geneid | 64241 |
---|---|
ensemblid | ENSG00000143921.9 |
hgncid | 13887 |
symbol | ABCG8 |
name | ATP binding cassette subfamily G member 8 |
refseq_nuc | NM_022437.3 |
refseq_prot | NP_071882.1 |
ensembl_nuc | ENST00000272286.4 |
ensembl_prot | ENSP00000272286.2 |
mane_status | MANE Select |
chr | chr2 |
start | 43838971 |
end | 43882988 |
strand | + |
ver | v1.2 |
region | chr2:43838971-43882988 |
region5000 | chr2:43833971-43887988 |
regionname0 | ABCG8_chr2_43838971_43882988 |
regionname5000 | ABCG8_chr2_43833971_43887988 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 673 | 111 | 14 | 14 | 66 | 1 | 16 | 43 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002 | 0/0 | 673 | 78 | 23 | 20 | 22 | 4 | 9 | 19 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003 | 0/0 | 673 | 66 | 26 | 21 | 9 | 3 | 7 | 9 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0004 | 0/0 | 673 | 12 | 0 | 9 | 0 | 1 | 2 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005 | 1/1 | 673 | 12 | 2 | 6 | 0 | 1 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006 | 0/0 | 673 | 12 | 4 | 2 | 4 | 0 | 2 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007 | 0/0 | 673 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008 | 0/0 | 673 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0009 | 0/0 | 673 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0010 | 0/0 | 673 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0011 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0012 | 0/0 | 673 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0013 | 0/0 | 673 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0014 | 0/0 | 673 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0015 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0016 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0017 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0018 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2022 | 102 | 12 | 11 | 66 | 1 | 12 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0002 | 0/0 | 2022 | 51 | 18 | 16 | 9 | 3 | 5 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0003 | 0/0 | 2022 | 49 | 14 | 12 | 16 | 2 | 5 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0004 | 0/0 | 2022 | 27 | 9 | 8 | 5 | 2 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0005 | 0/0 | 2022 | 12 | 4 | 2 | 4 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0006 | 1/1 | 2022 | 12 | 2 | 6 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0007 | 0/0 | 2022 | 12 | 0 | 9 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0008 | 0/0 | 2022 | 9 | 2 | 3 | 0 | 0 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0009 | 0/0 | 2022 | 6 | 5 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0010 | 0/0 | 2022 | 4 | 1 | 1 | 0 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0011 | 0/0 | 2022 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0012 | 0/0 | 2022 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0013 | 0/0 | 2022 | 3 | 0 | 2 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0014 | 0/0 | 2022 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0015 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0016 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0017 | 0/0 | 2022 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0018 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0019 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0020 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0021 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0022 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0023 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0024 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0025 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0026 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0027 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0028 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0029 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0030 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
c0031 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5158 | 17 | 0 | 1 | 16 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0002 | 0/0 | 5155 | 17 | 6 | 9 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0003 | 0/0 | 5162 | 16 | 4 | 3 | 2 | 1 | 6 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0004 | 0/0 | 5162 | 15 | 0 | 3 | 7 | 1 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0005 | 0/0 | 5163 | 13 | 0 | 2 | 11 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0006 | 0/0 | 5158 | 13 | 0 | 7 | 6 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0007 | 0/0 | 5159 | 10 | 0 | 8 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0008 | 0/0 | 5159 | 9 | 3 | 4 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0009 | 0/0 | 5162 | 7 | 0 | 0 | 7 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0010 | 0/0 | 5162 | 7 | 6 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0011 | 0/0 | 5160 | 7 | 0 | 4 | 1 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0012 | 0/0 | 5159 | 7 | 7 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0013 | 0/0 | 5159 | 6 | 6 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0014 | 0/0 | 5160 | 5 | 0 | 1 | 0 | 0 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0015 | 0/0 | 5155 | 5 | 2 | 3 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0016 | 0/0 | 5164 | 5 | 0 | 0 | 5 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0017 | 0/0 | 5156 | 5 | 0 | 3 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0018 | 0/0 | 5158 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0019 | 0/0 | 5163 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0020 | 0/0 | 5156 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0021 | 0/0 | 5162 | 4 | 3 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0022 | 0/0 | 5155 | 4 | 2 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0023 | 0/0 | 5163 | 4 | 0 | 1 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0024 | 0/0 | 5160 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0025 | 0/0 | 5154 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0026 | 0/0 | 5159 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0027 | 0/0 | 5163 | 3 | 0 | 1 | 1 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0028 | 0/0 | 5156 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0029 | 0/0 | 5158 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0030 | 0/0 | 5160 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0031 | 0/0 | 5159 | 2 | 1 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0032 | 0/0 | 5159 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0033 | 0/0 | 5162 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0034 | 0/0 | 5163 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0035 | 0/0 | 5163 | 2 | 0 | 1 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0036 | 0/0 | 5163 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0037 | 0/0 | 5156 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0038 | 0/0 | 5162 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0039 | 0/0 | 5158 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0040 | 1/0 | 5159 | 2 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0041 | 0/0 | 5160 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0042 | 0/0 | 5161 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0043 | 0/0 | 5159 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0044 | 0/1 | 5159 | 2 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0045 | 0/0 | 5159 | 2 | 0 | 0 | 1 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0046 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0047 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0048 | 0/0 | 5165 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0049 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0050 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0051 | 0/0 | 5160 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0052 | 0/0 | 5159 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0053 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0054 | 0/0 | 5161 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0055 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0056 | 0/0 | 5160 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0057 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0058 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0059 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0060 | 0/0 | 5160 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0061 | 0/0 | 5159 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0062 | 0/0 | 5159 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0063 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0064 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0065 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0066 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0067 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0068 | 0/0 | 5163 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0069 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0070 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0071 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0072 | 0/0 | 5164 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0073 | 0/0 | 5160 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0074 | 0/0 | 5161 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0075 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0076 | 0/0 | 5163 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0077 | 0/0 | 5163 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0078 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0079 | 0/0 | 5160 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0080 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0081 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0082 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0083 | 0/0 | 5159 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0084 | 0/0 | 5160 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0085 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0086 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0087 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0088 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0089 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0090 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0091 | 0/0 | 5161 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0092 | 0/0 | 5160 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0093 | 0/0 | 5163 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0094 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0095 | 0/0 | 5160 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0096 | 0/0 | 5159 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0097 | 0/0 | 5158 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0098 | 0/0 | 5163 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0099 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0100 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0101 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0102 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0103 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0104 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0105 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0106 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0107 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0108 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0109 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0110 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0111 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0112 | 0/0 | 5160 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0113 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0114 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0115 | 0/0 | 5163 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0116 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0117 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0118 | 0/0 | 5163 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0119 | 0/0 | 5163 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0120 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0121 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0122 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
t0123 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
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 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2022 | 102 | 12 | 11 | 66 | 1 | 12 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008 | 0/0 | 2022 | 9 | 2 | 3 | 0 | 0 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003 | 0/0 | 2022 | 49 | 14 | 12 | 16 | 2 | 5 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004 | 0/0 | 2022 | 27 | 9 | 8 | 5 | 2 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0024 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0026 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002 | 0/0 | 2022 | 51 | 18 | 16 | 9 | 3 | 5 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0010 | 0/0 | 2022 | 4 | 1 | 1 | 0 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0011 | 0/0 | 2022 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0014 | 0/0 | 2022 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0017 | 0/0 | 2022 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0021 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0022 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0004c0007 | 0/0 | 2022 | 12 | 0 | 9 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006 | 1/1 | 2022 | 12 | 2 | 6 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005 | 0/0 | 2022 | 12 | 4 | 2 | 4 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007c0009 | 0/0 | 2022 | 6 | 5 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007c0020 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0015 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0016 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0018 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0009c0012 | 0/0 | 2022 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0010c0013 | 0/0 | 2022 | 3 | 0 | 2 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0011c0031 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0012c0030 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0013c0029 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0014c0027 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0015c0023 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0016c0025 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0017c0028 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0018c0019 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7179 | 17 | 0 | 1 | 16 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0004 | 0/0 | 7183 | 13 | 0 | 3 | 5 | 1 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0005 | 0/0 | 7184 | 11 | 0 | 2 | 9 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0009 | 0/0 | 7183 | 6 | 0 | 0 | 6 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0010 | 0/0 | 7183 | 7 | 6 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0014 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0015 | 0/0 | 7176 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0018 | 0/0 | 7179 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0019 | 0/0 | 7184 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0020 | 0/0 | 7177 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0031 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0032 | 0/0 | 7180 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0033 | 0/0 | 7183 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0034 | 0/0 | 7184 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0035 | 0/0 | 7184 | 2 | 0 | 1 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0036 | 0/0 | 7184 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0037 | 0/0 | 7177 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0038 | 0/0 | 7183 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0052 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0057 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0059 | 0/0 | 7179 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0060 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0061 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0062 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0063 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0064 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0065 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0067 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0069 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0071 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0072 | 0/0 | 7185 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0073 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0074 | 0/0 | 7182 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0075 | 0/0 | 7176 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0076 | 0/0 | 7184 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0001t0077 | 0/0 | 7184 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008t0008 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008t0014 | 0/0 | 7181 | 4 | 0 | 1 | 0 | 0 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008t0031 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008t0054 | 0/0 | 7182 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008t0058 | 0/0 | 7184 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0001c0008t0079 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0002 | 0/0 | 7176 | 7 | 3 | 3 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0003 | 0/0 | 7183 | 4 | 0 | 1 | 0 | 0 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0006 | 0/0 | 7179 | 10 | 0 | 6 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0012 | 0/0 | 7180 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0016 | 0/0 | 7185 | 5 | 0 | 0 | 5 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0017 | 0/0 | 7177 | 3 | 0 | 1 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0023 | 0/0 | 7184 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0027 | 0/0 | 7184 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0039 | 0/0 | 7179 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0045 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0048 | 0/0 | 7186 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0094 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0096 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0099 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0103 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0105 | 0/0 | 7185 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0106 | 0/0 | 7177 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0107 | 0/0 | 7179 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0111 | 0/0 | 7184 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0113 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0115 | 0/0 | 7184 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0003t0119 | 0/0 | 7184 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0008 | 0/0 | 7180 | 7 | 3 | 3 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0011 | 0/0 | 7181 | 7 | 0 | 4 | 1 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0013 | 0/0 | 7180 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0041 | 0/0 | 7181 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0042 | 0/0 | 7182 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0084 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0085 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0088 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0004t0091 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0024t0117 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0002c0026t0095 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0002 | 0/0 | 7176 | 7 | 1 | 5 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0003 | 0/0 | 7183 | 6 | 1 | 2 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0004 | 0/0 | 7183 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0005 | 0/0 | 7184 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0006 | 0/0 | 7179 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0008 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0009 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0017 | 0/0 | 7177 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0021 | 0/0 | 7183 | 4 | 3 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0022 | 0/0 | 7176 | 4 | 2 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0027 | 0/0 | 7184 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0028 | 0/0 | 7177 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0029 | 0/0 | 7179 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0046 | 0/0 | 7175 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0050 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0068 | 0/0 | 7184 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0081 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0092 | 0/0 | 7181 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0093 | 0/0 | 7184 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0098 | 0/0 | 7184 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0101 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0102 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0104 | 0/0 | 7185 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0110 | 0/0 | 7177 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0112 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0114 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0116 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0002t0120 | 0/0 | 7175 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0010t0023 | 0/0 | 7184 | 3 | 0 | 1 | 0 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0010t0123 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0011t0012 | 0/0 | 7180 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0011t0100 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0014t0047 | 0/0 | 7175 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0014t0086 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0014t0087 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0017t0015 | 0/0 | 7176 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0021t0015 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0003c0022t0013 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0004c0007t0007 | 0/0 | 7180 | 10 | 0 | 8 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0004c0007t0055 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0004c0007t0056 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0026 | 0/0 | 7180 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0040 | 1/0 | 7180 | 2 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0043 | 0/0 | 7180 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0044 | 0/1 | 7180 | 2 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0082 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0083 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0005c0006t0089 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005t0002 | 0/0 | 7176 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005t0003 | 0/0 | 7183 | 6 | 3 | 0 | 2 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005t0027 | 0/0 | 7184 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005t0045 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005t0097 | 0/0 | 7179 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0006c0005t0118 | 0/0 | 7184 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007c0009t0024 | 0/0 | 7181 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007c0009t0030 | 0/0 | 7181 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007c0009t0053 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0007c0020t0066 | 0/0 | 7175 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0015t0012 | 0/0 | 7180 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0016t0108 | 0/0 | 7175 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0016t0109 | 0/0 | 7175 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0008c0018t0002 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0009c0012t0025 | 0/0 | 7175 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0009c0012t0078 | 0/0 | 7177 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0010c0013t0006 | 0/0 | 7179 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0010c0013t0017 | 0/0 | 7177 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0010c0013t0121 | 0/0 | 7177 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0011c0031t0049 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0012c0030t0051 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0013c0029t0070 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0014c0027t0006 | 0/0 | 7179 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0015c0023t0090 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0016c0025t0080 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0017c0028t0047 | 0/0 | 7175 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
