| geneid | 9619 |
|---|---|
| ensemblid | ENSG00000160179.19 |
| hgncid | 73 |
| symbol | ABCG1 |
| name | ATP binding cassette subfamily G member 1 |
| refseq_nuc | NM_016818.3 |
| refseq_prot | NP_058198.2 |
| ensembl_nuc | ENST00000398449.8 |
| ensembl_prot | ENSP00000381467.3 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 42219140 |
| end | 42297244 |
| strand | + |
| ver | v1.2 |
| region | chr21:42219140-42297244 |
| region5000 | chr21:42214140-42302244 |
| regionname0 | ABCG1_chr21_42219140_42297244 |
| regionname5000 | ABCG1_chr21_42214140_42302244 |
| 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 | 1/1 | 666 | 351 | 94 | 74 | 124 | 18 | 39 | 82 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0002 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0003 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0004 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| 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 | 1/1 | 2001 | 314 | 75 | 69 | 113 | 17 | 38 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0002 | 0/0 | 2001 | 13 | 13 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0003 | 0/0 | 2001 | 10 | 0 | 2 | 8 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0004 | 0/0 | 2001 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0005 | 0/0 | 2001 | 3 | 1 | 0 | 0 | 1 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0006 | 0/0 | 2001 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0007 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0008 | 0/0 | 2001 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0009 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0010 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0011 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0012 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| c0013 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| 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 | 1/0 | 976 | 81 | 18 | 13 | 40 | 5 | 4 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0002 | 0/1 | 977 | 78 | 16 | 18 | 29 | 6 | 8 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0003 | 0/0 | 978 | 56 | 7 | 13 | 22 | 3 | 11 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0004 | 0/0 | 976 | 35 | 29 | 6 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0005 | 0/0 | 971 | 21 | 0 | 4 | 14 | 1 | 2 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0006 | 0/0 | 970 | 19 | 2 | 1 | 12 | 0 | 4 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0007 | 0/0 | 972 | 11 | 1 | 1 | 6 | 0 | 3 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0008 | 0/0 | 976 | 7 | 2 | 3 | 0 | 1 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0009 | 0/0 | 977 | 6 | 5 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0010 | 0/0 | 979 | 6 | 0 | 4 | 0 | 2 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0011 | 0/0 | 970 | 5 | 0 | 5 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0012 | 0/0 | 983 | 4 | 1 | 1 | 0 | 0 | 2 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0013 | 0/0 | 978 | 3 | 0 | 0 | 0 | 0 | 3 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0014 | 0/0 | 970 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0015 | 0/0 | 973 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0016 | 0/0 | 973 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0017 | 0/0 | 984 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0018 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0019 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0020 | 0/0 | 971 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0021 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0022 | 0/0 | 973 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0023 | 0/0 | 974 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0024 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0025 | 0/0 | 977 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0026 | 0/0 | 979 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0027 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0028 | 0/0 | 982 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0029 | 0/0 | 982 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0030 | 0/0 | 994 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| t0031 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| 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 | 1/1 | 2001 | 314 | 75 | 69 | 113 | 17 | 38 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0002 | 0/0 | 2001 | 13 | 13 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003 | 0/0 | 2001 | 10 | 0 | 2 | 8 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0004 | 0/0 | 2001 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0005 | 0/0 | 2001 | 3 | 1 | 0 | 0 | 1 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0006 | 0/0 | 2001 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0007 | 0/0 | 2001 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0008 | 0/0 | 2001 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0011 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0012 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0002c0013 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0003c0010 | 0/0 | 2001 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0004c0009 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2976 | 76 | 18 | 11 | 37 | 5 | 4 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0002 | 0/1 | 2977 | 69 | 7 | 18 | 29 | 6 | 8 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0003 | 0/0 | 2978 | 50 | 7 | 13 | 17 | 3 | 10 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0004 | 0/0 | 2976 | 29 | 23 | 6 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0005 | 0/0 | 2971 | 18 | 0 | 3 | 12 | 1 | 2 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0006 | 0/0 | 2970 | 18 | 2 | 1 | 11 | 0 | 4 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0007 | 0/0 | 2972 | 10 | 1 | 1 | 5 | 0 | 3 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0008 | 0/0 | 2976 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0009 | 0/0 | 2977 | 6 | 5 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0010 | 0/0 | 2979 | 6 | 0 | 4 | 0 | 2 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0011 | 0/0 | 2970 | 4 | 0 | 4 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0012 | 0/0 | 2983 | 4 | 1 | 1 | 0 | 0 | 2 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0013 | 0/0 | 2978 | 3 | 0 | 0 | 0 | 0 | 3 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0014 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0015 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0017 | 0/0 | 2984 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0018 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0020 | 0/0 | 2971 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0021 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0022 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0023 | 0/0 | 2974 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0024 | 0/0 | 2975 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0025 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0026 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0027 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0028 | 0/0 | 2982 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0029 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0030 | 0/0 | 2994 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0001t0031 | 0/0 | 2996 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0002t0002 | 0/0 | 2977 | 9 | 9 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0002t0004 | 0/0 | 2976 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0002t0016 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0003 | 0/0 | 2978 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0005 | 0/0 | 2971 | 3 | 0 | 1 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0006 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0007 | 0/0 | 2972 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0008 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0003t0019 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0004t0003 | 0/0 | 2978 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0005t0008 | 0/0 | 2976 | 3 | 1 | 0 | 0 | 1 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0006t0001 | 0/0 | 2976 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0006t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0007t0015 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0007t0016 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0008t0011 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0011t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0001c0012t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0002c0013t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0003c0010t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| a0004c0009t0003 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | copy fasta | chr21 | 42214140 | 42302244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0009g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0010g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0010g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0010g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0010g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0011g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0011g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0011g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0012g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0012g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0012g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0013g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0013g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0013g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0014g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0015g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0017g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0018g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0020g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0021g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0022g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0023g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0024g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0025g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0026g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0027g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0028g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0029g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0030g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0001t0031g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0002t0016g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0003t0019g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0004t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0004t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0005t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0005t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0005t0008g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0006t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0006t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0007t0015g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0007t0016g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0008t0011g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0011t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0001c0012t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0002c0013t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0003c0010t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| a0004c0009t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00099 | hp2 | a0001 | c0005 | t0008 | g0131 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0305 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0236 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0017 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00408 | hp1 | a0001 | c0003 | t0005 | g0048 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00558 | hp1 | a0001 | c0003 | t0003 | g0259 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00609 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0302 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0194 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0307 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01070 | hp2 | a0001 | c0006 | t0001 | g0006 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01071 | hp1 | a0001 | c0006 | t0001 | g0006 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0329 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0005 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0195 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01243 | hp1 | a0001 | c0001 | t0025 | g0070 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0019 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01257 | hp2 | a0001 | c0001 | t0011 | g0043 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0267 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01346 | hp2 | a0001 | c0001 | t0023 | g0023 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01515 | hp2 | a0001 | c0001 | t0010 | g0303 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0193 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01517 | hp1 | a0001 | c0001 | t0010 | g0301 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0196 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01891 | hp2 | a0001 | c0005 | t0008 | g0170 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01934 | hp2 | a0001 | c0008 | t0011 | g0042 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0037 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01975 | hp2 | a0001 | c0003 | t0008 | g0117 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0045 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01981 | hp2 | a0001 | c0001 | t0010 | g0167 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0346 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02004 | hp1 | a0001 | c0001 | t0027 | g0344 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02015 | hp2 | a0001 | c0003 | t0019 | g0029 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0333 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02132 | hp1 | a0001 | c0003 | t0006 | g0044 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0085 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02148 | hp1 | a0001 | c0003 | t0005 | g0041 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0036 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0040 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02273 | hp2 | a0001 | c0001 | t0011 | g0057 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02280 | hp1 | a0001 | c0006 | t0004 | g0321 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0039 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02293 | hp2 | a0001 | c0001 | t0022 | g0022 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0330 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02602 | hp1 | a0004 | c0009 | t0003 | g0258 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02602 | hp2 | a0001 | c0001 | t0013 | g0294 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0143 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02615 | hp2 | a0001 | c0002 | t0016 | g0343 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0315 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0287 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0038 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0285 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0046 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02738 | hp1 | a0001 | c0001 | t0013 | g0295 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0061 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0275 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0062 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0323 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0322 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0332 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0065 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03098 | hp2 | a0001 | c0001 | t0026 | g0318 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0005 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0337 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03490 | hp1 | a0001 | c0005 | t0008 | g0314 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03490 | hp2 | a0001 | c0001 | t0012 | g0140 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0223 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0027 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0026 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0141 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03516 | hp1 | a0001 | c0007 | t0015 | g0348 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03516 | hp2 | a0001 | c0007 | t0016 | g0347 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03540 | hp1 | a0001 | c0011 | t0004 | g0087 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0056 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0296 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03704 | hp1 | a0001 | c0001 | t0028 | g0306 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0324 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | CHB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0274 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0339 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0212 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18962 | hp1 | a0001 | c0001 | t0020 | g0014 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0032 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18980 | hp2 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18981 | hp2 | a0001 | c0003 | t0005 | g0052 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18989 | hp1 | a0001 | c0001 | t0021 | g0008 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19003 | hp2 | a0001 | c0004 | t0003 | g0126 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19004 | hp1 | a0001 | c0004 | t0003 | g0074 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19067 | hp2 | a0003 | c0010 | t0001 | g0249 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19070 | hp2 | a0001 | c0004 | t0003 | g0127 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19087 | hp2 | a0002 | c0013 | t0001 | g0099 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19091 | hp1 | a0001 | c0003 | t0007 | g0054 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA19240 | hp2 | a0001 | c0012 | t0004 | g0276 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ASW | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ASW | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0217 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0304 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0299 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0016 | SAS | GIH | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0292 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0144 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02486 | hp1 | a0001 | c0001 | t0024 | g0101 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02559 | hp1 | a0001 | c0001 | t0030 | g0312 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0325 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG03471 | hp2 | a0001 | c0001 | t0029 | g0262 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0331 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0345 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| NA21309 | hp2 | a0001 | c0001 | t0031 | g0077 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0188 | REF | REF | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0160 | REF | REF | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:42225697
|
G | T | 1 | a0002 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.69G>T | p.Met23Ile | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/15 | 192/2976 | 69/2001 | 23/666 | chr21 | 42225697 | ||
| chr21:42225779
|
G | A | 1 | a0004 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.151G>A | p.Gly51Arg | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/15 | 274/2976 | 151/2001 | 51/666 | chr21 | 42225779 | ||
| chr21:42287931
|
G | A | 1 | a0003 | 1 | NA19067.hp2 | missense_variant | MODERATE | c.1016G>A | p.Arg339Gln | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/15 | 1139/2976 | 1016/2001 | 339/666 | chr21 | 42287931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:42219271
|
T | C | 1 | a0001c0007 | 2 | HG03516.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.9T>C | p.Cys3Cys | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 132/2976 | 9/2001 | 3/666 | chr21 | 42219271 | ||
| chr21:42225724
|
G | A | 1 | a0001c0008 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.96G>A | p.Ser32Ser | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/15 | 219/2976 | 96/2001 | 32/666 | chr21 | 42225724 | ||
| chr21:42271122
|
G | A | 1 | a0001c0003 | 10 | HG00408.hp1 HG00558.hp1 HG01975.hp2 others(7): Show |
synonymous_variant | LOW | c.339G>A | p.Leu113Leu | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/15 | 462/2976 | 339/2001 | 113/666 | chr21 | 42271122 | ||
| chr21:42273345
|
C | G | 1 | a0001c0006 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
synonymous_variant | LOW | c.447C>G | p.Pro149Pro | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/15 | 570/2976 | 447/2001 | 149/666 | chr21 | 42273345 | ||
| chr21:42287908
|
C | T | 1 | a0001c0005 | 3 | HG00099.hp2 HG01891.hp2 HG03490.hp1 |
synonymous_variant | LOW | c.993C>T | p.Gly331Gly | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/15 | 1116/2976 | 993/2001 | 331/666 | chr21 | 42287908 | ||
| chr21:42288312
|
G | A | 1 | a0001c0011 | 1 | HG03540.hp1 | splice_region_variant&synonymous_variant | LOW | c.1224G>A | p.Ser408Ser | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/15 | 1347/2976 | 1224/2001 | 408/666 | chr21 | 42288312 | ||
| chr21:42290193
|
G | C | 1 | a0001c0002 | 13 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(10): Show |
synonymous_variant | LOW | c.1368G>C | p.Ala456Ala | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/15 | 1491/2976 | 1368/2001 | 456/666 | chr21 | 42290193 | ||
| chr21:42294610
|
C | T | 1 | a0001c0004 | 3 | NA19003.hp2 NA19004.hp1 NA19070.hp2 |
synonymous_variant | LOW | c.1722C>T | p.Phe574Phe | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/15 | 1845/2976 | 1722/2001 | 574/666 | chr21 | 42294610 | ||
| chr21:42296233
|
C | T | 1 | a0001c0012 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1842C>T | p.Asp614Asp | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 1965/2976 | 1842/2001 | 614/666 | chr21 | 42296233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:42219222
|
C | CCCGCCG | 4 | a0001c0001t0012a0001c0001t0017a0001c0001t0028others(1): Show | 8 | HG01069.hp1 HG01109.hp2 HG02630.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-9dupGCCGCC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 8 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | ||||
| chr21:42219222
|
C | CCCGCCGC others(11): Show |
2 | a0001c0001t0030a0001c0001t0031 | 2 | HG02559.hp1 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-26_-9dupGCCGCCGCC others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 8 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | ||||
| chr21:42219222
|
CCCG | C | 7 | a0001c0001t0015a0001c0001t0022a0001c0001t0023others(4): Show | 7 | HG01346.hp2 HG02293.hp2 HG02486.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-11_-9delGCC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 9 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | ||||
| chr21:42219222
|
CCCGCCG | C | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(10): Show | 62 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-9delGCCGCC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 9 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | ||||
| chr21:42296444
|
G | A | 6 | a0001c0001t0008a0001c0001t0011a0001c0001t0022others(3): Show | 13 | HG00099.hp2 HG00741.hp1 HG01192.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*52G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 52 | chr21 | 42296444 | |||||
| chr21:42296450
|
A | C | 1 | a0001c0001t0027 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 58 | chr21 | 42296450 | |||||
| chr21:42296473
|
C | T | 1 | a0001c0001t0013 | 3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*81C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 81 | chr21 | 42296473 | |||||
| chr21:42296478
|
G | A | 1 | a0001c0001t0018 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 86 | chr21 | 42296478 | |||||
| chr21:42296538
|
G | A | 1 | a0001c0003t0019 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 146 | chr21 | 42296538 | |||||
| chr21:42296567
|
G | A | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 175 | chr21 | 42296567 | |||||
| chr21:42296624
|
G | GT | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(6): Show | 112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*245dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 246 | INFO_REALIGN_3_PRIME | chr21 | 42296624 | ||||
| chr21:42296624
|
G | GTT | 10 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(7): Show | 74 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*244_*245dupTT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 246 | INFO_REALIGN_3_PRIME | chr21 | 42296624 | ||||
| chr21:42296624
|
G | GTTT | 3 | a0001c0001t0010a0001c0001t0021a0001c0001t0026 | 8 | HG00642.hp1 HG01123.hp1 HG01123.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*243_*245dupTTT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 246 | INFO_REALIGN_3_PRIME | chr21 | 42296624 | ||||
| chr21:42296791
|
A | G | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*399A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 399 | chr21 | 42296791 | |||||
| chr21:42297077
|
C | T | 1 | a0001c0001t0020 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 685 | chr21 | 42297077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:42219366
|
C | T | 2 | a0001c0007t0015g0348a0001c0007t0016g0347 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.42+62C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219366 | ||||||
| chr21:42219406
|
G | T | 3 | a0001c0001t0003g0346a0001c0001t0008g0345a0001c0001t0027g0344 | 3 | HG01993.hp2 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.42+102G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219406 | ||||||
| chr21:42219443
|
T | A | 62 | a0001c0001t0005g0001a0001c0001t0005g0009a0001c0001t0005g0010others(59): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+139T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219443 | ||||||
| chr21:42219481
|
A | C | 62 | a0001c0001t0005g0001a0001c0001t0005g0009a0001c0001t0005g0010others(59): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+177A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219481 | ||||||
| chr21:42219631
|
C | G | 62 | a0001c0001t0005g0001a0001c0001t0005g0009a0001c0001t0005g0010others(59): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+327C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219631 | ||||||
| chr21:42219691
|
G | A | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 5 | HG00735.hp2 HG01106.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+387G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219691 | ||||||
| chr21:42219733
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.42+429T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219733 | ||||||
| chr21:42219897
|
C | T | 1 | a0001c0002t0016g0343 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.42+593C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219897 | ||||||
| chr21:42219956
|
C | G | 63 | a0001c0001t0001g0342a0001c0001t0005g0001a0001c0001t0005g0009others(60): Show | 64 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.42+652C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219956 | ||||||
| chr21:42220059
|
T | C | 62 | a0001c0001t0005g0001a0001c0001t0005g0009a0001c0001t0005g0010others(59): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+755T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220059 | ||||||
| chr21:42220073
|
G | A | 62 | a0001c0001t0005g0001a0001c0001t0005g0009a0001c0001t0005g0010others(59): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+769G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220073 | ||||||
| chr21:42220307
|
G | A | 2 | a0001c0001t0002g0075a0001c0004t0003g0074 | 2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.42+1003G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220307 | ||||||
| chr21:42220320
|
C | T | 2 | a0001c0001t0002g0340a0001c0001t0002g0341 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.42+1016C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220320 | ||||||
| chr21:42220334
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42+1030T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220334 | ||||||
| chr21:42220415
|
T | G | 2 | a0001c0001t0031g0077a0001c0002t0002g0078 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.42+1111T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220415 | ||||||
| chr21:42220421
|
G | GA | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0080others(3): Show | 7 | HG01081.hp2 HG01109.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+1129dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42220421 | |||||
| chr21:42220421
|
GA | G | 30 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0327others(27): Show | 32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.42+1129delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42220421 | |||||
| chr21:42220593
|
G | T | 1 | a0001c0001t0004g0339 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.42+1289G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220593 | ||||||
| chr21:42220606
|
G | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0096others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.42+1302G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220606 | ||||||
| chr21:42220854
|
GTTATAGA others(3): Show |
G | 1 | a0002c0013t0001g0099 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.42+1552_42+1561del others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42220854 | |||||
| chr21:42220999
|
T | C | 1 | a0001c0001t0003g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.42+1695T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220999 | ||||||
| chr21:42221237
|
G | A | 66 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0005g0001others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.42+1933G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221237 | ||||||
| chr21:42221258
|
C | T | 4 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0001t0004g0337others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1954C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221258 | ||||||
| chr21:42221283
|
G | A | 1 | a0001c0001t0024g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+1979G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221283 | ||||||
| chr21:42221348
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.42+2044C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221348 | ||||||
| chr21:42221475
|
A | T | 25 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0327others(22): Show | 26 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.42+2171A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221475 | ||||||
| chr21:42221495
|
G | A | 45 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0108others(42): Show | 46 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.42+2191G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221495 | ||||||
| chr21:42221547
|
G | A | 65 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0005g0001others(62): Show | 66 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.42+2243G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221547 | ||||||
| chr21:42221563
|
A | G | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.42+2259A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221563 | ||||||
| chr21:42221603
|
A | T | 1 | a0001c0001t0031g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+2299A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221603 | ||||||
| chr21:42221864
|
G | A | 1 | a0001c0001t0031g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+2560G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221864 | ||||||
| chr21:42221949
|
A | G | 1 | a0001c0001t0030g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.42+2645A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221949 | ||||||
| chr21:42222166
|
T | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.42+2862T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222166 | ||||||
| chr21:42222317
|
C | T | 2 | a0001c0001t0003g0310a0001c0001t0004g0311 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.42+3013C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222317 | ||||||
| chr21:42222328
|
C | T | 47 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0108others(44): Show | 48 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.42+3024C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222328 | ||||||
| chr21:42222477
|
C | G | 1 | a0001c0001t0002g0309 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.42+3173C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222477 | ||||||
| chr21:42222552
|
T | C | 1 | a0001c0001t0004g0313 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43-3119T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222552 | ||||||
| chr21:42222646
|
T | C | 3 | a0001c0001t0003g0320a0001c0001t0004g0319a0001c0001t0026g0318 | 3 | HG02572.hp1 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.43-3025T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222646 | ||||||
| chr21:42222700
|
G | A | 2 | a0001c0001t0012g0140a0001c0001t0012g0141 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.43-2971G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222700 | ||||||
| chr21:42222753
|
G | A | 1 | a0001c0001t0004g0339 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43-2918G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222753 | ||||||
| chr21:42222937
|
A | C | 138 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(135): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.43-2734A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222937 | ||||||
| chr21:42222990
|
T | G | 73 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0096others(70): Show | 77 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-2681T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222990 | ||||||
| chr21:42223154
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0003g0261 | 2 | NA18977.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.43-2517C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223154 | ||||||
| chr21:42223172
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0002g0308a0001c0001t0012g0140others(4): Show | 7 | HG01069.hp1 HG01496.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-2499C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223172 | ||||||
| chr21:42223178
|
G | A | 1 | a0001c0001t0005g0001 | 2 | NA18973.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.43-2493G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223178 | ||||||
| chr21:42223328
|
C | T | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.43-2343C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223328 | ||||||
| chr21:42223473
|
G | A | 1 | a0001c0002t0002g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-2198G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223473 | ||||||
| chr21:42223473
|
G | C | 34 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(31): Show | 35 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.43-2198G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223473 | ||||||
| chr21:42223481
|
G | T | 148 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0096others(145): Show | 153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.43-2190G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223481 | ||||||
| chr21:42223505
|
C | T | 1 | a0001c0001t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43-2166C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223505 | ||||||
| chr21:42223668
|
A | T | 2 | a0001c0001t0007g0026a0001c0001t0007g0027 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.43-2003A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223668 | ||||||
| chr21:42223681
|
G | A | 3 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0006g0011 | 3 | NA18612.hp1 NA18939.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.43-1990G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223681 | ||||||
| chr21:42223899
|
T | C | 184 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(181): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.43-1772T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223899 | ||||||
| chr21:42223917
|
C | T | 103 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0142others(100): Show | 105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.43-1754C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223917 | ||||||
| chr21:42223956
|
C | G | 2 | a0001c0001t0005g0024a0001c0001t0005g0025 | 2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.43-1715C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223956 | ||||||
| chr21:42224164
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.43-1507G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224164 | ||||||
| chr21:42224167
|
T | C | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.43-1504T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224167 | ||||||
| chr21:42224197
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.43-1474C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224197 | ||||||
| chr21:42224221
|
T | C | 183 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(180): Show | 188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.43-1450T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224221 | ||||||
| chr21:42224275
|
T | C | 1 | a0001c0001t0005g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.43-1396T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224275 | ||||||
