chr11:17450320
|
T | C | 20 | a0001c0004t0001g0296a0001c0006t0001g0102a0001c0007t0001g0116others(17): Show | 20 | HG00621.hp2 HG00735.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1177-1649A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450320 | ||||||
| chr11:17450322
|
CTT | C | 17 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(14): Show | 17 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1177-1653_1177-165 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450322 | ||||||
| chr11:17450323
|
T | TTTCTTTC others(6): Show |
1 | a0001c0012t0001g0245 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1177-1653_1177-165 others(17): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450323 | ||||||
| chr11:17450324
|
T | C | 107 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(104): Show | 107 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.1177-1653A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450324 | ||||||
| chr11:17450324
|
T | TTC | 3 | a0001c0004t0001g0293a0001c0012t0001g0212a0001c0077t0001g0313 | 3 | HG00639.hp1 HG01517.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1177-1655_1177-165 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450324 | ||||||
| chr11:17450324
|
TTC | T | 13 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0002others(10): Show | 15 | HG01106.hp1 HG01358.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1177-1655_1177-165 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450324 | ||||||
| chr11:17450326
|
C | CTT | 3 | a0001c0001t0001g0225a0001c0004t0001g0261a0001c0023t0001g0253 | 3 | HG01934.hp1 HG02056.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1177-1656_1177-165 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450326 | ||||||
| chr11:17450328
|
C | T | 48 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(45): Show | 49 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1177-1657G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450328 | ||||||
| chr11:17450330
|
C | T | 3 | a0001c0001t0001g0225a0001c0004t0001g0261a0001c0023t0001g0253 | 3 | HG01934.hp1 HG02056.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1177-1659G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450330 | ||||||
| chr11:17450332
|
C | T | 13 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 13 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177-1661G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450332 | ||||||
| chr11:17450334
|
C | T | 3 | a0001c0001t0001g0225a0001c0004t0001g0261a0001c0023t0001g0253 | 3 | HG01934.hp1 HG02056.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1177-1663G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450334 | ||||||
| chr11:17450334
|
CTCT | C | 5 | a0001c0006t0001g0102a0001c0007t0001g0116a0001c0013t0001g0069others(2): Show | 5 | HG00621.hp2 HG02145.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-1666_1177-166 others(7): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450334 | ||||||
| chr11:17450335
|
TC | T | 3 | a0001c0021t0001g0232a0002c0002t0001g0065a0003c0069t0001g0195 | 3 | HG02071.hp1 NA18945.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1177-1665delG | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450335 | ||||||
| chr11:17450335
|
TCTTTC | T | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177-1669_1177-166 others(9): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450335 | ||||||
| chr11:17450338
|
T | C | 13 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0137others(10): Show | 13 | HG00423.hp2 HG00597.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177-1667A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450338 | ||||||
| chr11:17450339
|
T | C | 2 | a0001c0021t0001g0232a0002c0002t0001g0065 | 2 | HG02071.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1177-1668A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450339 | ||||||
| chr11:17450340
|
C | T | 2 | a0001c0021t0001g0232a0002c0002t0001g0065 | 2 | HG02071.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1177-1669G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450340 | ||||||
| chr11:17450341
|
C | T | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0137others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1177-1670G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450341 | ||||||
| chr11:17450343
|
T | C | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 15 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1177-1672A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450343 | ||||||
| chr11:17450344
|
T | C | 13 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0137others(10): Show | 13 | HG00423.hp2 HG00597.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177-1673A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450344 | ||||||
| chr11:17450347
|
T | C | 16 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 16 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1177-1676A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450347 | ||||||
| chr11:17450351
|
T | C | 1 | a0001c0004t0001g0261 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1177-1680A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450351 | ||||||
| chr11:17450352
|
T | C | 1 | a0002c0002t0001g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1177-1681A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450352 | ||||||
| chr11:17450354
|
T | C | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1177-1683A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450354 | ||||||
| chr11:17450356
|
TCCTTCCT others(3): Show |
T | 13 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0137others(10): Show | 13 | HG00423.hp2 HG00597.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177-1695_1177-168 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450356 | ||||||
| chr11:17450357
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1177-1686G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450357 | ||||||
| chr11:17450358
|
C | T | 1 | a0002c0002t0001g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1177-1687G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450358 | ||||||
| chr11:17450361
|
C | T | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 15 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1177-1690G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450361 | ||||||
| chr11:17450361
|
CCTTTCCT others(7): Show |
C | 34 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0207others(31): Show | 34 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1177-1704_1177-169 others(18): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450361 | ||||||
| chr11:17450365
|
TC | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG00408.hp1 HG01169.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1177-1695delG | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450365 | ||||||
| chr11:17450366
|
C | T | 1 | a0002c0002t0001g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1177-1695G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450366 | ||||||
| chr11:17450375
|
T | C | 29 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1177-1704A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450375 | ||||||
| chr11:17450377
|
T | C | 79 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(76): Show | 79 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-1706A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450377 | ||||||
| chr11:17450380
|
CCT | C | 79 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(76): Show | 79 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-1711_1177-171 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450380 | ||||||
| chr11:17450385
|
C | T | 79 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(76): Show | 79 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-1714G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450385 | ||||||
| chr11:17450393
|
TCTTTCTT others(3): Show |
T | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1177-1732_1177-172 others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450393 | ||||||
| chr11:17450394
|
C | T | 75 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(72): Show | 75 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1177-1723G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450394 | ||||||
| chr11:17450395
|
TTTCTTTC others(1): Show |
T | 70 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(67): Show | 70 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1177-1732_1177-172 others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450395 | ||||||
| chr11:17450399
|
T | C | 1 | a0002c0044t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1177-1728A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450399 | ||||||
| chr11:17450402
|
C | T | 1 | a0002c0044t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1177-1731G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450402 | ||||||
| chr11:17450403
|
C | CT | 7 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-1733dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450403 | ||||||
| chr11:17450403
|
C | CTT | 8 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(5): Show | 8 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1177-1734_1177-173 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450403 | ||||||
| chr11:17450403
|
C | T | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0002c0044t0001g0117 | 3 | HG03098.hp1 HG03669.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-1732G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450403 | ||||||
| chr11:17450449
|
C | T | 5 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0201others(2): Show | 5 | HG01106.hp1 HG01358.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-1778G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450449 | ||||||
| chr11:17450455
|
T | C | 146 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0001t0001g0182others(143): Show | 149 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(146): Show |
intron_variant | MODIFIER | c.1177-1784A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450455 | ||||||
| chr11:17450509
|
C | T | 1 | a0004c0041t0001g0145 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1177-1838G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450509 | ||||||
| chr11:17450599
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1177-1928T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450599 | ||||||
| chr11:17450632
|
T | C | 6 | a0001c0004t0001g0293a0001c0010t0001g0298a0001c0022t0001g0292others(3): Show | 6 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177-1961A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450632 | ||||||