a0018c0019t0122 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | copy fasta | chr2 | 43833971 | 43887988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0010g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0010g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0015g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0018g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0018g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0019g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0019g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0019g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0020g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0020g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0020g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0020g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0031g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0032g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0032g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0033g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0033g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0034g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0034g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0035g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0035g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0036g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0036g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0037g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0037g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0038g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0038g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0052g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0057g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0059g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0060g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0061g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0062g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0063g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0064g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0065g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0067g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0069g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0071g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0072g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0073g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0074g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0075g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0076g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0001t0077g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0014g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0014g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0014g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0014g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0031g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0054g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0058g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0001c0008t0079g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0016g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0016g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0016g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0016g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0017g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0017g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0017g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0023g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0027g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0039g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0045g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0048g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0048g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0094g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0096g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0099g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0103g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0105g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0106g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0107g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0111g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0113g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0115g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0003t0119g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0008g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0011g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0041g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0042g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0042g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0084g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0085g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0088g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0004t0091g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0024t0117g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0002c0026t0095g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0008g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0017g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0021g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0021g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0021g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0021g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0022g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0022g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0027g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0028g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0028g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0028g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0029g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0029g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0046g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0050g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0068g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0081g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0092g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0093g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0098g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0101g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0102g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0104g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0110g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0112g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0114g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0116g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0002t0120g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0010t0023g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0010t0023g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0010t0023g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0010t0123g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0011t0012g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0011t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0011t0100g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0014t0047g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0014t0086g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0014t0087g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0017t0015g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0021t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0003c0022t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0055g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0004c0007t0056g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0026g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0026g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0026g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0040g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0040g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0043g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0043g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0044g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0044g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0082g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0083g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0005c0006t0089g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0027g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0045g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0097g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0006c0005t0118g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0007c0009t0024g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0007c0009t0024g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0007c0009t0030g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0007c0009t0030g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0007c0009t0053g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0007c0020t0066g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0008c0015t0012g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0008c0016t0108g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0008c0016t0109g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0008c0018t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0009c0012t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0009c0012t0025g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0009c0012t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0009c0012t0078g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0010c0013t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0010c0013t0017g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0010c0013t0121g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0011c0031t0049g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0012c0030t0051g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0013c0029t0070g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0014c0027t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0015c0023t0090g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0016c0025t0080g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0017c0028t0047g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
a0018c0019t0122g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | GBR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00099 | hp2 | a0003 | c0002 | t0002 | g0264 | EUR | GBR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00280 | hp1 | a0004 | c0007 | t0007 | g0064 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00280 | hp2 | a0002 | c0003 | t0023 | g0251 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00323 | hp1 | a0002 | c0004 | t0008 | g0272 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00323 | hp2 | a0005 | c0006 | t0083 | g0269 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00438 | hp1 | a0006 | c0005 | t0027 | g0220 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00438 | hp2 | a0001 | c0001 | t0018 | g0100 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00558 | hp1 | a0001 | c0001 | t0020 | g0084 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00597 | hp1 | a0001 | c0001 | t0033 | g0111 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00621 | hp1 | a0002 | c0003 | t0045 | g0169 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00621 | hp2 | a0001 | c0001 | t0020 | g0010 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00639 | hp1 | a0001 | c0001 | t0074 | g0049 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00639 | hp2 | a0003 | c0002 | t0017 | g0174 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00642 | hp1 | a0003 | c0014 | t0086 | g0276 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00642 | hp2 | a0003 | c0017 | t0015 | g0014 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00673 | hp1 | a0001 | c0001 | t0020 | g0145 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00733 | hp1 | a0004 | c0007 | t0007 | g0148 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00733 | hp2 | a0003 | c0002 | t0092 | g0279 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00735 | hp1 | a0003 | c0002 | t0002 | g0284 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00735 | hp2 | a0004 | c0007 | t0055 | g0013 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00738 | hp1 | a0002 | c0003 | t0017 | g0019 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00738 | hp2 | a0002 | c0004 | t0008 | g0182 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00741 | hp1 | a0003 | c0014 | t0087 | g0288 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG00741 | hp2 | a0006 | c0005 | t0002 | g0260 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01069 | hp1 | a0004 | c0007 | t0007 | g0006 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01069 | hp2 | a0002 | c0004 | t0011 | g0262 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01070 | hp1 | a0002 | c0003 | t0002 | g0197 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01070 | hp2 | a0003 | c0002 | t0002 | g0282 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01071 | hp1 | a0004 | c0007 | t0007 | g0006 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01071 | hp2 | a0003 | c0002 | t0002 | g0290 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01074 | hp1 | a0003 | c0002 | t0022 | g0015 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01074 | hp2 | a0003 | c0002 | t0002 | g0287 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01081 | hp1 | a0004 | c0007 | t0007 | g0013 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01099 | hp1 | a0003 | c0002 | t0022 | g0015 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01099 | hp2 | a0003 | c0017 | t0015 | g0014 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01106 | hp1 | a0002 | c0003 | t0006 | g0198 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01106 | hp2 | a0001 | c0001 | t0010 | g0011 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01109 | hp1 | a0002 | c0004 | t0008 | g0271 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01109 | hp2 | a0003 | c0002 | t0021 | g0163 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01167 | hp1 | a0004 | c0007 | t0007 | g0143 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01167 | hp2 | a0003 | c0002 | t0110 | g0283 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01168 | hp1 | a0004 | c0007 | t0007 | g0124 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01168 | hp2 | a0005 | c0006 | t0026 | g0043 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01169 | hp1 | a0004 | c0007 | t0007 | g0055 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01169 | hp2 | a0003 | c0002 | t0002 | g0275 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01175 | hp1 | a0003 | c0002 | t0003 | g0268 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01175 | hp2 | a0003 | c0002 | t0028 | g0270 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01192 | hp1 | a0003 | c0010 | t0023 | g0039 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01192 | hp2 | a0001 | c0008 | t0014 | g0144 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01255 | hp1 | a0005 | c0006 | t0089 | g0062 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01255 | hp2 | a0001 | c0008 | t0054 | g0141 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01256 | hp1 | a0002 | c0004 | t0011 | g0187 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01256 | hp2 | a0003 | c0002 | t0120 | g0266 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0231 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01261 | hp2 | a0005 | c0006 | t0026 | g0263 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01346 | hp1 | a0005 | c0006 | t0043 | g0253 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01346 | hp2 | a0007 | c0009 | t0053 | g0031 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01361 | hp1 | a0005 | c0006 | t0026 | g0289 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01361 | hp2 | a0001 | c0001 | t0035 | g0008 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01433 | hp1 | a0002 | c0004 | t0011 | g0225 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01433 | hp2 | a0003 | c0002 | t0028 | g0164 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01496 | hp1 | a0001 | c0008 | t0008 | g0274 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01496 | hp2 | a0002 | c0004 | t0011 | g0188 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01515 | hp1 | a0003 | c0002 | t0003 | g0205 | EUR | IBS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01515 | hp2 | a0002 | c0004 | t0011 | g0185 | EUR | IBS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01884 | hp1 | a0002 | c0003 | t0111 | g0178 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01884 | hp2 | a0003 | c0002 | t0102 | g0161 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01891 | hp1 | a0005 | c0006 | t0044 | g0277 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01891 | hp2 | a0002 | c0004 | t0013 | g0258 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01928 | hp1 | a0002 | c0003 | t0006 | g0193 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01934 | hp2 | a0001 | c0001 | t0077 | g0102 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01943 | hp1 | a0010 | c0013 | t0017 | g0167 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01943 | hp2 | a0002 | c0003 | t0006 | g0200 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01952 | hp1 | a0002 | c0003 | t0003 | g0248 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01952 | hp2 | a0002 | c0004 | t0042 | g0247 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01975 | hp1 | a0002 | c0003 | t0006 | g0199 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01975 | hp2 | a0010 | c0013 | t0006 | g0168 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01978 | hp1 | a0003 | c0002 | t0003 | g0286 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01978 | hp2 | a0006 | c0005 | t0097 | g0246 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01981 | hp1 | a0005 | c0006 | t0043 | g0241 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01981 | hp2 | a0002 | c0004 | t0008 | g0265 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01993 | hp2 | a0015 | c0023 | t0090 | g0208 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02015 | hp1 | a0002 | c0003 | t0017 | g0195 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02015 | hp2 | a0001 | c0001 | t0009 | g0060 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02027 | hp2 | a0001 | c0001 | t0033 | g0113 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02040 | hp2 | a0001 | c0001 | t0020 | g0112 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02055 | hp1 | a0001 | c0008 | t0058 | g0068 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02055 | hp2 | a0002 | c0003 | t0106 | g0255 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02056 | hp2 | a0001 | c0001 | t0019 | g0132 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02074 | hp1 | a0001 | c0001 | t0062 | g0010 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02074 | hp2 | a0006 | c0005 | t0118 | g0221 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02080 | hp2 | a0001 | c0001 | t0019 | g0066 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02083 | hp1 | a0002 | c0026 | t0095 | g0192 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02083 | hp2 | a0001 | c0001 | t0057 | g0107 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02132 | hp1 | a0006 | c0005 | t0003 | g0023 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02135 | hp2 | a0001 | c0001 | t0034 | g0074 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02148 | hp1 | a0002 | c0003 | t0027 | g0235 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02148 | hp2 | a0004 | c0007 | t0007 | g0103 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02165 | hp1 | a0006 | c0005 | t0003 | g0023 | EAS | CDX | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0086 | EAS | CDX | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02257 | hp1 | a0003 | c0002 | t0022 | g0159 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02257 | hp2 | a0002 | c0003 | t0002 | g0044 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02280 | hp1 | a0003 | c0002 | t0022 | g0158 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02280 | hp2 | a0005 | c0006 | t0082 | g0281 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02293 | hp1 | a0002 | c0003 | t0006 | g0201 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0127 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02300 | hp1 | a0002 | c0003 | t0006 | g0256 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02451 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02451 | hp2 | a0003 | c0021 | t0015 | g0030 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0118 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02572 | hp2 | a0002 | c0003 | t0105 | g0184 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02602 | hp1 | a0002 | c0003 | t0119 | g0186 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02602 | hp2 | a0013 | c0029 | t0070 | g0119 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02622 | hp1 | a0003 | c0002 | t0050 | g0149 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02622 | hp2 | a0002 | c0004 | t0085 | g0018 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02630 | hp1 | a0007 | c0009 | t0030 | g0033 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02630 | hp2 | a0002 | c0004 | t0013 | g0212 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02647 | hp1 | a0016 | c0025 | t0080 | g0156 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02647 | hp2 | a0003 | c0011 | t0012 | g0001 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02683 | hp1 | a0002 | c0003 | t0002 | g0234 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02683 | hp2 | a0001 | c0001 | t0031 | g0046 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02698 | hp1 | a0003 | c0002 | t0027 | g0280 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02698 | hp2 | a0003 | c0002 | t0008 | g0175 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02717 | hp1 | a0003 | c0002 | t0114 | g0217 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02717 | hp2 | a0017 | c0028 | t0047 | g0291 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02723 | hp2 | a0003 | c0002 | t0021 | g0157 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0093 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02735 | hp2 | a0002 | c0004 | t0084 | g0226 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02738 | hp1 | a0002 | c0004 | t0091 | g0257 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02738 | hp2 | a0001 | c0008 | t0014 | g0069 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02809 | hp1 | a0002 | c0003 | t0099 | g0035 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02809 | hp2 | a0003 | c0002 | t0046 | g0016 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02818 | hp1 | a0003 | c0002 | t0002 | g0209 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02818 | hp2 | a0003 | c0022 | t0013 | g0261 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02886 | hp1 | a0003 | c0002 | t0104 | g0242 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0117 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02895 | hp1 | a0001 | c0001 | t0038 | g0052 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02895 | hp2 | a0003 | c0010 | t0123 | g0038 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02896 | hp1 | a0007 | c0009 | t0030 | g0034 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02896 | hp2 | a0008 | c0016 | t0109 | g0207 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02897 | hp1 | a0008 | c0016 | t0108 | g0206 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02897 | hp2 | a0001 | c0001 | t0038 | g0053 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02922 | hp1 | a0002 | c0004 | t0008 | g0181 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02922 | hp2 | a0002 | c0003 | t0002 | g0254 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02965 | hp1 | a0002 | c0003 | t0012 | g0147 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02976 | hp1 | a0003 | c0002 | t0029 | g0150 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02976 | hp2 | a0002 | c0003 | t0012 | g0177 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0092 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03017 | hp2 | a0012 | c0030 | t0051 | g0078 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03041 | hp1 | a0003 | c0002 | t0021 | g0063 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03041 | hp2 | a0002 | c0003 | t0094 | g0170 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03098 | hp1 | a0009 | c0012 | t0078 | g0024 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03098 | hp2 | a0006 | c0005 | t0003 | g0219 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03130 | hp1 | a0003 | c0011 | t0012 | g0001 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03130 | hp2 | a0001 | c0001 | t0015 | g0057 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03195 | hp1 | a0001 | c0001 | t0064 | g0133 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03195 | hp2 | a0018 | c0019 | t0122 | g0215 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03209 | hp1 | a0009 | c0012 | t0025 | g0029 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03209 | hp2 | a0006 | c0005 | t0003 | g0259 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03225 | hp1 | a0002 | c0004 | t0013 | g0179 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03225 | hp2 | a0003 | c0002 | t0101 | g0040 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03453 | hp1 | a0003 | c0002 | t0046 | g0016 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03453 | hp2 | a0002 | c0004 | t0013 | g0211 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03490 | hp1 | a0003 | c0010 | t0023 | g0036 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03490 | hp2 | a0001 | c0008 | t0014 | g0072 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03491 | hp1 | a0003 | c0002 | t0003 | g0267 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03491 | hp2 | a0006 | c0005 | t0003 | g0218 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03492 | hp1 | a0003 | c0010 | t0023 | g0037 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03492 | hp2 | a0003 | c0002 | t0003 | g0278 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03516 | hp1 | a0008 | c0018 | t0002 | g0176 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03516 | hp2 | a0002 | c0004 | t0008 | g0213 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03540 | hp1 | a0003 | c0002 | t0081 | g0160 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03540 | hp2 | a0002 | c0003 | t0039 | g0022 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03579 | hp1 | a0003 | c0002 | t0021 | g0165 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0012 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03654 | hp1 | a0005 | c0006 | t0040 | g0166 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03654 | hp2 | a0004 | c0007 | t0007 | g0131 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03704 | hp1 | a0001 | c0008 | t0014 | g0071 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03704 | hp2 | a0002 | c0003 | t0003 | g0222 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03710 | hp1 | a0001 | c0001 | t0071 | g0106 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03710 | hp2 | a0001 | c0001 | t0069 | g0109 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03831 | hp1 | a0001 | c0001 | t0063 | g0104 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03831 | hp2 | a0001 | c0001 | t0035 | g0138 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03834 | hp2 | a0010 | c0013 | t0121 | g0183 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04115 | hp1 | a0001 | c0001 | t0076 | g0085 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04115 | hp2 | a0003 | c0002 | t0116 | g0162 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04184 | hp1 | a0006 | c0005 | t0045 | g0243 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04184 | hp2 | a0001 | c0001 | t0014 | g0065 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04199 | hp1 | a0002 | c0004 | t0011 | g0042 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04199 | hp2 | a0004 | c0007 | t0056 | g0155 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04204 | hp2 | a0002 | c0003 | t0003 | g0223 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04228 | hp1 | a0001 | c0001 | t0073 | g0067 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG04228 | hp2 | a0001 | c0008 | t0079 | g0073 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18522 | hp1 | a0002 | c0003 | t0103 | g0019 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18522 | hp2 | a0007 | c0009 | t0024 | g0032 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18906 | hp1 | a0002 | c0004 | t0013 | g0018 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18906 | hp2 | a0007 | c0009 | t0024 | g0005 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18939 | hp2 | a0003 | c0002 | t0005 | g0189 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18942 | hp1 | a0002 | c0003 | t0006 | g0194 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18944 | hp2 | a0002 | c0004 | t0041 | g0020 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18948 | hp1 | a0002 | c0003 | t0016 | g0239 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18952 | hp1 | a0002 | c0003 | t0016 | g0252 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18952 | hp2 | a0001 | c0001 | t0019 | g0051 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18954 | hp1 | a0001 | c0001 | t0036 | g0076 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18954 | hp2 | a0002 | c0003 | t0017 | g0237 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18957 | hp1 | a0003 | c0002 | t0004 | g0021 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18959 | hp1 | a0002 | c0004 | t0088 | g0227 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18962 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18964 | hp2 | a0002 | c0003 | t0006 | g0233 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18969 | hp2 | a0002 | c0004 | t0041 | g0020 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18970 | hp1 | a0001 | c0001 | t0059 | g0136 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18970 | hp2 | a0001 | c0001 | t0018 | g0003 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18972 | hp1 | a0001 | c0001 | t0067 | g0120 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18972 | hp2 | a0002 | c0004 | t0042 | g0228 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18974 | hp1 | a0002 | c0003 | t0048 | g0004 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18974 | hp2 | a0003 | c0002 | t0005 | g0021 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18981 | hp1 | a0002 | c0003 | t0048 | g0236 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18982 | hp1 | a0001 | c0001 | t0034 | g0088 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18983 | hp2 | a0001 | c0001 | t0032 | g0126 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18986 | hp1 | a0001 | c0001 | t0065 | g0048 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18987 | hp1 | a0014 | c0027 | t0006 | g0232 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18998 | hp1 | a0001 | c0001 | t0075 | g0090 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18998 | hp2 | a0002 | c0003 | t0016 | g0004 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19000 | hp1 | a0001 | c0001 | t0061 | g0135 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19000 | hp2 | a0003 | c0002 | t0068 | g0146 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19003 | hp1 | a0003 | c0002 | t0098 | g0191 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19005 | hp1 | a0002 | c0003 | t0096 | g0249 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19005 | hp2 | a0001 | c0001 | t0072 | g0096 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19007 | hp1 | a0001 | c0001 | t0052 | g0081 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19007 | hp2 | a0003 | c0002 | t0004 | g0214 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19009 | hp1 | a0001 | c0001 | t0009 | g0114 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19009 | hp2 | a0002 | c0003 | t0006 | g0229 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19011 | hp1 | a0003 | c0002 | t0006 | g0224 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19011 | hp2 | a0001 | c0001 | t0036 | g0007 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19012 | hp1 | a0003 | c0002 | t0093 | g0238 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19030 | hp1 | a0003 | c0002 | t0003 | g0172 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19030 | hp2 | a0003 | c0011 | t0100 | g0001 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0210 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19043 | hp2 | a0002 | c0003 | t0107 | g0171 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19062 | hp1 | a0002 | c0003 | t0016 | g0004 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19062 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19066 | hp1 | a0002 | c0003 | t0006 | g0230 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19066 | hp2 | a0001 | c0001 | t0009 | g0097 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19070 | hp2 | a0001 | c0001 | t0060 | g0087 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19085 | hp1 | a0001 | c0001 | t0018 | g0003 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19085 | hp2 | a0002 | c0004 | t0011 | g0190 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19086 | hp1 | a0002 | c0003 | t0113 | g0203 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19089 | hp1 | a0001 | c0001 | t0032 | g0070 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19089 | hp2 | a0003 | c0002 | t0009 | g0202 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19090 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19091 | hp1 | a0001 | c0001 | t0018 | g0003 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19240 | hp1 | a0001 | c0001 | t0037 | g0056 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA19240 | hp2 | a0003 | c0002 | t0028 | g0041 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20129 | hp1 | a0003 | c0014 | t0047 | g0216 | AFR | ASW | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20129 | hp2 | a0006 | c0005 | t0002 | g0245 | AFR | ASW | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20752 | hp1 | a0003 | c0002 | t0112 | g0204 | EUR | TSI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20752 | hp2 | a0002 | c0003 | t0115 | g0173 | EUR | TSI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20905 | hp1 | a0002 | c0024 | t0117 | g0250 | SAS | GIH | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20905 | hp2 | a0002 | c0003 | t0003 | g0196 | SAS | GIH | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01123 | hp1 | a0002 | c0003 | t0002 | g0045 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG01123 | hp2 | a0001 | c0001 | t0015 | g0142 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02109 | hp1 | a0001 | c0008 | t0031 | g0152 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02109 | hp2 | a0009 | c0012 | t0025 | g0028 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02486 | hp1 | a0007 | c0009 | t0024 | g0005 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02486 | hp2 | a0001 | c0001 | t0037 | g0121 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02559 | hp1 | a0002 | c0003 | t0039 | g0022 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG02559 | hp2 | a0011 | c0031 | t0049 | g0025 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03471 | hp1 | a0006 | c0005 | t0003 | g0244 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG03471 | hp2 | a0003 | c0002 | t0029 | g0151 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG06807 | hp1 | a0008 | c0015 | t0012 | g0017 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
HG06807 | hp2 | a0003 | c0011 | t0012 | g0061 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18955 | hp1 | a0002 | c0003 | t0016 | g0240 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA18955 | hp2 | a0001 | c0001 | t0019 | g0079 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20300 | hp1 | a0008 | c0015 | t0012 | g0017 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA20300 | hp2 | a0009 | c0012 | t0025 | g0027 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA21309 | hp1 | a0007 | c0020 | t0066 | g0026 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
NA21309 | hp2 | a0002 | c0004 | t0008 | g0180 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
homoSapiens_chm13v2 | hp1 | a0005 | c0006 | t0044 | g0285 | REF | REF | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
homoSapiens_grch38 | hp1 | a0005 | c0006 | t0040 | g0273 | REF | REF | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43839108
|
G | C | 2 | a0006a0010 | 15 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(12): Show |
missense_variant | MODERATE | c.55G>C | p.Asp19His | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 138/7180 | 55/2022 | 19/673 | chr2 | 43839108 | ||
chr2:43844537
|
A | G | 2 | a0009a0011 | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.94A>G | p.Ser32Gly | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/13 | 177/7180 | 94/2022 | 32/673 | chr2 | 43844537 | ||
chr2:43844597
|
C | G | 2 | a0008a0018 | 6 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(3): Show |
missense_variant | MODERATE | c.154C>G | p.Leu52Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/13 | 237/7180 | 154/2022 | 52/673 | chr2 | 43844597 | ||
chr2:43844604
|
A | G | 4 | a0001a0004a0012others(1): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
missense_variant | MODERATE | c.161A>G | p.Tyr54Cys | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/13 | 244/7180 | 161/2022 | 54/673 | chr2 | 43844604 | ||
chr2:43846228
|
G | A | 3 | a0007a0009a0011 | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
missense_variant | MODERATE | c.239G>A | p.Cys80Tyr | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/13 | 322/7180 | 239/2022 | 80/673 | chr2 | 43846228 | ||
chr2:43852420
|
G | A | 1 | a0007 | 7 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.628G>A | p.Val210Met | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/13 | 711/7180 | 628/2022 | 210/673 | chr2 | 43852420 | ||
chr2:43852601
|
A | G | 1 | a0017 | 1 | HG02717.hp2 | missense_variant&splice_region_variant | MODERATE | c.697A>G | p.Ile233Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 780/7180 | 697/2022 | 233/673 | chr2 | 43852601 | ||
chr2:43852626
|
C | T | 1 | a0012 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.722C>T | p.Ser241Phe | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 805/7180 | 722/2022 | 241/673 | chr2 | 43852626 | ||
chr2:43852664
|
A | G | 1 | a0014 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.760A>G | p.Thr254Ala | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 843/7180 | 760/2022 | 254/673 | chr2 | 43852664 | ||
chr2:43871979
|
A | T | 1 | a0013 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.968A>T | p.Asp323Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 7/13 | 1051/7180 | 968/2022 | 323/673 | chr2 | 43871979 | ||
chr2:43872294
|
C | A | 5 | a0002a0008a0010others(2): Show | 88 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(85): Show |
missense_variant | MODERATE | c.1199C>A | p.Thr400Lys | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/13 | 1282/7180 | 1199/2022 | 400/673 | chr2 | 43872294 | ||
chr2:43877786
|
T | C | 15 | a0001a0002a0003others(12): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
missense_variant | MODERATE | c.1895T>C | p.Val632Ala | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1978/7180 | 1895/2022 | 632/673 | chr2 | 43877786 | ||
chr2:43877854
|
A | G | 2 | a0011a0016 | 2 | HG02559.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.1963A>G | p.Met655Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2046/7180 | 1963/2022 | 655/673 | chr2 | 43877854 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43839104
|
C | A | 4 | a0008c0015a0008c0016a0008c0018others(1): Show | 6 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.51C>A | p.Pro17Pro | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 134/7180 | 51/2022 | 17/673 | chr2 | 43839104 | ||
chr2:43851714
|
G | A | 4 | a0003c0021a0003c0022a0006c0005others(1): Show | 17 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(14): Show |
synonymous_variant | LOW | c.453G>A | p.Val151Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/13 | 536/7180 | 453/2022 | 151/673 | chr2 | 43851714 | ||
chr2:43852467
|
G | A | 1 | a0003c0010 | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
synonymous_variant | LOW | c.675G>A | p.Val225Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/13 | 758/7180 | 675/2022 | 225/673 | chr2 | 43852467 | ||
chr2:43852774
|
C | T | 1 | a0002c0026 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.870C>T | p.Thr290Thr | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 953/7180 | 870/2022 | 290/673 | chr2 | 43852774 | ||
chr2:43873940
|
C | T | 1 | a0003c0011 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.1365C>T | p.Ile455Ile | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/13 | 1448/7180 | 1365/2022 | 455/673 | chr2 | 43873940 | ||
chr2:43873961
|
C | T | 1 | a0012c0030 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1386C>T | p.Asn462Asn | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/13 | 1469/7180 | 1386/2022 | 462/673 | chr2 | 43873961 | ||
chr2:43875226
|
A | G | 1 | a0002c0024 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1569A>G | p.Pro523Pro | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1652/7180 | 1569/2022 | 523/673 | chr2 | 43875226 | ||
chr2:43875313
|
G | A | 1 | a0011c0031 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1656G>A | p.Leu552Leu | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1739/7180 | 1656/2022 | 552/673 | chr2 | 43875313 | ||
chr2:43875352
|
C | T | 8 | a0001c0008a0002c0004a0003c0014others(5): Show | 45 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(42): Show |
synonymous_variant | LOW | c.1695C>T | p.Ala565Ala | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1778/7180 | 1695/2022 | 565/673 | chr2 | 43875352 | ||
chr2:43875373
|
C | T | 1 | a0008c0015 | 2 | HG06807.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1716C>T | p.Leu572Leu | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1799/7180 | 1716/2022 | 572/673 | chr2 | 43875373 | ||
chr2:43877586
|
C | T | 1 | a0003c0017 | 2 | HG00642.hp2 HG01099.hp2 |
synonymous_variant | LOW | c.1782C>T | p.Ser594Ser | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 12/13 | 1865/7180 | 1782/2022 | 594/673 | chr2 | 43877586 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43839035
|
T | G | 65 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(62): Show | 158 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(155): Show |
5_prime_UTR_variant | MODIFIER | c.-19T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 19 | chr2 | 43839035 | |||||
chr2:43839039
|
A | C | 4 | a0003c0002t0021a0003c0002t0022a0003c0002t0081others(1): Show | 10 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-15A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 15 | chr2 | 43839039 | |||||
chr2:43878065
|
A | G | 1 | a0001c0008t0079 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 152 | chr2 | 43878065 | |||||
chr2:43878663
|
C | T | 1 | a0009c0012t0078 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 750 | chr2 | 43878663 | |||||
chr2:43878728
|
T | C | 1 | a0011c0031t0049 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 815 | chr2 | 43878728 | |||||
chr2:43878748
|
T | C | 3 | a0002c0003t0039a0003c0002t0029a0003c0002t0050 | 5 | HG02559.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*835T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 835 | chr2 | 43878748 | |||||
chr2:43878817
|
C | G | 1 | a0001c0001t0077 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 904 | chr2 | 43878817 | |||||
chr2:43878916
|
G | A | 2 | a0007c0009t0024a0007c0009t0030 | 5 | HG02486.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1003G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1003 | chr2 | 43878916 | |||||
chr2:43878918
|
C | T | 94 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(91): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1005C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1005 | chr2 | 43878918 | |||||
chr2:43878919
|
G | A | 1 | a0016c0025t0080 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1006G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1006 | chr2 | 43878919 | |||||
chr2:43878943
|
C | T | 1 | a0003c0010t0123 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1030C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1030 | chr2 | 43878943 | |||||
chr2:43879038
|
T | C | 1 | a0001c0001t0063 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1125T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1125 | chr2 | 43879038 | |||||
chr2:43879060
|
T | C | 1 | a0003c0002t0098 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1147T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1147 | chr2 | 43879060 | |||||
chr2:43879076
|
T | C | 1 | a0002c0003t0099 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1163 | chr2 | 43879076 | |||||
chr2:43879311
|
C | A | 6 | a0001c0001t0064a0002c0003t0012a0003c0002t0101others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1398C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1398 | chr2 | 43879311 | |||||
chr2:43879402
|
A | T | 17 | a0001c0001t0001a0001c0001t0018a0001c0001t0032others(14): Show | 47 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1489A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1489 | chr2 | 43879402 | |||||
chr2:43879414
|
T | G | 2 | a0003c0002t0046a0003c0002t0102 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1501T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1501 | chr2 | 43879414 | |||||
chr2:43879462
|
G | C | 4 | a0002c0003t0103a0003c0002t0102a0007c0009t0024others(1): Show | 7 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1549G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1549 | chr2 | 43879462 | |||||
chr2:43879518
|
G | A | 1 | a0003c0002t0104 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1605G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1605 | chr2 | 43879518 | |||||
chr2:43879568
|
A | G | 1 | a0001c0001t0062 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1655A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1655 | chr2 | 43879568 | |||||
chr2:43879579
|
T | A | 1 | a0002c0003t0105 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1666 | chr2 | 43879579 | |||||
chr2:43879759
|
C | G | 3 | a0001c0001t0076a0002c0003t0023a0003c0010t0023 | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1846C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1846 | chr2 | 43879759 | |||||
chr2:43879801
|
T | C | 1 | a0002c0003t0106 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1888T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1888 | chr2 | 43879801 | |||||
chr2:43879815
|
C | G | 2 | a0011c0031t0049a0016c0025t0080 | 2 | HG02559.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1902C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1902 | chr2 | 43879815 | |||||
chr2:43879963
|
C | G | 1 | a0006c0005t0097 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2050C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2050 | chr2 | 43879963 | |||||
chr2:43880029
|
T | G | 1 | a0001c0001t0065 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2116T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2116 | chr2 | 43880029 | |||||
chr2:43880085
|
C | A | 1 | a0001c0001t0018 | 4 | HG00438.hp2 NA18970.hp2 NA19085.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2172C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2172 | chr2 | 43880085 | |||||
chr2:43880091
|
C | T | 1 | a0003c0010t0123 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2178C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2178 | chr2 | 43880091 | |||||
chr2:43880121
|
C | A | 1 | a0012c0030t0051 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2208 | chr2 | 43880121 | |||||
chr2:43880156
|
T | C | 3 | a0001c0001t0076a0002c0003t0023a0003c0010t0023 | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2243T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2243 | chr2 | 43880156 | |||||
chr2:43880166
|
A | AT | 4 | a0001c0001t0010a0001c0001t0038a0003c0002t0081others(1): Show | 11 | HG01106.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2259dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2260 | INFO_REALIGN_3_PRIME | chr2 | 43880166 | ||||
chr2:43880172
|
TG | T | 15 | a0001c0001t0015a0001c0001t0018a0001c0001t0037others(12): Show | 41 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2260delG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2260 | chr2 | 43880172 | |||||
chr2:43880173
|
G | GT | 39 | a0001c0001t0004a0001c0001t0009a0001c0001t0019others(36): Show | 83 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2264dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | INFO_REALIGN_3_PRIME | chr2 | 43880173 | ||||
chr2:43880173
|
G | GTT | 12 | a0001c0001t0005a0001c0001t0036a0001c0001t0074others(9): Show | 27 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2263_*2264dupTT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | INFO_REALIGN_3_PRIME | chr2 | 43880173 | ||||
chr2:43880173
|
G | T | 10 | a0001c0001t0010a0001c0001t0020a0001c0001t0038others(7): Show | 22 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2260G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2260 | chr2 | 43880173 | |||||
chr2:43880177
|
TG | T | 33 | a0001c0001t0001a0001c0001t0052a0001c0001t0059others(30): Show | 68 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2265delG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | chr2 | 43880177 | |||||
chr2:43880178
|
G | T | 112 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(109): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*2265G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | chr2 | 43880178 | |||||
chr2:43880180
|
T | G | 6 | a0001c0001t0064a0002c0003t0012a0003c0002t0101others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2267T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2267 | chr2 | 43880180 | |||||
chr2:43880183
|
T | G | 1 | a0002c0003t0107 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2270T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2270 | chr2 | 43880183 | |||||
chr2:43880214
|
C | T | 1 | a0011c0031t0049 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2301C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2301 | chr2 | 43880214 | |||||
chr2:43880218
|
G | T | 1 | a0002c0003t0105 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2305 | chr2 | 43880218 | |||||
chr2:43880332
|
CCTGG | C | 28 | a0001c0001t0015a0001c0001t0020a0001c0001t0037others(25): Show | 57 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2425delGGCT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2422 | INFO_REALIGN_3_PRIME | chr2 | 43880332 | ||||
chr2:43880336
|
G | C | 3 | a0002c0003t0039a0003c0002t0029a0003c0002t0050 | 5 | HG02559.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2423G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2423 | chr2 | 43880336 | |||||
chr2:43880562
|
T | C | 57 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(54): Show | 127 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2649T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2649 | chr2 | 43880562 | |||||
chr2:43880596
|
T | A | 139 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(136): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*2683T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2683 | chr2 | 43880596 | |||||
chr2:43880603
|
G | T | 46 | a0001c0001t0015a0001c0001t0020a0001c0001t0037others(43): Show | 84 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2690G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2690 | chr2 | 43880603 | |||||
chr2:43880630
|
T | C | 1 | a0002c0003t0111 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2717T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2717 | chr2 | 43880630 | |||||
chr2:43880649
|
A | AGT | 43 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(40): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2750_*2751dupTG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2752 | INFO_REALIGN_3_PRIME | chr2 | 43880649 | ||||
chr2:43880649
|
A | AGTGT | 4 | a0001c0001t0072a0002c0003t0016a0002c0003t0048others(1): Show | 9 | HG02572.hp2 NA18948.hp1 NA18952.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2748_*2751dupTGTG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2752 | INFO_REALIGN_3_PRIME | chr2 | 43880649 | ||||
chr2:43880649
|
A | T | 1 | a0001c0001t0073 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2736A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2736 | chr2 | 43880649 | |||||
chr2:43880663
|
T | C | 30 | a0001c0001t0015a0001c0001t0020a0001c0001t0037others(27): Show | 59 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2750T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2750 | chr2 | 43880663 | |||||
chr2:43880663
|
T | TGC | 7 | a0001c0001t0060a0001c0008t0054a0001c0008t0058others(4): Show | 7 | HG01255.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2765_*2766dupGC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2767 | INFO_REALIGN_3_PRIME | chr2 | 43880663 | ||||
chr2:43880665
|
C | T | 72 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(69): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2752C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2752 | chr2 | 43880665 | |||||
chr2:43880667
|
C | T | 2 | a0001c0001t0038a0016c0025t0080 | 3 | HG02647.hp1 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2754C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2754 | chr2 | 43880667 | |||||
chr2:43880670
|
G | A | 4 | a0001c0001t0009a0001c0001t0067a0002c0003t0113others(1): Show | 9 | HG02015.hp2 NA18962.hp1 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2757G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2757 | chr2 | 43880670 | |||||
chr2:43880675
|
C | T | 38 | a0001c0001t0015a0001c0001t0020a0001c0001t0037others(35): Show | 72 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2762C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2762 | chr2 | 43880675 | |||||
chr2:43880677
|
C | T | 1 | a0003c0010t0123 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2764C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2764 | chr2 | 43880677 | |||||
chr2:43880686
|
A | G | 9 | a0001c0001t0076a0002c0003t0023a0002c0003t0039others(6): Show | 13 | HG00280.hp2 HG01192.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2773A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2773 | chr2 | 43880686 | |||||
chr2:43880726
|
C | T | 3 | a0001c0001t0076a0002c0003t0023a0003c0010t0023 | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2813C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2813 | chr2 | 43880726 | |||||
chr2:43880822
|
C | T | 1 | a0007c0009t0030 | 2 | HG02630.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2909C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2909 | chr2 | 43880822 | |||||
chr2:43880962
|
A | G | 1 | a0001c0001t0067 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3049A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3049 | chr2 | 43880962 | |||||
chr2:43880982
|
C | T | 1 | a0011c0031t0049 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3069 | chr2 | 43880982 | |||||
chr2:43881194
|
G | A | 6 | a0002c0003t0103a0003c0002t0102a0003c0002t0114others(3): Show | 9 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3281G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3281 | chr2 | 43881194 | |||||
chr2:43881243
|
A | T | 1 | a0001c0001t0057 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3330A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3330 | chr2 | 43881243 | |||||
chr2:43881261
|
A | T | 1 | a0001c0001t0063 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3348A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3348 | chr2 | 43881261 | |||||
chr2:43881438
|
C | T | 1 | a0003c0002t0104 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3525C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3525 | chr2 | 43881438 | |||||
chr2:43881521
|
C | T | 1 | a0003c0002t0104 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3608C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3608 | chr2 | 43881521 | |||||
chr2:43881525
|
A | G | 1 | a0015c0023t0090 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3612A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3612 | chr2 | 43881525 | |||||
chr2:43881669
|
A | C | 2 | a0003c0002t0046a0011c0031t0049 | 3 | HG02559.hp2 HG02809.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3756A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3756 | chr2 | 43881669 | |||||
chr2:43881697
|
T | G | 141 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(138): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*3784T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3784 | chr2 | 43881697 | |||||
chr2:43881707
|
C | CA | 54 | a0001c0001t0014a0001c0001t0015a0001c0001t0019others(51): Show | 96 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3812dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3813 | INFO_REALIGN_3_PRIME | chr2 | 43881707 | ||||
chr2:43881707
|
C | CAA | 8 | a0001c0001t0037a0002c0003t0103a0002c0004t0042others(5): Show | 15 | HG01175.hp2 HG01433.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3811_*3812dupAA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3813 | INFO_REALIGN_3_PRIME | chr2 | 43881707 | ||||
chr2:43881726
|
C | A | 55 | a0001c0001t0015a0001c0001t0019a0001c0001t0020others(52): Show | 100 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3813C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3813 | chr2 | 43881726 | |||||
chr2:43881898
|
C | T | 1 | a0003c0010t0123 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3985C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3985 | chr2 | 43881898 | |||||
chr2:43881953
|
G | A | 4 | a0002c0003t0039a0002c0003t0107a0003c0002t0029others(1): Show | 6 | HG02559.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4040G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4040 | chr2 | 43881953 | |||||
chr2:43881965
|
T | A | 1 | a0003c0010t0123 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4052 | chr2 | 43881965 | |||||
chr2:43882019
|
