geneid | 64240 |
---|---|
ensemblid | ENSG00000138075.14 |
hgncid | 13886 |
symbol | ABCG5 |
name | ATP binding cassette subfamily G member 5 |
refseq_nuc | NM_022436.3 |
refseq_prot | NP_071881.1 |
ensembl_nuc | ENST00000405322.8 |
ensembl_prot | ENSP00000384513.2 |
mane_status | MANE Select |
chr | chr2 |
start | 43812472 |
end | 43838839 |
strand | - |
ver | v1.2 |
region | chr2:43812472-43838839 |
region5000 | chr2:43807472-43843839 |
regionname0 | ABCG5_chr2_43812472_43838839 |
regionname5000 | ABCG5_chr2_43807472_43843839 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 651 | 224 | 46 | 52 | 75 | 15 | 34 | 57 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002 | 0/0 | 651 | 70 | 27 | 18 | 13 | 3 | 9 | 12 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0003 | 0/0 | 651 | 12 | 4 | 3 | 3 | 0 | 2 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0004 | 0/0 | 651 | 6 | 2 | 2 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0005 | 0/0 | 651 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0006 | 0/0 | 651 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0007 | 0/0 | 651 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0008 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0009 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0010 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0011 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0012 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0013 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1956 | 221 | 46 | 52 | 73 | 15 | 33 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0002 | 0/0 | 1956 | 68 | 26 | 17 | 13 | 3 | 9 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0003 | 0/0 | 1956 | 12 | 4 | 3 | 3 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0004 | 0/0 | 1956 | 6 | 2 | 2 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0005 | 0/0 | 1956 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0006 | 0/0 | 1956 | 5 | 4 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0007 | 0/0 | 1956 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0008 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0009 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0010 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0011 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0012 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0013 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0014 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0015 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0016 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0017 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
c0018 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 805 | 171 | 20 | 42 | 74 | 9 | 24 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0002 | 0/0 | 805 | 80 | 33 | 20 | 14 | 3 | 10 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0003 | 0/0 | 805 | 33 | 15 | 7 | 2 | 5 | 4 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0004 | 0/0 | 805 | 12 | 6 | 2 | 3 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0005 | 0/0 | 805 | 9 | 5 | 3 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0006 | 0/0 | 805 | 7 | 6 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0007 | 0/0 | 805 | 6 | 4 | 0 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0008 | 0/0 | 804 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0009 | 0/0 | 805 | 3 | 0 | 0 | 0 | 0 | 3 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0010 | 0/0 | 805 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0011 | 0/0 | 805 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
t0012 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
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 | 16 | 0 | 4 | 11 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0015 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1956 | 221 | 46 | 52 | 73 | 15 | 33 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0010 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0013 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0016 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0002 | 0/0 | 1956 | 68 | 26 | 17 | 13 | 3 | 9 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0009 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0015 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0003c0003 | 0/0 | 1956 | 12 | 4 | 3 | 3 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0004c0004 | 0/0 | 1956 | 6 | 2 | 2 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0005c0005 | 0/0 | 1956 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0006c0006 | 0/0 | 1956 | 5 | 4 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0007c0007 | 0/0 | 1956 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0008c0008 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0009c0018 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0010c0017 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0011c0012 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0012c0011 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0013c0014 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2760 | 157 | 16 | 39 | 69 | 9 | 22 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0003 | 0/0 | 2760 | 31 | 14 | 7 | 2 | 5 | 3 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0004 | 0/0 | 2760 | 10 | 5 | 2 | 2 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0005 | 0/0 | 2760 | 9 | 5 | 3 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0006 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0007 | 0/0 | 2760 | 5 | 4 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0009 | 0/0 | 2760 | 3 | 0 | 0 | 0 | 0 | 3 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0010 | 0/0 | 2760 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0011 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0001t0012 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0010t0004 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0013t0001 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0001c0016t0001 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0002t0002 | 0/0 | 2760 | 66 | 25 | 17 | 12 | 3 | 9 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0002t0007 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0002t0008 | 0/0 | 2759 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0009t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0002c0015t0002 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0003c0003t0001 | 0/0 | 2760 | 9 | 2 | 3 | 3 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0003c0003t0003 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0003c0003t0006 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0004c0004t0002 | 0/0 | 2760 | 6 | 2 | 2 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0005c0005t0002 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0005c0005t0008 | 0/0 | 2759 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0006c0006t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0006c0006t0006 | 0/0 | 2760 | 4 | 3 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0007c0007t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0007c0007t0003 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0008c0008t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0009c0018t0004 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0010c0017t0002 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0011c0012t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0012c0011t0001 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