| chr11:17450636
|
A | G | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1177-1965T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450636 | ||||||
| chr11:17450640
|
A | G | 1 | a0001c0004t0002g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1177-1969T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450640 | ||||||
| chr11:17450677
|
A | G | 8 | a0001c0033t0001g0001a0001c0058t0001g0046a0002c0002t0001g0216others(5): Show | 9 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1177-2006T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450677 | ||||||
| chr11:17450685
|
C | CT | 37 | a0001c0001t0001g0234a0001c0004t0001g0258a0001c0004t0001g0261others(34): Show | 37 | HG00140.hp2 HG01074.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1177-2015dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450685 | ||||||
| chr11:17450685
|
C | CTTTTT | 7 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0026t0001g0034others(4): Show | 7 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-2019_1177-201 others(9): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450685 | ||||||
| chr11:17450685
|
C | CTTTTTT | 10 | a0001c0003t0001g0164a0001c0004t0002g0012a0001c0006t0001g0044others(7): Show | 10 | HG01496.hp1 HG02559.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177-2020_1177-201 others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450685 | ||||||
| chr11:17450685
|
C | CTTTTTTT | 63 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(60): Show | 63 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1177-2021_1177-201 others(11): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450685 | ||||||
| chr11:17450685
|
C | CTTTTTTT others(1): Show |
17 | a0001c0003t0001g0095a0001c0003t0001g0105a0001c0003t0001g0106others(14): Show | 17 | HG00738.hp1 HG00741.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1177-2022_1177-201 others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450685 | ||||||
| chr11:17450685
|
CT | C | 6 | a0001c0020t0001g0043a0001c0025t0001g0054a0001c0025t0001g0056others(3): Show | 6 | HG02896.hp2 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-2015delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17450685 | ||||||
| chr11:17451166
|
T | C | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1176+1953A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451166 | ||||||
| chr11:17451166
|
T | G | 137 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(134): Show | 139 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.1176+1953A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451166 | ||||||
| chr11:17451171
|
A | G | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1176+1948T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451171 | ||||||
| chr11:17451302
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1176+1817C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451302 | ||||||
| chr11:17451322
|
C | T | 1 | a0001c0071t0001g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1176+1797G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451322 | ||||||
| chr11:17451498
|
C | T | 3 | a0001c0003t0001g0167a0001c0046t0001g0166a0003c0029t0002g0011 | 3 | HG00735.hp2 HG01070.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1176+1621G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451498 | ||||||
| chr11:17451540
|
C | A | 1 | a0002c0018t0001g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1176+1579G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451540 | ||||||
| chr11:17451599
|
G | A | 19 | a0001c0003t0001g0302a0001c0008t0001g0039a0001c0008t0001g0040others(16): Show | 20 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1176+1520C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451599 | ||||||
| chr11:17451769
|
G | A | 6 | a0001c0001t0001g0219a0001c0001t0001g0235a0001c0001t0001g0286others(3): Show | 6 | HG00597.hp2 HG02071.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1176+1350C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451769 | ||||||
| chr11:17451850
|
G | T | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1176+1269C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451850 | ||||||
| chr11:17451875
|
T | C | 100 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(97): Show | 101 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1176+1244A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451875 | ||||||
| chr11:17451890
|
C | T | 69 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1176+1229G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451890 | ||||||
| chr11:17451953
|
C | T | 3 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0009t0001g0201 | 3 | HG01358.hp1 HG04204.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1176+1166G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17451953 | ||||||
| chr11:17452224
|
A | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1176+895T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452224 | ||||||
| chr11:17452308
|
A | C | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1176+811T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452308 | ||||||
| chr11:17452393
|
G | A | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1176+726C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452393 | ||||||
| chr11:17452617
|
C | T | 5 | a0001c0004t0001g0144a0001c0008t0001g0041a0001c0008t0001g0042others(2): Show | 5 | HG01891.hp1 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1176+502G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452617 | ||||||
| chr11:17452642
|
G | A | 10 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1176+477C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452642 | ||||||
| chr11:17452730
|
C | T | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1176+389G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452730 | ||||||
| chr11:17452771
|
T | G | 150 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(147): Show | 153 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.1176+348A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17452771 | ||||||
| chr11:17453034
|
G | A | 1 | a0002c0011t0001g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1176+85C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17453034 | ||||||
| chr11:17453067
|
T | C | 1 | a0002c0047t0001g0112 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1176+52A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 7/38 | chr11 | 17453067 | ||||||
| chr11:17453389
|
C | T | 5 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(2): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1012-106G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453389 | ||||||
| chr11:17453391
|
T | C | 3 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049 | 4 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-108A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453391 | ||||||
| chr11:17453405
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1012-122C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453405 | ||||||
| chr11:17453421
|
T | G | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1012-138A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453421 | ||||||
| chr11:17453430
|
A | C | 10 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1012-147T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453430 | ||||||
| chr11:17453554
|
T | G | 1 | a0003c0029t0002g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1012-271A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453554 | ||||||
| chr11:17453600
|
T | C | 7 | a0001c0010t0001g0192a0001c0010t0001g0204a0002c0018t0001g0193others(4): Show | 7 | HG00642.hp1 HG01175.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1012-317A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453600 | ||||||
| chr11:17453653
|
C | T | 2 | a0001c0065t0001g0288a0001c0068t0001g0048 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1012-370G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453653 | ||||||
| chr11:17453736
|
G | A | 94 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(91): Show | 95 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1012-453C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453736 | ||||||
| chr11:17453896
|
G | A | 128 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(125): Show | 131 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.1012-613C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17453896 | ||||||
| chr11:17454067
|
A | G | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1012-784T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454067 | ||||||
| chr11:17454251
|
A | G | 1 | a0001c0006t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1012-968T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454251 | ||||||
| chr11:17454387
|
C | T | 2 | a0002c0005t0001g0025a0002c0005t0001g0026 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1012-1104G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454387 | ||||||
| chr11:17454388
|
G | A | 7 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012-1105C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454388 | ||||||
| chr11:17454470
|
A | G | 47 | a0001c0001t0001g0180a0001c0004t0001g0293a0001c0004t0001g0296others(44): Show | 49 | HG00639.hp1 HG01243.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1012-1187T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454470 | ||||||
| chr11:17454607
|
G | C | 2 | a0001c0017t0001g0070a0001c0022t0001g0072 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1012-1324C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454607 | ||||||
| chr11:17454667
|
A | G | 1 | a0001c0046t0001g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1012-1384T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454667 | ||||||
| chr11:17454841
|
C | T | 94 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(91): Show | 95 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1012-1558G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454841 | ||||||
| chr11:17454913
|
C | G | 10 | a0001c0001t0001g0137a0001c0001t0001g0254a0001c0003t0001g0115others(7): Show | 10 | HG00423.hp2 HG00642.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1012-1630G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454913 | ||||||
| chr11:17454969
|
T | G | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 142 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.1012-1686A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17454969 | ||||||
| chr11:17455004
|