G | C | 74 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(71): Show | 169 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*4106G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4106 | chr2 | 43882019 | |||||
chr2:43882069
|
C | T | 1 | a0016c0025t0080 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4156C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4156 | chr2 | 43882069 | |||||
chr2:43882142
|
A | G | 74 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(71): Show | 173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*4229A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4229 | chr2 | 43882142 | |||||
chr2:43882368
|
C | A | 46 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(43): Show | 109 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*4455C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4455 | chr2 | 43882368 | |||||
chr2:43882405
|
C | G | 1 | a0001c0001t0061 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4492C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4492 | chr2 | 43882405 | |||||
chr2:43882468
|
G | A | 1 | a0003c0002t0101 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4555G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4555 | chr2 | 43882468 | |||||
chr2:43882485
|
T | C | 9 | a0001c0001t0014a0001c0008t0014a0001c0008t0079others(6): Show | 19 | HG01069.hp2 HG01192.hp2 HG01256.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4572T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4572 | chr2 | 43882485 | |||||
chr2:43882611
|
C | A | 1 | a0003c0010t0123 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4698C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4698 | chr2 | 43882611 | |||||
chr2:43882641
|
G | A | 1 | a0001c0001t0069 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4728G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4728 | chr2 | 43882641 | |||||
chr2:43882731
|
C | G | 1 | a0011c0031t0049 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4818C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4818 | chr2 | 43882731 | |||||
chr2:43882863
|
A | G | 1 | a0003c0002t0116 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4950A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4950 | chr2 | 43882863 | |||||
chr2:43882954
|
G | A | 6 | a0001c0001t0064a0002c0003t0012a0003c0002t0101others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5041G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 5041 | chr2 | 43882954 | |||||
chr2:43882957
|
C | A | 6 | a0001c0001t0064a0002c0003t0012a0003c0002t0101others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5044C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 5044 | chr2 | 43882957 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43839282
|
C | G | 1 | a0017c0028t0047g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+166C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839282 | ||||||
chr2:43839403
|
C | CT | 9 | a0001c0008t0008g0274a0003c0002t0002g0275a0003c0002t0002g0282others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+328dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
C | CTT | 8 | a0003c0002t0002g0284a0003c0002t0002g0287a0003c0002t0002g0290others(5): Show | 8 | HG00735.hp1 HG00741.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+327_63+328dupTT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTT | C | 17 | a0002c0003t0002g0254a0002c0003t0003g0248a0002c0003t0006g0256others(14): Show | 17 | HG00280.hp2 HG01346.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+327_63+328delTT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTT | C | 30 | a0002c0003t0002g0231a0002c0003t0002g0234a0002c0003t0003g0222others(27): Show | 32 | HG00438.hp1 HG01261.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+326_63+328delTT others(1): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTT | C | 39 | a0002c0003t0002g0197a0002c0003t0002g0210a0002c0003t0003g0196others(36): Show | 41 | HG00738.hp1 HG01070.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.63+325_63+328delTT others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTT | C | 15 | a0002c0003t0012g0177a0002c0003t0107g0171a0002c0003t0111g0178others(12): Show | 16 | HG00639.hp2 HG00738.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+324_63+328delTT others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0003t0094g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.63+319_63+328delTT others(8): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(4): Show |
C | 3 | a0002c0003t0045g0169a0010c0013t0006g0168a0010c0013t0017g0167 | 3 | HG00621.hp1 HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.63+318_63+328delTT others(9): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(7): Show |
C | 3 | a0003c0002t0021g0165a0003c0002t0028g0164a0005c0006t0040g0166 | 3 | HG01433.hp2 HG03579.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.63+315_63+328delTT others(12): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(8): Show |
C | 18 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0008t0031g0152others(15): Show | 21 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+314_63+328delTT others(13): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(9): Show |
C | 100 | a0001c0001t0001g0082a0001c0001t0001g0098a0001c0001t0001g0099others(97): Show | 108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.63+313_63+328delTT others(14): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(10): Show |
C | 19 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(16): Show | 20 | HG00558.hp2 HG00639.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+312_63+328delTT others(15): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(11): Show |
C | 2 | a0002c0003t0002g0044a0002c0003t0002g0045 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.63+311_63+328delTT others(16): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(13): Show |
C | 7 | a0002c0004t0011g0042a0003c0002t0028g0041a0003c0002t0101g0040others(4): Show | 7 | HG01168.hp2 HG01192.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+309_63+328delTT others(18): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(14): Show |
C | 2 | a0002c0003t0099g0035a0003c0010t0023g0036 | 2 | HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.63+308_63+328delTT others(19): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(17): Show |
C | 2 | a0007c0009t0030g0033a0007c0009t0030g0034 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+305_63+328delTT others(22): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839403
|
CTTTTTTT others(18): Show |
C | 10 | a0003c0021t0015g0030a0007c0009t0024g0005a0007c0009t0024g0032others(7): Show | 11 | HG01346.hp2 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+304_63+328delTT others(23): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | |||||
chr2:43839489
|
T | C | 1 | a0003c0002t0021g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+373T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839489 | ||||||
chr2:43839642
|
A | G | 1 | a0004c0007t0007g0148 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+526A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839642 | ||||||
chr2:43839723
|
G | A | 1 | a0018c0019t0122g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63+607G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839723 | ||||||
chr2:43839737
|
G | A | 298 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(295): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.63+621G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839737 | ||||||
chr2:43839860
|
G | T | 2 | a0003c0002t0021g0163a0003c0002t0021g0165 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.63+744G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839860 | ||||||
chr2:43840030
|
G | A | 120 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(117): Show | 129 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.63+914G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840030 | ||||||
chr2:43840081
|
T | A | 2 | a0004c0007t0007g0006a0004c0007t0007g0064 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.63+965T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840081 | ||||||
chr2:43840519
|
C | T | 2 | a0001c0001t0009g0060a0001c0001t0020g0145 | 2 | HG00673.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.63+1403C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840519 | ||||||
chr2:43840639
|
C | G | 1 | a0003c0002t0004g0214 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.63+1523C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840639 | ||||||
chr2:43840680
|
T | G | 158 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(155): Show | 171 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+1564T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840680 | ||||||
chr2:43840711
|
G | C | 1 | a0006c0005t0045g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.63+1595G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840711 | ||||||
chr2:43840712
|
C | T | 4 | a0001c0001t0015g0142a0001c0008t0014g0144a0001c0008t0054g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1596C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840712 | ||||||
chr2:43840743
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0139others(1): Show | 4 | NA18962.hp2 NA18969.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1627C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840743 | ||||||
chr2:43840810
|
A | C | 1 | a0006c0005t0003g0023 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.63+1694A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840810 | ||||||
chr2:43840857
|
C | G | 2 | a0002c0004t0008g0271a0002c0004t0008g0272 | 2 | HG00323.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.63+1741C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840857 | ||||||
chr2:43841152
|
C | T | 4 | a0001c0001t0015g0142a0001c0008t0014g0144a0001c0008t0054g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2036C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841152 | ||||||
chr2:43841202
|
C | G | 6 | a0003c0002t0028g0041a0003c0002t0101g0040a0003c0010t0023g0036others(3): Show | 6 | HG01192.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2086C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841202 | ||||||
chr2:43841220
|
A | C | 1 | a0001c0001t0018g0003 | 3 | NA18970.hp2 NA19085.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.63+2104A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841220 | ||||||
chr2:43841260
|
C | G | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+2144C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841260 | ||||||
chr2:43841650
|
G | A | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2534G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841650 | ||||||
chr2:43841728
|
T | G | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2612T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841728 | ||||||
chr2:43841755
|
C | T | 1 | a0003c0002t0028g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.63+2639C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841755 | ||||||
chr2:43841837
|
C | A | 6 | a0003c0002t0028g0041a0003c0002t0101g0040a0003c0010t0023g0036others(3): Show | 6 | HG01192.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-2670C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841837 | ||||||
chr2:43841857
|
C | A | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-2650C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841857 | ||||||
chr2:43841873
|
G | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2634G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841873 | ||||||
chr2:43841932
|
T | C | 1 | a0009c0012t0078g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64-2575T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841932 | ||||||
chr2:43841975
|
GC | G | 4 | a0001c0001t0015g0142a0001c0008t0014g0144a0001c0008t0054g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2531delC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841975 | ||||||
chr2:43842013
|
AT | A | 134 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(131): Show | 144 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.64-2481delT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43842013 | |||||
chr2:43842075
|
C | T | 1 | a0002c0004t0008g0213 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.64-2432C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842075 | ||||||
chr2:43842199
|
G | C | 1 | a0006c0005t0045g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-2308G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842199 | ||||||
chr2:43842292
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0059g0136a0001c0001t0061g0135 | 3 | HG00597.hp2 NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.64-2215C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842292 | ||||||
chr2:43842304
|
C | T | 1 | a0004c0007t0056g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-2203C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842304 | ||||||
chr2:43842378
|
C | T | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-2129C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842378 | ||||||
chr2:43842415
|
C | G | 9 | a0003c0002t0021g0063a0003c0002t0021g0157a0003c0002t0021g0163others(6): Show | 10 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2092C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842415 | ||||||
chr2:43842563
|
C | A | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-1944C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842563 | ||||||
chr2:43842601
|
A | T | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-1906A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842601 | ||||||
chr2:43842621
|
G | A | 1 | a0002c0003t0107g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-1886G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842621 | ||||||
chr2:43842633
|
G | A | 17 | a0003c0002t0003g0172a0003c0021t0015g0030a0003c0022t0013g0261others(14): Show | 18 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-1874G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842633 | ||||||
chr2:43842642
|
A | T | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-1865A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842642 | ||||||
chr2:43842779
|
A | AT | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-1721dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43842779 | |||||
chr2:43842891
|
C | T | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-1616C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842891 | ||||||
chr2:43843073
|
C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1434C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843073 | ||||||
chr2:43843112
|
T | C | 132 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(129): Show | 143 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-1395T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843112 | ||||||
chr2:43843158
|
G | A | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.64-1349G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843158 | ||||||
chr2:43843188
|
A | AGCTTTT | 3 | a0001c0001t0015g0057a0001c0001t0037g0056a0001c0001t0064g0133 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.64-1318_64-1313dup others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43843188 | |||||
chr2:43843255
|
A | G | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-1252A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843255 | ||||||
chr2:43843358
|
T | A | 1 | a0011c0031t0049g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-1149T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843358 | ||||||
chr2:43843391
|
T | C | 1 | a0002c0004t0011g0262 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.64-1116T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843391 | ||||||
chr2:43843414
|
C | T | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1093C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843414 | ||||||
chr2:43843500
|
T | C | 174 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(171): Show | 188 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.64-1007T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843500 | ||||||
chr2:43843641
|
G | A | 143 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.64-866G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843641 | ||||||
chr2:43843754
|
A | T | 12 | a0002c0003t0002g0210a0002c0003t0012g0147a0002c0004t0008g0180others(9): Show | 12 | HG00738.hp2 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-753A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843754 | ||||||
chr2:43843796
|
A | G | 132 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(129): Show | 143 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-711A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843796 | ||||||
chr2:43843892
|
C | T | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-615C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843892 | ||||||
chr2:43843915
|
C | G | 1 | a0006c0005t0045g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-592C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843915 | ||||||
chr2:43843930
|
A | C | 1 | a0001c0001t0019g0132 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64-577A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843930 | ||||||
chr2:43843947
|
G | A | 1 | a0001c0001t0014g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-560G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843947 | ||||||
chr2:43844213
|
T | A | 17 | a0003c0002t0021g0063a0003c0002t0021g0157a0003c0002t0021g0163others(14): Show | 19 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-294T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844213 | ||||||
chr2:43844251
|
G | C | 3 | a0002c0003t0017g0019a0002c0003t0103g0019a0002c0003t0105g0184 | 3 | HG00738.hp1 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64-256G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844251 | ||||||
chr2:43844313
|
G | T | 2 | a0002c0003t0012g0177a0002c0003t0111g0178 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.64-194G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844313 | ||||||
chr2:43844394
|
A | G | 5 | a0002c0003t0099g0035a0003c0002t0104g0242a0003c0002t0114g0217others(2): Show | 5 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-113A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844394 | ||||||
chr2:43844486
|
C | A | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-21C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844486 | ||||||
chr2:43844500
|
C | T | 143 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
splice_region_variant&intron_variant | LOW | c.64-7C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844500 | ||||||
chr2:43844621
|
C | T | 3 | a0001c0001t0001g0130a0004c0007t0007g0131a0004c0007t0007g0148 | 3 | HG00733.hp1 HG01934.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.165+13C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844621 | ||||||
chr2:43844649
|
G | A | 2 | a0003c0002t0002g0264a0005c0006t0026g0263 | 2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.165+41G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844649 | ||||||
chr2:43844694
|
A | C | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 154 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.165+86A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844694 | ||||||
chr2:43844713
|
G | C | 143 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.165+105G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844713 | ||||||
chr2:43844963
|
G | A | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.165+355G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844963 | ||||||
chr2:43845006
|
T | G | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.165+398T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845006 | ||||||
chr2:43845080
|
ATG | A | 15 | a0002c0003t0006g0229a0002c0004t0011g0190a0002c0004t0041g0020others(12): Show | 17 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+490_165+491del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845080 | |||||
chr2:43845082
|
G | A | 2 | a0001c0001t0019g0066a0001c0001t0073g0067 | 2 | HG02080.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.165+474G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845082 | ||||||
chr2:43845094
|
G | GTA | 4 | a0009c0012t0025g0028a0009c0012t0025g0029a0009c0012t0078g0024others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+487_165+488ins others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845094 | |||||
chr2:43845096
|
G | A | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+488G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845096 | ||||||
chr2:43845096
|
G | GTA | 6 | a0001c0001t0005g0002a0001c0001t0005g0054a0001c0001t0005g0123others(3): Show | 8 | HG00558.hp2 HG02486.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+489_165+490ins others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | |||||
chr2:43845096
|
G | GTATA | 3 | a0001c0001t0005g0125a0001c0001t0005g0127a0001c0001t0032g0126 | 3 | HG01081.hp2 HG02293.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.165+489_165+490ins others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | |||||
chr2:43845096
|
GTGTA | G | 11 | a0002c0003t0003g0222a0002c0003t0003g0223a0002c0003t0119g0186others(8): Show | 11 | HG01256.hp1 HG01433.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+490_165+493del others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | |||||
chr2:43845096
|
GTGTATA | G | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+490_165+495del others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | |||||
chr2:43845098
|
G | A | 136 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(133): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.165+490G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845098 | ||||||
chr2:43845098
|
G | GTA | 7 | a0003c0002t0028g0041a0003c0002t0028g0164a0003c0011t0012g0001others(4): Show | 9 | HG01433.hp2 HG02647.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+511_165+512dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845098 | |||||
chr2:43845098
|
GTA | G | 87 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(84): Show | 90 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.165+511_165+512del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845098 | |||||
chr2:43845100
|
A | G | 1 | a0002c0004t0091g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.165+492A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845100 | ||||||
chr2:43845118
|
AT | A | 4 | a0001c0008t0031g0152a0001c0008t0058g0068a0004c0007t0007g0006others(1): Show | 5 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+511delT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845118 | ||||||
chr2:43845119
|
T | TATA | 10 | a0001c0001t0015g0057a0001c0001t0019g0066a0001c0001t0037g0056others(7): Show | 10 | HG00735.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+512_165+513ins others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845119 | |||||
chr2:43845121
|
A | AT | 15 | a0001c0001t0001g0130a0001c0001t0010g0011a0001c0001t0010g0012others(12): Show | 17 | HG00733.hp1 HG01106.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+523dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845121 | |||||
chr2:43845121
|
A | T | 14 | a0001c0001t0015g0057a0001c0001t0019g0066a0001c0001t0037g0056others(11): Show | 15 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+513A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845121 | ||||||
chr2:43845184
|
G | C | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+576G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845184 | ||||||
chr2:43845301
|
G | A | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+693G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845301 | ||||||
chr2:43845349
|
C | A | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+741C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845349 | ||||||
chr2:43845412
|
C | G | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-743C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845412 | ||||||
chr2:43845435
|
G | C | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-720G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845435 | ||||||
chr2:43845437
|
G | T | 262 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(259): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.166-718G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845437 | ||||||
chr2:43845487
|
T | C | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-668T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845487 | ||||||
chr2:43845748
|
A | G | 6 | a0003c0002t0028g0041a0003c0002t0101g0040a0003c0010t0023g0036others(3): Show | 6 | HG01192.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-407A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845748 | ||||||
chr2:43845811
|
G | A | 1 | a0007c0020t0066g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-344G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845811 | ||||||
chr2:43845827
|
G | A | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-328G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845827 | ||||||
chr2:43845852
|
C | A | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-303C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845852 | ||||||
chr2:43845946
|
T | C | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-209T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845946 | ||||||
chr2:43846014
|
G | A | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-141G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43846014 | ||||||
chr2:43846068
|
C | T | 1 | a0007c0020t0066g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-87C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43846068 | ||||||
chr2:43846444
|
G | C | 1 | a0001c0008t0058g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322+133G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846444 | ||||||
chr2:43846454
|
C | G | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.322+143C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846454 | ||||||
chr2:43846517
|
T | C | 22 | a0002c0003t0094g0170a0003c0002t0003g0172a0003c0002t0104g0242others(19): Show | 23 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.322+206T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846517 | ||||||
chr2:43846533
|
G | A | 2 | a0008c0016t0108g0206a0008c0016t0109g0207 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322+222G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846533 | ||||||
chr2:43846620
|
A | T | 1 | a0003c0002t0101g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322+309A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846620 | ||||||
chr2:43846679
|
T | G | 2 | a0008c0016t0108g0206a0008c0016t0109g0207 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322+368T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846679 | ||||||
chr2:43846742
|
T | C | 262 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(259): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.322+431T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846742 | ||||||
chr2:43846813
|
C | T | 1 | a0002c0003t0002g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.322+502C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846813 | ||||||
chr2:43846814
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.322+503A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846814 | ||||||
chr2:43846861
|
G | A | 17 | a0003c0002t0003g0172a0003c0021t0015g0030a0003c0022t0013g0261others(14): Show | 18 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.322+550G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846861 | ||||||
chr2:43846936
|
G | A | 2 | a0001c0001t0015g0142a0001c0008t0054g0141 | 2 | HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.322+625G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846936 | ||||||
chr2:43846980
|
A | ACG | 3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.322+676_322+677dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846980 | |||||
chr2:43846987
|