a0013c0014t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | copy fasta | chr2 | 43807472 | 43843839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 16 | 0 | 4 | 11 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0015 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0009g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0009g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0010g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0011g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0011g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0001t0012g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0010t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0013t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0001c0016t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0002t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0009t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0002c0015t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0003c0003t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0004c0004t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0004c0004t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0004c0004t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0004c0004t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0004c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0004c0004t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0005c0005t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0005c0005t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0005c0005t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0005c0005t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0005c0005t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0006c0006t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0006c0006t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0006c0006t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0006c0006t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0006c0006t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0007c0007t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0007c0007t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0008c0008t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0009c0018t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0010c0017t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0011c0012t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0012c0011t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
a0013c0014t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0126 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0136 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0062 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00438 | hp1 | a0004 | c0004 | t0002 | g0267 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00609 | hp1 | a0012 | c0011 | t0001 | g0230 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0172 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0191 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0030 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01168 | hp1 | a0002 | c0015 | t0002 | g0058 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0142 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01243 | hp1 | a0006 | c0006 | t0006 | g0163 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0066 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0088 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0067 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01884 | hp1 | a0005 | c0005 | t0008 | g0045 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01884 | hp2 | a0005 | c0005 | t0002 | g0036 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0076 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0264 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01975 | hp1 | a0004 | c0004 | t0002 | g0266 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01978 | hp2 | a0004 | c0004 | t0002 | g0260 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0041 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0263 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02132 | hp1 | a0010 | c0017 | t0002 | g0255 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02145 | hp1 | a0006 | c0006 | t0006 | g0164 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0256 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02258 | hp2 | a0006 | c0006 | t0006 | g0162 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0258 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0073 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0075 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0128 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02717 | hp2 | a0002 | c0009 | t0002 | g0035 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0236 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02809 | hp1 | a0005 | c0005 | t0002 | g0037 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02818 | hp1 | a0007 | c0007 | t0003 | g0271 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0253 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02895 | hp2 | a0006 | c0006 | t0006 | g0161 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02896 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02922 | hp1 | a0009 | c0018 | t0004 | g0272 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02922 | hp2 | a0011 | c0012 | t0002 | g0116 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0174 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02976 | hp2 | a0005 | c0005 | t0008 | g0044 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0218 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0241 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03139 | hp2 | a0013 | c0014 | t0002 | g0168 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0190 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03195 | hp2 | a0008 | c0008 | t0002 | g0034 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03209 | hp1 | a0003 | c0003 | t0006 | g0031 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0158 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03225 | hp2 | a0006 | c0006 | t0001 | g0166 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03453 | hp1 | a0005 | c0005 | t0008 | g0038 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03490 | hp2 | a0001 | c0001 | t0011 | g0274 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03491 | hp2 | a0004 | c0004 | t0002 | g0268 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0103 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0030 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0141 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03704 | hp1 | a0001 | c0001 | t0011 | g0273 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03710 | hp1 | a0001 | c0001 | t0009 | g0032 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0275 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03834 | hp1 | a0003 | c0003 | t0003 | g0265 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03942 | hp2 | a0001 | c0001 | t0007 | g0239 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04115 | hp1 | a0001 | c0001 | t0009 | g0032 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0127 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0214 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0254 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0215 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04228 | hp1 | a0001 | c0016 | t0001 | g0231 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0210 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18982 | hp2 | a0001 | c0013 | t0001 | g0211 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19005 | hp1 | a0002 | c0002 | t0007 | g0124 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19012 | hp2 | a0001 | c0010 | t0004 | g0197 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19030 | hp2 | a0004 | c0004 | t0002 | g0252 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19043 | hp2 | a0007 | c0007 | t0001 | g0270 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0200 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20129 | hp1 | a0004 | c0004 | t0002 | g0257 | AFR | ASW | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0130 | AFR | ASW | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0018 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0059 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0269 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | GIH | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20905 | hp2 | a0001 | c0001 | t0012 | g0033 | SAS | GIH | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0238 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0157 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0170 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG03471 | hp2 | a0003 | c0003 | t0006 | g0031 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
NA21309 | hp2 | a0002 | c0002 | t0008 | g0148 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0015 | REF | REF | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0085 | REF | REF | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43813262
|
G | C | 7 | a0002a0004a0005others(4): Show | 85 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(82): Show |
missense_variant | MODERATE | c.1810C>G | p.Gln604Glu | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 1970/2760 | 1810/1956 | 604/651 | chr2 | 43813262 | ||
chr2:43819994
|
C | T | 1 | a0012 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1570G>A | p.Val524Ile | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/13 | 1730/2760 | 1570/1956 | 524/651 | chr2 | 43819994 | ||
chr2:43820014
|
G | C | 2 | a0009a0011 | 2 | HG02922.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.1550C>G | p.Thr517Ser | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/13 | 1710/2760 | 1550/1956 | 517/651 | chr2 | 43820014 | ||
chr2:43820036
|
G | T | 1 | a0010 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1528C>A | p.His510Asn | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/13 | 1688/2760 | 1528/1956 | 510/651 | chr2 | 43820036 | ||
chr2:43824009
|
T | G | 1 | a0005 | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.1228A>C | p.Asn410His | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/13 | 1388/2760 | 1228/1956 | 410/651 | chr2 | 43824009 | ||
chr2:43825008
|
T | C | 2 | a0006a0013 | 6 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
missense_variant | MODERATE | c.785A>G | p.Lys262Arg | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/13 | 945/2760 | 785/1956 | 262/651 | chr2 | 43825008 | ||
chr2:43837951
|
G | A | 3 | a0003a0004a0010 | 19 | HG00438.hp1 HG00741.hp2 HG01943.hp2 others(16): Show |
missense_variant | MODERATE | c.148C>T | p.Arg50Cys | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/13 | 308/2760 | 148/1956 | 50/651 | chr2 | 43837951 | ||
chr2:43838541
|
C | A | 2 | a0007a0009 | 3 | HG02818.hp1 HG02922.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.139G>T | p.Val47Phe | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 299/2760 | 139/1956 | 47/651 | chr2 | 43838541 | ||
chr2:43838630
|
A | C | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.50T>G | p.Val17Gly | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 210/2760 | 50/1956 | 17/651 | chr2 | 43838630 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43822835
|
G | A | 1 | a0001c0013 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.1425C>T | p.Ser475Ser | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/13 | 1585/2760 | 1425/1956 | 475/651 | chr2 | 43822835 | ||
chr2:43826460
|
G | A | 1 | a0002c0015 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.696C>T | p.Val232Val | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/13 | 856/2760 | 696/1956 | 232/651 | chr2 | 43826460 | ||
chr2:43828011
|
G | A | 1 | a0001c0016 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.606C>T | p.Ser202Ser | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/13 | 766/2760 | 606/1956 | 202/651 | chr2 | 43828011 | ||
chr2:43832010
|
C | T | 1 | a0001c0010 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.339G>A | p.Val113Val | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 3/13 | 499/2760 | 339/1956 | 113/651 | chr2 | 43832010 | ||
chr2:43838581
|