C | T | 1 | a0001c0071t0001g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1012-1721G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455004 | ||||||
| chr11:17455265
|
T | C | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012-1982A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455265 | ||||||
| chr11:17455278
|
A | T | 4 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014others(1): Show | 4 | HG00735.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-1995T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455278 | ||||||
| chr11:17455471
|
G | A | 4 | a0001c0003t0001g0130a0001c0007t0001g0129a0001c0009t0001g0268others(1): Show | 4 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-2188C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455471 | ||||||
| chr11:17455475
|
C | G | 1 | a0001c0006t0001g0044 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1012-2192G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455475 | ||||||
| chr11:17455488
|
C | G | 2 | a0001c0013t0001g0189a0003c0069t0001g0195 | 2 | HG01346.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1012-2205G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455488 | ||||||
| chr11:17455868
|
G | A | 1 | a0002c0011t0001g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1012-2585C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455868 | ||||||
| chr11:17455937
|
C | CA | 19 | a0001c0001t0001g0061a0001c0003t0001g0118a0001c0004t0001g0187others(16): Show | 19 | HG00423.hp2 HG01175.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1012-2655dupT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455937 | ||||||
| chr11:17455937
|
CA | C | 24 | a0001c0003t0001g0115a0001c0007t0001g0126a0001c0008t0001g0039others(21): Show | 25 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1012-2655delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455937 | ||||||
| chr11:17455937
|
CAAAAAAA others(5): Show |
C | 16 | a0001c0004t0001g0296a0001c0015t0001g0018a0001c0015t0001g0019others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1012-2666_1012-265 others(16): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455937 | ||||||
| chr11:17455957
|
A | AG | 3 | a0001c0017t0001g0003a0001c0017t0001g0051a0003c0063t0001g0052 | 4 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-2675_1012-267 others(5): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455957 | ||||||
| chr11:17455963
|
G | A | 4 | a0001c0014t0002g0009a0001c0017t0001g0179a0001c0017t0001g0186others(1): Show | 4 | HG01256.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012-2680C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17455963 | ||||||
| chr11:17456036
|
G | A | 1 | a0001c0009t0001g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1012-2753C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456036 | ||||||
| chr11:17456087
|
C | A | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1012-2804G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456087 | ||||||
| chr11:17456094
|
C | T | 1 | a0001c0012t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1012-2811G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456094 | ||||||
| chr11:17456283
|
C | T | 92 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(89): Show | 92 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1012-3000G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456283 | ||||||
| chr11:17456361
|
T | TGA | 35 | a0001c0004t0001g0293a0001c0009t0001g0002a0001c0009t0001g0050others(32): Show | 37 | HG00639.hp1 HG00735.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-3080_1012-307 others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456361 | ||||||
| chr11:17456452
|
G | A | 5 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0035t0002g0013others(2): Show | 5 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012-3169C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456452 | ||||||
| chr11:17456457
|
G | T | 2 | a0001c0007t0001g0119a0001c0007t0001g0163 | 2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1012-3174C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456457 | ||||||
| chr11:17456470
|
G | C | 1 | a0001c0076t0002g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1012-3187C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456470 | ||||||
| chr11:17456522
|
T | C | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012-3239A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456522 | ||||||
| chr11:17456541
|
A | C | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-3258T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456541 | ||||||
| chr11:17456576
|
G | A | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012-3293C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456576 | ||||||
| chr11:17456610
|
C | T | 90 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(87): Show | 90 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1012-3327G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456610 | ||||||
| chr11:17456614
|
C | T | 1 | a0001c0015t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1012-3331G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456614 | ||||||
| chr11:17456647
|
C | T | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-3364G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456647 | ||||||
| chr11:17456657
|
G | C | 37 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0009t0001g0002others(34): Show | 39 | HG00639.hp1 HG00735.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1012-3374C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456657 | ||||||
| chr11:17456913
|
G | A | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1011+3575C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17456913 | ||||||
| chr11:17457063
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1011+3425A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457063 | ||||||
| chr11:17457214
|
T | C | 6 | a0001c0006t0001g0103a0001c0009t0001g0002a0001c0009t0001g0050others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1011+3274A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457214 | ||||||
| chr11:17457243
|
A | C | 29 | a0001c0006t0001g0103a0001c0009t0001g0002a0001c0009t0001g0050others(26): Show | 31 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1011+3245T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457243 | ||||||
| chr11:17457285
|
C | T | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1011+3203G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457285 | ||||||
| chr11:17457339
|
C | A | 1 | a0001c0015t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1011+3149G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457339 | ||||||
| chr11:17457365
|
T | G | 2 | a0001c0009t0001g0150a0002c0011t0001g0149 | 2 | NA18948.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1011+3123A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457365 | ||||||
| chr11:17457442
|
C | T | 23 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(20): Show | 24 | HG01123.hp2 HG01361.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1011+3046G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457442 | ||||||
| chr11:17457685
|
G | A | 1 | a0001c0004t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1011+2803C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457685 | ||||||
| chr11:17457779
|
G | A | 28 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(25): Show | 30 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1011+2709C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457779 | ||||||
| chr11:17457847
|
C | T | 3 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014 | 3 | HG00735.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1011+2641G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17457847 | ||||||
| chr11:17458031
|
C | G | 17 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(14): Show | 18 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1011+2457G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458031 | ||||||
| chr11:17458041
|
G | A | 1 | a0001c0009t0001g0150 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1011+2447C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458041 | ||||||
| chr11:17458190
|
G | A | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1011+2298C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458190 | ||||||
| chr11:17458201
|
G | T | 2 | a0001c0007t0001g0036a0001c0053t0001g0158 | 2 | HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1011+2287C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458201 | ||||||
| chr11:17458308
|
C | T | 2 | a0001c0001t0001g0241a0002c0002t0001g0240 | 2 | HG01361.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1011+2180G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458308 | ||||||
| chr11:17458481
|
G | A | 1 | a0001c0012t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1011+2007C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458481 | ||||||
| chr11:17458618
|
C | A | 28 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0009t0001g0289others(25): Show | 30 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1011+1870G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458618 | ||||||
| chr11:17458728
|
A | C | 1 | a0001c0001t0001g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1011+1760T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458728 | ||||||
| chr11:17458789
|
T | C | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1011+1699A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458789 | ||||||
| chr11:17458987
|
G | C | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+1501C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17458987 | ||||||
| chr11:17459138
|
C | T | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1011+1350G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459138 | ||||||
| chr11:17459288
|
T | C | 117 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(114): Show | 119 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1011+1200A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459288 | ||||||
| chr11:17459421
|
A | C | 1 | a0001c0007t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1011+1067T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459421 | ||||||
| chr11:17459427
|
C | T | 1 | a0002c0011t0001g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1011+1061G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459427 | ||||||
| chr11:17459462
|
A | G | 2 | a0001c0033t0001g0001a0002c0027t0001g0027 | 3 | HG01123.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1011+1026T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459462 | ||||||
| chr11:17459463