| chr21:42224308
|
G | A | 1 | a0001c0001t0030g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.43-1363G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224308 | ||||||
| chr21:42224317
|
C | T | 5 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-1354C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224317 | ||||||
| chr21:42224424
|
C | T | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.43-1247C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224424 | ||||||
| chr21:42224477
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.43-1194G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224477 | ||||||
| chr21:42224520
|
G | C | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-1151G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224520 | ||||||
| chr21:42224614
|
C | T | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.43-1057C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224614 | ||||||
| chr21:42224763
|
A | G | 1 | a0001c0002t0004g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.43-908A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224763 | ||||||
| chr21:42224944
|
C | CT | 9 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0002g0305others(6): Show | 9 | HG00140.hp1 HG01975.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.43-713dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42224944 | |||||
| chr21:42224944
|
CT | C | 25 | a0001c0001t0001g0155a0001c0001t0001g0327a0001c0001t0001g0328others(22): Show | 26 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.43-713delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42224944 | |||||
| chr21:42225096
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.43-575T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225096 | ||||||
| chr21:42225202
|
T | C | 2 | a0001c0001t0012g0307a0001c0001t0028g0306 | 2 | HG01069.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-469T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225202 | ||||||
| chr21:42225319
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.43-352T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225319 | ||||||
| chr21:42225613
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.43-58T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225613 | ||||||
| chr21:42225918
|
G | A | 4 | a0001c0001t0005g0001a0001c0001t0005g0015a0001c0001t0005g0066others(1): Show | 5 | HG02129.hp2 NA18962.hp1 NA18969.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.286+4G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42225918 | ||||||
| chr21:42225925
|
C | T | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+11C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42225925 | ||||||
| chr21:42225960
|
G | A | 1 | a0001c0001t0006g0012 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.286+46G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42225960 | ||||||
| chr21:42226215
|
G | C | 1 | a0001c0001t0010g0144 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.286+301G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226215 | ||||||
| chr21:42226272
|
C | A | 1 | a0002c0013t0001g0099 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.286+358C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226272 | ||||||
| chr21:42226316
|
C | T | 6 | a0001c0001t0001g0263a0001c0001t0002g0266a0001c0001t0004g0264others(3): Show | 6 | HG01261.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+402C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226316 | ||||||
| chr21:42226490
|
C | T | 1 | a0001c0001t0005g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.286+576C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226490 | ||||||
| chr21:42226606
|
G | A | 1 | a0001c0003t0019g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.286+692G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226606 | ||||||
| chr21:42226632
|
T | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0316a0001c0001t0009g0085 | 3 | HG02145.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.286+718T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226632 | ||||||
| chr21:42226696
|
T | C | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+782T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226696 | ||||||
| chr21:42226716
|
G | A | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+802G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226716 | ||||||
| chr21:42226717
|
A | T | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+803A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226717 | ||||||
| chr21:42226884
|
G | A | 4 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+970G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226884 | ||||||
| chr21:42227340
|
A | G | 34 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0124others(31): Show | 35 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.286+1426A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227340 | ||||||
| chr21:42227408
|
A | T | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.286+1494A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227408 | ||||||
| chr21:42227454
|
T | C | 4 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+1540T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227454 | ||||||
| chr21:42227638
|
G | A | 38 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0124others(35): Show | 39 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.286+1724G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227638 | ||||||
| chr21:42227748
|
G | A | 4 | a0001c0001t0001g0155a0001c0001t0003g0153a0001c0001t0004g0154others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+1834G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227748 | ||||||
| chr21:42227757
|
G | T | 1 | a0001c0007t0015g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.286+1843G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227757 | ||||||
| chr21:42227839
|
GGAGA | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0004g0269others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+1939_286+1942d others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42227839 | |||||
| chr21:42227842
|
G | T | 2 | a0001c0001t0001g0338a0001c0001t0004g0337 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.286+1928G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227842 | ||||||
| chr21:42227848
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.286+1934G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227848 | ||||||
| chr21:42227984
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.286+2070G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227984 | ||||||
| chr21:42228028
|
C | T | 1 | a0004c0009t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.286+2114C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228028 | ||||||
| chr21:42228033
|
C | T | 4 | a0001c0001t0004g0329a0001c0002t0002g0330a0001c0002t0002g0331others(1): Show | 4 | HG01081.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+2119C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228033 | ||||||
| chr21:42228256
|
G | A | 68 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0260others(65): Show | 68 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.286+2342G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228256 | ||||||
| chr21:42228313
|
A | G | 187 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(184): Show | 192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.286+2399A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228313 | ||||||
| chr21:42228320
|
C | G | 187 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(184): Show | 192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.286+2406C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228320 | ||||||
| chr21:42228443
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0004g0283 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.286+2529C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228443 | ||||||
| chr21:42228628
|
G | A | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+2714G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228628 | ||||||
| chr21:42228643
|
C | A | 15 | a0001c0001t0001g0155a0001c0001t0001g0327a0001c0001t0001g0328others(12): Show | 16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+2729C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228643 | ||||||
| chr21:42228825
|
G | C | 187 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(184): Show | 192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.286+2911G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228825 | ||||||
| chr21:42229062
|
A | C | 1 | a0001c0001t0002g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+3148A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229062 | ||||||
| chr21:42229105
|
G | A | 2 | a0001c0001t0004g0158a0001c0002t0002g0143 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.286+3191G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229105 | ||||||
| chr21:42229264
|
T | G | 1 | a0001c0001t0027g0344 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.286+3350T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229264 | ||||||
| chr21:42229284
|
T | C | 4 | a0001c0001t0001g0155a0001c0001t0003g0153a0001c0001t0004g0154others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3370T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229284 | ||||||
| chr21:42229442
|
G | A | 2 | a0001c0001t0005g0024a0001c0001t0005g0025 | 2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.286+3528G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229442 | ||||||
| chr21:42229457
|
C | G | 1 | a0001c0001t0003g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.286+3543C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229457 | ||||||
| chr21:42229501
|
C | T | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+3587C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229501 | ||||||
| chr21:42229551
|
C | G | 1 | a0001c0001t0003g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.286+3637C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229551 | ||||||
| chr21:42229564
|
A | C | 2 | a0001c0001t0001g0255a0001c0001t0003g0256 | 2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.286+3650A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229564 | ||||||
| chr21:42229588
|
C | T | 1 | a0001c0002t0002g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.286+3674C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229588 | ||||||
| chr21:42229667
|
T | C | 15 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0326others(12): Show | 16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+3753T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229667 | ||||||
| chr21:42229670
|
G | C | 1 | a0001c0001t0005g0030 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.286+3756G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229670 | ||||||
| chr21:42229674
|
C | A | 4 | a0001c0001t0001g0155a0001c0001t0003g0153a0001c0001t0004g0154others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3760C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229674 | ||||||
| chr21:42229719
|
C | CAA | 15 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0326others(12): Show | 16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+3814_286+3815d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42229719 | |||||
| chr21:42230060
|
T | C | 3 | a0001c0001t0001g0335a0001c0001t0003g0310a0001c0001t0004g0311 | 3 | HG02055.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.286+4146T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230060 | ||||||
| chr21:42230081
|
G | A | 3 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141 | 3 | HG01496.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.286+4167G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230081 | ||||||
| chr21:42230132
|
A | T | 1 | a0001c0006t0004g0321 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.286+4218A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230132 | ||||||
| chr21:42230160
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0002g0104a0001c0001t0002g0121 | 3 | NA18962.hp2 NA18989.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.286+4246G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230160 | ||||||
| chr21:42230228
|
A | G | 1 | a0001c0001t0003g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.286+4314A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230228 | ||||||
| chr21:42230277
|
A | G | 186 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(183): Show | 190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.286+4363A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230277 | ||||||
| chr21:42230346
|
A | G | 341 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(338): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.286+4432A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230346 | ||||||
| chr21:42230362
|
C | T | 15 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0326others(12): Show | 16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+4448C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230362 | ||||||
| chr21:42230590
|
G | A | 15 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0326others(12): Show | 16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+4676G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230590 | ||||||
| chr21:42230620
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+4706G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230620 | ||||||
| chr21:42230623
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0003g0261 | 2 | NA18977.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.286+4709A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230623 | ||||||
| chr21:42230656
|
C | A | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+4742C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230656 | ||||||
| chr21:42230666
|
C | T | 6 | a0001c0001t0005g0001a0001c0001t0005g0015a0001c0001t0005g0024others(3): Show | 7 | HG02129.hp2 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+4752C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230666 | ||||||
| chr21:42230669
|
G | A | 69 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0260others(66): Show | 69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.286+4755G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230669 | ||||||
| chr21:42230770
|
C | T | 15 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0326others(12): Show | 16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+4856C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230770 | ||||||
| chr21:42230940
|
G | A | 7 | a0001c0001t0001g0260a0001c0001t0002g0146a0001c0001t0002g0147others(4): Show | 7 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+5026G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230940 | ||||||
| chr21:42230948
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286+5034G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230948 | ||||||
| chr21:42230952
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0003c0010t0001g0249 | 3 | HG02056.hp1 NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.286+5038C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230952 | ||||||
| chr21:42231006
|
C | T | 1 | a0001c0001t0003g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.286+5092C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231006 | ||||||
| chr21:42231189
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0004g0154 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.286+5275G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231189 | ||||||
| chr21:42231191
|
GC | G | 5 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+5278delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231191 | ||||||
| chr21:42231203
|
A | G | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+5289A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231203 | ||||||
| chr21:42231370
|
C | T | 2 | a0001c0001t0022g0022a0001c0001t0023g0023 | 2 | HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.286+5456C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231370 | ||||||
| chr21:42231412
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.286+5498C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231412 | ||||||
| chr21:42231446
|
C | T | 171 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(168): Show | 174 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.286+5532C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231446 | ||||||
| chr21:42231481
|
C | T | 3 | a0001c0001t0010g0301a0001c0001t0010g0302a0001c0001t0010g0303 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.286+5567C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231481 | ||||||
| chr21:42231486
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+5572T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231486 | ||||||
| chr21:42231546
|
C | T | 5 | a0001c0001t0001g0083a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 5 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+5632C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231546 | ||||||
| chr21:42231566
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0009g0085 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.286+5652G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231566 | ||||||
| chr21:42231567
|
A | G | 1 | a0001c0001t0011g0057 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.286+5653A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231567 | ||||||
| chr21:42231595
|
T | C | 192 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.286+5681T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231595 | ||||||
| chr21:42231626
|
A | G | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+5712A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231626 | ||||||
| chr21:42231736
|
T | G | 4 | a0001c0001t0002g0291a0001c0001t0002g0293a0001c0001t0002g0305others(1): Show | 4 | HG00140.hp1 HG01123.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+5822T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231736 | ||||||
| chr21:42231847
|
C | T | 169 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.286+5933C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231847 | ||||||
| chr21:42231861
|
C | A | 1 | a0001c0001t0010g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.286+5947C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231861 | ||||||
| chr21:42231863
|
T | C | 1 | a0001c0002t0004g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.286+5949T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231863 | ||||||
| chr21:42231991
|
G | C | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+6077G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231991 | ||||||
| chr21:42232204
|
T | A | 191 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.286+6290T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232204 | ||||||
| chr21:42232300
|
C | T | 121 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(118): Show | 122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.286+6386C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232300 | ||||||
| chr21:42232397
|
G | T | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+6483G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232397 | ||||||
| chr21:42232420
|
G | A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+6506G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232420 | ||||||
| chr21:42232672
|
C | G | 126 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.286+6758C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232672 | ||||||
| chr21:42232943
|
C | T | 166 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(163): Show | 168 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.286+7029C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232943 | ||||||
| chr21:42233090
|
C | G | 166 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(163): Show | 168 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.286+7176C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233090 | ||||||
| chr21:42233340
|
G | A | 3 | a0001c0001t0003g0346a0001c0001t0008g0345a0001c0001t0027g0344 | 3 | HG01993.hp2 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.286+7426G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233340 | ||||||
| chr21:42233347
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.286+7433G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233347 | ||||||
| chr21:42233565
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.286+7651C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233565 | ||||||
| chr21:42233951
|
G | T | 20 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0097others(17): Show | 22 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.286+8037G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233951 | ||||||
| chr21:42233996
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286+8082C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233996 | ||||||
| chr21:42234023
|
G | GT | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0243others(11): Show | 14 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+8118dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42234023 | |||||
| chr21:42234023
|
GT | G | 173 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(170): Show | 178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.286+8118delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42234023 | |||||
| chr21:42234585
|
C | A | 4 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+8671C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234585 | ||||||
| chr21:42234796
|
G | A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+8882G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234796 | ||||||
| chr21:42234807
|
C | T | 1 | a0001c0001t0004g0339 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.286+8893C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234807 | ||||||
| chr21:42234970
|
C | A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+9056C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234970 | ||||||
| chr21:42235109
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.286+9195C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235109 | ||||||
| chr21:42235157
|
G | A | 128 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(125): Show | 131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.286+9243G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235157 | ||||||
| chr21:42235158
|
G | C | 4 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0337others(1): Show | 4 | HG02055.hp1 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+9244G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235158 | ||||||
| chr21:42235309
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0002g0164 | 2 | NA18971.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.286+9395G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235309 | ||||||
| chr21:42235340
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.286+9426G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235340 | ||||||
| chr21:42235522
|
T | C | 2 | a0001c0001t0002g0340a0001c0001t0002g0341 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.286+9608T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235522 | ||||||
| chr21:42235531
|
C | T | 8 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0313others(5): Show | 8 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+9617C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235531 | ||||||
| chr21:42235540
|
G | A | 2 | a0001c0001t0022g0022a0001c0001t0023g0023 | 2 | HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.286+9626G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235540 | ||||||
| chr21:42235949
|
G | T | 4 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+10035G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235949 | ||||||
| chr21:42236020
|
T | C | 2 | a0001c0002t0002g0078a0001c0002t0016g0343 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.286+10106T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236020 | ||||||
| chr21:42236112
|
G | A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+10198G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236112 | ||||||
| chr21:42236181
|
C | T | 5 | a0001c0001t0001g0260a0001c0001t0002g0148a0001c0001t0002g0150others(2): Show | 5 | HG00423.hp1 HG00621.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+10267C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236181 | ||||||
| chr21:42236241
|
G | A | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0328others(11): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+10327G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236241 | ||||||
| chr21:42236375
|
G | T | 8 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0313others(5): Show | 8 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+10461G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236375 | ||||||
| chr21:42236484
|
A | T | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0254others(16): Show | 20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+10570A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236484 | ||||||
| chr21:42236544
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0002g0120a0001c0001t0003g0123 | 3 | HG02738.hp2 HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.286+10630G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236544 | ||||||
| chr21:42236621
|
T | C | 3 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.286+10707T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236621 | ||||||
| chr21:42236724
|
G | A | 2 | a0001c0001t0005g0060a0001c0001t0006g0059 | 2 | HG02523.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.286+10810G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236724 | ||||||
| chr21:42236826
|
G | A | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+10912G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236826 | ||||||
| chr21:42236971
|
G | A | 2 | a0001c0001t0001g0317a0001c0001t0001g0336 | 2 | HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.286+11057G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236971 | ||||||
| chr21:42237048
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286+11134C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237048 | ||||||
| chr21:42237138
|
G | A | 126 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.286+11224G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237138 | ||||||
| chr21:42237160
|
T | G | 1 | a0001c0001t0003g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.286+11246T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237160 | ||||||
| chr21:42237285
|
T | G | 2 | a0001c0001t0003g0105a0001c0001t0003g0106 | 2 | NA18939.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.286+11371T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237285 | ||||||
| chr21:42237310
|
A | G | 1 | a0001c0001t0026g0318 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+11396A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237310 | ||||||
| chr21:42237604
|
C | G | 5 | a0001c0001t0005g0051a0001c0001t0006g0053a0001c0001t0007g0055others(2): Show | 5 | NA18952.hp2 NA18980.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+11690C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237604 | ||||||
| chr21:42237679
|
C | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0342a0001c0001t0002g0237others(3): Show | 6 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+11765C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237679 | ||||||
| chr21:42237705
|
A | G | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0002t0002g0078others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+11791A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237705 | ||||||
| chr21:42237886
|
C | T | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0254others(16): Show | 20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+11972C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237886 | ||||||
| chr21:42238005
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.286+12091G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238005 | ||||||
| chr21:42238096
|
G | A | 153 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(150): Show | 157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.286+12182G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238096 | ||||||
| chr21:42238116
|
G | C | 190 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(187): Show | 195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12202G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238116 | ||||||
| chr21:42238214
|
T | G | 1 | a0001c0001t0014g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.286+12300T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238214 | ||||||
| chr21:42238334
|
T | C | 190 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(187): Show | 195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12420T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238334 | ||||||
| chr21:42238380
|
G | T | 1 | a0001c0001t0021g0008 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.286+12466G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238380 | ||||||
| chr21:42238391
|
A | G | 5 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+12477A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238391 | ||||||
| chr21:42238398
|
C | T | 190 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(187): Show | 195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12484C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238398 | ||||||
| chr21:42238693
|
C | T | 5 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0337others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+12779C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238693 | ||||||
| chr21:42238748
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.286+12834C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238748 | ||||||
| chr21:42238760
|
T | C | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.286+12846T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238760 | ||||||
| chr21:42238869
|
A | G | 190 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(187): Show | 195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12955A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238869 | ||||||
| chr21:42238899
|
T | C | 1 | a0001c0001t0002g0107 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286+12985T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238899 | ||||||
| chr21:42238979
|
G | A | 20 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0097others(17): Show | 21 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+13065G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238979 | ||||||
| chr21:42239194
|
C | T | 4 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0003g0135others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13280C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239194 | ||||||
| chr21:42239487
|
G | A | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13573G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239487 | ||||||
| chr21:42239518
|
G | T | 2 | a0001c0001t0001g0235a0001c0001t0002g0236 | 2 | HG00323.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.286+13604G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239518 | ||||||
| chr21:42239530
|
G | A | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286+13616G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239530 | ||||||
| chr21:42239720
|
T | C | 154 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(151): Show | 158 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.286+13806T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239720 | ||||||
| chr21:42239866
|
C | T | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+13952C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239866 | ||||||
| chr21:42239870
|
G | A | 5 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0337others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+13956G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239870 | ||||||
| chr21:42239900
|
G | A | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.286+13986G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239900 | ||||||
| chr21:42240027
|
G | A | 22 | a0001c0001t0001g0278a0001c0001t0001g0327a0001c0001t0002g0273others(19): Show | 23 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+14113G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240027 | ||||||
| chr21:42240169
|
C | T | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0254others(16): Show | 20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+14255C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240169 | ||||||
| chr21:42240183
|
C | T | 5 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+14269C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240183 | ||||||
| chr21:42240203
|
C | T | 13 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(10): Show | 13 | HG00639.hp2 HG01069.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.286+14289C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240203 | ||||||
| chr21:42240216
|
C | G | 1 | a0001c0001t0003g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+14302C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240216 | ||||||
| chr21:42240481
|
C | T | 139 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.286+14567C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240481 | ||||||
| chr21:42240482
|
G | T | 9 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0313others(6): Show | 9 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+14568G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240482 | ||||||
| chr21:42240578
|
G | A | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0254others(16): Show | 20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+14664G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240578 | ||||||
| chr21:42240607
|
C | T | 4 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0004g0337others(1): Show | 4 | HG02055.hp1 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+14693C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240607 | ||||||
| chr21:42240630
|
T | C | 1 | a0001c0001t0031g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286+14716T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240630 | ||||||
| chr21:42240662
|
G | A | 2 | a0001c0001t0004g0158a0001c0002t0002g0143 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.286+14748G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240662 | ||||||
| chr21:42240694
|
C | T | 3 | a0001c0001t0002g0233a0001c0001t0003g0232a0001c0001t0006g0028 | 3 | HG00558.hp2 NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.286+14780C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240694 | ||||||
| chr21:42240777
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.286+14863G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240777 | ||||||
| chr21:42240936
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0002g0230 | 2 | HG00544.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.286+15022C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240936 | ||||||
| chr21:42241179
|
G | A | 1 | a0001c0001t0006g0016 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.286+15265G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241179 | ||||||
| chr21:42241271
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+15357G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241271 | ||||||
| chr21:42241367
|
G | A | 5 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+15453G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241367 | ||||||
| chr21:42241376
|
G | A | 139 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(136): Show | 143 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.286+15462G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241376 | ||||||
| chr21:42241510
|
C | A | 5 | a0001c0001t0002g0308a0001c0001t0012g0140a0001c0001t0012g0141others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+15596C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241510 | ||||||
| chr21:42241604
|
CA | C | 127 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.286+15702delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241604 | |||||
| chr21:42241617
|
T | A | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286+15703T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241617 | ||||||
| chr21:42241620
|
CA | C | 178 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(175): Show | 183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.286+15716delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241620 | |||||
| chr21:42241705
|
T | G | 1 | a0001c0003t0019g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.286+15791T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241705 | ||||||
| chr21:42241810
|
C | A | 113 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(110): Show | 116 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.286+15896C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241810 | ||||||
| chr21:42241820
|
TA | T | 153 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(150): Show | 156 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.286+15920delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241820 | |||||
| chr21:42241862
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.286+15948C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241862 | ||||||
| chr21:42241977
|
C | CA | 24 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0108others(21): Show | 24 | HG01070.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+16082dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | |||||
| chr21:42241977
|
C | CAA | 10 | a0001c0001t0001g0155a0001c0001t0002g0120a0001c0001t0002g0137others(7): Show | 10 | HG01069.hp2 HG01167.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+16081_286+1608 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | |||||
| chr21:42241977
|
C | CAAA | 86 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.286+16080_286+1608 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | |||||
| chr21:42241977
|
C | CAAAA | 27 | a0001c0001t0001g0122a0001c0001t0001g0278a0001c0001t0001g0284others(24): Show | 28 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.286+16079_286+1608 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | |||||