CGT | C | 26 | a0003c0002t0002g0209a0003c0002t0003g0172a0003c0002t0104g0242others(23): Show | 27 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.322+678_322+679del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846987 | |||||
chr2:43846988
|
GTGCA | G | 13 | a0003c0002t0021g0063a0003c0002t0021g0157a0003c0002t0021g0163others(10): Show | 15 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.322+678_322+681del others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | ||||||
chr2:43846988
|
GTGCACAC others(1): Show |
G | 4 | a0002c0003t0006g0256a0002c0003t0099g0035a0002c0026t0095g0192others(1): Show | 4 | HG02083.hp1 HG02300.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+678_322+685del others(8): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | ||||||
chr2:43846988
|
GTGCACAC others(3): Show |
G | 85 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(82): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.322+678_322+687del others(10): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | ||||||
chr2:43846988
|
GTGCACAC others(7): Show |
G | 1 | a0002c0003t0113g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.322+678_322+691del others(14): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | ||||||
chr2:43846989
|
T | C | 18 | a0003c0002t0028g0041a0003c0002t0046g0016a0003c0002t0101g0040others(15): Show | 21 | HG01192.hp1 HG01346.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.322+678T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846989 | ||||||
chr2:43846990
|
G | A | 3 | a0003c0002t0046g0016a0003c0002t0102g0161a0003c0014t0047g0216 | 4 | HG01884.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+679G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846990 | ||||||
chr2:43846990
|
G | GCA | 58 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0082others(55): Show | 62 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.322+713_322+714dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
G | GCACA | 8 | a0001c0001t0001g0134a0001c0001t0009g0060a0001c0001t0010g0011others(5): Show | 9 | HG00597.hp2 HG00673.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.322+711_322+714dup others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
G | GCACACA | 7 | a0001c0001t0010g0118a0001c0001t0038g0052a0001c0001t0038g0053others(4): Show | 8 | HG02572.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.322+709_322+714dup others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
G | GCACACAC others(1): Show |
5 | a0001c0001t0010g0116a0001c0001t0010g0117a0007c0009t0024g0032others(2): Show | 5 | HG01346.hp2 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+707_322+714dup others(8): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
G | GCACACAC others(3): Show |
1 | a0007c0009t0024g0005 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322+705_322+714dup others(10): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
GCA | G | 22 | a0001c0001t0001g0050a0001c0001t0001g0105a0001c0001t0001g0108others(19): Show | 22 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.322+713_322+714del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
GCACA | G | 4 | a0001c0001t0033g0113a0001c0001t0073g0067a0003c0002t0002g0287others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+711_322+714del others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846990
|
GCACACA | G | 9 | a0001c0001t0001g0115a0001c0001t0009g0114a0001c0001t0019g0051others(6): Show | 9 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.322+709_322+714del others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | |||||
chr2:43846992
|
A | G | 2 | a0007c0020t0066g0026a0010c0013t0121g0183 | 2 | HG03834.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.322+681A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846992 | ||||||
chr2:43846996
|
A | G | 1 | a0001c0001t0015g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.322+685A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846996 | ||||||
chr2:43846998
|
A | G | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.322+687A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846998 | ||||||
chr2:43847039
|
A | T | 1 | a0003c0010t0023g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.322+728A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847039 | ||||||
chr2:43847121
|
T | C | 1 | a0002c0003t0003g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.322+810T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847121 | ||||||
chr2:43847219
|
G | A | 1 | a0002c0003t0003g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.322+908G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847219 | ||||||
chr2:43847289
|
T | G | 1 | a0001c0001t0004g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.322+978T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847289 | ||||||
chr2:43847292
|
C | T | 266 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(263): Show | 284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.322+981C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847292 | ||||||
chr2:43847325
|
T | A | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.322+1014T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847325 | ||||||
chr2:43847342
|
T | C | 1 | a0002c0003t0002g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.322+1031T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847342 | ||||||
chr2:43847413
|
A | G | 3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.322+1102A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847413 | ||||||
chr2:43847473
|
C | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.322+1162C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847473 | ||||||
chr2:43847503
|
C | G | 139 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(136): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.322+1192C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847503 | ||||||
chr2:43847508
|
C | T | 1 | a0005c0006t0026g0043 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.322+1197C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847508 | ||||||
chr2:43847534
|
C | T | 125 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(122): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.322+1223C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847534 | ||||||
chr2:43847557
|
A | T | 4 | a0003c0002t0104g0242a0003c0002t0114g0217a0003c0014t0047g0216others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+1246A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847557 | ||||||
chr2:43847565
|
G | C | 10 | a0003c0002t0002g0209a0003c0002t0021g0063a0003c0002t0021g0157others(7): Show | 11 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.322+1254G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847565 | ||||||
chr2:43847624
|
G | A | 1 | a0002c0003t0113g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.322+1313G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847624 | ||||||
chr2:43847719
|
G | A | 1 | a0002c0003t0003g0223 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.322+1408G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847719 | ||||||
chr2:43847750
|
G | GT | 5 | a0003c0002t0022g0015a0003c0002t0029g0150a0003c0002t0029g0151others(2): Show | 7 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+1447dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43847750 | |||||
chr2:43847778
|
T | C | 1 | a0003c0010t0123g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.322+1467T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847778 | ||||||
chr2:43847845
|
G | A | 2 | a0003c0010t0023g0036a0003c0010t0023g0037 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.322+1534G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847845 | ||||||
chr2:43847924
|
C | A | 1 | a0002c0003t0039g0022 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.322+1613C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847924 | ||||||
chr2:43847927
|
A | AT | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.322+1625dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43847927 | |||||
chr2:43847954
|
A | G | 140 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(137): Show | 150 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.322+1643A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847954 | ||||||
chr2:43848023
|
T | C | 141 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(138): Show | 152 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.322+1712T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848023 | ||||||
chr2:43848078
|
T | A | 5 | a0003c0002t0002g0275a0003c0002t0002g0284a0003c0002t0110g0283others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1767T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848078 | ||||||
chr2:43848251
|
C | G | 1 | a0001c0001t0020g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.322+1940C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848251 | ||||||
chr2:43848344
|
T | C | 17 | a0003c0002t0003g0172a0003c0021t0015g0030a0003c0022t0013g0261others(14): Show | 18 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.322+2033T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848344 | ||||||
chr2:43848407
|
T | G | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.322+2096T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848407 | ||||||
chr2:43848596
|
A | G | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+2285A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848596 | ||||||
chr2:43848670
|
C | G | 1 | a0003c0002t0114g0217 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.322+2359C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848670 | ||||||
chr2:43848756
|
C | T | 1 | a0003c0002t0028g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.322+2445C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848756 | ||||||
chr2:43848813
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.322+2502C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848813 | ||||||
chr2:43848831
|
C | T | 1 | a0011c0031t0049g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.322+2520C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848831 | ||||||
chr2:43848853
|
TA | T | 11 | a0002c0003t0099g0035a0003c0002t0002g0209a0003c0002t0021g0063others(8): Show | 12 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2552delA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43848853 | |||||
chr2:43848882
|
C | T | 1 | a0003c0014t0047g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322+2571C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848882 | ||||||
chr2:43848928
|
G | A | 1 | a0002c0004t0011g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.322+2617G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848928 | ||||||
chr2:43849021
|
T | TA | 21 | a0001c0001t0001g0105a0001c0001t0010g0116a0001c0001t0032g0070others(18): Show | 23 | HG01884.hp2 HG01891.hp1 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.323-2538dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | |||||
chr2:43849021
|
T | TAAA | 11 | a0003c0002t0028g0041a0007c0009t0024g0005a0007c0009t0024g0032others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.323-2540_323-2538d others(5): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | |||||
chr2:43849021
|
TA | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0115a0001c0001t0004g0047others(15): Show | 18 | HG00323.hp1 HG01515.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.323-2538delA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | |||||
chr2:43849021
|
TAAAAAAA | T | 10 | a0003c0002t0002g0264a0003c0002t0002g0282a0003c0002t0002g0287others(7): Show | 10 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-2544_323-2538d others(9): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | |||||
chr2:43849021
|
TAAAAAAA others(3): Show |
T | 1 | a0003c0002t0021g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.323-2547_323-2538d others(12): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | |||||
chr2:43849105
|
C | G | 10 | a0002c0003t0099g0035a0003c0002t0028g0041a0003c0002t0101g0040others(7): Show | 11 | HG01192.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.323-2479C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849105 | ||||||
chr2:43849217
|
G | A | 3 | a0006c0005t0003g0219a0006c0005t0003g0244a0006c0005t0003g0259 | 3 | HG03098.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.323-2367G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849217 | ||||||
chr2:43849283
|
CTCAGAGT | C | 92 | a0001c0001t0005g0002a0001c0001t0005g0054a0001c0001t0005g0123others(89): Show | 98 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.323-2298_323-2292d others(9): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849283 | |||||
chr2:43849490
|
A | G | 6 | a0002c0003t0099g0035a0008c0015t0012g0017a0008c0016t0108g0206others(3): Show | 7 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-2094A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849490 | ||||||
chr2:43849583
|
TCTCCCCA others(7): Show |
T | 2 | a0001c0008t0014g0071a0001c0008t0014g0072 | 2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.323-1999_323-1986d others(16): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849583 | |||||
chr2:43849592
|
A | G | 10 | a0003c0002t0002g0209a0003c0002t0021g0063a0003c0002t0021g0157others(7): Show | 11 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.323-1992A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849592 | ||||||
chr2:43849713
|
T | C | 1 | a0003c0002t0114g0217 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.323-1871T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849713 | ||||||
chr2:43849933
|
C | G | 12 | a0003c0002t0028g0041a0007c0009t0024g0005a0007c0009t0024g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.323-1651C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849933 | ||||||
chr2:43850010
|
G | A | 3 | a0001c0001t0004g0092a0001c0001t0004g0093a0001c0001t0004g0094 | 3 | HG02735.hp1 HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.323-1574G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850010 | ||||||
chr2:43850032
|
G | A | 1 | a0006c0005t0027g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.323-1552G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850032 | ||||||
chr2:43850086
|
T | C | 294 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(291): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.323-1498T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850086 | ||||||
chr2:43850184
|
C | T | 3 | a0010c0013t0006g0168a0010c0013t0017g0167a0010c0013t0121g0183 | 3 | HG01943.hp1 HG01975.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.323-1400C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850184 | ||||||
chr2:43850314
|
T | C | 297 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(294): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.323-1270T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850314 | ||||||
chr2:43850501
|
A | G | 1 | a0004c0007t0007g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.323-1083A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850501 | ||||||
chr2:43850545
|
T | C | 1 | a0008c0015t0012g0017 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.323-1039T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850545 | ||||||
chr2:43850603
|
A | G | 1 | a0001c0001t0010g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.323-981A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850603 | ||||||
chr2:43850629
|
C | T | 179 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(176): Show | 191 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.323-955C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850629 | ||||||
chr2:43850909
|
C | CA | 7 | a0001c0001t0014g0065a0001c0001t0060g0087a0001c0008t0054g0141others(4): Show | 7 | HG01255.hp2 HG02055.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-658dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43850909 | |||||
chr2:43850921
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.323-663A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850921 | ||||||
chr2:43851023
|
A | G | 135 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(132): Show | 142 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.323-561A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851023 | ||||||
chr2:43851053
|
T | C | 5 | a0003c0002t0003g0172a0003c0010t0023g0036a0003c0010t0023g0037others(2): Show | 5 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.323-531T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851053 | ||||||
chr2:43851079
|
G | C | 2 | a0002c0003t0107g0171a0009c0012t0025g0027 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.323-505G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851079 | ||||||
chr2:43851209
|
C | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.323-375C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851209 | ||||||
chr2:43851260
|
C | G | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.323-324C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851260 | ||||||
chr2:43851356
|
C | T | 1 | a0001c0001t0073g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.323-228C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851356 | ||||||
chr2:43851384
|
G | A | 1 | a0001c0001t0071g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.323-200G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851384 | ||||||
chr2:43851449
|
C | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.323-135C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851449 | ||||||
chr2:43851537
|
C | A | 6 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(3): Show | 7 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-47C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851537 | ||||||
chr2:43851574
|
G | A | 1 | a0016c0025t0080g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.323-10G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851574 | ||||||
chr2:43851865
|
T | C | 181 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(178): Show | 193 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.561+43T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43851865 | ||||||
chr2:43852061
|
G | A | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.561+239G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852061 | ||||||
chr2:43852150
|
C | T | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-204C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852150 | ||||||
chr2:43852164
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.562-190C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852164 | ||||||
chr2:43852169
|
C | T | 1 | a0001c0001t0077g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.562-185C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852169 | ||||||
chr2:43852171
|
C | A | 29 | a0003c0002t0003g0172a0003c0002t0028g0041a0003c0021t0015g0030others(26): Show | 31 | HG00438.hp1 HG00741.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-183C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852171 | ||||||
chr2:43852177
|
G | C | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.562-177G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852177 | ||||||
chr2:43852262
|
G | A | 24 | a0001c0001t0005g0002a0001c0001t0005g0054a0001c0001t0005g0123others(21): Show | 26 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.562-92G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852262 | ||||||
chr2:43852269
|
C | T | 1 | a0003c0002t0008g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.562-85C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852269 | ||||||
chr2:43852532
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+46C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/12 | chr2 | 43852532 | ||||||
chr2:43852581
|
CCT | C | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-13_695-12delCT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43852581 | |||||
chr2:43852914
|
C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+46C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43852914 | ||||||
chr2:43852946
|
G | GAAAGATT others(312): Show |
4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+94_964+95insGG others(317): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43852946 | |||||
chr2:43852991
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+123G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43852991 | ||||||
chr2:43853046
|
G | A | 2 | a0003c0002t0017g0174a0003c0002t0112g0204 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964+178G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853046 | ||||||
chr2:43853103
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+235A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853103 | ||||||
chr2:43853171
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+303C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853171 | ||||||
chr2:43853185
|
A | G | 42 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(39): Show | 44 | HG00438.hp1 HG00741.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.964+317A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853185 | ||||||
chr2:43853200
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+332T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853200 | ||||||
chr2:43853338
|
C | T | 1 | a0005c0006t0043g0241 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.964+470C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853338 | ||||||
chr2:43853366
|
G | C | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+498G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853366 | ||||||
chr2:43853499
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+631G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853499 | ||||||
chr2:43853517
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.964+649C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853517 | ||||||
chr2:43853541
|
T | TA | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+674dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43853541 | |||||
chr2:43853576
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+708C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853576 | ||||||
chr2:43853660
|
A | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+792A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853660 | ||||||
chr2:43853700
|
C | T | 3 | a0002c0004t0008g0265a0002c0004t0008g0271a0002c0004t0008g0272 | 3 | HG00323.hp1 HG01109.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.964+832C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853700 | ||||||
chr2:43853748
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+880T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853748 | ||||||
chr2:43853750
|
G | A | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+882G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853750 | ||||||
chr2:43853752
|
A | G | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+884A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853752 | ||||||
chr2:43853828
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+960G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853828 | ||||||
chr2:43853903
|
T | C | 190 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(187): Show | 204 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.964+1035T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853903 | ||||||
chr2:43853953
|
C | A | 81 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(78): Show | 85 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.964+1085C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853953 | ||||||
chr2:43854041
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1173G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854041 | ||||||
chr2:43854052
|
C | T | 74 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(71): Show | 77 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.964+1184C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854052 | ||||||
chr2:43854111
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1243A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854111 | ||||||
chr2:43854156
|
C | T | 1 | a0002c0004t0008g0213 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.964+1288C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854156 | ||||||
chr2:43854226
|
T | G | 5 | a0002c0003t0099g0035a0003c0010t0023g0036a0003c0010t0023g0037others(2): Show | 5 | HG01192.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+1358T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854226 | ||||||
chr2:43854287
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1419T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854287 | ||||||
chr2:43854296
|
C | G | 1 | a0001c0001t0019g0066 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.964+1428C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854296 | ||||||
chr2:43854349
|
C | T | 134 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(131): Show | 141 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.964+1481C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854349 | ||||||
chr2:43854436
|
T | A | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+1568T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854436 | ||||||
chr2:43854488
|
T | G | 40 | a0002c0003t0006g0194a0002c0003t0006g0230a0003c0002t0003g0172others(37): Show | 42 | HG00438.hp1 HG00741.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.964+1620T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854488 | ||||||
chr2:43854498
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1630T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854498 | ||||||
chr2:43854534
|
C | T | 5 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+1666C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854534 | ||||||
chr2:43854626
|
C | CA | 147 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(144): Show | 159 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.964+1777dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43854626 | |||||
chr2:43854626
|
C | CAA | 8 | a0001c0001t0004g0092a0001c0008t0079g0073a0003c0002t0029g0150others(5): Show | 9 | HG00642.hp2 HG01099.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+1776_964+1777d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43854626 | |||||
chr2:43854640
|
A | AG | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+1772_964+1773i others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854640 | ||||||
chr2:43854759
|
C | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+1891C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854759 | ||||||
chr2:43854837
|
C | T | 1 | a0002c0003t0094g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964+1969C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854837 | ||||||
chr2:43854919
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2051G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854919 | ||||||
chr2:43854972
|
G | T | 1 | a0001c0001t0018g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.964+2104G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854972 | ||||||
chr2:43854979
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2111C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854979 | ||||||
chr2:43855170
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2302C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855170 | ||||||
chr2:43855212
|
A | G | 3 | a0002c0003t0017g0019a0002c0003t0103g0019a0002c0003t0105g0184 | 3 | HG00738.hp1 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.964+2344A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855212 | ||||||
chr2:43855218
|
A | G | 1 | a0002c0004t0013g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964+2350A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855218 | ||||||
chr2:43855223
|
A | G | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.964+2355A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855223 | ||||||
chr2:43855334
|
C | T | 4 | a0003c0002t0104g0242a0003c0002t0114g0217a0003c0014t0047g0216others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2466C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855334 | ||||||