|
C | T | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1011+1025G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459463 | ||||||
| chr11:17459522
|
T | C | 2 | a0001c0007t0001g0139a0001c0008t0001g0140 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1011+966A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459522 | ||||||
| chr11:17459718
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1011+770G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459718 | ||||||
| chr11:17459724
|
C | T | 2 | a0001c0034t0001g0176a0001c0034t0001g0177 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1011+764G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459724 | ||||||
| chr11:17459801
|
C | T | 1 | a0001c0004t0002g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1011+687G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459801 | ||||||
| chr11:17459809
|
G | C | 7 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+679C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459809 | ||||||
| chr11:17459864
|
A | G | 3 | a0001c0012t0001g0210a0001c0012t0001g0211a0001c0012t0001g0212 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1011+624T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459864 | ||||||
| chr11:17459926
|
A | G | 8 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1011+562T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17459926 | ||||||
| chr11:17460023
|
G | A | 1 | a0002c0002t0001g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1011+465C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17460023 | ||||||
| chr11:17460033
|
TTC | T | 5 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(2): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1011+453_1011+454d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17460033 | ||||||
| chr11:17460265
|
G | A | 5 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0035t0002g0013others(2): Show | 5 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1011+223C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17460265 | ||||||
| chr11:17460395
|
T | C | 1 | a0001c0019t0001g0321 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1011+93A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17460395 | ||||||
| chr11:17460401
|
T | C | 115 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(112): Show | 117 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.1011+87A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 6/38 | chr11 | 17460401 | ||||||
| chr11:17460725
|
C | T | 3 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0049t0001g0141 | 3 | HG01106.hp1 HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.823-49G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17460725 | ||||||
| chr11:17460781
|
T | C | 115 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(112): Show | 117 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.823-105A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17460781 | ||||||
| chr11:17460782
|
G | A | 69 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.823-106C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17460782 | ||||||
| chr11:17460783
|
G | T | 31 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(28): Show | 32 | HG00639.hp1 HG01123.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.823-107C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17460783 | ||||||
| chr11:17460997
|
C | T | 1 | a0001c0076t0002g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.823-321G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17460997 | ||||||
| chr11:17461033
|
G | T | 18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.823-357C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461033 | ||||||
| chr11:17461072
|
A | G | 116 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(113): Show | 118 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.823-396T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461072 | ||||||
| chr11:17461178
|
A | G | 1 | a0001c0012t0001g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.822+405T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461178 | ||||||
| chr11:17461367
|
C | T | 3 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014 | 3 | HG00735.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.822+216G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461367 | ||||||
| chr11:17461417
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.822+166G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461417 | ||||||
| chr11:17461491
|
C | T | 30 | a0001c0009t0001g0150a0001c0009t0001g0201a0001c0010t0001g0135others(27): Show | 30 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+92G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461491 | ||||||
| chr11:17461548
|
C | T | 2 | a0001c0012t0001g0171a0001c0012t0001g0259 | 2 | NA18940.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.822+35G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 5/38 | chr11 | 17461548 | ||||||
| chr11:17461942
|
C | T | 7 | a0001c0026t0001g0034a0001c0026t0001g0035a0001c0026t0004g0326others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-117G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17461942 | ||||||
| chr11:17462139
|
A | G | 5 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0035t0002g0013others(2): Show | 5 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-314T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462139 | ||||||
| chr11:17462195
|
A | G | 20 | a0001c0003t0001g0302a0001c0008t0001g0039a0001c0008t0001g0040others(17): Show | 21 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.580-370T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462195 | ||||||
| chr11:17462198
|
C | T | 1 | a0002c0016t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.580-373G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462198 | ||||||
| chr11:17462336
|
T | C | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-511A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462336 | ||||||
| chr11:17462536
|
C | T | 3 | a0001c0004t0001g0144a0001c0010t0001g0142a0001c0010t0001g0143 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.580-711G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462536 | ||||||
| chr11:17462609
|
A | G | 3 | a0001c0017t0001g0003a0001c0017t0001g0051a0003c0063t0001g0052 | 4 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-784T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462609 | ||||||
| chr11:17462767
|
T | A | 132 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(129): Show | 134 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.579+671A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462767 | ||||||
| chr11:17462799
|
C | CAG | 153 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(150): Show | 156 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.579+638_579+639ins others(2): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462799 | ||||||
| chr11:17462820
|
T | C | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+618A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462820 | ||||||
| chr11:17462930
|
C | G | 22 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(19): Show | 22 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+508G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17462930 | ||||||
| chr11:17463044
|
A | G | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.579+394T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463044 | ||||||
| chr11:17463081
|
C | G | 132 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(129): Show | 134 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.579+357G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463081 | ||||||
| chr11:17463152
|
C | A | 3 | a0001c0009t0003g0015a0001c0021t0001g0138a0001c0021t0003g0014 | 3 | HG00735.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.579+286G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463152 | ||||||
| chr11:17463184
|
C | T | 102 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.579+254G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463184 | ||||||
| chr11:17463234
|
C | G | 94 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.579+204G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463234 | ||||||
| chr11:17463251
|
C | T | 9 | a0001c0001t0001g0137a0001c0001t0001g0254a0002c0002t0001g0216others(6): Show | 9 | HG00423.hp2 HG00642.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+187G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463251 | ||||||
| chr11:17463273
|
T | A | 1 | a0001c0028t0001g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.579+165A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463273 | ||||||
| chr11:17463300
|
C | T | 1 | a0001c0004t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.579+138G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463300 | ||||||
| chr11:17463306
|
T | A | 9 | a0001c0033t0001g0001a0001c0034t0001g0176a0001c0034t0001g0177others(6): Show | 10 | HG01123.hp2 HG01361.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+132A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463306 | ||||||
| chr11:17463409
|
C | G | 2 | a0001c0035t0002g0013a0003c0036t0001g0045 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.579+29G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463409 | ||||||
| chr11:17463424
|
G | A | 153 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(150): Show | 156 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.579+14C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 4/38 | chr11 | 17463424 | ||||||
| chr11:17463790
|
G | A | 1 | a0001c0003t0001g0100 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.413-186C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17463790 | ||||||
| chr11:17463922
|
C | T | 5 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0035t0002g0013others(2): Show | 5 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-318G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17463922 | ||||||
| chr11:17463992
|
G | A | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-388C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17463992 | ||||||
| chr11:17464093
|
C | T | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-489G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464093 | ||||||
| chr11:17464281
|
G | A | 5 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0035t0002g0013others(2): Show | 5 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-677C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464281 | ||||||
| chr11:17464341
|