| chr21:42241977
|
C | CAAAAA | 7 | a0001c0001t0004g0329a0001c0001t0007g0031a0001c0002t0002g0330others(4): Show | 7 | HG01081.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+16078_286+1608 others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | |||||
| chr21:42241977
|
CA | C | 6 | a0001c0001t0001g0271a0001c0001t0002g0229a0001c0001t0002g0308others(3): Show | 7 | HG00099.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+16082delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | |||||
| chr21:42241978
|
A | G | 2 | a0001c0001t0012g0307a0001c0001t0028g0306 | 2 | HG01069.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.286+16064A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241978 | ||||||
| chr21:42241979
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.286+16065A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241979 | ||||||
| chr21:42242035
|
T | C | 3 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.286+16121T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242035 | ||||||
| chr21:42242213
|
T | A | 3 | a0001c0001t0001g0155a0001c0001t0003g0153a0001c0001t0004g0154 | 3 | HG02257.hp1 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.286+16299T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242213 | ||||||
| chr21:42242231
|
C | T | 86 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0124others(83): Show | 89 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.286+16317C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242231 | ||||||
| chr21:42242380
|
A | T | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+16466A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242380 | ||||||
| chr21:42242466
|
A | G | 1 | a0001c0001t0003g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.286+16552A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242466 | ||||||
| chr21:42242484
|
C | T | 2 | a0001c0001t0003g0227a0001c0001t0003g0228 | 2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.286+16570C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242484 | ||||||
| chr21:42242516
|
C | A | 149 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(146): Show | 152 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.286+16602C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242516 | ||||||
| chr21:42242686
|
C | T | 141 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.286+16772C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242686 | ||||||
| chr21:42242721
|
G | A | 5 | a0001c0001t0004g0182a0001c0001t0004g0268a0001c0001t0004g0313others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+16807G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242721 | ||||||
| chr21:42242970
|
C | A | 5 | a0001c0001t0002g0183a0001c0001t0002g0286a0001c0001t0002g0288others(2): Show | 5 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17056C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242970 | ||||||
| chr21:42242971
|
C | A | 5 | a0001c0001t0002g0183a0001c0001t0002g0286a0001c0001t0002g0288others(2): Show | 5 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17057C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242971 | ||||||
| chr21:42242972
|
A | C | 5 | a0001c0001t0002g0183a0001c0001t0002g0286a0001c0001t0002g0288others(2): Show | 5 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17058A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242972 | ||||||
| chr21:42243027
|
C | A | 5 | a0001c0001t0004g0169a0001c0001t0004g0182a0001c0001t0004g0313others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17113C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243027 | ||||||
| chr21:42243066
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286+17152C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243066 | ||||||
| chr21:42243135
|
C | G | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.286+17221C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243135 | ||||||
| chr21:42243167
|
T | G | 1 | a0001c0002t0002g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286+17253T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243167 | ||||||
| chr21:42243208
|
G | A | 23 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0097others(20): Show | 25 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.286+17294G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243208 | ||||||
| chr21:42243249
|
C | A | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+17335C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243249 | ||||||
| chr21:42243365
|
A | G | 1 | a0001c0007t0015g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.286+17451A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243365 | ||||||
| chr21:42243435
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286+17521C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243435 | ||||||
| chr21:42243435
|
CGT | C | 5 | a0001c0001t0001g0159a0001c0001t0001g0316a0001c0001t0002g0236others(2): Show | 5 | HG00323.hp1 HG01106.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+17529_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243435 | |||||
| chr21:42243441
|
TGTGC | T | 91 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0133others(88): Show | 94 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.286+17529_286+1753 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243441 | |||||
| chr21:42243443
|
T | C | 10 | a0001c0001t0001g0142a0001c0001t0001g0327a0001c0001t0002g0180others(7): Show | 10 | HG01167.hp1 HG01257.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+17529T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243443 | ||||||
| chr21:42243443
|
TGC | T | 63 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0155others(60): Show | 65 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.286+17533_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243443 | |||||
| chr21:42243445
|
C | CGT | 8 | a0001c0001t0001g0248a0001c0001t0001g0335a0001c0001t0002g0222others(5): Show | 8 | HG02055.hp2 HG02056.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+17532_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | |||||
| chr21:42243445
|
C | T | 11 | a0001c0001t0001g0142a0001c0001t0001g0327a0001c0001t0002g0180others(8): Show | 11 | HG01167.hp1 HG01257.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+17531C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243445 | ||||||
| chr21:42243445
|
CGCGT | C | 42 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0145others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.286+17533_286+1753 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | |||||
| chr21:42243445
|
CGCGTGT | C | 9 | a0001c0001t0001g0165a0001c0001t0002g0162a0001c0001t0002g0164others(6): Show | 10 | HG00408.hp2 HG00558.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+17533_286+1753 others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | |||||
| chr21:42243445
|
CGCGTGTG others(1): Show |
C | 20 | a0001c0001t0001g0089a0001c0001t0001g0263a0001c0001t0001g0328others(17): Show | 20 | HG00609.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+17533_286+1754 others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | |||||
| chr21:42243445
|
CGCGTGTG others(3): Show |
C | 2 | a0001c0001t0030g0312a0001c0003t0006g0044 | 2 | HG02132.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.286+17533_286+1754 others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | |||||
| chr21:42243447
|
C | CGT | 8 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0157others(5): Show | 8 | HG02040.hp2 HG02080.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+17575_286+1757 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | |||||
| chr21:42243447
|
C | CGTGT | 3 | a0001c0001t0002g0114a0001c0001t0002g0203a0001c0001t0002g0309 | 3 | HG02129.hp1 NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.286+17573_286+1757 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | |||||
| chr21:42243447
|
C | T | 36 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0159others(33): Show | 36 | HG00323.hp1 HG01106.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.286+17533C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243447 | ||||||
| chr21:42243447
|
CGT | C | 21 | a0001c0001t0001g0124a0001c0001t0001g0172a0001c0001t0001g0186others(18): Show | 21 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+17575_286+1757 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | |||||
| chr21:42243447
|
CGTGT | C | 16 | a0001c0001t0001g0238a0001c0001t0001g0290a0001c0001t0001g0342others(13): Show | 16 | HG00280.hp1 HG00280.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+17573_286+1757 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | |||||
| chr21:42243447
|
CGTGTGT | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0002g0237 | 3 | HG00423.hp2 HG00741.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.286+17571_286+1757 others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | |||||
| chr21:42243451
|
T | C | 4 | a0001c0001t0004g0169a0001c0001t0004g0313a0001c0001t0009g0322others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+17537T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243451 | ||||||
| chr21:42243451
|
T | TGC | 3 | a0001c0001t0001g0076a0001c0001t0001g0336a0001c0001t0012g0315 | 3 | HG02622.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.286+17538_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243451 | |||||
| chr21:42243453
|
T | C | 2 | a0001c0001t0004g0182a0001c0001t0009g0275 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.286+17539T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243453 | ||||||
| chr21:42243455
|
T | C | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0155others(16): Show | 21 | HG00738.hp2 HG01109.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+17541T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243455 | ||||||
| chr21:42243457
|
T | C | 6 | a0001c0001t0002g0251a0001c0001t0002g0286a0001c0001t0002g0288others(3): Show | 6 | HG00639.hp2 HG01099.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+17543T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243457 | ||||||
| chr21:42243485
|
TGTGTGC | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0260a0001c0001t0002g0173others(2): Show | 5 | NA18964.hp2 NA18968.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17573_286+1757 others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243485 | |||||
| chr21:42243487
|
T | C | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.286+17573T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243487 | ||||||
| chr21:42243487
|
TGTGC | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0297a0001c0001t0002g0277others(3): Show | 6 | HG01243.hp2 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+17575_286+1757 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243487 | |||||
| chr21:42243489
|
T | C | 15 | a0001c0001t0001g0186a0001c0001t0003g0256a0001c0001t0004g0169others(12): Show | 15 | HG01346.hp2 HG02040.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+17575T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243489 | ||||||
| chr21:42243489
|
TGC | T | 30 | a0001c0001t0001g0133a0001c0001t0001g0177a0001c0001t0001g0235others(27): Show | 31 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.286+17578_286+1757 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243489 | |||||
| chr21:42243491
|
C | T | 66 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0142others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.286+17577C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243491 | ||||||
| chr21:42243709
|
G | A | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.286+17795G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243709 | ||||||
| chr21:42243717
|
G | T | 28 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 29 | HG00099.hp2 HG00609.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.286+17803G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243717 | ||||||
| chr21:42243751
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.286+17837A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243751 | ||||||
| chr21:42243814
|
C | CT | 96 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0155others(93): Show | 97 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.286+17922dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243814 | |||||
| chr21:42243814
|
C | CTT | 18 | a0001c0001t0001g0091a0001c0001t0001g0142a0001c0001t0001g0215others(15): Show | 18 | HG00642.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.286+17921_286+1792 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243814 | |||||
| chr21:42243814
|
CT | C | 41 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0145others(38): Show | 43 | HG00609.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.286+17922delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243814 | |||||
| chr21:42243850
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.286+17936A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243850 | ||||||
| chr21:42243858
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+17944G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243858 | ||||||
| chr21:42243966
|
C | T | 2 | a0001c0001t0002g0308a0001c0001t0028g0306 | 2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+18052C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243966 | ||||||
| chr21:42243974
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.286+18060A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243974 | ||||||
| chr21:42243975
|
C | A | 6 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+18061C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243975 | ||||||
| chr21:42244066
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0243 | 2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.286+18152A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244066 | ||||||
| chr21:42244067
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0243 | 2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.286+18153T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244067 | ||||||
| chr21:42244146
|
A | C | 1 | a0001c0001t0012g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.286+18232A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244146 | ||||||
| chr21:42244536
|
C | T | 2 | a0001c0001t0002g0308a0001c0001t0028g0306 | 2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+18622C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244536 | ||||||
| chr21:42244537
|
T | A | 23 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0097others(20): Show | 25 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.286+18623T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244537 | ||||||
| chr21:42244542
|
T | C | 4 | a0001c0001t0004g0329a0001c0002t0002g0330a0001c0002t0002g0331others(1): Show | 4 | HG01081.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+18628T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244542 | ||||||
| chr21:42244668
|
A | G | 6 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+18754A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244668 | ||||||
| chr21:42244681
|
C | G | 41 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0142others(38): Show | 42 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.286+18767C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244681 | ||||||
| chr21:42244681
|
C | T | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0155others(16): Show | 20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+18767C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244681 | ||||||
| chr21:42244756
|
C | A | 1 | a0001c0001t0028g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+18842C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244756 | ||||||
| chr21:42244803
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.286+18889G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244803 | ||||||
| chr21:42244883
|
C | T | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+18969C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244883 | ||||||
| chr21:42244888
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.286+18974T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244888 | ||||||
| chr21:42244914
|
G | A | 20 | a0001c0001t0001g0278a0001c0001t0001g0284a0001c0001t0001g0316others(17): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+19000G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244914 | ||||||
| chr21:42245078
|
G | A | 9 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(6): Show | 9 | HG02056.hp1 NA18948.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+19164G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245078 | ||||||
| chr21:42245092
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.286+19178G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245092 | ||||||
| chr21:42245130
|
G | A | 8 | a0001c0001t0002g0180a0001c0001t0005g0040a0001c0001t0011g0039others(5): Show | 8 | HG01257.hp2 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+19216G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245130 | ||||||
| chr21:42245179
|
T | G | 1 | a0001c0001t0006g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+19265T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245179 | ||||||
| chr21:42245194
|
GA | G | 9 | a0001c0001t0001g0278a0001c0001t0001g0316a0001c0001t0002g0273others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+19282delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42245194 | |||||
| chr21:42245231
|
T | G | 1 | a0001c0001t0006g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.286+19317T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245231 | ||||||
| chr21:42245390
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.286+19476G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245390 | ||||||
| chr21:42245391
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286+19477C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245391 | ||||||
| chr21:42245523
|
G | A | 1 | a0001c0001t0006g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+19609G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245523 | ||||||
| chr21:42245668
|
G | A | 1 | a0001c0002t0004g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19754G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245668 | ||||||
| chr21:42245693
|
A | C | 1 | a0001c0001t0026g0318 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+19779A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245693 | ||||||
| chr21:42245757
|
A | G | 1 | a0001c0001t0003g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.286+19843A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245757 | ||||||
| chr21:42245773
|
A | T | 2 | a0001c0001t0002g0308a0001c0001t0028g0306 | 2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+19859A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245773 | ||||||
| chr21:42245807
|
T | C | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+19893T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245807 | ||||||
| chr21:42245818
|
T | TGGGGCAC others(29): Show |
140 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(137): Show | 144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.286+19937_286+1997 others(40): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42245818 | |||||
| chr21:42245818
|
T | TGGGGCAC others(65): Show |
3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0007g0007 | 3 | HG01891.hp1 HG03540.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.286+19972_286+1997 others(76): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42245818 | |||||
| chr21:42245955
|
T | C | 140 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(137): Show | 144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.286+20041T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245955 | ||||||
| chr21:42245960
|
G | A | 107 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(104): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.286+20046G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245960 | ||||||
| chr21:42246064
|
G | T | 2 | a0001c0002t0002g0078a0001c0002t0016g0343 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.286+20150G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246064 | ||||||
| chr21:42246498
|
G | A | 2 | a0001c0001t0004g0086a0001c0001t0004g0092 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.286+20584G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246498 | ||||||
| chr21:42246529
|
T | G | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+20615T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246529 | ||||||
| chr21:42246578
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.286+20664A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246578 | ||||||
| chr21:42246591
|
G | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 19 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+20677G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246591 | ||||||
| chr21:42246753
|
G | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0002g0073others(1): Show | 4 | HG00438.hp2 NA18943.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+20839G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246753 | ||||||
| chr21:42246972
|
G | A | 105 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0122others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.286+21058G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246972 | ||||||
| chr21:42247024
|
AC | A | 6 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+21111delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247024 | ||||||
| chr21:42247247
|
G | A | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.286+21333G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247247 | ||||||
| chr21:42247268
|
G | T | 2 | a0001c0001t0002g0308a0001c0001t0028g0306 | 2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+21354G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247268 | ||||||
| chr21:42247638
|
C | T | 1 | a0001c0006t0004g0321 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.286+21724C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247638 | ||||||
| chr21:42247693
|
G | T | 1 | a0001c0003t0003g0259 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.286+21779G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247693 | ||||||
| chr21:42247746
|
G | A | 19 | a0001c0001t0001g0089a0001c0001t0001g0155a0001c0001t0001g0278others(16): Show | 20 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+21832G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247746 | ||||||
| chr21:42247755
|
C | A | 14 | a0001c0001t0001g0089a0001c0001t0001g0278a0001c0001t0001g0328others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+21841C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247755 | ||||||
| chr21:42247789
|
G | A | 1 | a0001c0001t0012g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.286+21875G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247789 | ||||||
| chr21:42247851
|
G | A | 6 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+21937G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247851 | ||||||
| chr21:42247880
|
C | T | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286+21966C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247880 | ||||||
| chr21:42247881
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.286+21967G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247881 | ||||||
| chr21:42247908
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0015g0285 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.286+21994G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247908 | ||||||
| chr21:42247944
|
G | A | 5 | a0001c0001t0004g0169a0001c0001t0004g0182a0001c0001t0004g0313others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+22030G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247944 | ||||||
| chr21:42247953
|
C | T | 2 | a0001c0001t0002g0340a0001c0001t0002g0341 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.286+22039C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247953 | ||||||
| chr21:42248063
|
G | A | 1 | a0001c0001t0011g0057 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.286+22149G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248063 | ||||||
| chr21:42248087
|
C | T | 1 | a0001c0001t0028g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+22173C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248087 | ||||||
| chr21:42248104
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.286+22190G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248104 | ||||||
| chr21:42248163
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0015g0285 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.286+22249A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248163 | ||||||
| chr21:42248200
|
C | T | 47 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0142others(44): Show | 49 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.286+22286C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248200 | ||||||
| chr21:42248252
|
T | C | 1 | a0001c0001t0028g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+22338T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248252 | ||||||
| chr21:42248412
|
G | A | 49 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0142others(46): Show | 51 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.286+22498G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248412 | ||||||
| chr21:42248468
|
G | T | 1 | a0001c0001t0021g0008 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.286+22554G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248468 | ||||||
| chr21:42248616
|
G | A | 2 | a0001c0002t0002g0078a0001c0002t0016g0343 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.287-22454G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248616 | ||||||
| chr21:42248747
|
T | TA | 30 | a0001c0001t0001g0091a0001c0001t0001g0142a0001c0001t0001g0155others(27): Show | 32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-22312dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248747 | |||||
| chr21:42248806
|
C | G | 10 | a0001c0001t0001g0254a0001c0001t0002g0090a0001c0001t0002g0251others(7): Show | 10 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-22264C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248806 | ||||||
| chr21:42248814
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-22256G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248814 | ||||||
| chr21:42248902
|
C | CA | 46 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0096others(43): Show | 47 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-22150dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | |||||
| chr21:42248902
|
C | CAA | 84 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0133others(81): Show | 87 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.287-22151_287-2215 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | |||||
| chr21:42248902
|
C | CAAA | 10 | a0001c0001t0002g0230a0001c0001t0002g0286a0001c0001t0002g0288others(7): Show | 10 | HG00544.hp1 HG00639.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-22152_287-2215 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | |||||
| chr21:42248902
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-22159_287-2215 others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | |||||
| chr21:42249006
|
A | G | 1 | a0001c0001t0031g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-22064A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249006 | ||||||
| chr21:42249118
|
G | C | 23 | a0001c0001t0001g0284a0001c0001t0001g0316a0001c0001t0001g0327others(20): Show | 24 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.287-21952G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249118 | ||||||
| chr21:42249259
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.287-21811C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249259 | ||||||
| chr21:42249323
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.287-21747A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249323 | ||||||
| chr21:42249339
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-21731A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249339 | ||||||
| chr21:42249410
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-21660C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249410 | ||||||
| chr21:42249500
|
T | G | 16 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0254others(13): Show | 16 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.287-21570T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249500 | ||||||
| chr21:42249576
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0297a0001c0001t0003g0300 | 3 | HG04199.hp2 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.287-21494G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249576 | ||||||
| chr21:42249732
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-21338G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249732 | ||||||
| chr21:42249762
|
T | C | 23 | a0001c0001t0001g0284a0001c0001t0001g0316a0001c0001t0001g0327others(20): Show | 24 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.287-21308T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249762 | ||||||
| chr21:42249928
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.287-21142C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249928 | ||||||
| chr21:42249937
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0024g0101 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.287-21133G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249937 | ||||||
| chr21:42250088
|
T | G | 2 | a0001c0001t0001g0334a0001c0001t0009g0333 | 2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.287-20982T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250088 | ||||||
| chr21:42250212
|
C | T | 6 | a0001c0001t0001g0165a0001c0001t0002g0162a0001c0001t0002g0164others(3): Show | 6 | HG00408.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-20858C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250212 | ||||||
| chr21:42250215
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.287-20855G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250215 | ||||||
| chr21:42250265
|
G | A | 8 | a0001c0001t0004g0169a0001c0001t0004g0182a0001c0001t0004g0313others(5): Show | 8 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-20805G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250265 | ||||||
| chr21:42250547
|
C | G | 107 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0091others(104): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.287-20523C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250547 | ||||||
| chr21:42250735
|
T | C | 5 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(2): Show | 5 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-20335T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250735 | ||||||
| chr21:42250796
|
C | T | 4 | a0001c0001t0002g0286a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-20274C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250796 | ||||||
| chr21:42250886
|
G | A | 1 | a0001c0001t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-20184G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250886 | ||||||
| chr21:42251010
|
G | C | 5 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0304others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-20060G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251010 | ||||||
| chr21:42251050
|
A | AG | 309 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(306): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.287-20020_287-2001 others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251050 | ||||||
| chr21:42251061
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-20009A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251061 | ||||||
| chr21:42251084
|
C | T | 1 | a0001c0001t0031g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-19986C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251084 | ||||||
| chr21:42251110
|
C | T | 3 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG01099.hp2 HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.287-19960C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251110 | ||||||
| chr21:42251290
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.287-19780C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251290 | ||||||
| chr21:42251291
|
G | A | 1 | a0001c0007t0016g0347 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.287-19779G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251291 | ||||||
| chr21:42251338
|
G | A | 2 | a0001c0001t0003g0310a0001c0001t0004g0311 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.287-19732G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251338 | ||||||
| chr21:42251523
|
C | G | 166 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0096others(163): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.287-19547C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251523 | ||||||
| chr21:42251543
|
T | TGAG | 168 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0096others(165): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.287-19525_287-1952 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42251543 | |||||
| chr21:42251660
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.287-19410G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251660 | ||||||
| chr21:42251701
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.287-19369C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251701 | ||||||
| chr21:42251907
|
G | C | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.287-19163G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251907 | ||||||
| chr21:42251998
|
C | A | 1 | a0001c0001t0001g0111 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.287-19072C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251998 | ||||||
| chr21:42252103
|
C | T | 2 | a0001c0001t0003g0105a0001c0001t0003g0106 | 2 | NA18939.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.287-18967C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252103 | ||||||
| chr21:42252104
|
G | A | 10 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0178others(7): Show | 11 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-18966G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252104 | ||||||
| chr21:42252422
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-18648G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252422 | ||||||
| chr21:42252424
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-18646C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252424 | ||||||
| chr21:42252425
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.287-18645G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252425 | ||||||
| chr21:42252527
|
T | A | 34 | a0001c0001t0001g0122a0001c0001t0002g0162a0001c0001t0002g0189others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.287-18543T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252527 | ||||||
| chr21:42252528
|
C | A | 34 | a0001c0001t0001g0122a0001c0001t0002g0162a0001c0001t0002g0189others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.287-18542C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252528 | ||||||
| chr21:42252551
|
C | A | 1 | a0001c0001t0006g0028 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.287-18519C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252551 | ||||||
| chr21:42252703
|
C | T | 5 | a0001c0001t0001g0254a0001c0001t0004g0182a0001c0001t0004g0268others(2): Show | 5 | HG00738.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-18367C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252703 | ||||||
| chr21:42252783
|
C | T | 3 | a0001c0001t0002g0173a0001c0001t0002g0233a0001c0001t0003g0232 | 3 | HG00558.hp2 NA18942.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.287-18287C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252783 | ||||||
| chr21:42252839
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-18231G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252839 | ||||||
| chr21:42252859
|
C | G | 1 | a0001c0001t0005g0024 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.287-18211C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252859 | ||||||
| chr21:42253003
|
G | C | 10 | a0001c0001t0001g0260a0001c0001t0002g0110a0001c0001t0002g0146others(7): Show | 10 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-18067G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253003 | ||||||
| chr21:42253021
|
C | T | 3 | a0001c0001t0001g0317a0001c0001t0001g0336a0001c0002t0002g0270 | 3 | HG02622.hp1 HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.287-18049C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253021 | ||||||
| chr21:42253026
|
C | T | 4 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0002g0220others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-18044C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253026 | ||||||
| chr21:42253038
|
G | A | 2 | a0001c0001t0004g0086a0001c0001t0004g0092 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-18032G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253038 | ||||||
| chr21:42253073
|
C | T | 11 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0002g0220others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-17997C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253073 | ||||||
| chr21:42253265
|
A | G | 11 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0002g0220others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-17805A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253265 | ||||||
| chr21:42253367
|
G | C | 33 | a0001c0001t0001g0122a0001c0001t0002g0162a0001c0001t0002g0189others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.287-17703G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253367 | ||||||
| chr21:42253557
|
C | T | 4 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0006t0001g0006others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-17513C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253557 | ||||||
| chr21:42253568
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.287-17502C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253568 | ||||||
| chr21:42253801
|
G | GGAGGTCG others(1): Show |