chr2:43855414
|
C | G | 5 | a0002c0003t0099g0035a0003c0010t0023g0036a0003c0010t0023g0037others(2): Show | 5 | HG01192.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+2546C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855414 | ||||||
chr2:43855504
|
A | C | 2 | a0002c0003t0012g0177a0002c0003t0111g0178 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.964+2636A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855504 | ||||||
chr2:43855530
|
T | A | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.964+2662T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855530 | ||||||
chr2:43855550
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2682G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855550 | ||||||
chr2:43855564
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2696C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855564 | ||||||
chr2:43855568
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2700C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855568 | ||||||
chr2:43855572
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2704A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855572 | ||||||
chr2:43855576
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2708A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855576 | ||||||
chr2:43855718
|
C | T | 1 | a0002c0003t0012g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.964+2850C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855718 | ||||||
chr2:43855755
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2887C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855755 | ||||||
chr2:43855763
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2895T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855763 | ||||||
chr2:43855779
|
A | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2911A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855779 | ||||||
chr2:43855840
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2972G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855840 | ||||||
chr2:43855880
|
C | A | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+3012C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855880 | ||||||
chr2:43855930
|
C | T | 1 | a0001c0001t0032g0070 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.964+3062C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855930 | ||||||
chr2:43855961
|
TCTCA | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+3096_964+3099d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43855961 | |||||
chr2:43855984
|
T | C | 126 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(123): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.964+3116T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855984 | ||||||
chr2:43855988
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3120T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855988 | ||||||
chr2:43856137
|
T | C | 2 | a0001c0001t0034g0074a0001c0001t0034g0088 | 2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.964+3269T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856137 | ||||||
chr2:43856210
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3342G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856210 | ||||||
chr2:43856237
|
G | C | 1 | a0002c0003t0107g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.964+3369G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856237 | ||||||
chr2:43856285
|
A | G | 1 | a0009c0012t0078g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.964+3417A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856285 | ||||||
chr2:43856331
|
TCCCTGTC others(17): Show |
T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3487_964+3510d others(26): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43856331 | |||||
chr2:43856355
|
A | T | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+3487A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856355 | ||||||
chr2:43856405
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3537T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856405 | ||||||
chr2:43856515
|
G | A | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+3647G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856515 | ||||||
chr2:43856518
|
C | CTCTCACT others(13): Show |
1 | a0003c0017t0015g0014 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.964+3662_964+3681d others(22): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43856518 | |||||
chr2:43856588
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.964+3720C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856588 | ||||||
chr2:43856616
|
T | C | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+3748T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856616 | ||||||
chr2:43856623
|
C | CTCTA | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3758_964+3761d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43856623 | |||||
chr2:43856665
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3797A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856665 | ||||||
chr2:43856713
|
A | G | 2 | a0003c0002t0003g0172a0003c0022t0013g0261 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.964+3845A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856713 | ||||||
chr2:43856744
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3876G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856744 | ||||||
chr2:43856746
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3878T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856746 | ||||||
chr2:43856826
|
C | A | 1 | a0004c0007t0056g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.964+3958C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856826 | ||||||
chr2:43856863
|
G | A | 1 | a0003c0002t0101g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.964+3995G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856863 | ||||||
chr2:43856873
|
T | C | 3 | a0006c0005t0003g0219a0006c0005t0003g0244a0006c0005t0003g0259 | 3 | HG03098.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.964+4005T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856873 | ||||||
chr2:43856913
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4045T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856913 | ||||||
chr2:43856973
|
A | G | 1 | a0003c0002t0093g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.964+4105A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856973 | ||||||
chr2:43857023
|
C | A | 5 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+4155C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857023 | ||||||
chr2:43857041
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4173C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857041 | ||||||
chr2:43857050
|
A | T | 195 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(192): Show | 210 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.964+4182A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857050 | ||||||
chr2:43857117
|
A | AGATAGAA others(37): Show |
4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4273_964+4274i others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43857117 | |||||
chr2:43857117
|
AGATAGAA others(37): Show |
A | 1 | a0002c0003t0003g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.964+4276_964+4319d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43857117 | |||||
chr2:43857133
|
A | G | 12 | a0003c0002t0028g0041a0007c0009t0024g0005a0007c0009t0024g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+4265A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857133 | ||||||
chr2:43857140
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.964+4272T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857140 | ||||||
chr2:43857177
|
A | G | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+4309A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857177 | ||||||
chr2:43857193
|
T | C | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+4325T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857193 | ||||||
chr2:43857328
|
C | T | 2 | a0001c0008t0031g0152a0001c0008t0058g0068 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.964+4460C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857328 | ||||||
chr2:43857345
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4477T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857345 | ||||||
chr2:43857351
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4483A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857351 | ||||||
chr2:43857364
|
A | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4496A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857364 | ||||||
chr2:43857422
|
G | GATAGAAC others(31): Show |
2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+4573_964+4610d others(40): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43857422 | |||||
chr2:43857461
|
A | T | 25 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(22): Show | 26 | HG00741.hp2 HG01943.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.964+4593A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857461 | ||||||
chr2:43857547
|
A | T | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.964+4679A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857547 | ||||||
chr2:43857549
|
A | G | 2 | a0002c0003t0002g0044a0002c0003t0002g0045 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.964+4681A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857549 | ||||||
chr2:43857726
|
C | G | 1 | a0005c0006t0044g0277 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.964+4858C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857726 | ||||||
chr2:43857836
|
C | T | 27 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(24): Show | 28 | HG00280.hp2 HG01070.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.964+4968C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857836 | ||||||
chr2:43857872
|
C | T | 1 | a0001c0001t0004g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.964+5004C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857872 | ||||||
chr2:43857873
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5005G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857873 | ||||||
chr2:43857896
|
C | A | 3 | a0003c0002t0002g0275a0003c0002t0002g0284a0003c0002t0110g0283 | 3 | HG00735.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.964+5028C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857896 | ||||||
chr2:43857955
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5087G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857955 | ||||||
chr2:43858025
|
T | A | 8 | a0001c0001t0001g0050a0001c0001t0005g0075a0001c0001t0005g0086others(5): Show | 8 | HG01081.hp2 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+5157T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858025 | ||||||
chr2:43858105
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5237A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858105 | ||||||
chr2:43858127
|
T | C | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+5259T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858127 | ||||||
chr2:43858402
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5534C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858402 | ||||||
chr2:43858500
|
A | G | 5 | a0003c0002t0004g0021a0003c0002t0004g0214a0003c0002t0005g0021others(2): Show | 5 | NA18939.hp2 NA18957.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+5632A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858500 | ||||||
chr2:43858507
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5639T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858507 | ||||||
chr2:43858567
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5699C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858567 | ||||||
chr2:43858724
|
G | A | 1 | a0008c0018t0002g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.964+5856G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858724 | ||||||
chr2:43858741
|
A | AC | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.964+5874dupC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43858741 | |||||
chr2:43858849
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5981A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858849 | ||||||
chr2:43858988
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6120C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858988 | ||||||
chr2:43859008
|
G | A | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.964+6140G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859008 | ||||||
chr2:43859082
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6214C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859082 | ||||||
chr2:43859084
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6216G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859084 | ||||||
chr2:43859180
|
ACTGT | A | 12 | a0003c0002t0028g0041a0007c0009t0024g0005a0007c0009t0024g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+6315_964+6318d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43859180 | |||||
chr2:43859201
|
C | G | 1 | a0001c0001t0076g0085 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.964+6333C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859201 | ||||||
chr2:43859207
|
C | T | 2 | a0005c0006t0043g0241a0005c0006t0043g0253 | 2 | HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.964+6339C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859207 | ||||||
chr2:43859300
|
G | T | 1 | a0001c0001t0020g0084 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.964+6432G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859300 | ||||||
chr2:43859423
|
A | G | 1 | a0013c0029t0070g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.964+6555A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859423 | ||||||
chr2:43859452
|
G | A | 25 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(22): Show | 26 | HG00741.hp2 HG01943.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.964+6584G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859452 | ||||||
chr2:43859535
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6667C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859535 | ||||||
chr2:43859584
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6716G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859584 | ||||||
chr2:43859656
|
G | T | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.964+6788G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859656 | ||||||
chr2:43859776
|
G | A | 1 | a0002c0003t0003g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.964+6908G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859776 | ||||||
chr2:43859824
|
T | A | 1 | a0002c0003t0003g0196 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964+6956T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859824 | ||||||
chr2:43859885
|
C | G | 25 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(22): Show | 26 | HG00741.hp2 HG01943.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.964+7017C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859885 | ||||||
chr2:43859929
|
C | G | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+7061C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859929 | ||||||
chr2:43860007
|
C | G | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+7139C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860007 | ||||||
chr2:43860019
|
G | A | 2 | a0004c0007t0007g0006a0004c0007t0007g0064 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.964+7151G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860019 | ||||||
chr2:43860077
|
CCCTCTGG others(33): Show |
C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7218_964+7257d others(42): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860077 | |||||
chr2:43860168
|
G | A | 1 | a0001c0001t0015g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.964+7300G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860168 | ||||||
chr2:43860169
|
A | G | 1 | a0001c0001t0004g0140 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.964+7301A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860169 | ||||||
chr2:43860234
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7366A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860234 | ||||||
chr2:43860347
|
A | ACTAT | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7480_964+7483d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860347 | |||||
chr2:43860352
|
T | C | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.964+7484T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860352 | ||||||
chr2:43860385
|
TCA | T | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+7519_964+7520d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860385 | |||||
chr2:43860404
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7536G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860404 | ||||||
chr2:43860412
|
G | T | 5 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(2): Show | 6 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+7544G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860412 | ||||||
chr2:43860473
|
A | G | 3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964+7605A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860473 | ||||||
chr2:43860501
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7633A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860501 | ||||||
chr2:43860608
|
T | C | 8 | a0001c0001t0001g0050a0001c0001t0005g0075a0001c0001t0005g0086others(5): Show | 8 | HG01081.hp2 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+7740T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860608 | ||||||
chr2:43860711
|
C | A | 1 | a0002c0003t0017g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.964+7843C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860711 | ||||||
chr2:43860721
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7853G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860721 | ||||||
chr2:43860777
|
GCTGTATA others(37): Show |
G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7942_964+7985d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860777 | |||||
chr2:43860824
|
G | T | 1 | a0001c0008t0014g0144 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.964+7956G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860824 | ||||||
chr2:43860843
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0139 | 3 | NA18962.hp2 NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.964+7975T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860843 | ||||||
chr2:43860894
|
C | G | 4 | a0001c0001t0035g0138a0001c0001t0076g0085a0001c0008t0014g0071others(1): Show | 4 | HG03490.hp2 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+8026C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860894 | ||||||
chr2:43860902
|
C | CTATCTGG others(37): Show |
21 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(18): Show | 22 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.964+8045_964+8088d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860902 | |||||
chr2:43860934
|
A | T | 4 | a0001c0001t0009g0060a0001c0001t0020g0145a0001c0001t0033g0111others(1): Show | 4 | HG00597.hp1 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+8066A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860934 | ||||||
chr2:43860957
|
T | G | 4 | a0003c0002t0104g0242a0003c0002t0114g0217a0003c0014t0047g0216others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8089T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860957 | ||||||
chr2:43861008
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8140A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861008 | ||||||
chr2:43861014
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8146T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861014 | ||||||
chr2:43861026
|
C | G | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+8158C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861026 | ||||||
chr2:43861028
|
A | G | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.964+8160A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861028 | ||||||
chr2:43861039
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8171T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861039 | ||||||
chr2:43861057
|
G | T | 2 | a0003c0021t0015g0030a0006c0005t0002g0260 | 2 | HG00741.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.964+8189G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861057 | ||||||
chr2:43861064
|
C | G | 3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964+8196C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861064 | ||||||
chr2:43861123
|
T | C | 1 | a0002c0003t0016g0239 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.964+8255T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861123 | ||||||
chr2:43861172
|
T | C | 1 | a0002c0003t0107g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.964+8304T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861172 | ||||||
chr2:43861176
|
C | A | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+8308C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861176 | ||||||
chr2:43861179
|
C | A | 6 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(3): Show | 7 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+8311C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861179 | ||||||
chr2:43861251
|
T | C | 5 | a0001c0001t0018g0003a0003c0010t0023g0036a0003c0010t0023g0037others(2): Show | 7 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+8383T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861251 | ||||||
chr2:43861359
|
T | G | 1 | a0003c0002t0101g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.964+8491T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861359 | ||||||
chr2:43861367
|
T | G | 1 | a0015c0023t0090g0208 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.964+8499T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861367 | ||||||
chr2:43861670
|
C | T | 1 | a0003c0002t0008g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.964+8802C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861670 | ||||||
chr2:43861684
|
T | A | 1 | a0001c0001t0009g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.964+8816T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861684 | ||||||
chr2:43861712
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8844C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861712 | ||||||
chr2:43861739
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8871A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861739 | ||||||
chr2:43861808
|
C | T | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+8940C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861808 | ||||||
chr2:43861890
|
A | G | 1 | a0005c0006t0083g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.964+9022A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861890 | ||||||
chr2:43861909
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9041T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861909 | ||||||
chr2:43861942
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9074C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861942 | ||||||
chr2:43862086
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9218T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862086 | ||||||
chr2:43862087
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9219G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862087 | ||||||
chr2:43862115
|
G | T | 1 | a0006c0005t0118g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.964+9247G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862115 | ||||||
chr2:43862216
|
A | C | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+9348A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862216 | ||||||
chr2:43862216
|
A | G | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.964+9348A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862216 | ||||||
chr2:43862294
|
C | G | 1 | a0001c0001t0073g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.964+9426C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862294 | ||||||
chr2:43862333
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9465T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862333 | ||||||
chr2:43862358
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9490G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862358 | ||||||
chr2:43862360
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9492G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862360 | ||||||
chr2:43862361
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9493T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862361 | ||||||
chr2:43862376
|
T | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9508T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862376 | ||||||
chr2:43862381
|
T | TCTCTATA others(712): Show |
4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9517_964+9518i others(721): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43862381 | |||||
chr2:43862403
|
T | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9535T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862403 | ||||||
chr2:43862408
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9540A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862408 | ||||||
chr2:43862413
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9545G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862413 | ||||||
chr2:43862420
|
A | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9552A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862420 | ||||||
chr2:43862421
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9553T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862421 | ||||||
chr2:43862426
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9550A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862426 | ||||||
chr2:43862427
|
A | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9549A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862427 | ||||||
chr2:43862431
|
T | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9545T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862431 | ||||||
chr2:43862451
|
A | AATAGAAT others(77): Show |
1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.965-9514_965-9431d others(86): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43862451 | |||||
chr2:43862462
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9514C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862462 | ||||||
chr2:43862468
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9508C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862468 | ||||||
chr2:43862477
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9499A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862477 | ||||||
chr2:43862478
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9498T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862478 | ||||||
chr2:43862480
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9496C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862480 | ||||||
chr2:43862546
|
T | TCC | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9430_965-9429i others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862546 | ||||||
chr2:43862547
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9429A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862547 | ||||||
chr2:43862553
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9423A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862553 | ||||||
chr2:43862554
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9422A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862554 | ||||||
chr2:43862559
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9417A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862559 | ||||||
chr2:43862560
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9416C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862560 | ||||||
chr2:43862570
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9406G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862570 | ||||||
chr2:43862579
|
T | CAGAACTC others(2864): Show |