G | C | 3 | a0001c0021t0001g0221a0001c0021t0001g0232a0001c0023t0001g0253 | 3 | HG02056.hp1 HG02071.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.413-737C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464341 | ||||||
| chr11:17464467
|
T | C | 16 | a0001c0008t0001g0041a0001c0008t0001g0042a0001c0017t0001g0070others(13): Show | 16 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.413-863A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464467 | ||||||
| chr11:17464559
|
GC | G | 7 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-956delG | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464559 | ||||||
| chr11:17464692
|
C | T | 7 | a0001c0008t0001g0041a0001c0008t0001g0042a0001c0017t0001g0003others(4): Show | 8 | HG01891.hp1 HG02622.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-1088G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464692 | ||||||
| chr11:17464934
|
G | A | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-1330C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17464934 | ||||||
| chr11:17465004
|
G | C | 3 | a0001c0003t0001g0164a0001c0004t0002g0012a0001c0008t0001g0165 | 3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.413-1400C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465004 | ||||||
| chr11:17465049
|
C | T | 4 | a0001c0007t0001g0139a0001c0017t0001g0003a0001c0017t0001g0051others(1): Show | 5 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-1445G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465049 | ||||||
| chr11:17465050
|
G | T | 3 | a0001c0017t0001g0003a0001c0017t0001g0051a0003c0063t0001g0052 | 4 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-1446C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465050 | ||||||
| chr11:17465059
|
G | A | 12 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(9): Show | 14 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.413-1455C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465059 | ||||||
| chr11:17465075
|
G | A | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-1471C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465075 | ||||||
| chr11:17465081
|
T | G | 95 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.413-1477A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465081 | ||||||
| chr11:17465097
|
G | C | 95 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.413-1493C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465097 | ||||||
| chr11:17465131
|
T | C | 140 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(137): Show | 142 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.413-1527A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465131 | ||||||
| chr11:17465177
|
G | A | 3 | a0001c0033t0001g0001a0002c0027t0001g0027a0002c0074t0001g0214 | 4 | HG01123.hp2 HG01361.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-1573C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465177 | ||||||
| chr11:17465190
|
C | T | 95 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.413-1586G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465190 | ||||||
| chr11:17465202
|
G | C | 1 | a0001c0071t0001g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.413-1598C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465202 | ||||||
| chr11:17465276
|
G | T | 14 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.413-1672C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465276 | ||||||
| chr11:17465306
|
A | G | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.413-1702T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465306 | ||||||
| chr11:17465421
|
C | G | 141 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(138): Show | 143 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.413-1817G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465421 | ||||||
| chr11:17465506
|
A | G | 1 | a0001c0003t0001g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.413-1902T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465506 | ||||||
| chr11:17465532
|
C | T | 95 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.413-1928G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465532 | ||||||
| chr11:17465540
|
G | A | 4 | a0001c0026t0001g0034a0001c0026t0001g0035a0001c0026t0004g0326others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-1936C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465540 | ||||||
| chr11:17465714
|
C | T | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-2110G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465714 | ||||||
| chr11:17465715
|
G | A | 3 | a0001c0003t0001g0101a0001c0006t0001g0080a0001c0006t0001g0102 | 3 | HG00621.hp2 NA18971.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.413-2111C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465715 | ||||||
| chr11:17465731
|
C | A | 141 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(138): Show | 143 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.413-2127G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465731 | ||||||
| chr11:17465802
|
G | A | 109 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(106): Show | 109 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.413-2198C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465802 | ||||||
| chr11:17465898
|
C | T | 138 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(135): Show | 139 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.413-2294G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17465898 | ||||||
| chr11:17466149
|
C | T | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0071t0001g0071 | 3 | HG03098.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.413-2545G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466149 | ||||||
| chr11:17466260
|
G | A | 112 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.413-2656C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466260 | ||||||
| chr11:17466286
|
T | C | 146 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(143): Show | 148 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.413-2682A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466286 | ||||||
| chr11:17466321
|
C | A | 3 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0049t0001g0141 | 3 | HG01106.hp1 HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.413-2717G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466321 | ||||||
| chr11:17466340
|
G | A | 150 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(147): Show | 153 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.413-2736C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466340 | ||||||
| chr11:17466344
|
A | G | 1 | a0001c0071t0001g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.413-2740T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466344 | ||||||
| chr11:17466398
|
C | CA | 52 | a0001c0001t0001g0172a0001c0001t0001g0254a0001c0001t0001g0255others(49): Show | 54 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.413-2795dupT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466398 | ||||||
| chr11:17466398
|
C | CAA | 11 | a0001c0004t0001g0257a0001c0004t0001g0296a0001c0026t0001g0034others(8): Show | 11 | HG00741.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-2796_413-2795d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466398 | ||||||
| chr11:17466398
|
CA | C | 15 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0004t0001g0258others(12): Show | 15 | HG01169.hp2 HG02280.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.413-2795delT | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466398 | ||||||
| chr11:17466443
|
T | A | 1 | a0001c0007t0001g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.413-2839A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466443 | ||||||
| chr11:17466478
|
A | G | 150 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(147): Show | 153 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.413-2874T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466478 | ||||||
| chr11:17466491
|
T | C | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-2887A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466491 | ||||||
| chr11:17466494
|
T | C | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-2890A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466494 | ||||||
| chr11:17466554
|
C | T | 115 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(112): Show | 116 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.413-2950G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466554 | ||||||
| chr11:17466620
|
T | G | 1 | a0001c0003t0001g0323 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.413-3016A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466620 | ||||||
| chr11:17466642
|
G | A | 3 | a0001c0017t0001g0003a0001c0017t0001g0051a0003c0063t0001g0052 | 4 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-3038C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466642 | ||||||
| chr11:17466660
|
A | AGGCTGGA others(18): Show |
104 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(101): Show | 104 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.413-3081_413-3057d others(27): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466660 | ||||||
| chr11:17466670
|
G | A | 9 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.413-3066C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466670 | ||||||
| chr11:17466679
|
C | T | 7 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-3075G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466679 | ||||||
| chr11:17466854
|
C | T | 12 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+3247G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466854 | ||||||
| chr11:17466864
|
G | C | 136 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(133): Show | 137 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.412+3237C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466864 | ||||||
| chr11:17466872
|
G | T | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+3229C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466872 | ||||||
| chr11:17466885
|
C | A | 29 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0007t0001g0139others(26): Show | 30 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.412+3216G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17466885 | ||||||
| chr11:17467042
|
C | CACACACA others(10): Show |