6 | a0001c0001t0001g0165a0001c0001t0002g0164a0001c0001t0002g0230others(3): Show | 6 | HG00408.hp2 HG00544.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-17267_287-1726 others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42253801 | |||||
| chr21:42253931
|
C | G | 1 | a0001c0001t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-17139C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253931 | ||||||
| chr21:42254012
|
G | C | 226 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.287-17058G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254012 | ||||||
| chr21:42254111
|
A | G | 79 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.287-16959A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254111 | ||||||
| chr21:42254118
|
A | G | 79 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.287-16952A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254118 | ||||||
| chr21:42254145
|
C | G | 1 | a0001c0002t0002g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.287-16925C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254145 | ||||||
| chr21:42254153
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-16917C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254153 | ||||||
| chr21:42254289
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0004g0269a0001c0001t0029g0262 | 3 | HG02451.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.287-16781C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254289 | ||||||
| chr21:42254481
|
A | T | 2 | a0001c0001t0002g0162a0001c0001t0005g0015 | 2 | NA18969.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.287-16589A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254481 | ||||||
| chr21:42254574
|
T | C | 77 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.287-16496T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254574 | ||||||
| chr21:42254597
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-16473G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254597 | ||||||
| chr21:42254609
|
G | A | 2 | a0001c0001t0009g0085a0001c0001t0030g0312 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.287-16461G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254609 | ||||||
| chr21:42254632
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.287-16438G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254632 | ||||||
| chr21:42254726
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-16344G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254726 | ||||||
| chr21:42254749
|
G | A | 79 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.287-16321G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254749 | ||||||
| chr21:42254760
|
G | C | 1 | a0001c0001t0012g0307 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.287-16310G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254760 | ||||||
| chr21:42254847
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.287-16223C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254847 | ||||||
| chr21:42254872
|
G | A | 45 | a0001c0001t0001g0122a0001c0001t0001g0263a0001c0001t0002g0162others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.287-16198G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254872 | ||||||
| chr21:42255113
|
C | T | 4 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0006t0001g0006others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15957C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255113 | ||||||
| chr21:42255184
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0254a0001c0001t0003g0109others(2): Show | 5 | HG00738.hp2 HG02735.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15886C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255184 | ||||||
| chr21:42255238
|
C | T | 48 | a0001c0001t0001g0122a0001c0001t0001g0263a0001c0001t0001g0271others(45): Show | 50 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.287-15832C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255238 | ||||||
| chr21:42255255
|
G | A | 1 | a0001c0001t0003g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.287-15815G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255255 | ||||||
| chr21:42255324
|
G | T | 4 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0006t0001g0006others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15746G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255324 | ||||||
| chr21:42255393
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-15677C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255393 | ||||||
| chr21:42255482
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.287-15588A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255482 | ||||||
| chr21:42255500
|
G | T | 4 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0006t0001g0006others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15570G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255500 | ||||||
| chr21:42255563
|
C | T | 1 | a0001c0003t0005g0048 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.287-15507C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255563 | ||||||
| chr21:42255571
|
T | C | 3 | a0001c0001t0009g0275a0001c0002t0002g0078a0001c0002t0004g0274 | 3 | HG02109.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-15499T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255571 | ||||||
| chr21:42255584
|
A | G | 170 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(167): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.287-15486A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255584 | ||||||
| chr21:42255661
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287-15409T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255661 | ||||||
| chr21:42255724
|
T | C | 3 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG01099.hp2 HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.287-15346T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255724 | ||||||
| chr21:42255741
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.287-15329T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255741 | ||||||
| chr21:42255777
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0159 | 2 | HG02027.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.287-15293G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255777 | ||||||
| chr21:42255830
|
C | T | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-15240C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255830 | ||||||
| chr21:42255918
|
T | G | 1 | a0001c0001t0006g0049 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.287-15152T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255918 | ||||||
| chr21:42256258
|
C | T | 2 | a0001c0006t0001g0006a0001c0006t0004g0321 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-14812C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256258 | ||||||
| chr21:42256277
|
G | A | 32 | a0001c0001t0001g0097a0001c0001t0001g0142a0001c0001t0001g0317others(29): Show | 33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.287-14793G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256277 | ||||||
| chr21:42256436
|
T | C | 1 | a0001c0001t0022g0022 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.287-14634T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256436 | ||||||
| chr21:42256476
|
A | T | 35 | a0001c0001t0001g0122a0001c0001t0002g0162a0001c0001t0002g0189others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-14594A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256476 | ||||||
| chr21:42256724
|
G | A | 1 | a0001c0001t0006g0034 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.287-14346G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256724 | ||||||
| chr21:42257008
|
C | T | 2 | a0001c0007t0015g0348a0001c0007t0016g0347 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-14062C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257008 | ||||||
| chr21:42257164
|
G | A | 1 | a0001c0001t0007g0032 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.287-13906G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257164 | ||||||
| chr21:42257257
|
G | A | 2 | a0001c0001t0009g0085a0001c0001t0030g0312 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.287-13813G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257257 | ||||||
| chr21:42257330
|
G | C | 6 | a0001c0001t0001g0254a0001c0001t0002g0134a0001c0001t0002g0137others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13740G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257330 | ||||||
| chr21:42257355
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0150 | 2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.287-13715C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257355 | ||||||
| chr21:42257370
|
A | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-13700A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257370 | ||||||
| chr21:42257557
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0003g0088a0001c0002t0002g0094 | 3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-13513C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257557 | ||||||
| chr21:42257563
|
G | A | 2 | a0001c0001t0003g0300a0004c0009t0003g0258 | 2 | HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.287-13507G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257563 | ||||||
| chr21:42257661
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287-13409T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257661 | ||||||
| chr21:42257721
|
C | A | 215 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.287-13349C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257721 | ||||||
| chr21:42257813
|
G | T | 1 | a0001c0001t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-13257G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257813 | ||||||
| chr21:42257899
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.287-13171C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257899 | ||||||
| chr21:42257932
|
C | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0102a0001c0001t0004g0103others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13138C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257932 | ||||||
| chr21:42257955
|
TCCATCCC others(189): Show |
T | 3 | a0001c0001t0001g0263a0001c0001t0004g0265a0001c0001t0004g0267 | 3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-13114_287-1291 others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257955 | ||||||
| chr21:42257956
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-13114C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257956 | ||||||
| chr21:42257956
|
CCATCCCT others(189): Show |
C | 172 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.287-13058_287-1286 others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42257956 | |||||
| chr21:42257989
|
C | T | 5 | a0001c0001t0001g0271a0001c0001t0001g0328a0001c0001t0012g0315others(2): Show | 6 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13081C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257989 | ||||||
| chr21:42258214
|
C | T | 2 | a0001c0006t0001g0006a0001c0006t0004g0321 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-12856C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258214 | ||||||
| chr21:42258440
|
A | G | 142 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(139): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.287-12630A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258440 | ||||||
| chr21:42258680
|
A | G | 1 | a0002c0013t0001g0099 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.287-12390A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258680 | ||||||
| chr21:42258698
|
C | T | 67 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-12372C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258698 | ||||||
| chr21:42258753
|
G | A | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287-12317G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258753 | ||||||
| chr21:42258934
|
G | A | 29 | a0001c0001t0001g0097a0001c0001t0001g0142a0001c0001t0001g0317others(26): Show | 29 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.287-12136G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258934 | ||||||
| chr21:42258997
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-12073A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258997 | ||||||
| chr21:42259013
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.287-12057C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259013 | ||||||
| chr21:42259328
|
T | C | 70 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.287-11742T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259328 | ||||||
| chr21:42259403
|
C | T | 68 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(65): Show | 69 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-11667C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259403 | ||||||
| chr21:42259444
|
C | T | 70 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.287-11626C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259444 | ||||||
| chr21:42259523
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.287-11547G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259523 | ||||||
| chr21:42259534
|
G | A | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11536G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259534 | ||||||
| chr21:42259642
|
A | G | 4 | a0001c0001t0001g0328a0001c0001t0012g0315a0001c0001t0015g0285others(1): Show | 5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-11428A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259642 | ||||||
| chr21:42259752
|
G | A | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11318G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259752 | ||||||
| chr21:42259960
|
C | G | 5 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(2): Show | 6 | HG01099.hp2 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-11110C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259960 | ||||||
| chr21:42259996
|
CGGCATCC others(8): Show |
C | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11072_287-1105 others(19): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42259996 | |||||
| chr21:42259997
|
G | A | 6 | a0001c0001t0001g0338a0001c0001t0004g0269a0001c0001t0009g0275others(3): Show | 6 | HG02109.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-11073G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259997 | ||||||
| chr21:42260034
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-11036C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260034 | ||||||
| chr21:42260058
|
A | C | 1 | a0001c0001t0003g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.287-11012A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260058 | ||||||
| chr21:42260222
|
T | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-10848T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260222 | ||||||
| chr21:42260288
|
C | T | 5 | a0001c0001t0001g0328a0001c0001t0001g0338a0001c0001t0012g0315others(2): Show | 6 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-10782C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260288 | ||||||
| chr21:42260305
|
C | A | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-10765C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260305 | ||||||
| chr21:42260310
|
C | G | 10 | a0001c0001t0001g0254a0001c0001t0001g0284a0001c0001t0002g0134others(7): Show | 10 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-10760C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260310 | ||||||
| chr21:42260354
|
C | A | 21 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(18): Show | 21 | HG01167.hp1 HG01884.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-10716C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260354 | ||||||
| chr21:42260569
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.287-10501C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260569 | ||||||
| chr21:42260608
|
A | T | 1 | a0001c0001t0001g0327 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.287-10462A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260608 | ||||||
| chr21:42260700
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-10370A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260700 | ||||||
| chr21:42260829
|
C | CT | 12 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(9): Show | 12 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-10230dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42260829 | |||||
| chr21:42260967
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10103G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260967 | ||||||
| chr21:42260968
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10102C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260968 | ||||||
| chr21:42260969
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10101C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260969 | ||||||
| chr21:42260970
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10100A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260970 | ||||||
| chr21:42261120
|
C | T | 7 | a0001c0001t0001g0328a0001c0001t0001g0338a0001c0001t0004g0086others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-9950C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261120 | ||||||
| chr21:42261195
|
C | A | 1 | a0001c0001t0012g0307 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.287-9875C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261195 | ||||||
| chr21:42261213
|
CT | C | 8 | a0001c0001t0004g0269a0001c0001t0009g0085a0001c0001t0009g0275others(5): Show | 9 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-9856delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261213 | ||||||
| chr21:42261215
|
C | G | 8 | a0001c0001t0004g0269a0001c0001t0009g0085a0001c0001t0009g0275others(5): Show | 9 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-9855C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261215 | ||||||
| chr21:42261287
|
A | C | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-9783A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261287 | ||||||
| chr21:42261373
|
C | T | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.287-9697C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261373 | ||||||
| chr21:42261527
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-9543G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261527 | ||||||
| chr21:42261588
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-9482T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261588 | ||||||
| chr21:42261589
|
C | T | 2 | a0001c0007t0015g0348a0001c0007t0016g0347 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-9481C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261589 | ||||||
| chr21:42261793
|
G | A | 4 | a0001c0001t0009g0085a0001c0001t0009g0322a0001c0001t0009g0323others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-9277G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261793 | ||||||
| chr21:42261840
|
T | C | 2 | a0001c0001t0001g0334a0001c0001t0009g0333 | 2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.287-9230T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261840 | ||||||
| chr21:42261841
|
T | A | 1 | a0001c0001t0003g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.287-9229T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261841 | ||||||
| chr21:42261846
|
A | G | 32 | a0001c0001t0001g0122a0001c0001t0001g0177a0001c0001t0002g0162others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-9224A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261846 | ||||||
| chr21:42261973
|
G | A | 8 | a0001c0001t0001g0328a0001c0001t0001g0338a0001c0001t0009g0275others(5): Show | 9 | HG02109.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.287-9097G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261973 | ||||||
| chr21:42262026
|
C | A | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-9044C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262026 | ||||||
| chr21:42262067
|
G | A | 67 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-9003G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262067 | ||||||
| chr21:42262099
|
G | A | 2 | a0001c0006t0001g0006a0001c0006t0004g0321 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-8971G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262099 | ||||||
| chr21:42262124
|
G | C | 1 | a0001c0001t0006g0050 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.287-8946G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262124 | ||||||
| chr21:42262134
|
C | T | 144 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.287-8936C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262134 | ||||||
| chr21:42262217
|
G | C | 2 | a0001c0001t0003g0149a0001c0001t0007g0007 | 2 | NA18964.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.287-8853G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262217 | ||||||
| chr21:42262255
|
G | A | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-8815G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262255 | ||||||
| chr21:42262260
|
G | C | 67 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0142others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-8810G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262260 | ||||||
| chr21:42262284
|
G | A | 139 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.287-8786G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262284 | ||||||
| chr21:42262291
|
ATTC | A | 4 | a0001c0001t0002g0293a0001c0001t0006g0047a0001c0001t0006g0049others(1): Show | 4 | HG01433.hp1 HG02083.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-8773_287-8771d others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42262291 | |||||
| chr21:42262420
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0004g0265a0001c0001t0004g0267 | 3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-8650C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262420 | ||||||
| chr21:42262429
|
C | T | 32 | a0001c0001t0001g0122a0001c0001t0001g0177a0001c0001t0002g0162others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-8641C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262429 | ||||||
| chr21:42262576
|
G | A | 143 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-8494G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262576 | ||||||
| chr21:42262600
|
A | G | 3 | a0001c0001t0009g0275a0001c0002t0002g0078a0001c0002t0004g0274 | 3 | HG02109.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-8470A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262600 | ||||||
| chr21:42262601
|
A | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-8469A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262601 | ||||||
| chr21:42262691
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0004g0265a0001c0001t0004g0267 | 3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-8379C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262691 | ||||||
| chr21:42262698
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.287-8372A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262698 | ||||||
| chr21:42262757
|
C | A | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-8313C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262757 | ||||||
| chr21:42262810
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-8260T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262810 | ||||||
| chr21:42262828
|
A | G | 158 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(155): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.287-8242A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262828 | ||||||
| chr21:42262849
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.287-8221G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262849 | ||||||
| chr21:42262942
|
C | T | 3 | a0001c0003t0003g0212a0001c0003t0005g0052a0001c0003t0007g0054 | 3 | NA18952.hp1 NA18981.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.287-8128C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262942 | ||||||
| chr21:42262943
|
A | G | 140 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(137): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.287-8127A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262943 | ||||||
| chr21:42263151
|
C | T | 1 | a0001c0001t0004g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287-7919C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263151 | ||||||
| chr21:42263290
|
C | T | 2 | a0001c0001t0004g0269a0001c0001t0014g0061 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-7780C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263290 | ||||||
| chr21:42263312
|
C | T | 1 | a0001c0001t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-7758C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263312 | ||||||
| chr21:42263412
|
C | T | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0012t0004g0276 | 3 | HG01168.hp1 HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.287-7658C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263412 | ||||||
| chr21:42263493
|
C | T | 1 | a0001c0002t0002g0331 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.287-7577C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263493 | ||||||
| chr21:42263533
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.287-7537C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263533 | ||||||
| chr21:42263569
|
T | C | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-7501T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263569 | ||||||
| chr21:42263587
|
C | T | 2 | a0001c0001t0004g0283a0001c0001t0004g0337 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.287-7483C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263587 | ||||||
| chr21:42263631
|
C | T | 6 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0251others(3): Show | 6 | HG01099.hp2 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-7439C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263631 | ||||||
| chr21:42263742
|
T | C | 2 | a0001c0001t0006g0063a0001c0001t0014g0062 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.287-7328T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263742 | ||||||
| chr21:42263759
|
G | A | 21 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(18): Show | 21 | HG01167.hp1 HG01884.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-7311G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263759 | ||||||
| chr21:42263859
|
C | T | 39 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(36): Show | 40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-7211C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263859 | ||||||
| chr21:42263870
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.287-7200C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263870 | ||||||
| chr21:42263871
|
G | A | 3 | a0001c0001t0001g0263a0001c0001t0004g0265a0001c0001t0004g0267 | 3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-7199G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263871 | ||||||
| chr21:42263991
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-7079G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263991 | ||||||
| chr21:42264094
|
G | A | 2 | a0001c0001t0004g0086a0001c0001t0004g0092 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-6976G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264094 | ||||||
| chr21:42264186
|
G | A | 2 | a0001c0006t0001g0006a0001c0006t0004g0321 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-6884G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264186 | ||||||
| chr21:42264189
|
A | G | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-6881A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264189 | ||||||
| chr21:42264211
|
C | T | 39 | a0001c0001t0001g0133a0001c0001t0001g0156a0001c0001t0001g0165others(36): Show | 39 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.287-6859C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264211 | ||||||
| chr21:42264305
|
G | A | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-6765G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264305 | ||||||
| chr21:42264346
|
G | A | 139 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.287-6724G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264346 | ||||||
| chr21:42264438
|
C | T | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-6632C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264438 | ||||||
| chr21:42264439
|
G | A | 144 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.287-6631G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264439 | ||||||
| chr21:42264442
|
A | C | 1 | a0001c0001t0005g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.287-6628A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264442 | ||||||
| chr21:42264469
|
T | A | 1 | a0004c0009t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.287-6601T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264469 | ||||||
| chr21:42264475
|
A | G | 226 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.287-6595A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264475 | ||||||
| chr21:42264489
|
CCATCCAT others(1): Show |
C | 144 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.287-6557_287-6550d others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42264489 | |||||
| chr21:42264557
|
C | T | 1 | a0001c0001t0006g0028 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.287-6513C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264557 | ||||||
| chr21:42264558
|
G | A | 6 | a0001c0001t0001g0254a0001c0001t0002g0134a0001c0001t0002g0137others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-6512G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264558 | ||||||
| chr21:42264582
|
CAGG | C | 39 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(36): Show | 40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-6487_287-6485d others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264582 | ||||||
| chr21:42264586
|
G | C | 39 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(36): Show | 40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-6484G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264586 | ||||||
| chr21:42264681
|
G | A | 144 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.287-6389G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264681 | ||||||
| chr21:42264800
|
C | T | 1 | a0001c0001t0006g0016 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.287-6270C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264800 | ||||||
| chr21:42264931
|
C | T | 2 | a0001c0007t0015g0348a0001c0007t0016g0347 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-6139C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264931 | ||||||
| chr21:42264952
|
C | T | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-6118C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264952 | ||||||
| chr21:42265012
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.287-6058G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265012 | ||||||
| chr21:42265013
|
A | G | 187 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(184): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.287-6057A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265013 | ||||||
| chr21:42265269
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.287-5801C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265269 | ||||||
| chr21:42265494
|
G | A | 14 | a0001c0001t0001g0328a0001c0001t0001g0335a0001c0001t0001g0338others(11): Show | 15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.287-5576G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265494 | ||||||
| chr21:42265527
|
C | T | 16 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0260others(13): Show | 17 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.287-5543C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265527 | ||||||
| chr21:42265554
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-5516C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265554 | ||||||
| chr21:42265642
|
C | T | 25 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-5428C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265642 | ||||||
| chr21:42265643
|
G | A | 141 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(138): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.287-5427G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265643 | ||||||
| chr21:42265644
|
G | A | 184 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.287-5426G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265644 | ||||||
| chr21:42265655
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.287-5415G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265655 | ||||||
| chr21:42265698
|
G | A | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-5372G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265698 | ||||||
| chr21:42265764
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.287-5306G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265764 | ||||||
| chr21:42265798
|
G | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0327a0001c0001t0001g0336others(3): Show | 6 | HG01167.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5272G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265798 | ||||||
| chr21:42265838
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-5232C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265838 | ||||||
| chr21:42265875
|
C | T | 143 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-5195C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265875 | ||||||
| chr21:42265897
|
C | T | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287-5173C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265897 | ||||||
| chr21:42266118
|
A | G | 2 | a0001c0001t0009g0085a0001c0001t0030g0312 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.287-4952A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266118 | ||||||
| chr21:42266171
|
C | T | 4 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-4899C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266171 | ||||||
| chr21:42266172
|
G | A | 4 | a0001c0001t0004g0269a0001c0001t0009g0085a0001c0001t0014g0061others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-4898G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266172 | ||||||
| chr21:42266216
|
G | A | 2 | a0001c0001t0004g0269a0001c0001t0014g0061 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-4854G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266216 | ||||||
| chr21:42266258
|
G | A | 3 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.287-4812G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266258 | ||||||
| chr21:42266261
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-4809A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266261 | ||||||
| chr21:42266309
|
T | TAAATA | 13 | a0001c0001t0001g0083a0001c0001t0001g0097a0001c0001t0001g0112others(10): Show | 13 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-4737_287-4733d others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42266309 | |||||
| chr21:42266309
|
T | TAAATAAA others(3): Show |
18 | a0001c0001t0001g0317a0001c0001t0001g0327a0001c0001t0001g0336others(15): Show | 18 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-4742_287-4733d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42266309 | |||||
| chr21:42266328
|
T | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-4742T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266328 | ||||||
| chr21:42266333
|
T | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-4737T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266333 | ||||||
| chr21:42266373
|
A | G | 1 | a0001c0001t0002g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.287-4697A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266373 | ||||||
| chr21:42266439
|
G | T | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.287-4631G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266439 | ||||||
| chr21:42266572
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-4498C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266572 | ||||||
| chr21:42266601
|
A | G | 1 | a0001c0001t0030g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-4469A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266601 | ||||||
| chr21:42266660
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-4410G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266660 | ||||||
| chr21:42266731
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.287-4339A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266731 | ||||||
| chr21:42266756
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0009g0085a0001c0001t0030g0312 | 3 | HG02145.hp1 HG02559.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.287-4314G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266756 | ||||||
| chr21:42266757
|
T | C | 1 | a0001c0001t0006g0049 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.287-4313T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266757 | ||||||
| chr21:42266882
|
T | C | 223 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.287-4188T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266882 | ||||||
| chr21:42266924
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-4146C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266924 | ||||||
| chr21:42267032
|
G | T | 40 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(37): Show | 42 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-4038G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267032 | ||||||
| chr21:42267212
|
C | T | 25 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-3858C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267212 | ||||||
| chr21:42267244
|
C | T | 140 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(137): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.287-3826C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267244 | ||||||
| chr21:42267276
|
T | C | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-3794T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267276 | ||||||
| chr21:42267297
|
G | C | 3 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0003g0234 | 3 | HG02258.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.287-3773G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267297 | ||||||
| chr21:42267332
|
C | T | 7 | a0001c0001t0001g0254a0001c0001t0002g0134a0001c0001t0002g0137others(4): Show | 7 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-3738C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267332 | ||||||
| chr21:42267343
|
CTGGGTTC others(15): Show |