C | T | 1 | a0002c0009 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.99G>A | p.Pro33Pro | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 259/2760 | 99/1956 | 33/651 | chr2 | 43838581 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43812494
|
G | A | 15 | a0001c0001t0004a0001c0001t0010a0001c0010t0004others(12): Show | 98 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 622 | chr2 | 43812494 | |||||
chr2:43812581
|
G | A | 3 | a0001c0001t0006a0003c0003t0006a0006c0006t0006 | 7 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 535 | chr2 | 43812581 | |||||
chr2:43812594
|
C | T | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(2): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*522G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 522 | chr2 | 43812594 | |||||
chr2:43812700
|
C | T | 12 | a0001c0001t0010a0002c0002t0002a0002c0002t0008others(9): Show | 86 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 416 | chr2 | 43812700 | |||||
chr2:43812717
|
G | A | 1 | a0001c0001t0005 | 9 | HG01074.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*399C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 399 | chr2 | 43812717 | |||||
chr2:43812736
|
A | C | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(20): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*380T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 380 | chr2 | 43812736 | |||||
chr2:43812896
|
TA | T | 2 | a0002c0002t0008a0005c0005t0008 | 4 | HG01884.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*219delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 219 | chr2 | 43812896 | |||||
chr2:43813044
|
C | T | 1 | a0001c0001t0010 | 2 | HG01109.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*72G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 72 | chr2 | 43813044 | |||||
chr2:43838781
|
C | T | 1 | a0001c0001t0012 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 102 | chr2 | 43838781 | |||||
chr2:43838797
|
T | G | 2 | a0001c0001t0009a0001c0001t0011 | 5 | HG03490.hp2 HG03704.hp1 HG03710.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-118A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 118 | chr2 | 43838797 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:43813358
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1763-49A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813358 | ||||||
chr2:43813423
|
G | C | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-114C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813423 | ||||||
chr2:43813426
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1763-117T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813426 | ||||||
chr2:43813519
|
A | G | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-210T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813519 | ||||||
chr2:43813542
|
A | C | 2 | a0001c0001t0003g0022a0001c0001t0003g0240 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1763-233T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813542 | ||||||
chr2:43813674
|
G | GT | 13 | a0001c0001t0003g0222a0001c0001t0004g0019a0001c0001t0004g0060others(10): Show | 14 | HG00597.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1763-366dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813674 | ||||||
chr2:43813693
|
T | G | 15 | a0001c0001t0001g0042a0001c0001t0003g0010a0001c0001t0003g0077others(12): Show | 17 | HG00738.hp1 HG00738.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1763-384A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813693 | ||||||
chr2:43813697
|
G | GT | 7 | a0001c0001t0001g0057a0001c0001t0001g0220a0001c0001t0001g0244others(4): Show | 7 | HG02083.hp1 HG02083.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1763-389dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813697 | ||||||
chr2:43813697
|
G | T | 70 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0009others(67): Show | 81 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1763-388C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813697 | ||||||
chr2:43813708
|
C | G | 1 | a0001c0001t0007g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1763-399G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813708 | ||||||
chr2:43813708
|
C | T | 6 | a0001c0001t0007g0154a0001c0001t0007g0160a0001c0001t0007g0239others(3): Show | 6 | HG02109.hp2 HG03041.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1763-399G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813708 | ||||||
chr2:43813708
|
CGTTTT | C | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-404_1763-400d others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813708 | ||||||
chr2:43813709
|
G | GT | 56 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0046others(53): Show | 61 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1763-401dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | ||||||
chr2:43813709
|
G | GTT | 35 | a0001c0001t0001g0165a0002c0002t0002g0005a0002c0002t0002g0009others(32): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1763-402_1763-401d others(4): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | ||||||
chr2:43813709
|
G | GTTT | 18 | a0002c0002t0002g0024a0002c0002t0002g0043a0002c0002t0002g0056others(15): Show | 19 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1763-403_1763-401d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | ||||||
chr2:43813709
|
G | T | 4 | a0001c0001t0007g0109a0001c0001t0007g0241a0001c0001t0011g0274others(1): Show | 4 | HG01168.hp1 HG02055.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1763-400C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | ||||||
chr2:43813709
|
GT | G | 33 | a0001c0001t0001g0203a0001c0001t0001g0221a0001c0001t0003g0010others(30): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1763-401delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | ||||||
chr2:43813709
|
GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0002g0003 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763-410_1763-401d others(12): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | ||||||
chr2:43813710
|
T | G | 2 | a0001c0001t0007g0241a0001c0001t0011g0274 | 2 | HG03041.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1763-401A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813710 | ||||||
chr2:43813714
|
T | A | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-405A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813714 | ||||||
chr2:43813771
|
G | T | 1 | a0002c0002t0002g0003 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763-462C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813771 | ||||||
chr2:43813881
|
G | A | 1 | a0002c0002t0002g0141 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1763-572C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813881 | ||||||