1 | a0001c0007t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.412+3058_412+3059i others(19): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCA | 61 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(58): Show | 62 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.412+3057_412+3058d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACA | 66 | a0001c0001t0001g0137a0001c0001t0001g0207a0001c0001t0001g0234others(63): Show | 66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.412+3055_412+3058d others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACA | 58 | a0001c0001t0001g0068a0001c0001t0001g0182a0001c0001t0001g0273others(55): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.412+3053_412+3058d others(8): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(1): Show |
39 | a0001c0001t0001g0185a0001c0003t0001g0082a0001c0003t0001g0094others(36): Show | 41 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.412+3051_412+3058d others(10): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(3): Show |
30 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0003t0001g0030others(27): Show | 30 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.412+3049_412+3058d others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(5): Show |
11 | a0001c0003t0001g0118a0001c0003t0001g0160a0001c0004t0002g0012others(8): Show | 11 | HG00738.hp1 HG02132.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+3047_412+3058d others(14): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(7): Show |
7 | a0001c0007t0001g0131a0001c0007t0001g0310a0001c0019t0001g0121others(4): Show | 7 | HG00140.hp1 HG01258.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+3045_412+3058d others(16): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(9): Show |
4 | a0001c0001t0001g0076a0001c0007t0001g0124a0001c0007t0001g0125others(1): Show | 4 | HG02027.hp1 HG02027.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+3043_412+3058d others(18): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(11): Show |
2 | a0001c0003t0001g0282a0001c0003t0001g0323 | 2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.412+3041_412+3058d others(20): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
C | CCACACAC others(13): Show |
1 | a0002c0005t0001g0283 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.412+3039_412+3058d others(22): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
CCA | C | 11 | a0001c0001t0001g0215a0001c0003t0001g0164a0001c0007t0001g0139others(8): Show | 11 | HG01256.hp2 HG01358.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.412+3057_412+3058d others(4): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
CCACA | C | 4 | a0001c0003t0001g0086a0001c0077t0001g0313a0002c0045t0001g0085others(1): Show | 4 | HG00639.hp1 HG02132.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+3055_412+3058d others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467042
|
CCACACAC others(3): Show |
C | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+3049_412+3058d others(12): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467042 | ||||||
| chr11:17467114
|
A | C | 94 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.412+2987T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467114 | ||||||
| chr11:17467139
|
G | C | 94 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.412+2962C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467139 | ||||||
| chr11:17467146
|
C | T | 1 | a0001c0010t0001g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.412+2955G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467146 | ||||||
| chr11:17467156
|
C | T | 94 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.412+2945G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467156 | ||||||
| chr11:17467183
|
T | C | 1 | a0001c0003t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.412+2918A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467183 | ||||||
| chr11:17467335
|
T | C | 29 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0007t0001g0139others(26): Show | 30 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.412+2766A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467335 | ||||||
| chr11:17467350
|
G | A | 8 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(5): Show | 9 | HG01123.hp2 HG01361.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+2751C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467350 | ||||||
| chr11:17467444
|
C | T | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0071t0001g0071 | 3 | HG03098.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412+2657G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467444 | ||||||
| chr11:17467529
|
G | A | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.412+2572C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467529 | ||||||
| chr11:17467559
|
C | T | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.412+2542G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467559 | ||||||
| chr11:17467577
|
A | G | 3 | a0001c0017t0001g0003a0001c0017t0001g0051a0003c0063t0001g0052 | 4 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+2524T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467577 | ||||||
| chr11:17467677
|
G | A | 1 | a0002c0016t0001g0276 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.412+2424C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467677 | ||||||
| chr11:17467720
|
T | C | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.412+2381A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467720 | ||||||
| chr11:17467732
|
C | T | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.412+2369G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467732 | ||||||
| chr11:17467743
|
T | G | 125 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(122): Show | 126 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.412+2358A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467743 | ||||||
| chr11:17467746
|
T | C | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.412+2355A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467746 | ||||||
| chr11:17467790
|
G | C | 85 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.412+2311C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467790 | ||||||
| chr11:17467816
|
T | C | 148 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(145): Show | 151 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.412+2285A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467816 | ||||||
| chr11:17467837
|
C | T | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+2264G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467837 | ||||||
| chr11:17467898
|
C | T | 33 | a0001c0004t0001g0144a0001c0009t0001g0150a0001c0009t0001g0201others(30): Show | 33 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.412+2203G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17467898 | ||||||
| chr11:17468013
|
C | CTGA | 3 | a0001c0017t0001g0003a0001c0017t0001g0051a0003c0063t0001g0052 | 4 | HG02622.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+2087_412+2088i others(5): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468013 | ||||||
| chr11:17468013
|
C | CTGG | 172 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(169): Show | 175 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(172): Show |
intron_variant | MODIFIER | c.412+2085_412+2087d others(5): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468013 | ||||||
| chr11:17468145
|
G | A | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.412+1956C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468145 | ||||||
| chr11:17468149
|
CT | C | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0071t0001g0071 | 3 | HG03098.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412+1951delA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468149 | ||||||
| chr11:17468234
|
G | C | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0071t0001g0071 | 3 | HG03098.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412+1867C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468234 | ||||||
| chr11:17468354
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+1747T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468354 | ||||||
| chr11:17468476
|
C | G | 1 | a0001c0003t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.412+1625G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468476 | ||||||
| chr11:17468531
|
G | A | 1 | a0001c0013t0001g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.412+1570C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468531 | ||||||
| chr11:17468630
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.412+1471A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468630 | ||||||
| chr11:17468717
|
T | C | 96 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.412+1384A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468717 | ||||||
| chr11:17468764
|
G | C | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0071t0001g0071 | 3 | HG03098.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412+1337C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468764 | ||||||
| chr11:17468954
|
C | T | 85 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.412+1147G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17468954 | ||||||
| chr11:17469024
|
C | T | 131 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(128): Show | 134 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.412+1077G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469024 | ||||||
| chr11:17469056
|
T | TC | 300 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(297): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.412+1044dupG | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469056 | ||||||
| chr11:17469056
|
T | TCCCTC | 10 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0047others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+1044_412+1045i others(7): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469056 | ||||||
| chr11:17469056
|
T | TCCCTCCC others(2): Show |
13 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.412+1044_412+1045i others(11): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469056 | ||||||
| chr11:17469056
|
T | TCCCTCCC others(6): Show |
1 | a0001c0081t0001g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.412+1044_412+1045i others(15): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469056 | ||||||
| chr11:17469060
|
C | T | 2 | a0001c0033t0001g0001a0002c0027t0001g0027 | 3 | HG01123.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.412+1041G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469060 | ||||||
| chr11:17469068
|
C | T | 8 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0047others(5): Show | 8 | HG00639.hp2 HG02602.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+1033G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469068 | ||||||
| chr11:17469075
|
C | T | 318 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(315): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.412+1026G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469075 | ||||||