C | 3 | a0001c0001t0001g0089a0001c0001t0003g0088a0001c0002t0002g0094 | 3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-3707_287-3686d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267343 | |||||
| chr21:42267437
|
G | GTGGTCCG others(15): Show |
3 | a0001c0001t0009g0275a0001c0002t0002g0078a0001c0002t0004g0274 | 3 | HG02109.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-3627_287-3606d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267437 | |||||
| chr21:42267443
|
CGAGTTCT others(59): Show |
C | 4 | a0001c0001t0001g0142a0001c0001t0001g0263a0001c0001t0004g0265others(1): Show | 4 | HG01261.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-3586_287-3521d others(68): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267443 | |||||
| chr21:42267457
|
G | A | 140 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(137): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.287-3613G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267457 | ||||||
| chr21:42267466
|
G | A | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-3604G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267466 | ||||||
| chr21:42267501
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0207a0001c0001t0003g0072others(1): Show | 4 | HG01243.hp1 HG01261.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-3569G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267501 | ||||||
| chr21:42267507
|
T | A | 3 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.287-3563T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267507 | ||||||
| chr21:42267528
|
G | C | 4 | a0001c0001t0001g0338a0001c0001t0012g0315a0001c0001t0015g0285others(1): Show | 5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-3542G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267528 | ||||||
| chr21:42267537
|
C | T | 136 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(133): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.287-3533C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267537 | ||||||
| chr21:42267635
|
G | C | 223 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.287-3435G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267635 | ||||||
| chr21:42267637
|
G | C | 223 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.287-3433G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267637 | ||||||
| chr21:42267833
|
C | G | 1 | a0001c0001t0002g0180 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.287-3237C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267833 | ||||||
| chr21:42267859
|
T | A | 1 | a0001c0001t0007g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.287-3211T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267859 | ||||||
| chr21:42267866
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-3204C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267866 | ||||||
| chr21:42267866
|
CTGGTCTG others(15): Show |
C | 35 | a0001c0001t0001g0122a0001c0001t0001g0177a0001c0001t0002g0162others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-3142_287-3121d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267866 | |||||
| chr21:42267890
|
G | C | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.287-3180G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267890 | ||||||
| chr21:42267903
|
T | C | 4 | a0001c0001t0001g0338a0001c0001t0012g0315a0001c0001t0015g0285others(1): Show | 5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-3167T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267903 | ||||||
| chr21:42267920
|
TTCTGTCT others(19): Show |
T | 4 | a0001c0001t0001g0142a0001c0001t0001g0263a0001c0001t0004g0265others(1): Show | 4 | HG01261.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-3146_287-3121d others(28): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267920 | |||||
| chr21:42268108
|
A | G | 1 | a0001c0001t0008g0345 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287-2962A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268108 | ||||||
| chr21:42268362
|
G | GGT | 6 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0003g0106others(3): Show | 6 | HG01975.hp1 NA18943.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-2682_287-2681d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | |||||
| chr21:42268362
|
G | GGTGT | 16 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0207others(13): Show | 16 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-2684_287-2681d others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | |||||
| chr21:42268362
|
G | GGTGTGT | 17 | a0001c0001t0001g0334a0001c0001t0002g0180a0001c0001t0002g0188others(14): Show | 18 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-2686_287-2681d others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | |||||
| chr21:42268362
|
G | GGTGTGTG others(1): Show |
73 | a0001c0001t0001g0091a0001c0001t0001g0112a0001c0001t0001g0124others(70): Show | 73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.287-2688_287-2681d others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | |||||
| chr21:42268362
|
G | GGTGTGTG others(3): Show |
14 | a0001c0001t0001g0096a0001c0001t0001g0213a0001c0001t0002g0115others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-2690_287-2681d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | |||||
| chr21:42268362
|
G | GGTGTGTG others(5): Show |
4 | a0001c0001t0001g0290a0001c0001t0004g0182a0001c0001t0009g0085others(1): Show | 4 | HG00280.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-2692_287-2681d others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | |||||
| chr21:42268381
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0001g0089a0001c0001t0003g0088a0001c0002t0002g0094 | 3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-2682_287-2681i others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268381 | |||||
| chr21:42268386
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.287-2684T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268386 | ||||||
| chr21:42268386
|
T | TGCGC | 19 | a0001c0001t0001g0317a0001c0001t0001g0327a0001c0001t0001g0336others(16): Show | 19 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-2683_287-2682i others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268386 | |||||
| chr21:42268388
|
T | C | 21 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(18): Show | 21 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-2682T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268388 | ||||||
| chr21:42268388
|
T | TGCGCGC | 4 | a0001c0001t0003g0153a0001c0001t0004g0339a0001c0002t0002g0282others(1): Show | 4 | HG02818.hp1 HG02922.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-2675_287-2670d others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGCG others(1): Show |
9 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0004g0102others(6): Show | 10 | HG01891.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(1): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0271a0001c0001t0002g0183others(4): Show | 7 | HG02683.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-2681_287-2680i others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(3): Show |
26 | a0001c0001t0001g0122a0001c0001t0001g0177a0001c0001t0002g0162others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(5): Show |
2 | a0001c0001t0004g0269a0001c0001t0014g0061 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-2681_287-2680i others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(5): Show |
13 | a0001c0001t0001g0142a0001c0001t0001g0254a0001c0001t0002g0134others(10): Show | 14 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(13): Show |
2 | a0001c0001t0004g0265a0001c0001t0004g0267 | 2 | HG01261.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.287-2681_287-2680i others(22): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268388
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.287-2681_287-2680i others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | |||||
| chr21:42268390
|
C | T | 19 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0207others(16): Show | 19 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-2680C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268390 | ||||||
| chr21:42268392
|
C | T | 58 | a0001c0001t0001g0083a0001c0001t0001g0122a0001c0001t0001g0139others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.287-2678C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268392 | ||||||
| chr21:42268395
|
G | A | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-2675G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268395 | ||||||
| chr21:42268397
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.287-2673G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268397 | ||||||
| chr21:42268398
|
C | T | 3 | a0001c0004t0003g0074a0001c0004t0003g0126a0001c0004t0003g0127 | 3 | NA19003.hp2 NA19004.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.287-2672C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268398 | ||||||
| chr21:42268405
|
T | C | 27 | a0001c0001t0001g0097a0001c0001t0001g0317a0001c0001t0001g0327others(24): Show | 27 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.287-2665T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268405 | ||||||
| chr21:42268426
|
A | G | 2 | a0001c0006t0001g0006a0001c0006t0004g0321 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-2644A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268426 | ||||||
| chr21:42268484
|
G | C | 209 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.287-2586G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268484 | ||||||
| chr21:42268602
|
A | T | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-2468A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268602 | ||||||
| chr21:42268679
|
G | T | 1 | a0001c0001t0003g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.287-2391G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268679 | ||||||
| chr21:42268719
|
C | T | 3 | a0001c0001t0004g0313a0001c0001t0009g0322a0001c0001t0009g0323 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.287-2351C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268719 | ||||||
| chr21:42268835
|
C | G | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.287-2235C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268835 | ||||||
| chr21:42269005
|
G | T | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0286others(4): Show | 7 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-2065G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269005 | ||||||
| chr21:42269065
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.287-2005G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269065 | ||||||
| chr21:42269067
|
C | T | 2 | a0001c0007t0015g0348a0001c0007t0016g0347 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-2003C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269067 | ||||||
| chr21:42269284
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-1786G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269284 | ||||||
| chr21:42269381
|
C | T | 99 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(96): Show | 100 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.287-1689C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269381 | ||||||
| chr21:42269408
|
C | A | 10 | a0001c0003t0001g0250a0001c0003t0003g0212a0001c0003t0003g0259others(7): Show | 10 | HG00408.hp1 HG00558.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-1662C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269408 | ||||||
| chr21:42269410
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.287-1660C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269410 | ||||||
| chr21:42269493
|
G | T | 2 | a0001c0007t0015g0348a0001c0007t0016g0347 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-1577G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269493 | ||||||
| chr21:42269583
|
TC | T | 4 | a0001c0001t0002g0134a0001c0001t0002g0137a0001c0001t0002g0340others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-1484delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42269583 | |||||
| chr21:42269616
|
G | T | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.287-1454G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269616 | ||||||
| chr21:42269647
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-1423G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269647 | ||||||
| chr21:42269703
|
G | A | 1 | a0001c0001t0004g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287-1367G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269703 | ||||||
| chr21:42269740
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-1330T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269740 | ||||||
| chr21:42269760
|
A | G | 100 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(97): Show | 101 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.287-1310A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269760 | ||||||
| chr21:42270016
|
A | G | 2 | a0001c0001t0004g0269a0001c0001t0014g0061 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-1054A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270016 | ||||||
| chr21:42270259
|
C | CA | 8 | a0001c0001t0002g0226a0001c0001t0002g0266a0001c0001t0002g0288others(5): Show | 8 | HG01123.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-789dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | |||||
| chr21:42270259
|
C | CAAA | 7 | a0001c0001t0001g0156a0001c0001t0001g0206a0001c0001t0002g0221others(4): Show | 7 | HG01070.hp1 HG01975.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-791_287-789dup others(3): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | |||||
| chr21:42270259
|
C | CAAAA | 61 | a0001c0001t0001g0133a0001c0001t0001g0165a0001c0001t0001g0166others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.287-792_287-789dup others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | |||||
| chr21:42270259
|
C | CAAAAA | 31 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0317others(28): Show | 31 | HG01106.hp2 HG01167.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.287-793_287-789dup others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | |||||
| chr21:42270259
|
C | CAAAAAA | 8 | a0001c0001t0001g0338a0001c0001t0002g0090a0001c0001t0002g0277others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-794_287-789dup others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | |||||
| chr21:42270259
|
CA | C | 97 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0089others(94): Show | 98 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.287-789delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | |||||
| chr21:42270309
|
A | C | 1 | a0001c0001t0003g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-761A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270309 | ||||||
| chr21:42270330
|
T | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-740T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270330 | ||||||
| chr21:42270528
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-542C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270528 | ||||||
| chr21:42270748
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.287-322G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270748 | ||||||
| chr21:42270768
|
G | C | 1 | a0001c0001t0030g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-302G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270768 | ||||||
| chr21:42270828
|
T | G | 7 | a0001c0001t0001g0335a0001c0001t0004g0269a0001c0001t0009g0085others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-242T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270828 | ||||||
| chr21:42270831
|
A | G | 1 | a0001c0001t0002g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.287-239A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270831 | ||||||
| chr21:42270902
|
A | G | 6 | a0001c0001t0001g0271a0001c0001t0001g0328a0001c0001t0001g0338others(3): Show | 7 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-168A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270902 | ||||||
| chr21:42270956
|
A | G | 1 | a0001c0001t0012g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-114A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270956 | ||||||
| chr21:42270984
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0006g0011 | 2 | NA18939.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.287-86C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270984 | ||||||
| chr21:42271029
|
A | G | 5 | a0001c0001t0001g0271a0001c0001t0001g0338a0001c0001t0012g0315others(2): Show | 6 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-41A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42271029 | ||||||
| chr21:42271212
|
A | G | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.404+25A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271212 | ||||||
| chr21:42271359
|
G | C | 37 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0091others(34): Show | 37 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.404+172G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271359 | ||||||
| chr21:42271466
|
T | TCAGGGAG others(16): Show |
4 | a0001c0001t0003g0310a0001c0001t0009g0275a0001c0001t0017g0005others(1): Show | 5 | HG01109.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+281_404+303dup others(23): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr21 | 42271466 | |||||
| chr21:42271656
|
C | T | 2 | a0001c0001t0004g0086a0001c0001t0004g0092 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.404+469C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271656 | ||||||
| chr21:42271657
|
G | A | 4 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0015g0285others(1): Show | 5 | HG01167.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+470G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271657 | ||||||
| chr21:42271662
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.404+475A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271662 | ||||||
| chr21:42271930
|
G | A | 27 | a0001c0001t0002g0162a0001c0001t0002g0180a0001c0001t0002g0229others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.404+743G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271930 | ||||||
| chr21:42271931
|
T | C | 27 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0263others(24): Show | 29 | HG01070.hp2 HG01071.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.404+744T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271931 | ||||||
| chr21:42272055
|
T | C | 1 | a0001c0007t0016g0347 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.404+868T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272055 | ||||||
| chr21:42272269
|
T | A | 3 | a0001c0001t0002g0090a0001c0001t0004g0086a0001c0001t0004g0092 | 3 | HG01167.hp2 HG01169.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.405-1034T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272269 | ||||||
| chr21:42272314
|
T | C | 4 | a0001c0001t0001g0338a0001c0001t0012g0315a0001c0001t0015g0285others(1): Show | 5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-989T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272314 | ||||||
| chr21:42272431
|
A | G | 3 | a0001c0001t0001g0338a0001c0001t0012g0315a0001c0002t0004g0004 | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-872A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272431 | ||||||
| chr21:42272442
|
G | T | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.405-861G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272442 | ||||||
| chr21:42272563
|
G | A | 16 | a0001c0001t0001g0271a0001c0001t0001g0328a0001c0001t0001g0335others(13): Show | 17 | HG01496.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-740G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272563 | ||||||
| chr21:42272704
|
G | C | 9 | a0001c0001t0001g0335a0001c0001t0002g0277a0001c0001t0004g0269others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-599G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272704 | ||||||
| chr21:42272712
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.405-591G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272712 | ||||||
| chr21:42272731
|
T | C | 81 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0096others(78): Show | 82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.405-572T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272731 | ||||||
| chr21:42272917
|
C | T | 2 | a0001c0001t0009g0275a0001c0002t0002g0143 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.405-386C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272917 | ||||||
| chr21:42272996
|
C | G | 2 | a0001c0001t0009g0322a0001c0001t0009g0323 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405-307C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272996 | ||||||
| chr21:42273140
|
C | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0239 | 2 | HG01496.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.405-163C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42273140 | ||||||
| chr21:42273159
|
G | T | 3 | a0001c0001t0001g0111a0001c0001t0002g0113a0001c0001t0005g0060 | 3 | HG02040.hp2 NA18944.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.405-144G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42273159 | ||||||
| chr21:42273218
|
C | T | 1 | a0001c0007t0015g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.405-85C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42273218 | ||||||
| chr21:42273454
|
C | T | 1 | a0001c0001t0002g0107 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.537+19C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273454 | ||||||
| chr21:42273474
|
G | C | 108 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0096others(105): Show | 109 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.537+39G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273474 | ||||||
| chr21:42273583
|
G | A | 53 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0254others(50): Show | 53 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.537+148G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273583 | ||||||
| chr21:42273631
|
A | T | 5 | a0001c0001t0002g0173a0001c0001t0002g0233a0001c0001t0003g0232others(2): Show | 5 | HG00558.hp2 HG01993.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+196A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273631 | ||||||
| chr21:42273693
|
A | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.537+258A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273693 | ||||||
| chr21:42273707
|
G | A | 1 | a0001c0001t0030g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.537+272G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273707 | ||||||
| chr21:42273791
|
T | G | 1 | a0002c0013t0001g0099 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.537+356T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273791 | ||||||
| chr21:42273808
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0006g0028 | 2 | NA18942.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.537+373G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273808 | ||||||
| chr21:42273927
|
T | G | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.537+492T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273927 | ||||||
| chr21:42274021
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.537+586G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274021 | ||||||
| chr21:42274023
|
G | T | 1 | a0001c0003t0006g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.537+588G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274023 | ||||||
| chr21:42274162
|
C | T | 4 | a0001c0001t0001g0335a0001c0001t0031g0077a0001c0002t0002g0270others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+727C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274162 | ||||||
| chr21:42274199
|
A | T | 9 | a0001c0003t0001g0250a0001c0003t0003g0212a0001c0003t0005g0041others(6): Show | 9 | HG00408.hp1 HG01975.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+764A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274199 | ||||||
| chr21:42274291
|
A | G | 15 | a0001c0001t0001g0335a0001c0001t0002g0090a0001c0001t0002g0277others(12): Show | 16 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.537+856A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274291 | ||||||
| chr21:42274297
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0003g0088 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.537+862T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274297 | ||||||
| chr21:42274326
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.537+891G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274326 | ||||||
| chr21:42274393
|
G | C | 13 | a0001c0001t0001g0335a0001c0001t0002g0277a0001c0001t0004g0269others(10): Show | 14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.537+958G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274393 | ||||||
| chr21:42274436
|
G | A | 3 | a0001c0001t0002g0277a0001c0001t0009g0085a0001c0001t0030g0312 | 3 | HG02145.hp1 HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.537+1001G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274436 | ||||||
| chr21:42274438
|
G | A | 3 | a0001c0001t0001g0263a0001c0001t0001g0316a0001c0001t0004g0267 | 3 | HG01261.hp2 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.537+1003G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274438 | ||||||
| chr21:42274475
|
C | CT | 50 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0166others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.537+1056dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274475 | |||||
| chr21:42274475
|
C | CTT | 102 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0096others(99): Show | 104 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+1055_537+1056d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274475 | |||||
| chr21:42274475
|
C | CTTT | 34 | a0001c0001t0001g0243a0001c0001t0001g0317a0001c0001t0001g0336others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.537+1054_537+1056d others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274475 | |||||
| chr21:42274491
|
T | G | 3 | a0001c0001t0010g0301a0001c0001t0010g0302a0001c0001t0010g0303 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.537+1056T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274491 | ||||||
| chr21:42274492
|
G | T | 178 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0096others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.537+1057G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274492 | ||||||
| chr21:42274560
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.537+1125C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274560 | ||||||
| chr21:42274620
|
G | A | 90 | a0001c0001t0001g0133a0001c0001t0001g0165a0001c0001t0001g0166others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.537+1185G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274620 | ||||||
| chr21:42274635
|
C | T | 9 | a0001c0001t0001g0271a0001c0001t0001g0338a0001c0001t0004g0102others(6): Show | 10 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.537+1200C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274635 | ||||||
| chr21:42274690
|
G | T | 2 | a0001c0001t0001g0083a0001c0001t0002g0305 | 2 | HG00140.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.537+1255G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274690 | ||||||
| chr21:42274715
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.537+1280T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274715 | ||||||
| chr21:42274779
|
ATT | A | 127 | a0001c0001t0001g0133a0001c0001t0001g0165a0001c0001t0001g0166others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.537+1354_537+1355d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274779 | |||||
| chr21:42274870
|
G | A | 25 | a0001c0001t0001g0317a0001c0001t0001g0327a0001c0001t0001g0336others(22): Show | 25 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.537+1435G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274870 | ||||||
| chr21:42275030
|
T | A | 101 | a0001c0001t0001g0133a0001c0001t0001g0165a0001c0001t0001g0166others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.537+1595T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275030 | ||||||
| chr21:42275220
|
T | C | 11 | a0001c0001t0001g0328a0001c0001t0002g0277a0001c0001t0002g0308others(8): Show | 12 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.538-1675T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275220 | ||||||
| chr21:42275351
|
C | A | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.538-1544C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275351 | ||||||
| chr21:42275378
|
G | C | 101 | a0001c0001t0001g0133a0001c0001t0001g0165a0001c0001t0001g0166others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.538-1517G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275378 | ||||||
| chr21:42275423
|
G | A | 9 | a0001c0001t0002g0277a0001c0001t0004g0269a0001c0001t0006g0063others(6): Show | 10 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.538-1472G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275423 | ||||||
| chr21:42275636
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.538-1259T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275636 | ||||||
| chr21:42275674
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.538-1221A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275674 | ||||||
| chr21:42275729
|
C | T | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.538-1166C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275729 | ||||||
| chr21:42275772
|
C | T | 9 | a0001c0001t0002g0277a0001c0001t0004g0269a0001c0001t0006g0063others(6): Show | 10 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.538-1123C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275772 | ||||||
| chr21:42275815
|
C | T | 2 | a0001c0001t0004g0269a0001c0001t0014g0061 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.538-1080C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275815 | ||||||
| chr21:42275862
|
A | G | 2 | a0001c0001t0002g0277a0001c0001t0009g0085 | 2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.538-1033A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275862 | ||||||
| chr21:42276042
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.538-853C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276042 | ||||||
| chr21:42276122
|
G | A | 1 | a0001c0001t0021g0008 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.538-773G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276122 | ||||||
| chr21:42276215
|
C | A | 8 | a0001c0001t0001g0338a0001c0001t0004g0102a0001c0001t0004g0103others(5): Show | 9 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.538-680C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276215 | ||||||
| chr21:42276301
|
G | C | 2 | a0001c0001t0001g0334a0001c0001t0009g0333 | 2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.538-594G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276301 | ||||||
| chr21:42276335
|
C | G | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.538-560C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276335 | ||||||
| chr21:42276424
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.538-471C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276424 | ||||||
| chr21:42276447
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.538-448C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276447 | ||||||
| chr21:42276682
|
ATAGCTGC others(68): Show |
A | 9 | a0001c0001t0002g0277a0001c0001t0004g0269a0001c0001t0004g0339others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.538-199_538-125del others(75): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42276682 | |||||
| chr21:42276692
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.538-203C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276692 | ||||||
| chr21:42276707
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.538-188C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276707 | ||||||
| chr21:42276723
|
G | A | 27 | a0001c0001t0002g0162a0001c0001t0002g0180a0001c0001t0002g0229others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.538-172G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276723 | ||||||
| chr21:42276840
|
A | G | 3 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0003g0116 | 3 | HG02080.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.538-55A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276840 | ||||||
| chr21:42276889
|
C | T | 26 | a0001c0001t0001g0172a0001c0001t0001g0177a0001c0001t0001g0185others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.538-6C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276889 | ||||||
| chr21:42277008
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+63G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277008 | ||||||
| chr21:42277070
|
G | A | 10 | a0001c0001t0001g0271a0001c0001t0001g0328a0001c0001t0002g0308others(7): Show | 11 | HG01109.hp2 HG01496.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+125G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277070 | ||||||
| chr21:42277085
|
A | G | 104 | a0001c0001t0001g0133a0001c0001t0001g0165a0001c0001t0001g0166others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.588+140A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277085 | ||||||
| chr21:42277182
|
G | C | 13 | a0001c0001t0001g0271a0001c0001t0001g0328a0001c0001t0002g0277others(10): Show | 14 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+237G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277182 | ||||||
| chr21:42277300
|
A | G | 10 | a0001c0001t0002g0277a0001c0001t0004g0269a0001c0001t0004g0339others(7): Show | 11 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+355A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277300 | ||||||
| chr21:42277426
|
A | G | 1 | a0001c0006t0004g0321 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+481A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277426 | ||||||
| chr21:42277468
|
A | AT | 63 | a0001c0001t0001g0317a0001c0001t0001g0327a0001c0001t0001g0336others(60): Show | 65 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.588+533dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr21 | 42277468 | |||||
| chr21:42277963
|
T | G | 55 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0278others(52): Show | 56 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.588+1018T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277963 | ||||||
| chr21:42277968
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.588+1023T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277968 | ||||||
| chr21:42277997
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.588+1052G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277997 | ||||||
| chr21:42278123
|
A | T | 1 | a0001c0003t0005g0041 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.588+1178A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278123 | ||||||
| chr21:42278137
|
G | A | 1 | a0001c0006t0001g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.588+1192G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278137 | ||||||
| chr21:42278141
|
G | A | 125 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0111others(122): Show | 127 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+1196G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278141 | ||||||
| chr21:42278145
|
A | C | 159 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0111others(156): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.588+1200A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278145 | ||||||
| chr21:42278183
|
G | C | 5 | a0001c0001t0002g0277a0001c0001t0004g0339a0001c0001t0006g0064others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1238G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278183 | ||||||
| chr21:42278293
|
C | A | 2 | a0001c0001t0004g0264a0001c0001t0006g0063 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.588+1348C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278293 | ||||||
| chr21:42278402
|
A | G | 241 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.588+1457A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278402 | ||||||
| chr21:42278419
|
A | T | 245 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.588+1474A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278419 | ||||||
| chr21:42278518
|
G | A | 2 | a0001c0001t0002g0095a0001c0001t0002g0308 | 2 | HG01496.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.588+1573G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278518 | ||||||
| chr21:42278603
|
C | T | 1 | a0001c0002t0002g0324 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.588+1658C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278603 | ||||||
| chr21:42278700
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.588+1755G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278700 | ||||||
| chr21:42278704
|
C | T | 9 | a0001c0003t0001g0250a0001c0003t0003g0212a0001c0003t0005g0041others(6): Show | 9 | HG00408.hp1 HG01975.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+1759C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278704 | ||||||
| chr21:42278705
|
A | G | 212 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.588+1760A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278705 | ||||||
| chr21:42278713
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.588+1768A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278713 | ||||||
| chr21:42278787
|
G | A | 3 | a0001c0001t0002g0277a0001c0001t0004g0339a0001c0001t0009g0085 | 3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.588+1842G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278787 | ||||||
| chr21:42278792
|
A | G | 89 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(86): Show | 91 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.588+1847A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278792 | ||||||
| chr21:42278804
|
G | C | 31 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0327others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.588+1859G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278804 | ||||||
| chr21:42278830
|
G | T | 1 | a0001c0002t0016g0343 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.588+1885G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278830 | ||||||
| chr21:42278840
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0004g0267 | 2 | HG01261.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.588+1895T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278840 | ||||||
| chr21:42278851
|