1 | a0003c0010t0123g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.965-9398_965-9397i others(2873): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862579 | ||||||
chr2:43862579
|
T | CAGAACTC others(2864): Show |
3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.965-9398_965-9397i others(2873): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862579 | ||||||
chr2:43862587
|
TTAC | T | 125 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(122): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.965-9385_965-9383d others(5): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43862587 | |||||
chr2:43862601
|
C | A | 1 | a0006c0005t0002g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.965-9375C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862601 | ||||||
chr2:43862648
|
C | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-9328C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862648 | ||||||
chr2:43862651
|
T | C | 2 | a0003c0014t0086g0276a0005c0006t0044g0285 | 2 | HG00642.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.965-9325T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862651 | ||||||
chr2:43862652
|
A | T | 2 | a0003c0014t0086g0276a0005c0006t0044g0285 | 2 | HG00642.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.965-9324A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862652 | ||||||
chr2:43862676
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9300T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862676 | ||||||
chr2:43862711
|
A | G | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-9265A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862711 | ||||||
chr2:43862789
|
C | A | 152 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(149): Show | 164 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.965-9187C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862789 | ||||||
chr2:43862790
|
T | G | 1 | a0001c0001t0005g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.965-9186T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862790 | ||||||
chr2:43862795
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9181G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862795 | ||||||
chr2:43862913
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9063T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862913 | ||||||
chr2:43863045
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8931G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863045 | ||||||
chr2:43863047
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8929G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863047 | ||||||
chr2:43863067
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8909C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863067 | ||||||
chr2:43863087
|
A | G | 1 | a0003c0002t0003g0205 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.965-8889A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863087 | ||||||
chr2:43863131
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8845C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863131 | ||||||
chr2:43863194
|
T | C | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-8782T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863194 | ||||||
chr2:43863338
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8638T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863338 | ||||||
chr2:43863351
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8625C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863351 | ||||||
chr2:43863621
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8355A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863621 | ||||||
chr2:43863762
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8214C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863762 | ||||||
chr2:43863798
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8178G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863798 | ||||||
chr2:43863857
|
T | G | 1 | a0001c0001t0018g0003 | 3 | NA18970.hp2 NA19085.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.965-8119T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863857 | ||||||
chr2:43863916
|
G | A | 9 | a0003c0002t0002g0209a0003c0002t0021g0063a0003c0002t0021g0157others(6): Show | 9 | HG01109.hp2 HG01192.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-8060G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863916 | ||||||
chr2:43863919
|
C | T | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.965-8057C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863919 | ||||||
chr2:43863944
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8032A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863944 | ||||||
chr2:43863958
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8018G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863958 | ||||||
chr2:43863980
|
A | G | 1 | a0013c0029t0070g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.965-7996A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863980 | ||||||
chr2:43863990
|
A | G | 1 | a0002c0003t0006g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.965-7986A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863990 | ||||||
chr2:43864120
|
T | C | 1 | a0008c0018t0002g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.965-7856T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864120 | ||||||
chr2:43864140
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7836T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864140 | ||||||
chr2:43864228
|
C | G | 12 | a0003c0002t0028g0041a0007c0009t0024g0005a0007c0009t0024g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.965-7748C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864228 | ||||||
chr2:43864281
|
C | G | 141 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(138): Show | 150 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.965-7695C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864281 | ||||||
chr2:43864283
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7693T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864283 | ||||||
chr2:43864367
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7609T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864367 | ||||||
chr2:43864468
|
A | G | 1 | a0003c0010t0023g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.965-7508A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864468 | ||||||
chr2:43864490
|
A | G | 7 | a0001c0001t0010g0011a0001c0001t0010g0012a0001c0001t0010g0116others(4): Show | 9 | HG01106.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-7486A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864490 | ||||||
chr2:43864499
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7477A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864499 | ||||||
chr2:43864502
|
C | A | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.965-7474C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864502 | ||||||
chr2:43864646
|
C | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-7330C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864646 | ||||||
chr2:43864868
|
A | ATAGGACT others(41): Show |
4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7108_965-7107i others(50): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864868 | ||||||
chr2:43864869
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7107C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864869 | ||||||
chr2:43864921
|
T | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-7055T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864921 | ||||||
chr2:43864927
|
C | T | 266 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(263): Show | 283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.965-7049C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864927 | ||||||
chr2:43864928
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7048A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864928 | ||||||
chr2:43865063
|
T | C | 1 | a0001c0001t0005g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.965-6913T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865063 | ||||||
chr2:43865106
|
C | G | 137 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.965-6870C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865106 | ||||||
chr2:43865190
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6786C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865190 | ||||||
chr2:43865194
|
CACTATCT others(161): Show |
C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6774_965-6607d others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865194 | |||||
chr2:43865262
|
A | G | 1 | a0007c0020t0066g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.965-6714A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865262 | ||||||
chr2:43865267
|
C | G | 190 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(187): Show | 205 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.965-6709C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865267 | ||||||
chr2:43865479
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6497C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865479 | ||||||
chr2:43865487
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6489C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865487 | ||||||
chr2:43865492
|
T | C | 1 | a0002c0003t0107g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.965-6484T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865492 | ||||||
chr2:43865555
|
C | A | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-6421C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865555 | ||||||
chr2:43865557
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6419C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865557 | ||||||
chr2:43865591
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6385C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865591 | ||||||
chr2:43865592
|
TCA | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6382_965-6381d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865592 | |||||
chr2:43865599
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6377C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865599 | ||||||
chr2:43865601
|
A | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6375A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865601 | ||||||
chr2:43865614
|
A | ACTCT | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6360_965-6359i others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865614 | |||||
chr2:43865634
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6342C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865634 | ||||||
chr2:43865635
|
C | T | 1 | a0001c0001t0074g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.965-6341C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865635 | ||||||
chr2:43865636
|
T | TG | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6340_965-6339i others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865636 | ||||||
chr2:43865637
|
A | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6339A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865637 | ||||||
chr2:43865639
|
T | TG | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6336dupG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865639 | |||||
chr2:43865653
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6323C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865653 | ||||||
chr2:43865655
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6321C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865655 | ||||||
chr2:43865659
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6317C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865659 | ||||||
chr2:43865661
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6315C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865661 | ||||||
chr2:43865671
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6305T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865671 | ||||||
chr2:43865679
|
G | GTCTA | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6294_965-6293i others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865679 | |||||
chr2:43865691
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6285C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865691 | ||||||
chr2:43865696
|
AATAT | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6279_965-6276d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865696 | ||||||
chr2:43865702
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6274T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865702 | ||||||
chr2:43865703
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6273A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865703 | ||||||
chr2:43865705
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6271G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865705 | ||||||
chr2:43865712
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6264G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865712 | ||||||
chr2:43865719
|
C | T | 1 | a0002c0003t0006g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.965-6257C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865719 | ||||||
chr2:43865723
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6253G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865723 | ||||||
chr2:43865820
|
G | C | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-6156G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865820 | ||||||
chr2:43865887
|
C | T | 9 | a0001c0001t0001g0130a0001c0001t0010g0011a0001c0001t0010g0012others(6): Show | 11 | HG00733.hp1 HG01106.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-6089C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865887 | ||||||
chr2:43865899
|
C | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-6077C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865899 | ||||||
chr2:43865912
|
G | C | 1 | a0003c0002t0093g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.965-6064G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865912 | ||||||
chr2:43865923
|
A | G | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-6053A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865923 | ||||||
chr2:43865941
|
C | G | 6 | a0002c0003t0016g0004a0002c0003t0016g0239a0002c0003t0016g0252others(3): Show | 7 | NA18948.hp1 NA18952.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-6035C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865941 | ||||||
chr2:43865977
|
G | C | 1 | a0006c0005t0045g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.965-5999G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865977 | ||||||
chr2:43866092
|
G | A | 2 | a0002c0003t0002g0231a0002c0003t0115g0173 | 2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.965-5884G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866092 | ||||||
chr2:43866137
|
G | C | 85 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(82): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.965-5839G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866137 | ||||||
chr2:43866210
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5766A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866210 | ||||||
chr2:43866211
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5765G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866211 | ||||||
chr2:43866239
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5737G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866239 | ||||||
chr2:43866282
|
CG | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5691delG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43866282 | |||||
chr2:43866284
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5692G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866284 | ||||||
chr2:43866333
|
A | G | 5 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.965-5643A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866333 | ||||||
chr2:43866352
|
A | C | 1 | a0007c0020t0066g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.965-5624A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866352 | ||||||
chr2:43866395
|
A | G | 1 | a0003c0022t0013g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.965-5581A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866395 | ||||||
chr2:43866400
|
G | A | 4 | a0001c0001t0035g0138a0001c0001t0076g0085a0001c0008t0014g0071others(1): Show | 4 | HG03490.hp2 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-5576G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866400 | ||||||
chr2:43866482
|
G | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5494G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866482 | ||||||
chr2:43866659
|
C | T | 3 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0053g0031 | 4 | HG01346.hp2 HG02486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-5317C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866659 | ||||||
chr2:43866682
|
G | A | 1 | a0002c0003t0006g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.965-5294G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866682 | ||||||
chr2:43866730
|
A | G | 1 | a0017c0028t0047g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965-5246A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866730 | ||||||
chr2:43866731
|
C | T | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-5245C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866731 | ||||||
chr2:43866751
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5225T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866751 | ||||||
chr2:43866782
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5194A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866782 | ||||||
chr2:43866809
|
C | T | 5 | a0003c0002t0002g0209a0003c0002t0021g0063a0003c0002t0021g0157others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-5167C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866809 | ||||||
chr2:43866819
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5157T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866819 | ||||||
chr2:43866824
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5152G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866824 | ||||||
chr2:43866879
|
A | G | 1 | a0001c0001t0005g0110 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.965-5097A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866879 | ||||||
chr2:43866896
|
C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-5080C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866896 | ||||||
chr2:43866899
|
A | G | 2 | a0002c0003t0006g0194a0002c0003t0006g0230 | 2 | NA18942.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.965-5077A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866899 | ||||||
chr2:43866926
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5050G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866926 | ||||||
chr2:43866951
|
G | A | 1 | a0014c0027t0006g0232 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.965-5025G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866951 | ||||||
chr2:43867001
|
G | A | 1 | a0006c0005t0045g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.965-4975G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867001 | ||||||
chr2:43867015
|
C | T | 12 | a0001c0001t0015g0142a0001c0008t0008g0274a0001c0008t0014g0144others(9): Show | 13 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.965-4961C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867015 | ||||||
chr2:43867017
|
T | C | 1 | a0009c0012t0078g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.965-4959T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867017 | ||||||
chr2:43867026
|
G | A | 5 | a0003c0002t0021g0165a0003c0010t0023g0036a0003c0010t0023g0037others(2): Show | 5 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-4950G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867026 | ||||||
chr2:43867175
|
G | A | 6 | a0001c0001t0038g0052a0001c0001t0038g0053a0003c0002t0029g0150others(3): Show | 7 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-4801G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867175 | ||||||
chr2:43867207
|
G | A | 2 | a0003c0002t0017g0174a0003c0002t0112g0204 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.965-4769G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867207 | ||||||
chr2:43867208
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.965-4768A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867208 | ||||||
chr2:43867216
|
G | A | 1 | a0003c0002t0098g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.965-4760G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867216 | ||||||
chr2:43867226
|
T | A | 1 | a0002c0003t0003g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.965-4750T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867226 | ||||||
chr2:43867260
|
C | T | 1 | a0003c0010t0123g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.965-4716C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867260 | ||||||
chr2:43867347
|
T | TA | 182 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(179): Show | 196 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.965-4617dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43867347 | |||||
chr2:43867477
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4499A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867477 | ||||||
chr2:43867513
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4463A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867513 | ||||||
chr2:43867547
|
C | G | 1 | a0005c0006t0044g0277 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.965-4429C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867547 | ||||||
chr2:43867560
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4416C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867560 | ||||||
chr2:43867582
|
G | A | 1 | a0003c0014t0047g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.965-4394G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867582 | ||||||
chr2:43867601
|
G | T | 1 | a0003c0002t0028g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.965-4375G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867601 | ||||||
chr2:43867619
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4357C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867619 | ||||||
chr2:43867706
|
G | A | 22 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(19): Show | 23 | HG00438.hp1 HG00741.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.965-4270G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867706 | ||||||
chr2:43867843
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0036g0076 | 2 | NA18942.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.965-4133C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867843 | ||||||
chr2:43867875
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.965-4101A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867875 | ||||||
chr2:43867884
|
T | C | 1 | a0005c0006t0026g0043 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.965-4092T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867884 | ||||||
chr2:43867914
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4062G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867914 | ||||||
chr2:43867938
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0033g0111a0001c0001t0033g0113 | 3 | HG00597.hp1 HG02027.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.965-4038T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867938 | ||||||
chr2:43868069
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3907C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868069 | ||||||
chr2:43868074
|
T | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3902T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868074 | ||||||
chr2:43868091
|
A | G | 2 | a0003c0002t0003g0172a0003c0022t0013g0261 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.965-3885A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868091 | ||||||
chr2:43868101
|
C | T | 2 | a0001c0001t0005g0089a0003c0002t0028g0041 | 2 | NA18957.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.965-3875C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868101 | ||||||
chr2:43868187
|
G | C | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.965-3789G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868187 | ||||||
chr2:43868193
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3783A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868193 | ||||||
chr2:43868227
|
A | C | 139 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(136): Show | 148 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.965-3749A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868227 | ||||||
chr2:43868337
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3639G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868337 | ||||||
chr2:43868347
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3629T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868347 | ||||||
chr2:43868426
|
G | A | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-3550G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868426 | ||||||
chr2:43868446
|
C | T | 1 | a0006c0005t0097g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.965-3530C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868446 | ||||||
chr2:43868482
|
A | G | 139 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(136): Show | 148 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.965-3494A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868482 | ||||||
chr2:43868492
|
T | TTATCTGT others(37): Show |
1 | a0017c0028t0047g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965-3462_965-3419d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43868492 | |||||
chr2:43868533
|
T | C | 3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.965-3443T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868533 | ||||||
chr2:43868558
|
G | C | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.965-3418G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868558 | ||||||
chr2:43868611
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3365G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868611 | ||||||
chr2:43868725
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3251C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868725 | ||||||
chr2:43868765
|
A | G | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-3211A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868765 | ||||||
chr2:43868824
|
G | A | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.965-3152G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868824 | ||||||
chr2:43868871
|
T | A | 138 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-3105T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868871 | ||||||
chr2:43868897
|
C | G | 11 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-3079C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868897 | ||||||
chr2:43868915
|
C | A | 4 | a0003c0002t0104g0242a0003c0002t0114g0217a0003c0014t0047g0216others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3061C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868915 | ||||||
chr2:43868919
|
C | G | 1 | a0006c0005t0003g0023 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.965-3057C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868919 | ||||||
chr2:43868999
|
C | T | 2 | a0002c0003t0016g0004a0002c0003t0048g0004 | 3 | NA18974.hp1 NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.965-2977C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868999 | ||||||
chr2:43869000
|
G | A | 261 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(258): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.965-2976G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869000 | ||||||
chr2:43869120
|
T | G | 263 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(260): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.965-2856T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869120 | ||||||
chr2:43869179
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2797G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869179 | ||||||