| chr11:17469079
|
C | T | 130 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(127): Show | 133 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.412+1022G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469079 | ||||||
| chr11:17469083
|
C | T | 8 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0047others(5): Show | 8 | HG00639.hp2 HG02602.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+1018G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469083 | ||||||
| chr11:17469083
|
CTCCT | C | 7 | a0001c0026t0001g0034a0001c0026t0001g0035a0001c0026t0004g0326others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+1014_412+1017d others(6): Show |
ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469083 | ||||||
| chr11:17469134
|
C | A | 1 | a0002c0002t0001g0271 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.412+967G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469134 | ||||||
| chr11:17469154
|
C | T | 1 | a0001c0061t0001g0311 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.412+947G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469154 | ||||||
| chr11:17469155
|
G | A | 1 | a0001c0076t0002g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.412+946C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469155 | ||||||
| chr11:17469326
|
C | T | 91 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(88): Show | 91 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.412+775G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469326 | ||||||
| chr11:17469344
|
C | T | 4 | a0001c0012t0001g0210a0001c0012t0001g0211a0001c0012t0001g0212others(1): Show | 4 | HG01515.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+757G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469344 | ||||||
| chr11:17469498
|
T | A | 9 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(6): Show | 11 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+603A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469498 | ||||||
| chr11:17469582
|
T | A | 93 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.412+519A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469582 | ||||||
| chr11:17469619
|
G | A | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+482C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469619 | ||||||
| chr11:17469652
|
G | T | 86 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.412+449C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469652 | ||||||
| chr11:17469715
|
C | T | 1 | a0001c0012t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.412+386G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469715 | ||||||
| chr11:17469789
|
T | G | 93 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.412+312A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469789 | ||||||
| chr11:17469800
|
A | G | 1 | a0001c0007t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.412+301T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469800 | ||||||
| chr11:17469804
|
C | G | 3 | a0001c0017t0001g0070a0001c0022t0001g0072a0001c0071t0001g0071 | 3 | HG03098.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412+297G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469804 | ||||||
| chr11:17469839
|
A | T | 93 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.412+262T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469839 | ||||||
| chr11:17469862
|
C | T | 7 | a0001c0026t0001g0034a0001c0026t0001g0035a0001c0026t0004g0326others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+239G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469862 | ||||||
| chr11:17469893
|
C | T | 18 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(15): Show | 21 | HG00639.hp1 HG01123.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.412+208G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17469893 | ||||||
| chr11:17470024
|
C | T | 139 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0003t0001g0030others(136): Show | 142 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.412+77G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 3/38 | chr11 | 17470024 | ||||||
| chr11:17470284
|
C | A | 28 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0014t0002g0009others(25): Show | 28 | HG01106.hp1 HG01256.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.291-62G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470284 | ||||||
| chr11:17470364
|
G | A | 7 | a0001c0007t0001g0139a0001c0008t0001g0140a0001c0014t0002g0009others(4): Show | 7 | HG01106.hp1 HG01256.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-142C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470364 | ||||||
| chr11:17470465
|
G | T | 15 | a0001c0026t0001g0034a0001c0026t0001g0035a0001c0026t0004g0326others(12): Show | 16 | HG01123.hp2 HG01361.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.291-243C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470465 | ||||||
| chr11:17470472
|
T | C | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.291-250A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470472 | ||||||
| chr11:17470556
|
C | T | 7 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-334G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470556 | ||||||
| chr11:17470579
|
A | G | 1 | a0003c0036t0001g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291-357T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470579 | ||||||
| chr11:17470617
|
C | T | 4 | a0001c0001t0001g0173a0001c0003t0001g0082a0001c0006t0001g0083others(1): Show | 4 | HG01168.hp2 HG01358.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-395G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470617 | ||||||
| chr11:17470732
|
C | G | 10 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(7): Show | 12 | HG01243.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-510G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470732 | ||||||
| chr11:17470831
|
A | G | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.291-609T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470831 | ||||||
| chr11:17470884
|
A | T | 14 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.291-662T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17470884 | ||||||
| chr11:17471117
|
T | C | 176 | a0001c0001t0001g0173a0001c0003t0001g0030a0001c0003t0001g0082others(173): Show | 180 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(177): Show |
intron_variant | MODIFIER | c.291-895A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471117 | ||||||
| chr11:17471250
|
G | A | 4 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(1): Show | 5 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-1028C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471250 | ||||||
| chr11:17471507
|
G | A | 5 | a0001c0025t0001g0054a0001c0025t0001g0056a0001c0025t0001g0075others(2): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-1285C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471507 | ||||||
| chr11:17471586
|
T | C | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.291-1364A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471586 | ||||||
| chr11:17471605
|
G | A | 7 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0010t0001g0298others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-1383C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471605 | ||||||
| chr11:17471635
|
A | G | 94 | a0001c0001t0001g0173a0001c0003t0001g0030a0001c0003t0001g0082others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.291-1413T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471635 | ||||||
| chr11:17471665
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.291-1443G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471665 | ||||||
| chr11:17471703
|
G | A | 1 | a0001c0012t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.291-1481C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471703 | ||||||
| chr11:17471752
|
C | T | 1 | a0001c0006t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.291-1530G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471752 | ||||||
| chr11:17471829
|
G | T | 1 | a0002c0060t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291-1607C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17471829 | ||||||
| chr11:17472150
|
C | T | 4 | a0001c0014t0002g0009a0001c0035t0002g0013a0003c0036t0001g0045others(1): Show | 4 | HG01256.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1928G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472150 | ||||||
| chr11:17472241
|
C | T | 1 | a0001c0077t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.291-2019G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472241 | ||||||
| chr11:17472277
|
T | C | 115 | a0001c0001t0001g0173a0001c0001t0001g0274a0001c0001t0001g0275others(112): Show | 115 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.291-2055A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472277 | ||||||
| chr11:17472513
|
T | A | 1 | a0001c0017t0001g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291-2291A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472513 | ||||||
| chr11:17472514
|
A | C | 1 | a0001c0017t0001g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291-2292T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472514 | ||||||
| chr11:17472515
|
A | T | 92 | a0001c0001t0001g0173a0001c0003t0001g0030a0001c0003t0001g0082others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.291-2293T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472515 | ||||||
| chr11:17472516
|
A | C | 1 | a0001c0017t0001g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291-2294T>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472516 | ||||||
| chr11:17472517
|
T | A | 1 | a0001c0017t0001g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291-2295A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472517 | ||||||
| chr11:17472518
|
T | C | 1 | a0001c0017t0001g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291-2296A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472518 | ||||||
| chr11:17472528
|
C | T | 6 | a0001c0009t0001g0002a0001c0009t0001g0050a0001c0010t0001g0049others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-2306G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472528 | ||||||
| chr11:17472908
|
T | C | 1 | a0001c0008t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.290+1978A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472908 | ||||||
| chr11:17472991
|
C | T | 4 | a0001c0008t0001g0041a0001c0008t0001g0042a0001c0020t0001g0043others(1): Show | 4 | HG01891.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+1895G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17472991 | ||||||