C | A | 16 | a0001c0001t0001g0172a0001c0001t0001g0185a0001c0001t0001g0209others(13): Show | 16 | HG00423.hp2 HG00639.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.588+1906C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278851 | ||||||
| chr21:42278851
|
C | T | 3 | a0001c0001t0002g0277a0001c0001t0004g0339a0001c0001t0009g0085 | 3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.588+1906C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278851 | ||||||
| chr21:42278857
|
T | A | 60 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(57): Show | 62 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.588+1912T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278857 | ||||||
| chr21:42278886
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0171a0001c0001t0001g0254others(8): Show | 11 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+1941C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278886 | ||||||
| chr21:42278958
|
C | T | 93 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0097others(90): Show | 96 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.588+2013C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278958 | ||||||
| chr21:42278986
|
G | A | 82 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0111others(79): Show | 83 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.588+2041G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278986 | ||||||
| chr21:42279038
|
C | T | 4 | a0001c0001t0001g0317a0001c0001t0001g0336a0001c0001t0029g0262others(1): Show | 4 | HG02622.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+2093C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279038 | ||||||
| chr21:42279057
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.588+2112T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279057 | ||||||
| chr21:42279120
|
G | A | 32 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0156others(29): Show | 33 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.588+2175G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279120 | ||||||
| chr21:42279144
|
A | G | 6 | a0001c0001t0001g0338a0001c0001t0002g0273a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+2199A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279144 | ||||||
| chr21:42279180
|
C | T | 63 | a0001c0001t0001g0096a0001c0001t0001g0142a0001c0001t0001g0155others(60): Show | 65 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.588+2235C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279180 | ||||||
| chr21:42279225
|
G | A | 101 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0111others(98): Show | 102 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.588+2280G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279225 | ||||||
| chr21:42279251
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0006g0064 | 2 | HG02683.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.588+2306C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279251 | ||||||
| chr21:42279278
|
G | GGAATTCT others(8): Show |
1 | a0001c0003t0005g0052 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.588+2336_588+2350d others(17): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr21 | 42279278 | |||||
| chr21:42279298
|
C | T | 3 | a0001c0001t0002g0277a0001c0001t0004g0339a0001c0001t0009g0085 | 3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.588+2353C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279298 | ||||||
| chr21:42279313
|
G | C | 2 | a0001c0001t0004g0086a0001c0001t0004g0092 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.588+2368G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279313 | ||||||
| chr21:42279318
|
G | C | 2 | a0001c0001t0018g0065a0001c0006t0001g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.588+2373G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279318 | ||||||
| chr21:42279325
|
C | T | 61 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(58): Show | 63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.588+2380C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279325 | ||||||
| chr21:42279344
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.588+2399G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279344 | ||||||
| chr21:42279386
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.588+2441G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279386 | ||||||
| chr21:42279398
|
T | G | 2 | a0001c0002t0002g0078a0001c0002t0004g0274 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.588+2453T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279398 | ||||||
| chr21:42279435
|
A | T | 69 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0133others(66): Show | 71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.588+2490A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279435 | ||||||
| chr21:42279497
|
G | A | 64 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(61): Show | 66 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.588+2552G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279497 | ||||||
| chr21:42279499
|
T | A | 29 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0156others(26): Show | 29 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.588+2554T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279499 | ||||||
| chr21:42279506
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+2561C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279506 | ||||||
| chr21:42279563
|
G | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0316a0001c0001t0004g0265 | 3 | HG02280.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.588+2618G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279563 | ||||||
| chr21:42279591
|
C | T | 4 | a0001c0001t0003g0071a0001c0001t0003g0193a0001c0001t0003g0196others(1): Show | 4 | HG01074.hp2 HG01106.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+2646C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279591 | ||||||
| chr21:42279598
|
G | A | 1 | a0001c0001t0023g0023 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.588+2653G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279598 | ||||||
| chr21:42279653
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589-2621T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279653 | ||||||
| chr21:42279693
|
G | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0316a0001c0001t0004g0265 | 3 | HG02280.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.589-2581G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279693 | ||||||
| chr21:42279711
|
C | T | 8 | a0001c0001t0001g0338a0001c0001t0002g0273a0001c0001t0004g0102others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.589-2563C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279711 | ||||||
| chr21:42279767
|
T | C | 63 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(60): Show | 65 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.589-2507T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279767 | ||||||
| chr21:42279794
|
C | T | 4 | a0001c0001t0004g0279a0001c0001t0009g0275a0001c0002t0002g0143others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-2480C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279794 | ||||||
| chr21:42279795
|
G | A | 61 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(58): Show | 63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.589-2479G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279795 | ||||||
| chr21:42279864
|
C | T | 61 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(58): Show | 63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.589-2410C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279864 | ||||||
| chr21:42279904
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.589-2370C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279904 | ||||||
| chr21:42279905
|
G | T | 31 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0156others(28): Show | 32 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.589-2369G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279905 | ||||||
| chr21:42279932
|
G | A | 2 | a0001c0001t0008g0194a0001c0001t0008g0195 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.589-2342G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279932 | ||||||
| chr21:42280132
|
A | C | 31 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0156others(28): Show | 32 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.589-2142A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280132 | ||||||
| chr21:42280209
|
G | T | 72 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(69): Show | 74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-2065G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280209 | ||||||
| chr21:42280221
|
T | C | 75 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0133others(72): Show | 77 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.589-2053T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280221 | ||||||
| chr21:42280250
|
C | G | 72 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(69): Show | 74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-2024C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280250 | ||||||
| chr21:42280301
|
G | C | 1 | a0001c0001t0002g0245 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.589-1973G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280301 | ||||||
| chr21:42280322
|
A | G | 72 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(69): Show | 74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-1952A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280322 | ||||||
| chr21:42280451
|
T | C | 90 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(87): Show | 92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.589-1823T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280451 | ||||||
| chr21:42280483
|
G | A | 82 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0111others(79): Show | 83 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.589-1791G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280483 | ||||||
| chr21:42280487
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.589-1787G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280487 | ||||||
| chr21:42280499
|
A | G | 72 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(69): Show | 74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-1775A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280499 | ||||||
| chr21:42280527
|
G | A | 2 | a0001c0001t0004g0182a0001c0001t0004g0313 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.589-1747G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280527 | ||||||
| chr21:42280596
|
C | T | 26 | a0001c0001t0001g0089a0001c0001t0001g0156a0001c0001t0001g0171others(23): Show | 27 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.589-1678C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280596 | ||||||
| chr21:42280632
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.589-1642A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280632 | ||||||
| chr21:42280666
|
C | T | 62 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(59): Show | 64 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.589-1608C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280666 | ||||||
| chr21:42280667
|
G | A | 6 | a0001c0001t0001g0338a0001c0001t0002g0273a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1607G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280667 | ||||||
| chr21:42280687
|
C | T | 18 | a0001c0001t0001g0328a0001c0001t0002g0090a0001c0001t0004g0093others(15): Show | 18 | HG01081.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-1587C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280687 | ||||||
| chr21:42280713
|
G | A | 3 | a0001c0001t0002g0277a0001c0001t0004g0339a0001c0001t0009g0085 | 3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-1561G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280713 | ||||||
| chr21:42280797
|
C | T | 159 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.589-1477C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280797 | ||||||
| chr21:42280815
|
G | A | 4 | a0001c0001t0015g0285a0001c0002t0002g0330a0001c0002t0002g0331others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-1459G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280815 | ||||||
| chr21:42280866
|
A | G | 90 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(87): Show | 92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.589-1408A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280866 | ||||||
| chr21:42280924
|
C | T | 90 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(87): Show | 92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.589-1350C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280924 | ||||||
| chr21:42281026
|
G | C | 6 | a0001c0001t0001g0338a0001c0001t0002g0273a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1248G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281026 | ||||||
| chr21:42281066
|
C | T | 69 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(66): Show | 71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.589-1208C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281066 | ||||||
| chr21:42281182
|
C | T | 7 | a0001c0001t0002g0188a0001c0001t0011g0039a0001c0001t0011g0043others(4): Show | 7 | HG01257.hp2 HG01934.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-1092C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281182 | ||||||
| chr21:42281236
|
G | A | 87 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(84): Show | 89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.589-1038G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281236 | ||||||
| chr21:42281379
|
G | T | 3 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0003g0310 | 3 | HG02258.hp2 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.589-895G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281379 | ||||||
| chr21:42281453
|
G | C | 6 | a0001c0001t0001g0338a0001c0001t0002g0273a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-821G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281453 | ||||||
| chr21:42281521
|
G | C | 1 | a0001c0001t0003g0119 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.589-753G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281521 | ||||||
| chr21:42281687
|
G | A | 6 | a0001c0001t0001g0338a0001c0001t0002g0273a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-587G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281687 | ||||||
| chr21:42281818
|
C | T | 1 | a0001c0001t0031g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.589-456C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281818 | ||||||
| chr21:42281867
|
A | G | 162 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.589-407A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281867 | ||||||
| chr21:42281913
|
C | T | 67 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(64): Show | 69 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.589-361C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281913 | ||||||
| chr21:42281975
|
A | C | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589-299A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281975 | ||||||
| chr21:42282141
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.589-133C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42282141 | ||||||
| chr21:42282453
|
G | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0316a0001c0001t0004g0265others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+34G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282453 | ||||||
| chr21:42282660
|
G | A | 1 | a0001c0001t0004g0329 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.734+241G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282660 | ||||||
| chr21:42282738
|
T | C | 249 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.734+319T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282738 | ||||||
| chr21:42282744
|
G | T | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.734+325G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282744 | ||||||
| chr21:42282812
|
A | G | 162 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0083others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.734+393A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282812 | ||||||
| chr21:42282826
|
G | A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734+407G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282826 | ||||||
| chr21:42282988
|
G | A | 88 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0142others(85): Show | 89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.734+569G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282988 | ||||||
| chr21:42283026
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.734+607G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283026 | ||||||
| chr21:42283029
|
G | A | 4 | a0001c0001t0015g0285a0001c0002t0002g0330a0001c0002t0002g0331others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.734+610G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283029 | ||||||
| chr21:42283083
|
G | A | 1 | a0001c0002t0002g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.734+664G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283083 | ||||||
| chr21:42283115
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.734+696A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283115 | ||||||
| chr21:42283214
|
G | T | 28 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0327others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.734+795G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283214 | ||||||
| chr21:42283246
|
CTTGGGCC others(13): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.734+828_734+847del others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283246 | ||||||
| chr21:42283369
|
G | A | 1 | a0001c0002t0004g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.734+950G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283369 | ||||||
| chr21:42283486
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.734+1067T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283486 | ||||||
| chr21:42283493
|
C | T | 1 | a0001c0001t0009g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.735-1067C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283493 | ||||||
| chr21:42283629
|
GCCTGCCT others(117): Show |
G | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735-908_735-785del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283629 | |||||
| chr21:42283633
|
GCCTGGAC others(54): Show |
G | 4 | a0001c0001t0001g0165a0001c0001t0002g0164a0001c0001t0023g0023others(1): Show | 4 | HG01346.hp2 HG01975.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-908_735-848del others(61): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283633 | |||||
| chr21:42283652
|
C | A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735-908C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283652 | ||||||
| chr21:42283657
|
C | A | 1 | a0001c0003t0005g0048 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.735-903C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283657 | ||||||
| chr21:42283658
|
CCACCCAA others(55): Show |
C | 1 | a0001c0002t0002g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.735-900_735-839del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283658 | |||||
| chr21:42283659
|
C | A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735-901C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283659 | ||||||
| chr21:42283660
|
A | AC | 7 | a0001c0001t0001g0342a0001c0001t0003g0071a0001c0001t0003g0193others(4): Show | 7 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-897dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283660 | |||||
| chr21:42283660
|
A | C | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.735-900A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283660 | ||||||
| chr21:42283660
|
ACCCAAAT others(359): Show |
A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735-895_735-530del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283660 | |||||
| chr21:42283661
|
CCCAAATG others(55): Show |
C | 16 | a0001c0001t0002g0229a0001c0001t0002g0242a0001c0001t0003g0125others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.735-896_735-835del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283661 | |||||
| chr21:42283665
|
A | G | 3 | a0001c0002t0004g0274a0001c0002t0016g0343a0001c0003t0005g0048 | 3 | HG00408.hp1 HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.735-895A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283665 | ||||||
| chr21:42283665
|
AATGAGTG others(56): Show |
A | 12 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0002g0080others(9): Show | 12 | HG01081.hp2 HG01167.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-883_735-821del others(63): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | |||||
| chr21:42283665
|
AATGAGTG others(419): Show |
A | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735-883_735-458del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | |||||
| chr21:42283665
|
AATGAGTG others(480): Show |
A | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.735-883_735-397del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | |||||
| chr21:42283665
|
AATGAGTG others(540): Show |
A | 4 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0316others(1): Show | 4 | HG02280.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-883_735-337del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | |||||
| chr21:42283676
|
AACCCCCA others(360): Show |
A | 2 | a0001c0001t0008g0194a0001c0001t0008g0195 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.735-883_735-517del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283676 | ||||||
| chr21:42283676
|
AACCCCCA others(481): Show |
A | 2 | a0001c0001t0002g0277a0001c0001t0009g0085 | 2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.735-883_735-396del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283676 | ||||||
| chr21:42283677
|
A | C | 5 | a0001c0001t0003g0071a0001c0001t0003g0193a0001c0001t0003g0196others(2): Show | 5 | HG00408.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-883A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283677 | ||||||
| chr21:42283677
|
ACCCCCAC others(299): Show |
A | 1 | a0001c0003t0005g0041 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.735-871_735-566del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283677 | |||||
| chr21:42283689
|
T | G | 5 | a0001c0001t0003g0071a0001c0001t0003g0193a0001c0001t0003g0196others(2): Show | 5 | HG00408.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-871T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283689 | ||||||
| chr21:42283693
|
C | T | 5 | a0001c0001t0003g0071a0001c0001t0003g0193a0001c0001t0003g0196others(2): Show | 5 | HG00408.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-867C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283693 | ||||||
| chr21:42283694
|
A | G | 10 | a0001c0001t0001g0096a0001c0001t0003g0071a0001c0001t0003g0193others(7): Show | 11 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-866A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283694 | ||||||
| chr21:42283694
|
ACCTGGAC others(56): Show |
A | 5 | a0001c0001t0002g0095a0001c0001t0003g0326a0001c0002t0002g0330others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-844_735-782del others(63): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283694 | |||||
| chr21:42283694
|
ACCTGGAC others(360): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.735-853_735-487del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283694 | |||||
| chr21:42283694
|
ACCTGGAC others(420): Show |
A | 1 | a0001c0001t0001g0342 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.735-853_735-427del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283694 | |||||
| chr21:42283707
|
T | C | 3 | a0001c0001t0003g0228a0001c0002t0004g0274a0001c0002t0016g0343 | 3 | HG02615.hp2 HG03831.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.735-853T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283707 | ||||||
| chr21:42283708
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.735-852G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283708 | ||||||
| chr21:42283712
|
TA | T | 30 | a0001c0001t0001g0082a0001c0001t0001g0181a0001c0001t0001g0186others(27): Show | 31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.735-847delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283712 | ||||||
| chr21:42283712
|
TAC | T | 14 | a0001c0001t0002g0090a0001c0001t0004g0098a0001c0001t0004g0158others(11): Show | 14 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.735-847_735-846del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283712 | ||||||
| chr21:42283712
|
TACCACCC others(58): Show |
T | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.735-847_735-783del others(65): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283712 | ||||||
| chr21:42283713
|
A | AC | 4 | a0001c0001t0001g0197a0001c0001t0001g0231a0001c0001t0001g0248others(1): Show | 4 | HG00597.hp1 HG02056.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-845dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283713 | |||||
| chr21:42283713
|
ACCACCCA others(298): Show |
A | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.735-844_735-540del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283713 | |||||
| chr21:42283713
|
ACCACCCA others(419): Show |
A | 14 | a0001c0001t0001g0155a0001c0001t0001g0278a0001c0001t0004g0086others(11): Show | 16 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.735-844_735-419del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283713 | |||||
| chr21:42283714
|
CCA | C | 68 | a0001c0001t0001g0091a0001c0001t0001g0108a0001c0001t0001g0145others(65): Show | 70 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.735-844_735-843del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283714 | |||||
| chr21:42283714
|
CCACCCAC others(358): Show |
C | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.735-844_735-480del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283714 | |||||
| chr21:42283716
|
A | C | 211 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(208): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.735-844A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283716 | ||||||
| chr21:42283717
|
C | CA | 4 | a0001c0001t0002g0147a0001c0001t0003g0224a0001c0001t0009g0322others(1): Show | 4 | HG00544.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-843_735-842ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283717 | ||||||
| chr21:42283720
|
ACC | A | 4 | a0001c0001t0002g0191a0001c0001t0018g0065a0001c0003t0005g0048others(1): Show | 4 | HG00408.hp1 HG02602.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-839_735-838del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283720 | ||||||
| chr21:42283722
|
CACCCAGA others(54): Show |
C | 5 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0003g0320others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-814_735-754del others(61): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283722 | |||||
| chr21:42283723
|
ACCCAGAT others(114): Show |
A | 7 | a0001c0001t0001g0096a0001c0001t0003g0234a0001c0001t0003g0298others(4): Show | 7 | HG00738.hp1 HG01934.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-814_735-694del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(171): Show |
A | 3 | a0001c0001t0002g0114a0001c0001t0002g0183a0001c0001t0003g0123 | 3 | HG02683.hp2 HG03704.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.735-834_735-657del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(174): Show |
A | 3 | a0001c0001t0001g0186a0001c0002t0002g0094a0001c0002t0002g0324 | 3 | NA18522.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.735-814_735-634del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(232): Show |
A | 3 | a0001c0001t0002g0189a0001c0001t0002g0220a0001c0001t0002g0293 | 3 | HG01433.hp1 HG01515.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.735-834_735-596del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(293): Show |
A | 39 | a0001c0001t0001g0108a0001c0001t0001g0145a0001c0001t0001g0159others(36): Show | 40 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.735-834_735-535del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(296): Show |
A | 63 | a0001c0001t0001g0083a0001c0001t0001g0111a0001c0001t0001g0112others(60): Show | 64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.735-814_735-512del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(353): Show |
A | 22 | a0001c0001t0001g0091a0001c0001t0001g0156a0001c0001t0001g0171others(19): Show | 22 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.735-834_735-475del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(356): Show |
A | 19 | a0001c0001t0001g0089a0001c0001t0001g0317a0001c0001t0002g0188others(16): Show | 19 | HG01074.hp2 HG01106.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.735-814_735-452del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(417): Show |
A | 4 | a0001c0001t0004g0182a0001c0001t0004g0337a0001c0001t0030g0312others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-814_735-391del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283723
|
ACCCAGAT others(477): Show |
A | 1 | a0001c0002t0004g0274 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.735-814_735-331del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | |||||
| chr21:42283725
|
CCAGATGA others(51): Show |
C | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-834_735-777del others(58): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283725 | ||||||
| chr21:42283728
|
G | A | 17 | a0001c0001t0002g0229a0001c0001t0002g0242a0001c0001t0003g0125others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.735-832G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283728 | ||||||
| chr21:42283739
|
A | AC | 7 | a0001c0001t0002g0132a0001c0001t0002g0219a0001c0001t0003g0224others(4): Show | 7 | HG00408.hp1 HG01168.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-815dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | |||||
| chr21:42283739
|
ACCCCCCA others(55): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.735-804_735-743del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | |||||
| chr21:42283739
|
ACCCCCCA others(115): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.735-804_735-683del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | |||||
| chr21:42283739
|
ACCCCCCA others(236): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.735-804_735-562del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | |||||
| chr21:42283739
|
ACCCCCCA others(297): Show |
A | 1 | a0001c0001t0013g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.735-804_735-501del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | |||||
| chr21:42283740
|
CCCCCCAC others(53): Show |
C | 2 | a0001c0001t0001g0231a0001c0001t0002g0291 | 2 | HG01192.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.735-814_735-755del others(60): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283740 | |||||
| chr21:42283740
|
CCCCCCAC others(295): Show |
C | 7 | a0001c0001t0001g0124a0001c0001t0001g0197a0001c0001t0001g0207others(4): Show | 7 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-814_735-513del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283740 | |||||
| chr21:42283740
|
CCCCCCAC others(355): Show |
C | 4 | a0001c0001t0001g0335a0001c0001t0002g0266a0001c0001t0011g0045others(1): Show | 4 | HG01978.hp1 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-814_735-453del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283740 | |||||
| chr21:42283756
|
T | C | 31 | a0001c0001t0001g0133a0001c0001t0001g0166a0001c0001t0001g0192others(28): Show | 32 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.735-804T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283756 | ||||||
| chr21:42283756
|
TGCCTGGA others(55): Show |
T | 2 | a0001c0001t0009g0322a0001c0001t0009g0323 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.735-790_735-729del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283756 | |||||
| chr21:42283770
|
T | C | 4 | a0001c0001t0002g0219a0001c0001t0006g0011a0001c0001t0029g0262others(1): Show | 4 | HG00408.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-790T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283770 | ||||||
| chr21:42283771
|
G | A | 3 | a0001c0001t0002g0219a0001c0001t0006g0011a0001c0003t0005g0048 | 3 | HG00408.hp1 HG02976.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.735-789G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283771 | ||||||
| chr21:42283775
|
TACCCCCC others(296): Show |
T | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.735-784_735-482del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283775 | ||||||
| chr21:42283776
|
A | C | 1 | a0001c0001t0002g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.735-784A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283776 | ||||||
| chr21:42283782
|
C | A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.735-778C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283782 | ||||||
| chr21:42283783
|
A | C | 4 | a0001c0001t0002g0219a0001c0001t0003g0228a0001c0001t0006g0011others(1): Show | 4 | HG00408.hp1 HG02976.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-777A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283783 | ||||||
| chr21:42283783
|
AACCCAGA others(357): Show |
A | 1 | a0001c0001t0018g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.735-776_735-413del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283783 | ||||||
| chr21:42283784
|
A | C | 1 | a0001c0001t0007g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.735-776A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283784 | ||||||
| chr21:42283784
|
A | G | 4 | a0001c0001t0002g0219a0001c0001t0003g0228a0001c0001t0006g0011others(1): Show | 4 | HG00408.hp1 HG02976.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-776A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283784 | ||||||
| chr21:42283784
|
ACCCAGAT others(174): Show |
A | 2 | a0001c0001t0013g0296a0001c0001t0023g0023 | 2 | HG01346.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.735-727_735-547del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | |||||
| chr21:42283784
|
ACCCAGAT others(235): Show |
A | 9 | a0001c0001t0002g0132a0001c0001t0002g0164a0001c0001t0002g0304others(6): Show | 9 | HG01069.hp1 HG01975.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.735-667_735-426del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | |||||
| chr21:42283784
|
ACCCAGAT others(295): Show |
A | 1 | a0001c0003t0008g0117 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.735-727_735-426del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | |||||
| chr21:42283784
|
ACCCAGAT others(356): Show |
A | 30 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0328others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.735-674_735-312del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | |||||
| chr21:42283789
|
G | A | 11 | a0001c0001t0004g0098a0001c0001t0004g0272a0001c0001t0004g0281others(8): Show | 11 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-771G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283789 | ||||||
| chr21:42283800
|
AC | A | 11 | a0001c0001t0003g0202a0001c0001t0004g0272a0001c0001t0004g0281others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-753delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283800 | |||||
| chr21:42283800
|
ACCCCCCC others(114): Show |
A | 1 | a0001c0001t0005g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.735-753_735-633del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283800 | |||||
| chr21:42283800
|
ACCCCCCC others(294): Show |
A | 1 | a0001c0001t0007g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.735-759_735-459del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283800 | ||||||
| chr21:42283800
|
ACCCCCCC others(357): Show |
A | 1 | a0001c0001t0004g0098 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.735-753_735-390del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283800 | |||||
| chr21:42283801
|
CCCCCCCA others(234): Show |
C | 4 | a0001c0001t0001g0248a0001c0001t0002g0115a0001c0001t0002g0180others(1): Show | 4 | HG01978.hp2 HG02056.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-752_735-512del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283801 | |||||
| chr21:42283801
|
CCCCCCCA others(355): Show |
C | 2 | a0001c0001t0001g0243a0001c0001t0002g0242 | 2 | HG00642.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.735-752_735-391del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283801 | |||||
| chr21:42283802
|
C | A | 8 | a0001c0001t0004g0272a0001c0001t0004g0281a0001c0001t0004g0319others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-758C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283802 | ||||||
| chr21:42283802
|
C | T | 1 | a0001c0001t0003g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.735-758C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283802 | ||||||
| chr21:42283814
|
G | T | 8 | a0001c0001t0004g0272a0001c0001t0004g0281a0001c0001t0004g0319others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-746G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283814 | ||||||
| chr21:42283818
|
C | T | 3 | a0001c0001t0003g0202a0001c0001t0004g0339a0001c0001t0007g0019 | 3 | HG01255.hp2 HG02148.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.735-742C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283818 | ||||||
| chr21:42283819
|
G | A | 8 | a0001c0001t0004g0272a0001c0001t0004g0281a0001c0001t0004g0319others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-741G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283819 | ||||||
| chr21:42283826
|
C | T | 1 | a0001c0001t0004g0339 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.735-734C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283826 | ||||||
| chr21:42283832
|
C | T | 14 | a0001c0001t0002g0090a0001c0001t0003g0002a0001c0001t0004g0272others(11): Show | 15 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.735-728C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283832 | ||||||
| chr21:42283833
|
A | G | 18 | a0001c0001t0002g0090a0001c0001t0002g0219a0001c0001t0003g0002others(15): Show | 19 | HG00408.hp1 HG01081.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.735-727A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283833 | ||||||
| chr21:42283833
|
AAAGTCCC others(113): Show |