chr2:43869194
|
T | C | 1 | a0001c0001t0004g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.965-2782T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869194 | ||||||
chr2:43869197
|
T | A | 263 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(260): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.965-2779T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869197 | ||||||
chr2:43869259
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2717G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869259 | ||||||
chr2:43869263
|
G | A | 271 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(268): Show | 289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.965-2713G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869263 | ||||||
chr2:43869318
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2658A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869318 | ||||||
chr2:43869420
|
T | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2556T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869420 | ||||||
chr2:43869631
|
T | A | 266 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(263): Show | 283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.965-2345T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869631 | ||||||
chr2:43869643
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2333C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869643 | ||||||
chr2:43869669
|
A | G | 1 | a0002c0003t0017g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.965-2307A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869669 | ||||||
chr2:43869975
|
A | C | 3 | a0003c0002t0003g0268a0003c0002t0092g0279a0005c0006t0089g0062 | 3 | HG00733.hp2 HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.965-2001A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869975 | ||||||
chr2:43869975
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2001A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869975 | ||||||
chr2:43870131
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1845G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870131 | ||||||
chr2:43870189
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1787C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870189 | ||||||
chr2:43870208
|
TCTCACTG others(13): Show |
T | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-1761_965-1742d others(22): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43870208 | |||||
chr2:43870221
|
A | G | 77 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(74): Show | 80 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.965-1755A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870221 | ||||||
chr2:43870228
|
C | T | 260 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(257): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.965-1748C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870228 | ||||||
chr2:43870249
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1727A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870249 | ||||||
chr2:43870293
|
C | CAATT | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1683_965-1682i others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870293 | ||||||
chr2:43870398
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1578G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870398 | ||||||
chr2:43870503
|
C | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1473C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870503 | ||||||
chr2:43870529
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1447T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870529 | ||||||
chr2:43870543
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1433C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870543 | ||||||
chr2:43870560
|
G | C | 8 | a0001c0001t0001g0050a0001c0001t0005g0075a0001c0001t0005g0086others(5): Show | 8 | HG01081.hp2 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-1416G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870560 | ||||||
chr2:43870571
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1405G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870571 | ||||||
chr2:43870573
|
C | T | 9 | a0002c0003t0003g0248a0002c0003t0006g0193a0002c0003t0006g0198others(6): Show | 9 | HG01106.hp1 HG01928.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-1403C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870573 | ||||||
chr2:43870574
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1402G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870574 | ||||||
chr2:43870640
|
G | T | 1 | a0003c0010t0123g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.965-1336G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870640 | ||||||
chr2:43870691
|
G | A | 1 | a0003c0002t0027g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.965-1285G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870691 | ||||||
chr2:43870755
|
C | T | 1 | a0002c0004t0011g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.965-1221C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870755 | ||||||
chr2:43870798
|
C | CACCATCT others(12): Show |
2 | a0003c0021t0015g0030a0006c0005t0002g0260 | 2 | HG00741.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.965-1176_965-1175i others(21): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43870798 | |||||
chr2:43870875
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1101A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870875 | ||||||
chr2:43870877
|
T | A | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-1099T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870877 | ||||||
chr2:43870890
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1086G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870890 | ||||||
chr2:43871016
|
C | T | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-960C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871016 | ||||||
chr2:43871020
|
G | GGATAGAA others(75): Show |
4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-921_965-920ins others(82): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871020 | |||||
chr2:43871120
|
C | G | 4 | a0001c0001t0015g0142a0001c0008t0014g0144a0001c0008t0054g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-856C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871120 | ||||||
chr2:43871129
|
T | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-847T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871129 | ||||||
chr2:43871140
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-836C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871140 | ||||||
chr2:43871162
|
ATCTATCT others(257): Show |
A | 3 | a0002c0004t0011g0185a0002c0004t0011g0188a0002c0004t0011g0225 | 3 | HG01433.hp1 HG01496.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.965-773_965-510del | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871162 | |||||
chr2:43871192
|
A | G | 117 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(114): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.965-784A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871192 | ||||||
chr2:43871195
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-781G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871195 | ||||||
chr2:43871282
|
C | T | 1 | a0003c0002t0116g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.965-694C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871282 | ||||||
chr2:43871286
|
A | C | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-690A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871286 | ||||||
chr2:43871308
|
C | G | 27 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(24): Show | 28 | HG00280.hp2 HG01070.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.965-668C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871308 | ||||||
chr2:43871374
|
A | AGAACTCT others(447): Show |
1 | a0003c0010t0023g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.965-587_965-586ins others(454): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871374 | |||||
chr2:43871374
|
A | AGAACTCT others(447): Show |
3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0123g0038 | 3 | HG02895.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.965-587_965-586ins others(454): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871374 | |||||
chr2:43871426
|
G | A | 146 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(143): Show | 156 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.965-550G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871426 | ||||||
chr2:43871457
|
T | C | 1 | a0003c0002t0029g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.965-519T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871457 | ||||||
chr2:43871467
|
G | A | 127 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(124): Show | 135 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.965-509G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871467 | ||||||
chr2:43871490
|
C | G | 11 | a0003c0002t0002g0209a0003c0002t0021g0063a0003c0002t0021g0157others(8): Show | 12 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.965-486C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871490 | ||||||
chr2:43871542
|
C | T | 3 | a0002c0003t0006g0233a0002c0003t0096g0249a0003c0002t0093g0238 | 3 | NA18964.hp2 NA19005.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.965-434C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871542 | ||||||
chr2:43871645
|
G | A | 4 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-331G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871645 | ||||||
chr2:43871687
|
G | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-289G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871687 | ||||||
chr2:43871716
|
T | C | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 152 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.965-260T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871716 | ||||||
chr2:43871902
|
G | A | 3 | a0002c0003t0012g0177a0002c0003t0111g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-74G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871902 | ||||||
chr2:43871917
|
C | T | 1 | a0003c0002t0029g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.965-59C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871917 | ||||||
chr2:43871918
|
A | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-58A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871918 | ||||||
chr2:43872191
|
C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-32C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 7/12 | chr2 | 43872191 | ||||||
chr2:43872348
|
C | G | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0100g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+42C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872348 | ||||||
chr2:43872406
|
G | A | 1 | a0015c0023t0090g0208 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1211+100G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872406 | ||||||
chr2:43872443
|
G | A | 85 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(82): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1211+137G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872443 | ||||||
chr2:43872454
|
G | C | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1211+148G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872454 | ||||||
chr2:43872495
|
G | A | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+189G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872495 | ||||||
chr2:43872652
|
A | G | 1 | a0001c0001t0004g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1211+346A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872652 | ||||||
chr2:43872687
|
C | G | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+381C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872687 | ||||||
chr2:43872754
|
C | T | 1 | a0002c0003t0006g0201 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1211+448C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872754 | ||||||
chr2:43872876
|
T | A | 26 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0197others(23): Show | 27 | HG00280.hp2 HG01070.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1211+570T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872876 | ||||||
chr2:43872924
|
C | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+618C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872924 | ||||||
chr2:43872938
|
G | A | 128 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(125): Show | 136 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1211+632G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872938 | ||||||
chr2:43872965
|
TAC | T | 4 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+665_1211+666d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43872965 | |||||
chr2:43872981
|
C | T | 1 | a0013c0029t0070g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1211+675C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872981 | ||||||
chr2:43873030
|
C | G | 142 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1211+724C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873030 | ||||||
chr2:43873189
|
A | AT | 22 | a0002c0003t0012g0147a0002c0003t0094g0170a0002c0003t0099g0035others(19): Show | 23 | HG00738.hp2 HG01891.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-581dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43873189 | |||||
chr2:43873189
|
A | ATT | 15 | a0002c0003t0003g0222a0002c0003t0003g0223a0002c0003t0006g0229others(12): Show | 16 | HG01256.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1212-582_1212-581d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43873189 | |||||
chr2:43873189
|
AT | A | 16 | a0001c0001t0001g0108a0001c0001t0001g0129a0001c0001t0010g0116others(13): Show | 17 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1212-581delT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43873189 | |||||
chr2:43873218
|
T | C | 141 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(138): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1212-569T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873218 | ||||||
chr2:43873244
|
A | G | 3 | a0001c0001t0004g0047a0001c0001t0004g0083a0001c0001t0065g0048 | 3 | NA18959.hp2 NA18986.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1212-543A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873244 | ||||||
chr2:43873457
|
G | T | 5 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-330G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873457 | ||||||
chr2:43873472
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0032g0070 | 2 | NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1212-315G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873472 | ||||||
chr2:43873488
|
A | G | 1 | a0002c0003t0106g0255 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1212-299A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873488 | ||||||
chr2:43873497
|
G | A | 1 | a0002c0003t0113g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1212-290G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873497 | ||||||
chr2:43873542
|
T | C | 2 | a0001c0001t0005g0125a0001c0001t0005g0127 | 2 | HG01081.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1212-245T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873542 | ||||||
chr2:43873563
|
G | C | 1 | a0003c0002t0101g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1212-224G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873563 | ||||||
chr2:43873601
|
A | G | 1 | a0002c0003t0113g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1212-186A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873601 | ||||||
chr2:43873620
|
C | G | 5 | a0003c0002t0029g0150a0003c0002t0029g0151a0003c0002t0050g0149others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-167C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873620 | ||||||
chr2:43873666
|
A | C | 1 | a0001c0001t0005g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1212-121A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873666 | ||||||
chr2:43873710
|
T | C | 29 | a0002c0003t0002g0234a0002c0003t0002g0254a0002c0004t0042g0247others(26): Show | 31 | HG00438.hp1 HG00741.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1212-77T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873710 | ||||||
chr2:43873732
|
G | A | 27 | a0003c0002t0003g0172a0003c0002t0004g0021a0003c0002t0004g0214others(24): Show | 29 | HG00438.hp1 HG00741.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1212-55G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873732 | ||||||
chr2:43874011
|
C | T | 1 | a0006c0005t0003g0023 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1411+25C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874011 | ||||||
chr2:43874075
|
CA | C | 279 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(276): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1411+90delA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874075 | ||||||
chr2:43874090
|
A | G | 35 | a0001c0008t0014g0144a0001c0008t0031g0152a0001c0008t0058g0068others(32): Show | 36 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1411+104A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874090 | ||||||
chr2:43874155
|
C | T | 2 | a0003c0002t0003g0267a0003c0002t0003g0278 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1411+169C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874155 | ||||||
chr2:43874233
|
A | G | 8 | a0002c0003t0111g0178a0003c0002t0114g0217a0003c0014t0047g0216others(5): Show | 9 | HG01884.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-174A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874233 | ||||||
chr2:43874255
|
A | G | 242 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(239): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1412-152A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874255 | ||||||
chr2:43874291
|
T | A | 2 | a0003c0002t0104g0242a0003c0010t0123g0038 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1412-116T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874291 | ||||||
chr2:43874291
|
T | G | 146 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(143): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1412-116T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874291 | ||||||
chr2:43874398
|
A | AT | 67 | a0001c0001t0001g0082a0001c0001t0001g0098a0001c0001t0001g0099others(64): Show | 73 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1412-9_1412-8insT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874398 | ||||||
chr2:43874399
|
C | T | 246 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(243): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
splice_region_variant&intron_variant | LOW | c.1412-8C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874399 | ||||||
chr2:43874510
|
G | GC | 85 | a0001c0001t0001g0130a0001c0001t0004g0047a0001c0001t0004g0092others(82): Show | 90 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1488+33dupC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874510 | |||||
chr2:43874510
|
G | GCC | 90 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(87): Show | 96 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1488+32_1488+33dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874510 | |||||
chr2:43874510
|
G | GCCC | 37 | a0001c0001t0004g0008a0001c0001t0004g0080a0001c0001t0004g0083others(34): Show | 38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1488+31_1488+33dup others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874510 | |||||
chr2:43874528
|
T | C | 1 | a0002c0003t0107g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1488+45T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874528 | ||||||
chr2:43874529
|
G | A | 7 | a0001c0001t0004g0009a0001c0001t0004g0095a0001c0001t0004g0128others(4): Show | 8 | HG00639.hp1 HG01928.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488+46G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874529 | ||||||
chr2:43874572
|
T | C | 44 | a0001c0001t0005g0054a0001c0001t0063g0104a0001c0001t0073g0067others(41): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1488+89T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874572 | ||||||
chr2:43874604
|
C | T | 3 | a0002c0003t0002g0231a0002c0003t0115g0173a0013c0029t0070g0119 | 3 | HG01261.hp1 HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1488+121C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874604 | ||||||
chr2:43874688
|
G | A | 218 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(215): Show | 231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1488+205G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874688 | ||||||
chr2:43874726
|
T | TA | 6 | a0003c0002t0046g0016a0003c0002t0102g0161a0003c0002t0104g0242others(3): Show | 7 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+251dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874726 | |||||
chr2:43874745
|
T | C | 19 | a0001c0001t0031g0046a0002c0003t0012g0147a0002c0003t0094g0170others(16): Show | 21 | HG00738.hp2 HG01346.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1488+262T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874745 | ||||||
chr2:43874804
|
C | G | 1 | a0002c0003t0003g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1488+321C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874804 | ||||||
chr2:43874825
|
G | A | 18 | a0001c0001t0009g0077a0001c0008t0014g0069a0001c0008t0014g0144others(15): Show | 19 | HG01069.hp2 HG01192.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1489-321G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874825 | ||||||
chr2:43874900
|
G | A | 4 | a0007c0009t0024g0005a0007c0009t0024g0032a0007c0009t0030g0033others(1): Show | 5 | HG02486.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-246G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874900 | ||||||
chr2:43874911
|
C | T | 3 | a0003c0010t0023g0036a0003c0010t0023g0037a0003c0010t0023g0039 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1489-235C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874911 | ||||||
chr2:43875027
|
C | T | 3 | a0001c0001t0005g0002a0001c0001t0005g0054a0001c0001t0005g0123 | 5 | HG00558.hp2 NA18939.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-119C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875027 | ||||||
chr2:43875058
|
T | C | 12 | a0001c0001t0052g0081a0001c0001t0076g0085a0002c0003t0023g0251others(9): Show | 13 | HG00280.hp2 HG01192.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489-88T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875058 | ||||||
chr2:43875085
|
G | A | 1 | a0002c0003t0016g0239 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1489-61G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875085 | ||||||
chr2:43875096
|
T | C | 101 | a0001c0001t0001g0137a0001c0001t0001g0153a0001c0001t0004g0008others(98): Show | 108 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1489-50T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875096 | ||||||
chr2:43875114
|
C | T | 2 | a0003c0002t0046g0016a0003c0002t0102g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1489-32C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875114 | ||||||
chr2:43875428
|
C | T | 3 | a0009c0012t0025g0027a0009c0012t0025g0028a0009c0012t0025g0029 | 3 | HG02109.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1756+15C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875428 | ||||||
chr2:43875435
|
T | C | 8 | a0001c0001t0064g0133a0002c0003t0012g0147a0002c0003t0012g0177others(5): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1756+22T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875435 | ||||||
chr2:43875495
|
C | T | 99 | a0001c0001t0001g0137a0001c0001t0001g0153a0001c0001t0004g0008others(96): Show | 106 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1756+82C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875495 | ||||||
chr2:43875520
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1756+107G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875520 | ||||||
chr2:43875522
|
C | A | 1 | a0016c0025t0080g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1756+109C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875522 | ||||||
chr2:43875814
|
G | C | 1 | a0003c0022t0013g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1756+401G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875814 | ||||||
chr2:43875878
|
T | C | 274 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(271): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1756+465T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875878 | ||||||
chr2:43876098
|
T | C | 76 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(73): Show | 81 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1756+685T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876098 | ||||||
chr2:43876221
|
G | A | 1 | a0011c0031t0049g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1756+808G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876221 | ||||||
chr2:43876289
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1756+876C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876289 | ||||||
chr2:43876419
|
A | G | 2 | a0008c0016t0108g0206a0008c0016t0109g0207 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1756+1006A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876419 | ||||||
chr2:43876422
|
G | A | 1 | a0002c0003t0099g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1756+1009G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876422 | ||||||
chr2:43876482
|
A | G | 3 | a0002c0004t0041g0020a0002c0004t0042g0228a0002c0004t0088g0227 | 4 | NA18944.hp2 NA18959.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756+1069A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876482 | ||||||
chr2:43876618
|
TGTGAGAA others(12): Show |
T | 2 | a0003c0014t0047g0216a0017c0028t0047g0291 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1757-924_1757-906d others(21): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 43876618 | |||||
chr2:43876867
|
T | C | 1 | a0001c0001t0020g0145 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1757-694T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876867 | ||||||
chr2:43876873
|
G | A | 1 | a0016c0025t0080g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1757-688G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876873 | ||||||
chr2:43876890
|
G | A | 5 | a0001c0001t0076g0085a0002c0003t0023g0251a0003c0010t0023g0036others(2): Show | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-671G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876890 | ||||||
chr2:43876928
|
G | A | 5 | a0001c0001t0076g0085a0002c0003t0023g0251a0003c0010t0023g0036others(2): Show | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-633G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876928 | ||||||
chr2:43877016
|
A | G | 79 | a0001c0001t0015g0057a0001c0001t0015g0142a0001c0001t0019g0051others(76): Show | 84 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1757-545A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877016 | ||||||
chr2:43877062
|
A | G | 238 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1757-499A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877062 | ||||||
chr2:43877172
|
A | G | 6 | a0001c0001t0076g0085a0002c0003t0023g0251a0003c0002t0104g0242others(3): Show | 6 | HG00280.hp2 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757-389A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877172 | ||||||
chr2:43877456
|
T | C | 1 | a0002c0003t0105g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1757-105T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877456 | ||||||
chr2:43877471
|
ACT | A | 49 | a0001c0001t0004g0047a0001c0001t0004g0080a0001c0001t0015g0057others(46): Show | 51 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1757-87_1757-86del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 43877471 | |||||
chr2:43877689
|
G | A | 2 | a0004c0007t0007g0055a0004c0007t0007g0124 | 2 | HG01168.hp1 HG01169.hp1 |
splice_donor_variant&intron_variant | HIGH | c.1884+1G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 12/12 | chr2 | 43877689 |