| chr11:17473012
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0273a0002c0002t0001g0272 | 3 | HG00408.hp1 NA18952.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.290+1874A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473012 | ||||||
| chr11:17473153
|
T | C | 9 | a0001c0015t0001g0018a0001c0015t0001g0019a0001c0015t0001g0020others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+1733A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473153 | ||||||
| chr11:17473187
|
G | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.290+1699C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473187 | ||||||
| chr11:17473415
|
T | C | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.290+1471A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473415 | ||||||
| chr11:17473503
|
C | T | 4 | a0001c0006t0001g0278a0001c0028t0001g0159a0002c0005t0001g0277others(1): Show | 4 | NA19000.hp1 NA19068.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+1383G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473503 | ||||||
| chr11:17473504
|
A | G | 173 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0180others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.290+1382T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473504 | ||||||
| chr11:17473633
|
G | A | 110 | a0001c0001t0001g0173a0001c0003t0001g0030a0001c0003t0001g0082others(107): Show | 110 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.290+1253C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473633 | ||||||
| chr11:17473663
|
G | A | 8 | a0001c0004t0001g0144a0001c0010t0001g0142a0001c0010t0001g0143others(5): Show | 8 | HG01243.hp1 HG02970.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+1223C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473663 | ||||||
| chr11:17473699
|
C | T | 17 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0181others(14): Show | 17 | HG00735.hp2 HG01070.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.290+1187G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473699 | ||||||
| chr11:17473789
|
C | T | 2 | a0001c0079t0001g0016a0001c0080t0001g0312 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.290+1097G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473789 | ||||||
| chr11:17473791
|
C | G | 1 | a0001c0001t0001g0207 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.290+1095G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473791 | ||||||
| chr11:17473810
|
A | G | 2 | a0001c0023t0001g0205a0001c0059t0001g0206 | 2 | HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.290+1076T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473810 | ||||||
| chr11:17473820
|
G | A | 22 | a0001c0003t0001g0302a0001c0007t0001g0036a0001c0008t0001g0039others(19): Show | 23 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.290+1066C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473820 | ||||||
| chr11:17473883
|
G | T | 128 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0180others(125): Show | 128 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.290+1003C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473883 | ||||||
| chr11:17473905
|
A | T | 1 | a0001c0004t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.290+981T>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473905 | ||||||
| chr11:17473977
|
C | A | 1 | a0001c0003t0001g0324 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290+909G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473977 | ||||||
| chr11:17473977
|
C | T | 22 | a0001c0003t0001g0302a0001c0007t0001g0036a0001c0008t0001g0039others(19): Show | 23 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.290+909G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17473977 | ||||||
| chr11:17474011
|
G | A | 1 | a0001c0007t0001g0131 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.290+875C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474011 | ||||||
| chr11:17474426
|
G | A | 47 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.290+460C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474426 | ||||||
| chr11:17474433
|
G | A | 4 | a0001c0009t0001g0289a0001c0009t0001g0290a0001c0009t0001g0291others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+453C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474433 | ||||||
| chr11:17474544
|
A | AT | 211 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0180others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.290+341dupA | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474544 | ||||||
| chr11:17474687
|
G | C | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+199C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474687 | ||||||
| chr11:17474688
|
G | T | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+198C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474688 | ||||||
| chr11:17474690
|
C | T | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+196G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474690 | ||||||
| chr11:17474691
|
T | A | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+195A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474691 | ||||||
| chr11:17474692
|
G | C | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+194C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474692 | ||||||
| chr11:17474695
|
G | A | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+191C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474695 | ||||||
| chr11:17474697
|
C | T | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+189G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474697 | ||||||
| chr11:17474698
|
A | G | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+188T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474698 | ||||||
| chr11:17474699
|
G | A | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+187C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474699 | ||||||
| chr11:17474700
|
G | T | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+186C>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474700 | ||||||
| chr11:17474702
|
C | T | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+184G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474702 | ||||||
| chr11:17474703
|
C | T | 1 | a0001c0012t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.290+183G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474703 | ||||||
| chr11:17474748
|
A | G | 1 | a0001c0061t0001g0311 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290+138T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 2/38 | chr11 | 17474748 | ||||||
| chr11:17475079
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.149-52C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475079 | ||||||
| chr11:17475183
|
A | G | 17 | a0001c0009t0003g0015a0001c0014t0001g0032a0001c0015t0001g0018others(14): Show | 17 | HG00735.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.149-156T>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475183 | ||||||
| chr11:17475329
|
C | T | 7 | a0001c0009t0001g0150a0001c0012t0001g0151a0001c0013t0001g0152others(4): Show | 7 | NA18942.hp2 NA18948.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-302G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475329 | ||||||
| chr11:17475392
|
T | A | 2 | a0001c0003t0001g0030a0001c0023t0001g0031 | 2 | HG02083.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.149-365A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475392 | ||||||
| chr11:17475417
|
T | C | 81 | a0001c0001t0001g0137a0001c0001t0001g0286a0001c0003t0001g0082others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.149-390A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475417 | ||||||
| chr11:17475440
|
T | C | 11 | a0001c0004t0001g0144a0001c0007t0001g0139a0001c0008t0001g0140others(8): Show | 11 | HG00735.hp1 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.149-413A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475440 | ||||||
| chr11:17475444
|
G | A | 1 | a0004c0041t0001g0145 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.149-417C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475444 | ||||||
| chr11:17475463
|
G | A | 323 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(320): Show | 327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.149-436C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475463 | ||||||
| chr11:17475638
|
T | G | 1 | a0001c0079t0001g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.149-611A>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475638 | ||||||
| chr11:17475753
|
T | A | 1 | a0001c0070t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.149-726A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475753 | ||||||
| chr11:17475766
|
G | C | 1 | a0001c0001t0001g0287 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.149-739C>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475766 | ||||||
| chr11:17475915
|
C | T | 17 | a0001c0003t0001g0030a0001c0015t0001g0018a0001c0015t0001g0019others(14): Show | 18 | HG01123.hp2 HG01361.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.148+714G>A | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17475915 | ||||||
| chr11:17476247
|
C | G | 166 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(163): Show | 170 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.148+382G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476247 | ||||||
| chr11:17476288
|
T | C | 1 | a0001c0010t0001g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.148+341A>G | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476288 | ||||||
| chr11:17476321
|
T | A | 11 | a0001c0004t0001g0293a0001c0004t0001g0296a0001c0009t0001g0289others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+308A>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476321 | ||||||
| chr11:17476429
|
G | A | 1 | a0002c0078t0001g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.148+200C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476429 | ||||||
| chr11:17476492
|
C | A | 1 | a0002c0030t0001g0300 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.148+137G>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476492 | ||||||
| chr11:17476510
|
G | A | 26 | a0001c0001t0001g0317a0001c0003t0001g0302a0001c0003t0001g0309others(23): Show | 27 | HG00639.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.148+119C>T | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476510 | ||||||
| chr11:17476602
|
C | G | 1 | a0001c0079t0001g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+27G>C | ABCC8 | ENSG00000006071.16 | transcript | ENST00000389817.8 | protein_coding | 1/38 | chr11 | 17476602 |