A | 1 | a0001c0005t0008g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.735-716_735-597del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283833 | |||||
| chr21:42283833
|
AAAGTCCC others(295): Show |
A | 1 | a0001c0001t0003g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.735-716_735-415del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283833 | |||||
| chr21:42283837
|
T | TAC | 8 | a0001c0001t0004g0272a0001c0001t0004g0281a0001c0001t0004g0319others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-723_735-722ins others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283837 | ||||||
| chr21:42283837
|
TCCCCCCG others(114): Show |
T | 19 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0238others(16): Show | 19 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.735-667_735-547del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283837 | |||||
| chr21:42283837
|
TCCCCCCG others(175): Show |
T | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.735-546_735-365del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283837 | |||||
| chr21:42283837
|
TCCCCCCG others(294): Show |
T | 4 | a0001c0001t0002g0090a0001c0001t0003g0002a0001c0001t0004g0329others(1): Show | 5 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-722_735-422del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283837 | ||||||
| chr21:42283837
|
TCCCCCCG others(296): Show |
T | 3 | a0001c0001t0003g0079a0001c0001t0003g0202a0001c0001t0027g0344 | 3 | HG01081.hp2 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.735-614_735-312del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283837 | |||||
| chr21:42283843
|
C | A | 8 | a0001c0001t0004g0272a0001c0001t0004g0281a0001c0001t0004g0319others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-717C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283843 | ||||||
| chr21:42283844
|
G | A | 8 | a0001c0001t0004g0272a0001c0001t0004g0281a0001c0001t0004g0319others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-716G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283844 | ||||||
| chr21:42283860
|
AC | A | 7 | a0001c0001t0001g0096a0001c0001t0004g0319a0001c0001t0012g0315others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-693delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283860 | |||||
| chr21:42283860
|
ACCCCCCC others(297): Show |
A | 2 | a0001c0001t0004g0272a0001c0001t0004g0281 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.735-693_735-390del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283860 | |||||
| chr21:42283861
|
CCCCCCCA others(113): Show |
C | 1 | a0001c0001t0003g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.735-692_735-573del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283861 | |||||
| chr21:42283861
|
CCCCCCCA others(174): Show |
C | 1 | a0001c0001t0002g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.735-692_735-512del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283861 | |||||
| chr21:42283862
|
C | A | 6 | a0001c0001t0004g0319a0001c0001t0012g0315a0001c0001t0014g0061others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-698C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283862 | ||||||
| chr21:42283877
|
C | T | 1 | a0001c0003t0006g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.735-683C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283877 | ||||||
| chr21:42283886
|
C | T | 8 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0002g0095others(5): Show | 8 | HG01167.hp1 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.735-674C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283886 | ||||||
| chr21:42283892
|
C | T | 22 | a0001c0001t0001g0133a0001c0001t0001g0166a0001c0001t0001g0192others(19): Show | 22 | HG01167.hp1 HG02040.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.735-668C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283892 | ||||||
| chr21:42283893
|
A | G | 37 | a0001c0001t0001g0097a0001c0001t0001g0133a0001c0001t0001g0166others(34): Show | 37 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.735-667A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283893 | ||||||
| chr21:42283897
|
T | TACCCCCC others(121): Show |
1 | a0001c0001t0002g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.735-663_735-662ins others(128): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283897 | ||||||
| chr21:42283897
|
T | TC | 11 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0003g0227others(8): Show | 11 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-657dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283897 | |||||
| chr21:42283897
|
TCCCCCCG others(113): Show |
T | 5 | a0001c0001t0001g0133a0001c0001t0001g0166a0001c0001t0001g0204others(2): Show | 5 | NA18956.hp2 NA18973.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-662_735-543del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283897 | ||||||
| chr21:42283897
|
TCCCCCCG others(234): Show |
T | 3 | a0001c0001t0001g0192a0001c0001t0001g0247a0001c0001t0002g0218 | 3 | HG02071.hp2 NA18948.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.735-662_735-422del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283897 | ||||||
| chr21:42283898
|
C | A | 3 | a0001c0001t0001g0206a0001c0001t0026g0318a0001c0003t0006g0044 | 3 | HG02132.hp1 HG03098.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.735-662C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283898 | ||||||
| chr21:42283898
|
CCCCCCGC others(113): Show |
C | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.735-656_735-537del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283898 | |||||
| chr21:42283898
|
CCCCCCGC others(174): Show |
C | 1 | a0001c0001t0014g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.735-656_735-476del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283898 | |||||
| chr21:42283898
|
CCCCCCGC others(295): Show |
C | 1 | a0001c0001t0002g0308 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.735-656_735-355del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283898 | |||||
| chr21:42283899
|
C | CCT | 7 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0002g0095others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-660_735-659ins others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283899 | |||||
| chr21:42283899
|
CCCCCGCC others(112): Show |
C | 1 | a0001c0001t0001g0206 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.735-656_735-538del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283899 | |||||
| chr21:42283899
|
CCCCCGCC others(173): Show |
C | 1 | a0001c0003t0006g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.735-656_735-477del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283899 | |||||
| chr21:42283900
|
CCCCGCCC others(111): Show |
C | 1 | a0001c0001t0026g0318 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.735-656_735-539del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283900 | |||||
| chr21:42283903
|
C | A | 2 | a0001c0001t0002g0219a0001c0003t0001g0250 | 2 | HG02040.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.735-657C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283903 | ||||||
| chr21:42283903
|
C | T | 7 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0002g0095others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-657C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283903 | ||||||
| chr21:42283904
|
G | A | 6 | a0001c0001t0002g0114a0001c0001t0002g0183a0001c0001t0002g0219others(3): Show | 6 | HG02040.hp1 HG02572.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-656G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283904 | ||||||
| chr21:42283908
|
A | G | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.735-652A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283908 | ||||||
| chr21:42283909
|
G | A | 1 | a0001c0001t0003g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-651G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283909 | ||||||
| chr21:42283921
|
CCCCCCCA others(295): Show |
C | 11 | a0001c0001t0002g0095a0001c0001t0003g0326a0001c0001t0004g0319others(8): Show | 11 | HG02280.hp1 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-632_735-331del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283921 | |||||
| chr21:42283922
|
C | A | 1 | a0001c0001t0003g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-638C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283922 | ||||||
| chr21:42283934
|
G | T | 1 | a0001c0001t0003g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-626G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283934 | ||||||
| chr21:42283938
|
C | T | 1 | a0001c0001t0005g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.735-622C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283938 | ||||||
| chr21:42283939
|
G | A | 1 | a0001c0001t0003g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-621G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283939 | ||||||
| chr21:42283946
|
C | T | 7 | a0001c0001t0001g0096a0001c0001t0004g0102a0001c0001t0004g0103others(4): Show | 8 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-614C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283946 | ||||||
| chr21:42283952
|
C | T | 17 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0338others(14): Show | 18 | HG00738.hp1 HG01109.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.735-608C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283952 | ||||||
| chr21:42283953
|
G | A | 18 | a0001c0001t0001g0082a0001c0001t0001g0186a0001c0001t0001g0213others(15): Show | 18 | HG00408.hp1 HG00642.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.735-607G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283953 | ||||||
| chr21:42283957
|
T | TACC | 4 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0004g0268others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-603_735-602ins others(3): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283957 | ||||||
| chr21:42283957
|
TC | T | 21 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0001g0231others(18): Show | 21 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.735-596delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283957 | |||||
| chr21:42283958
|
C | CCCCCCCG others(113): Show |
1 | a0001c0001t0006g0011 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.735-547_735-546ins others(120): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283958 | |||||
| chr21:42283958
|
CCCCCCCG others(235): Show |
C | 1 | a0001c0001t0001g0327 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.735-553_735-312del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283958 | |||||
| chr21:42283959
|
CCCCCCGC others(234): Show |
C | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-595_735-355del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283959 | |||||
| chr21:42283960
|
C | CT | 6 | a0001c0001t0001g0096a0001c0001t0001g0338a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-600_735-599ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283960 | ||||||
| chr21:42283962
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.735-598C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283962 | ||||||
| chr21:42283964
|
C | A | 2 | a0001c0001t0003g0298a0001c0001t0028g0306 | 2 | HG00738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.735-596C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283964 | ||||||
| chr21:42283964
|
C | T | 5 | a0001c0001t0001g0338a0001c0001t0004g0102a0001c0001t0004g0103others(2): Show | 5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-596C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283964 | ||||||
| chr21:42283965
|
G | A | 11 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0002g0189others(8): Show | 11 | HG00738.hp1 HG01109.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-595G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283965 | ||||||
| chr21:42283969
|
A | G | 3 | a0001c0001t0001g0338a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | HG01891.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.735-591A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283969 | ||||||
| chr21:42283970
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0003g0320others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-590G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283970 | ||||||
| chr21:42283981
|
A | C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.735-579A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283981 | ||||||
| chr21:42283982
|
CCCCCCCA others(174): Show |
C | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735-571_735-391del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283982 | |||||
| chr21:42283983
|
C | A | 5 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0003g0320others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-577C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283983 | ||||||
| chr21:42283995
|
G | T | 5 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0003g0320others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-565G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283995 | ||||||
| chr21:42284000
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0002g0222a0001c0001t0003g0320others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-560G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284000 | ||||||
| chr21:42284007
|
C | T | 3 | a0001c0001t0001g0338a0001c0001t0004g0339a0001c0008t0011g0042 | 3 | HG01934.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.735-553C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284007 | ||||||
| chr21:42284013
|
C | T | 15 | a0001c0001t0001g0097a0001c0001t0001g0186a0001c0001t0001g0338others(12): Show | 15 | HG00738.hp1 HG01891.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.735-547C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284013 | ||||||
| chr21:42284014
|
G | A | 10 | a0001c0001t0001g0082a0001c0001t0001g0213a0001c0001t0001g0290others(7): Show | 10 | HG00280.hp2 HG01109.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.735-546G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284014 | ||||||
| chr21:42284018
|
T | A | 5 | a0001c0001t0001g0133a0001c0001t0001g0166a0001c0001t0001g0204others(2): Show | 5 | NA18956.hp2 NA18973.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-542T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284018 | ||||||
| chr21:42284018
|
T | TA | 7 | a0001c0001t0001g0097a0001c0001t0001g0186a0001c0001t0002g0183others(4): Show | 7 | HG00738.hp1 HG01891.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-542_735-541ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284018 | ||||||
| chr21:42284018
|
T | TACC | 4 | a0001c0001t0002g0222a0001c0001t0003g0234a0001c0001t0003g0310others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-542_735-541ins others(3): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284018 | ||||||
| chr21:42284018
|
TC | T | 10 | a0001c0001t0001g0082a0001c0001t0001g0290a0001c0001t0002g0189others(7): Show | 10 | HG00280.hp2 HG00408.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.735-535delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284018 | |||||
| chr21:42284018
|
TCCCCCCC others(115): Show |
T | 1 | a0001c0001t0028g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.735-535_735-414del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284018 | |||||
| chr21:42284018
|
TCCCCCCC others(175): Show |
T | 1 | a0001c0001t0002g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.735-535_735-354del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284018 | |||||
| chr21:42284019
|
C | A | 1 | a0001c0002t0002g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.735-541C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284019 | ||||||
| chr21:42284022
|
C | T | 1 | a0001c0008t0011g0042 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.735-538C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284022 | ||||||
| chr21:42284022
|
CCCCGCCC others(50): Show |
C | 1 | a0001c0002t0002g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.735-534_735-478del others(57): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284022 | |||||
| chr21:42284023
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.735-537C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284023 | ||||||
| chr21:42284025
|
C | A | 13 | a0001c0001t0001g0097a0001c0001t0001g0133a0001c0001t0001g0166others(10): Show | 13 | HG01891.hp2 HG02040.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-535C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284025 | ||||||
| chr21:42284025
|
C | T | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.735-535C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284025 | ||||||
| chr21:42284026
|
G | A | 59 | a0001c0001t0001g0097a0001c0001t0001g0108a0001c0001t0001g0133others(56): Show | 60 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.735-534G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284026 | ||||||
| chr21:42284026
|
G | GCCCAGAT others(178): Show |
1 | a0001c0001t0010g0301 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.735-486_735-485ins others(185): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284026 | |||||
| chr21:42284026
|
G | GCCCAGAT others(179): Show |
1 | a0001c0001t0010g0303 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.735-486_735-485ins others(186): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284026 | |||||
| chr21:42284031
|
G | A | 5 | a0001c0001t0002g0222a0001c0001t0003g0234a0001c0001t0003g0310others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-529G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284031 | ||||||
| chr21:42284039
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.735-521G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284039 | ||||||
| chr21:42284042
|
A | ACCCCCCC others(179): Show |
1 | a0001c0001t0010g0302 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.735-486_735-485ins others(186): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284042 | |||||
| chr21:42284042
|
AC | A | 8 | a0001c0001t0002g0183a0001c0001t0002g0219a0001c0001t0002g0222others(5): Show | 8 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-511delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284042 | |||||
| chr21:42284044
|
C | A | 6 | a0001c0001t0002g0183a0001c0001t0002g0222a0001c0001t0003g0234others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-516C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284044 | ||||||
| chr21:42284056
|
G | T | 6 | a0001c0001t0002g0183a0001c0001t0002g0222a0001c0001t0003g0234others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-504G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284056 | ||||||
| chr21:42284060
|
C | T | 3 | a0001c0001t0002g0219a0001c0001t0008g0194a0001c0001t0008g0195 | 3 | HG00741.hp1 HG01192.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.735-500C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284060 | ||||||
| chr21:42284061
|
G | A | 6 | a0001c0001t0002g0183a0001c0001t0002g0222a0001c0001t0003g0234others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-499G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284061 | ||||||
| chr21:42284068
|
C | T | 2 | a0001c0001t0003g0224a0001c0001t0004g0339 | 2 | HG03942.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.735-492C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284068 | ||||||
| chr21:42284074
|
C | T | 10 | a0001c0001t0002g0183a0001c0001t0002g0219a0001c0001t0002g0222others(7): Show | 10 | HG02040.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.735-486C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284074 | ||||||
| chr21:42284075
|
A | G | 13 | a0001c0001t0001g0082a0001c0001t0001g0336a0001c0001t0002g0183others(10): Show | 13 | HG01109.hp1 HG02040.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-485A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284075 | ||||||
| chr21:42284079
|
T | C | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.735-481T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284079 | ||||||
| chr21:42284079
|
T | TAC | 5 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0003g0234others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-481_735-480ins others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284079 | ||||||
| chr21:42284079
|
TCCCCCCG others(52): Show |
T | 1 | a0001c0003t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.735-480_735-422del others(59): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284079 | ||||||
| chr21:42284079
|
TCCCCCCG others(54): Show |
T | 5 | a0001c0001t0003g0320a0001c0001t0009g0322a0001c0001t0009g0323others(2): Show | 5 | HG01123.hp1 HG01934.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-425_735-365del others(61): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284079 | |||||
| chr21:42284080
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.735-480C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284080 | ||||||
| chr21:42284080
|
CCCCCCGC others(52): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.735-474_735-416del others(59): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284080 | |||||
| chr21:42284080
|
CCCCCCGC others(113): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.735-474_735-355del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284080 | |||||
| chr21:42284085
|
C | A | 7 | a0001c0001t0002g0120a0001c0001t0002g0219a0001c0001t0002g0222others(4): Show | 7 | HG02132.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-475C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284085 | ||||||
| chr21:42284085
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735-475C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284085 | ||||||
| chr21:42284086
|
G | A | 33 | a0001c0001t0001g0091a0001c0001t0001g0156a0001c0001t0001g0171others(30): Show | 33 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.735-474G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284086 | ||||||
| chr21:42284091
|
G | A | 2 | a0001c0001t0003g0310a0001c0002t0002g0282 | 2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-469G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284091 | ||||||
| chr21:42284103
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735-457C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284103 | ||||||
| chr21:42284104
|
C | A | 2 | a0001c0001t0003g0310a0001c0002t0002g0282 | 2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-456C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284104 | ||||||
| chr21:42284109
|
C | A | 1 | a0001c0001t0005g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.735-451C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284109 | ||||||
| chr21:42284116
|
G | T | 2 | a0001c0001t0003g0310a0001c0002t0002g0282 | 2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-444G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284116 | ||||||
| chr21:42284120
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.735-440C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284120 | ||||||
| chr21:42284121
|
G | A | 2 | a0001c0001t0003g0310a0001c0002t0002g0282 | 2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-439G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284121 | ||||||
| chr21:42284128
|
C | T | 9 | a0001c0001t0001g0271a0001c0001t0001g0336a0001c0001t0001g0338others(6): Show | 9 | HG01433.hp1 HG01515.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.735-432C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284128 | ||||||
| chr21:42284134
|
C | T | 30 | a0001c0001t0001g0133a0001c0001t0001g0166a0001c0001t0001g0186others(27): Show | 30 | HG00280.hp2 HG00621.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.735-426C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284134 | ||||||
| chr21:42284135
|
G | A | 61 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0097others(58): Show | 61 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.735-425G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284135 | ||||||
| chr21:42284139
|
T | A | 8 | a0001c0001t0001g0192a0001c0001t0001g0247a0001c0001t0002g0090others(5): Show | 9 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.735-421T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284139 | ||||||
| chr21:42284139
|
T | TA | 19 | a0001c0001t0001g0133a0001c0001t0001g0166a0001c0001t0001g0186others(16): Show | 19 | HG00280.hp2 HG01074.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.735-421_735-420ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284139 | ||||||
| chr21:42284139
|
TC | T | 63 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0097others(60): Show | 63 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.735-414delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284139 | |||||
| chr21:42284140
|
C | CCCCCCCG others(53): Show |
1 | a0001c0001t0006g0011 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.735-371_735-312dup others(60): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284140 | |||||
| chr21:42284140
|
CCCCCCCG others(53): Show |
C | 4 | a0001c0001t0001g0213a0001c0001t0002g0309a0001c0002t0002g0094others(1): Show | 4 | HG01934.hp1 HG02129.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-371_735-312del others(60): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284140 | |||||
| chr21:42284142
|
C | CT | 5 | a0001c0001t0001g0271a0001c0001t0001g0338a0001c0001t0002g0273others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-418_735-417ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284142 | ||||||
| chr21:42284146
|
C | A | 45 | a0001c0001t0001g0133a0001c0001t0001g0155a0001c0001t0001g0166others(42): Show | 48 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.735-414C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284146 | ||||||
| chr21:42284146
|
C | G | 1 | a0001c0001t0003g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.735-414C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284146 | ||||||
| chr21:42284146
|
C | T | 5 | a0001c0001t0001g0271a0001c0001t0001g0338a0001c0001t0002g0273others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-414C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284146 | ||||||
| chr21:42284147
|
G | A | 46 | a0001c0001t0001g0133a0001c0001t0001g0155a0001c0001t0001g0166others(43): Show | 49 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.735-413G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284147 | ||||||
| chr21:42284151
|
A | G | 3 | a0001c0001t0002g0273a0001c0001t0004g0339a0001c0001t0015g0285 | 3 | HG02723.hp1 HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.735-409A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284151 | ||||||
| chr21:42284152
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735-408G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284152 | ||||||
| chr21:42284164
|
CCCCCCCA others(52): Show |
C | 2 | a0001c0001t0001g0338a0001c0001t0004g0339 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.735-389_735-331del others(59): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284164 | |||||
| chr21:42284165
|
C | A | 4 | a0001c0001t0003g0310a0001c0001t0004g0098a0001c0001t0004g0272others(1): Show | 4 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-395C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284165 | ||||||
| chr21:42284165
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.735-395C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284165 | ||||||
| chr21:42284181
|
C | T | 1 | a0001c0001t0007g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.735-379C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284181 | ||||||
| chr21:42284182
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.735-378G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284182 | ||||||
| chr21:42284189
|
C | T | 7 | a0001c0001t0002g0189a0001c0001t0002g0220a0001c0001t0002g0277others(4): Show | 7 | HG01433.hp1 HG01515.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-371C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284189 | ||||||
| chr21:42284195
|
C | T | 7 | a0001c0001t0002g0189a0001c0001t0002g0220a0001c0001t0002g0277others(4): Show | 7 | HG01433.hp1 HG01515.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-365C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284195 | ||||||
| chr21:42284196
|
A | G | 14 | a0001c0001t0001g0271a0001c0001t0002g0188a0001c0001t0002g0189others(11): Show | 14 | HG01257.hp2 HG01433.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.735-364A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284196 | ||||||
| chr21:42284202
|
C | T | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-358C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284202 | ||||||
| chr21:42284206
|
C | G | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.735-354C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284206 | ||||||
| chr21:42284206
|
C | T | 3 | a0001c0001t0015g0285a0001c0001t0017g0005a0001c0002t0016g0343 | 4 | HG01109.hp2 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-354C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284206 | ||||||
| chr21:42284206
|
CGCCCAGA others(55): Show |
C | 2 | a0001c0001t0004g0337a0001c0001t0030g0312 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.735-329_735-268del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284206 | |||||
| chr21:42284211
|
A | G | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-349A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284211 | ||||||
| chr21:42284223
|
A | C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.735-337A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284223 | ||||||
| chr21:42284225
|
C | A | 1 | a0001c0001t0003g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.735-335C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284225 | ||||||
| chr21:42284262
|
CCT | C | 26 | a0001c0001t0002g0229a0001c0001t0002g0242a0001c0001t0003g0071others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.735-296_735-295del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284262 | |||||
| chr21:42284268
|
T | C | 27 | a0001c0001t0002g0229a0001c0001t0002g0242a0001c0001t0003g0071others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.735-292T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284268 | ||||||
| chr21:42284285
|
A | AC | 29 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0159others(26): Show | 30 | HG00735.hp1 HG01081.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.735-266dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284285 | |||||
| chr21:42284320
|
C | T | 4 | a0001c0001t0001g0334a0001c0001t0004g0264a0001c0001t0006g0063others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-240C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284320 | ||||||
| chr21:42284344
|
A | T | 1 | a0001c0001t0006g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.735-216A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284344 | ||||||
| chr21:42284520
|
T | G | 3 | a0001c0001t0002g0273a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | HG01891.hp1 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735-40T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284520 | ||||||
| chr21:42284534
|
G | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0324 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.735-26G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284534 | ||||||
| chr21:42284536
|
C | T | 1 | a0001c0001t0006g0012 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.735-24C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284536 | ||||||
| chr21:42284540
|
C | T | 89 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0091others(86): Show | 90 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.735-20C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284540 | ||||||
| chr21:42284692
|
G | A | 1 | a0001c0001t0005g0030 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.858+9G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284692 | ||||||
| chr21:42284697
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.858+14G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284697 | ||||||
| chr21:42284739
|
AATGACAC others(47): Show |
A | 16 | a0001c0001t0001g0076a0001c0001t0001g0316a0001c0001t0002g0095others(13): Show | 16 | HG01884.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.858+82_858+135delT others(53): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr21 | 42284739 | |||||
| chr21:42284765
|
T | A | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+82T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284765 | ||||||
| chr21:42284781
|
G | A | 3 | a0001c0001t0001g0327a0001c0001t0002g0090a0001c0001t0004g0329 | 3 | HG01081.hp1 HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+98G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284781 | ||||||
| chr21:42284788
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+105G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284788 | ||||||
| chr21:42284788
|
GTCTTCAT others(47): Show |
G | 2 | a0001c0001t0004g0093a0001c0001t0029g0262 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.858+148_858+201del others(54): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr21 | 42284788 | |||||
| chr21:42284831
|
G | C | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+148G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284831 | ||||||
| chr21:42284835
|
A | G | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+152A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284835 | ||||||
| chr21:42284840
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+157G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284840 | ||||||
| chr21:42284841
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+158C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284841 | ||||||
| chr21:42284842
|
A | G | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+159A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284842 | ||||||
| chr21:42284854
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+171C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284854 | ||||||
| chr21:42284871
|
ACAGCCTT others(39): Show |
A | 1 | a0001c0001t0001g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.858+189_858+234del others(46): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284871 | ||||||
| chr21:42284872
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+189C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284872 | ||||||
| chr21:42284873
|
A | G | 2 | a0001c0001t0002g0090a0001c0001t0004g0329 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+190A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284873 | ||||||
| chr21:42284935
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0002g0219a0001c0001t0002g0222others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.858+252G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284935 | ||||||
| chr21:42285058
|
T | C | 1 | a0001c0001t0012g0307 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.858+375T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285058 | ||||||
| chr21:42285136
|
G | C | 1 | a0001c0001t0002g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.858+453G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285136 | ||||||
| chr21:42285173
|
C | T | 1 | a0001c0001t0010g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.858+490C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285173 | ||||||
| chr21:42285190
|
C | G | 15 | a0001c0001t0001g0096a0001c0001t0001g0317a0001c0001t0001g0336others(12): Show | 15 | HG01261.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.858+507C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285190 | ||||||
| chr21:42285196
|
G | C | 15 | a0001c0001t0001g0096a0001c0001t0001g0317a0001c0001t0001g0336others(12): Show | 15 | HG01261.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.858+513G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285196 | ||||||
| chr21:42285220
|
A | G | 202 | a0001c0001t0001g0108a0001c0001t0001g0133a0001c0001t0001g0142others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.858+537A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285220 | ||||||
| chr21:42285363
|
C | T | 15 | a0001c0001t0002g0090a0001c0001t0004g0093a0001c0001t0004g0098others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.859-517C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285363 | ||||||
| chr21:42285438
|
G | A | 46 | a0001c0001t0002g0229a0001c0001t0002g0242a0001c0001t0003g0071others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.859-442G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285438 | ||||||
| chr21:42285505
|
C | CA | 6 | a0001c0001t0002g0121a0001c0001t0002g0273a0001c0001t0004g0102others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-362dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr21 | 42285505 | |||||
| chr21:42285615
|
A | C | 203 | a0001c0001t0001g0108a0001c0001t0001g0133a0001c0001t0001g0142others(200): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.859-265A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285615 | ||||||
| chr21:42285741
|
G | C | 5 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0002t0002g0094others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-139G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285741 | ||||||
| chr21:42286063
|
G | T | 2 | a0001c0001t0001g0211a0001c0001t0006g0287 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.973+69G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286063 | ||||||
| chr21:42286204
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.973+210C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286204 | ||||||
| chr21:42286486
|
A | G | 4 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0002g0266others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+492A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286486 | ||||||
| chr21:42286618
|
C | T | 1 | a0001c0001t0004g0339 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.973+624C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286618 | ||||||
| chr21:42286637
|
G | A | 1 | a0001c0007t0015g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.973+643G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286637 | ||||||
| chr21:42286666
|
G | A | 70 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0091others(67): Show | 71 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.973+672G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286666 | ||||||
| chr21:42286723
|
C | G | 11 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0271others(8): Show | 12 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.973+729C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286723 | ||||||
| chr21:42286790
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.973+796A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286790 | ||||||
| chr21:42286834
|
T | C | 249 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0091others(246): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.973+840T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286834 | ||||||
| chr21:42286846
|
G | A | 1 | a0001c0001t0006g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.973+852G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286846 | ||||||
| chr21:42286885
|
G | A | 20 | a0001c0001t0001g0108a0001c0001t0001g0198a0001c0001t0002g0107others(17): Show | 21 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.973+891G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286885 | ||||||
| chr21:42286991
|
C | G | 183 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0096others(180): Show | 187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.974-898C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286991 | ||||||
| chr21:42287082
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.974-807G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287082 | ||||||
| chr21:42287216
|
C | T | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.974-673C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287216 | ||||||
| chr21:42287318
|
C | A | 2 | a0001c0001t0003g0071a0001c0001t0010g0144 | 2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.974-571C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287318 | ||||||
| chr21:42287345
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0005g0040 | 2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.974-544G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287345 | ||||||
| chr21:42287355
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0155a0001c0002t0002g0270 | 3 | HG02486.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.974-534A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287355 | ||||||
| chr21:42287356
|
C | T | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.974-533C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287356 | ||||||
| chr21:42287436
|
T | C | 27 | a0001c0001t0003g0002a0001c0001t0003g0225a0001c0001t0003g0239others(24): Show | 29 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.974-453T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287436 | ||||||
| chr21:42287481
|
G | A | 1 | a0001c0001t0003g0326 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.974-408G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287481 | ||||||
| chr21:42287663
|
T | C | 1 | a0001c0001t0012g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.974-226T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287663 | ||||||
| chr21:42287674
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.974-215G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287674 | ||||||
| chr21:42287871
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.974-18C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287871 | ||||||
| chr21:42288088
|
G | A | 2 | a0001c0001t0004g0269a0001c0012t0004g0276 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1122+51G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/14 | chr21 | 42288088 | ||||||
| chr21:42288170
|
G | A | 3 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0003g0116 | 3 | HG02080.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1123-41G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/14 | chr21 | 42288170 | ||||||
| chr21:42288321
|
G | GC | 113 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0284others(110): Show | 116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1224+12dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr21 | 42288321 | |||||
| chr21:42288380
|
C | T | 16 | a0001c0001t0002g0273a0001c0001t0004g0093a0001c0001t0004g0098others(13): Show | 16 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1224+68C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288380 | ||||||
| chr21:42288407
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+95G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288407 | ||||||
| chr21:42288640
|
G | A | 1 | a0001c0001t0005g0017 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1224+328G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288640 | ||||||
| chr21:42288656
|
C | T | 115 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0002g0073others(112): Show | 118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1224+344C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288656 | ||||||
| chr21:42288729
|
A | G | 7 | a0001c0001t0009g0085a0001c0001t0009g0275a0001c0001t0009g0322others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1224+417A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288729 | ||||||
| chr21:42288766
|
G | GAAGGA | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1224+467_1224+471d others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr21 | 42288766 | |||||
| chr21:42288814
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1224+502G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288814 | ||||||
| chr21:42288880
|
C | T | 132 | a0001c0001t0001g0096a0001c0001t0001g0155a0001c0001t0001g0198others(129): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1224+568C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288880 | ||||||
| chr21:42288927
|
A | T | 3 | a0001c0001t0013g0294a0001c0001t0013g0295a0001c0001t0013g0296 | 3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1224+615A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288927 | ||||||
| chr21:42288999
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1224+687G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288999 | ||||||
| chr21:42289074
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1224+762C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289074 | ||||||
| chr21:42289081
|
A | G | 6 | a0001c0001t0009g0085a0001c0001t0009g0275a0001c0001t0009g0322others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1224+769A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289081 | ||||||
| chr21:42289101
|
T | C | 19 | a0001c0001t0001g0155a0001c0001t0009g0085a0001c0001t0009g0275others(16): Show | 20 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1224+789T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289101 | ||||||
| chr21:42289277
|
G | A | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1225-773G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289277 | ||||||
| chr21:42289524
|
G | A | 1 | a0001c0011t0004g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1225-526G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289524 | ||||||
| chr21:42289544
|
G | A | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-506G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289544 | ||||||
| chr21:42289556
|
A | C | 105 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0002g0073others(102): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1225-494A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289556 | ||||||
| chr21:42289564
|
A | G | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1225-486A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289564 | ||||||
| chr21:42289572
|
T | G | 229 | a0001c0001t0001g0096a0001c0001t0001g0145a0001c0001t0001g0155others(226): Show | 234 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1225-478T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289572 | ||||||
| chr21:42289590
|
C | T | 86 | a0001c0001t0001g0145a0001c0001t0001g0284a0001c0001t0001g0328others(83): Show | 87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1225-460C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289590 | ||||||
| chr21:42289611
|
G | A | 1 | a0001c0001t0003g0002 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1225-439G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289611 | ||||||
| chr21:42289838
|
G | T | 1 | a0001c0001t0026g0318 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1225-212G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289838 | ||||||
| chr21:42289845
|
C | T | 2 | a0001c0001t0004g0279a0001c0001t0014g0062 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1225-205C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289845 | ||||||
| chr21:42289846
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1225-204G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289846 | ||||||
| chr21:42289900
|
T | A | 1 | a0001c0011t0004g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1225-150T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289900 | ||||||
| chr21:42289938
|
C | T | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-112C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289938 | ||||||
| chr21:42289942
|
C | T | 116 | a0001c0001t0001g0096a0001c0001t0002g0073a0001c0001t0002g0075others(113): Show | 119 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1225-108C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289942 | ||||||
| chr21:42289984
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1225-66C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289984 | ||||||
| chr21:42289986
|
G | T | 116 | a0001c0001t0001g0096a0001c0001t0002g0073a0001c0001t0002g0075others(113): Show | 119 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1225-64G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289986 | ||||||
| chr21:42290001
|
C | T | 3 | a0001c0001t0003g0109a0001c0001t0005g0010a0001c0001t0005g0025 | 3 | NA18612.hp1 NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1225-49C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42290001 | ||||||
| chr21:42290020
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1225-30G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42290020 | ||||||
| chr21:42290045
|
C | T | 1 | a0001c0003t0001g0250 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.1225-5C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42290045 | ||||||
| chr21:42290232
|
C | T | 1 | a0001c0002t0004g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1393+14C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290232 | ||||||
| chr21:42290266
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1393+48C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290266 | ||||||
| chr21:42290338
|
A | T | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1393+120A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290338 | ||||||
| chr21:42290549
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0171 | 2 | HG01070.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1393+331G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290549 | ||||||
| chr21:42290644
|
T | TG | 12 | a0001c0002t0002g0078a0001c0002t0002g0094a0001c0002t0002g0143others(9): Show | 13 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1393+428dupG | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr21 | 42290644 | |||||
| chr21:42290664
|
G | A | 84 | a0001c0001t0001g0145a0001c0001t0001g0284a0001c0001t0001g0328others(81): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1394-428G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290664 | ||||||
| chr21:42290752
|
C | A | 1 | a0001c0001t0003g0224 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1394-340C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290752 | ||||||
| chr21:42290799
|
C | G | 94 | a0001c0001t0001g0145a0001c0001t0001g0284a0001c0001t0001g0328others(91): Show | 95 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1394-293C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290799 | ||||||
| chr21:42290984
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0199a0001c0001t0001g0246others(1): Show | 4 | HG02080.hp1 HG02523.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-108G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290984 | ||||||
| chr21:42291002
|
G | A | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1394-90G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42291002 | ||||||
| chr21:42291258
|
A | T | 9 | a0001c0002t0002g0078a0001c0002t0002g0094a0001c0002t0002g0143others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+66A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 12/14 | chr21 | 42291258 | ||||||
| chr21:42291473
|
G | A | 1 | a0001c0001t0004g0267 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1495-25G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 12/14 | chr21 | 42291473 | ||||||
| chr21:42291475
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1495-23G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 12/14 | chr21 | 42291475 | ||||||
| chr21:42291695
|
T | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0135a0001c0001t0003g0136others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1653+39T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291695 | ||||||
| chr21:42291697
|
G | GGCTTCCC others(56): Show |
1 | a0001c0001t0007g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1653+42_1653+104du others(64): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42291697 | |||||
| chr21:42291748
|
C | A | 30 | a0001c0001t0001g0091a0001c0001t0002g0090a0001c0001t0002g0095others(27): Show | 30 | HG01081.hp1 HG01081.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1653+92C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291748 | ||||||
| chr21:42291857
|
C | A | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1653+201C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291857 | ||||||
| chr21:42291879
|
C | T | 13 | a0001c0001t0002g0090a0001c0001t0002g0095a0001c0001t0003g0079others(10): Show | 13 | HG01081.hp2 HG01255.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1653+223C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291879 | ||||||
| chr21:42291939
|
G | A | 1 | a0001c0001t0003g0326 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1653+283G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291939 | ||||||
| chr21:42291939
|
G | T | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1653+283G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291939 | ||||||
| chr21:42291940
|
T | G | 11 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0002t0002g0078others(8): Show | 11 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1653+284T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291940 | ||||||
| chr21:42292034
|
C | T | 8 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0001t0004g0169others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1653+378C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292034 | ||||||
| chr21:42292037
|
C | T | 47 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0095others(44): Show | 47 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.1653+381C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292037 | ||||||
| chr21:42292151
|
T | C | 1 | a0001c0011t0004g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653+495T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292151 | ||||||
| chr21:42292235
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1653+579C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292235 | ||||||
| chr21:42292375
|
C | T | 1 | a0001c0011t0004g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653+719C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292375 | ||||||
| chr21:42292456
|
A | G | 1 | a0001c0001t0003g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1653+800A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292456 | ||||||
| chr21:42292507
|
C | T | 4 | a0001c0001t0002g0095a0001c0001t0003g0079a0001c0001t0007g0019others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+851C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292507 | ||||||
| chr21:42292602
|
A | G | 1 | a0001c0001t0003g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1653+946A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292602 | ||||||
| chr21:42292631
|
A | C | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1653+975A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292631 | ||||||
| chr21:42292632
|
C | A | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1653+976C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292632 | ||||||
| chr21:42292713
|
ACACACTA others(53): Show |
A | 1 | a0001c0001t0007g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1653+1072_1653+113 others(64): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42292713 | |||||
| chr21:42292769
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1653+1113C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292769 | ||||||
| chr21:42292820
|
C | T | 11 | a0001c0001t0004g0003a0001c0001t0004g0154a0001c0001t0004g0169others(8): Show | 12 | HG01257.hp1 HG01258.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653+1164C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292820 | ||||||
| chr21:42292840
|
ACACAGTA others(12): Show |
A | 3 | a0001c0001t0013g0294a0001c0001t0013g0295a0001c0001t0013g0296 | 3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1653+1189_1653+120 others(23): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42292840 | |||||
| chr21:42292961
|
C | CTACACAC others(30): Show |
3 | a0001c0001t0013g0294a0001c0001t0013g0295a0001c0001t0013g0296 | 3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1653+1342_1653+137 others(41): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42292961 | |||||
| chr21:42293072
|
C | CACACACC others(5): Show |
223 | a0001c0001t0001g0096a0001c0001t0001g0155a0001c0001t0001g0200others(220): Show | 228 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1653+1427_1653+142 others(16): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293072 | |||||
| chr21:42293072
|
C | CACACACC others(489): Show |
1 | a0001c0011t0004g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653+1427_1653+142 others(500): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293072 | |||||
| chr21:42293081
|
CACACACT others(46): Show |
C | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1654-1415_1654-136 others(57): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293081 | |||||
| chr21:42293083
|
C | G | 1 | a0001c0007t0015g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1653+1427C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293083 | ||||||
| chr21:42293097
|
CACACGGT others(30): Show |
C | 1 | a0001c0001t0002g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1654-1440_1654-140 others(41): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293097 | |||||
| chr21:42293101
|
C | T | 3 | a0001c0002t0004g0004a0001c0002t0004g0274a0001c0002t0016g0343 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654-1441C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293101 | ||||||
| chr21:42293102
|
G | A | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1440G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293102 | ||||||
| chr21:42293103
|
G | C | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1439G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293103 | ||||||
| chr21:42293118
|
T | G | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1424T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293118 | ||||||
| chr21:42293119
|
A | G | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1423A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293119 | ||||||
| chr21:42293120
|
C | T | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1422C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293120 | ||||||
| chr21:42293141
|
T | C | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1401T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293141 | ||||||
| chr21:42293216
|
C | CACA | 53 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0095others(50): Show | 55 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1654-1325_1654-132 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293216 | |||||
| chr21:42293228
|
TACACACC others(4): Show |
T | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1654-1302_1654-129 others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293228 | |||||
| chr21:42293246
|
CACACTAC others(7): Show |
C | 38 | a0001c0001t0002g0277a0001c0001t0004g0003a0001c0001t0004g0086others(35): Show | 40 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1654-1284_1654-127 others(18): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293246 | |||||
| chr21:42293287
|
GTACACAC others(9): Show |
G | 5 | a0001c0001t0002g0095a0001c0001t0003g0079a0001c0001t0004g0269others(2): Show | 5 | HG01081.hp2 HG01255.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-1241_1654-122 others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293287 | |||||
| chr21:42293317
|
G | A | 10 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0273others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-1225G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293317 | ||||||
| chr21:42293406
|
C | T | 33 | a0001c0001t0004g0003a0001c0001t0004g0086a0001c0001t0004g0092others(30): Show | 35 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1654-1136C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293406 | ||||||
| chr21:42293407
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0129 | 2 | NA18944.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1654-1135G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293407 | ||||||
| chr21:42293407
|
G | GCACTACA others(9): Show |
1 | a0001c0003t0006g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1654-1124_1654-110 others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293407 | |||||
| chr21:42293421
|
CCACACTA others(7): Show |
C | 3 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0003g0116 | 3 | HG02080.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1654-1115_1654-110 others(18): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293421 | |||||
| chr21:42293496
|
C | T | 10 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0273others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-1046C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293496 | ||||||
| chr21:42293500
|
T | C | 225 | a0001c0001t0001g0096a0001c0001t0001g0155a0001c0001t0001g0200others(222): Show | 230 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1654-1042T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293500 | ||||||
| chr21:42293538
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0190 | 2 | HG00438.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1654-1004C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293538 | ||||||
| chr21:42293600
|
C | G | 8 | a0001c0001t0002g0188a0001c0001t0002g0237a0001c0001t0002g0240others(5): Show | 8 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1654-942C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293600 | ||||||
| chr21:42293603
|
T | TACACACC others(11): Show |
3 | a0001c0001t0003g0079a0001c0001t0004g0269a0001c0001t0007g0019 | 3 | HG01081.hp2 HG01255.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1654-928_1654-927i others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293603 | |||||
| chr21:42293609
|
CCACACTA | C | 63 | a0001c0001t0001g0096a0001c0001t0001g0200a0001c0001t0001g0328others(60): Show | 64 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1654-920_1654-914d others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293609 | |||||
| chr21:42293669
|
C | T | 162 | a0001c0001t0001g0096a0001c0001t0001g0200a0001c0001t0001g0328others(159): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1654-873C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293669 | ||||||
| chr21:42293719
|
A | C | 10 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0273others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-823A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293719 | ||||||
| chr21:42293750
|
A | G | 1 | a0001c0007t0015g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1654-792A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293750 | ||||||
| chr21:42293756
|
TACATACC | T | 12 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0273others(9): Show | 12 | HG01081.hp2 HG01255.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1654-775_1654-769d others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293756 | |||||
| chr21:42293791
|
C | T | 1 | a0001c0001t0017g0005 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1654-751C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293791 | ||||||
| chr21:42293831
|
G | A | 53 | a0001c0001t0001g0155a0001c0001t0002g0090a0001c0001t0002g0095others(50): Show | 55 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1654-711G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293831 | ||||||
| chr21:42293877
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1654-665A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293877 | ||||||
| chr21:42293891
|
C | A | 1 | a0001c0001t0001g0338 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1654-651C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293891 | ||||||
| chr21:42293921
|
A | G | 5 | a0001c0001t0002g0081a0001c0001t0002g0134a0001c0001t0002g0137others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-621A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293921 | ||||||
| chr21:42293923
|
A | C | 5 | a0001c0001t0002g0081a0001c0001t0002g0134a0001c0001t0002g0137others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-619A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293923 | ||||||
| chr21:42293927
|
ACCACACA others(29): Show |
A | 6 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0134others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1654-607_1654-572d others(38): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293927 | |||||
| chr21:42293950
|
A | ACCACACA others(6): Show |
3 | a0001c0001t0004g0003a0001c0001t0011g0039a0001c0001t0022g0022 | 4 | HG01257.hp1 HG01258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-557_1654-545d others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293950 | |||||
| chr21:42293950
|
ACCACACA others(6): Show |
A | 190 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0096others(187): Show | 194 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1654-557_1654-545d others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293950 | |||||
| chr21:42293998
|
C | A | 1 | a0001c0001t0002g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1654-544C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293998 | ||||||
| chr21:42294064
|
G | A | 2 | a0001c0002t0002g0078a0001c0002t0002g0270 | 2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1654-478G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294064 | ||||||
| chr21:42294095
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1654-447C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294095 | ||||||
| chr21:42294204
|
A | G | 2 | a0001c0001t0009g0322a0001c0001t0009g0323 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1654-338A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294204 | ||||||
| chr21:42294211
|
C | G | 14 | a0001c0001t0004g0003a0001c0001t0004g0086a0001c0001t0004g0092others(11): Show | 15 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1654-331C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294211 | ||||||
| chr21:42294407
|
A | C | 223 | a0001c0001t0001g0172a0001c0001t0001g0177a0001c0001t0001g0199others(220): Show | 228 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1654-135A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294407 | ||||||
| chr21:42294437
|
A | T | 4 | a0001c0001t0002g0277a0001c0001t0004g0279a0001c0001t0012g0315others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-105A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294437 | ||||||
| chr21:42294456
|
G | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0324 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1654-86G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294456 | ||||||
| chr21:42294469
|
G | A | 30 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0091others(27): Show | 31 | HG00738.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1654-73G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294469 | ||||||
| chr21:42294670
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1772+10G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294670 | ||||||
| chr21:42294733
|
G | A | 1 | a0001c0001t0004g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1772+73G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294733 | ||||||
| chr21:42294825
|
C | T | 8 | a0001c0001t0003g0071a0001c0001t0003g0187a0001c0001t0003g0193others(5): Show | 8 | HG01074.hp2 HG01106.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1772+165C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294825 | ||||||
| chr21:42294887
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0029g0262a0001c0002t0016g0343 | 3 | HG02615.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1772+227G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294887 | ||||||
| chr21:42294903
|
A | C | 217 | a0001c0001t0001g0200a0001c0001t0002g0073a0001c0001t0002g0075others(214): Show | 222 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1772+243A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294903 | ||||||
| chr21:42294937
|
C | T | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+277C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294937 | ||||||
| chr21:42294978
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1772+318C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294978 | ||||||
| chr21:42295019
|
T | C | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+359T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295019 | ||||||
| chr21:42295046
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0235others(1): Show | 4 | HG02027.hp2 HG02083.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1772+386C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295046 | ||||||
| chr21:42295059
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1772+399G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295059 | ||||||
| chr21:42295066
|
A | C | 3 | a0001c0001t0010g0144a0001c0001t0010g0167a0001c0001t0010g0292 | 3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+406A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295066 | ||||||
| chr21:42295191
|
C | T | 12 | a0001c0001t0004g0003a0001c0001t0004g0154a0001c0001t0004g0169others(9): Show | 13 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772+531C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295191 | ||||||
| chr21:42295195
|
C | T | 1 | a0001c0001t0002g0188 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1772+535C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295195 | ||||||
| chr21:42295228
|
C | T | 164 | a0001c0001t0001g0200a0001c0001t0002g0073a0001c0001t0002g0075others(161): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1772+568C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295228 | ||||||
| chr21:42295286
|
G | A | 9 | a0001c0001t0002g0090a0001c0001t0002g0273a0001c0002t0002g0078others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1772+626G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295286 | ||||||
| chr21:42295325
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1772+665C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295325 | ||||||
| chr21:42295333
|
T | TA | 17 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0001g0198others(14): Show | 17 | HG00609.hp1 HG01257.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1772+717dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1772+708_1772+717d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
T | TAAAAAAA others(4): Show |
3 | a0001c0001t0001g0139a0001c0001t0006g0016a0001c0001t0006g0038 | 3 | HG02698.hp1 NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1772+707_1772+717d others(13): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
T | TAAAAAAA others(5): Show |
1 | a0001c0003t0006g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1772+706_1772+717d others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TA | T | 16 | a0001c0001t0001g0128a0001c0001t0001g0159a0001c0001t0001g0186others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1772+717delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAA | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0155others(4): Show | 7 | HG01884.hp1 HG02922.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1772+716_1772+717d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0010g0144a0001c0001t0010g0167 | 2 | HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+708_1772+717d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0009g0322a0001c0001t0009g0333 | 2 | HG02055.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1772+707_1772+717d others(13): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(5): Show |
T | 5 | a0001c0001t0002g0305a0001c0001t0003g0326a0001c0001t0009g0085others(2): Show | 5 | HG00140.hp1 HG02145.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1772+706_1772+717d others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1772+705_1772+717d others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(7): Show |
T | 11 | a0001c0001t0001g0338a0001c0001t0002g0230a0001c0001t0002g0286others(8): Show | 11 | HG00544.hp1 HG01106.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1772+704_1772+717d others(16): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(8): Show |
T | 30 | a0001c0001t0002g0080a0001c0001t0002g0095a0001c0001t0002g0115others(27): Show | 30 | HG00423.hp1 HG00544.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1772+703_1772+717d others(17): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(9): Show |
T | 123 | a0001c0001t0001g0200a0001c0001t0002g0073a0001c0001t0002g0075others(120): Show | 126 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1772+702_1772+717d others(18): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(10): Show |
T | 11 | a0001c0001t0001g0124a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG00099.hp1 HG00597.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1772+701_1772+717d others(19): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(11): Show |
T | 4 | a0001c0001t0001g0157a0001c0001t0001g0207a0001c0001t0006g0049others(1): Show | 4 | HG01261.hp1 NA18957.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1772+700_1772+717d others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(12): Show |
T | 13 | a0001c0001t0001g0097a0001c0001t0001g0142a0001c0001t0001g0171others(10): Show | 13 | HG00738.hp2 HG01167.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772+699_1772+717d others(21): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(13): Show |
T | 20 | a0001c0001t0001g0156a0001c0001t0002g0090a0001c0001t0002g0273others(17): Show | 21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1772+698_1772+717d others(22): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(14): Show |
T | 3 | a0001c0001t0001g0328a0001c0002t0002g0143a0001c0002t0002g0330 | 3 | HG02451.hp1 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1772+697_1772+717d others(23): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(15): Show |
T | 5 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0001t0004g0279others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1772+696_1772+717d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(16): Show |
T | 4 | a0001c0002t0004g0004a0001c0002t0004g0274a0001c0002t0016g0343others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1772+695_1772+717d others(25): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(17): Show |
T | 17 | a0001c0001t0002g0277a0001c0001t0004g0093a0001c0001t0004g0098others(14): Show | 17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1772+694_1772+717d others(26): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295333
|
TAAAAAAA others(19): Show |
T | 1 | a0001c0001t0001g0260 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1772+692_1772+717d others(28): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | |||||
| chr21:42295345
|
A | T | 1 | a0001c0001t0009g0322 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1772+685A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295345 | ||||||
| chr21:42295346
|
A | T | 1 | a0001c0001t0009g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1772+686A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295346 | ||||||
| chr21:42295422
|
T | A | 1 | a0001c0001t0004g0339 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1773-742T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295422 | ||||||
| chr21:42295463
|
A | T | 2 | a0001c0002t0002g0094a0001c0002t0002g0324 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1773-701A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295463 | ||||||
| chr21:42295479
|
C | T | 1 | a0001c0001t0005g0010 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1773-685C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295479 | ||||||
| chr21:42295485
|
G | A | 13 | a0001c0001t0004g0003a0001c0001t0004g0154a0001c0001t0004g0169others(10): Show | 14 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1773-679G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295485 | ||||||
| chr21:42295629
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1773-535A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295629 | ||||||
| chr21:42295691
|
T | C | 50 | a0001c0001t0002g0090a0001c0001t0002g0273a0001c0001t0002g0277others(47): Show | 52 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.1773-473T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295691 | ||||||
| chr21:42295749
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1773-415C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295749 | ||||||
| chr21:42295912
|
G | A | 165 | a0001c0001t0002g0073a0001c0001t0002g0075a0001c0001t0002g0080others(162): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1773-252G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295912 | ||||||
| chr21:42295988
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1773-176C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295988 | ||||||
| chr21:42296131
|
A | G | 52 | a0001c0001t0002g0090a0001c0001t0002g0273a0001c0001t0002g0277others(49): Show | 54 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.1773-33A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42296131 |