chr2:43813970
|
A | C | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+507T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813970 | ||||||
chr2:43813971
|
C | T | 7 | a0001c0001t0007g0109a0001c0001t0007g0154a0001c0001t0007g0160others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1762+506G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813971 | ||||||
chr2:43814007
|
T | C | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+470A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814007 | ||||||
chr2:43814051
|
T | C | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+426A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814051 | ||||||
chr2:43814065
|
A | G | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+412T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814065 | ||||||
chr2:43814069
|
G | A | 5 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0069others(2): Show | 5 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762+408C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814069 | ||||||
chr2:43814086
|
G | T | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+391C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814086 | ||||||
chr2:43814118
|
G | A | 4 | a0002c0002t0008g0148a0005c0005t0008g0038a0005c0005t0008g0044others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762+359C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814118 | ||||||
chr2:43814122
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1762+355C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814122 | ||||||
chr2:43814140
|
C | T | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+337G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814140 | ||||||
chr2:43814160
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0150 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1762+317G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814160 | ||||||
chr2:43814269
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1762+208G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814269 | ||||||
chr2:43814345
|
A | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0225 | 2 | HG02523.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1762+132T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814345 | ||||||
chr2:43814669
|
T | C | 1 | a0010c0017t0002g0255 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1650-80A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43814669 | ||||||
chr2:43814755
|
T | G | 12 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(9): Show | 13 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1650-166A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43814755 | ||||||
chr2:43814925
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1650-336T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43814925 | ||||||
chr2:43815027
|
T | C | 1 | a0001c0001t0004g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1650-438A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815027 | ||||||
chr2:43815047
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0115a0001c0001t0001g0122 | 3 | NA18942.hp2 NA18959.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1650-458C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815047 | ||||||
chr2:43815076
|
C | A | 5 | a0002c0002t0002g0142a0002c0002t0002g0190a0002c0002t0002g0200others(2): Show | 5 | HG01192.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650-487G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815076 | ||||||
chr2:43815124
|
C | T | 134 | a0001c0001t0003g0010a0001c0001t0003g0022a0001c0001t0003g0059others(131): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1650-535G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815124 | ||||||
chr2:43815139
|
C | G | 1 | a0001c0001t0010g0030 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1650-550G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815139 | ||||||
chr2:43815178
|
A | G | 61 | a0001c0001t0001g0068a0001c0001t0001g0094a0001c0001t0004g0019others(58): Show | 72 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1650-589T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815178 | ||||||
chr2:43815222
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1650-633T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815222 | ||||||
chr2:43815292
|
G | A | 134 | a0001c0001t0003g0010a0001c0001t0003g0022a0001c0001t0003g0059others(131): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1650-703C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815292 | ||||||
chr2:43815303
|
T | C | 1 | a0002c0002t0002g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1650-714A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815303 | ||||||
chr2:43815421
|
T | C | 11 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650-832A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815421 | ||||||
chr2:43815454
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1650-865T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815454 | ||||||
chr2:43815575
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1650-986C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815575 | ||||||
chr2:43815700
|
G | C | 4 | a0001c0001t0004g0019a0001c0001t0004g0096a0001c0001t0004g0153others(1): Show | 5 | HG00738.hp1 HG02572.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1111C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815700 | ||||||
chr2:43815707
|
A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0040others(4): Show | 10 | HG00735.hp1 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-1118T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815707 | ||||||
chr2:43815757
|
A | G | 22 | a0002c0002t0002g0018a0002c0002t0002g0041a0002c0002t0002g0050others(19): Show | 23 | HG00639.hp2 HG01074.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1650-1168T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815757 | ||||||
chr2:43815765
|
C | A | 58 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(55): Show | 69 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1650-1176G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815765 | ||||||
chr2:43815790
|
TG | T | 2 | a0001c0001t0003g0022a0001c0001t0003g0240 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1650-1202delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815790 | ||||||
chr2:43815861
|
C | T | 1 | a0002c0002t0002g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1650-1272G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815861 | ||||||
chr2:43815910
|
G | GA | 13 | a0001c0001t0001g0047a0001c0001t0001g0250a0001c0001t0007g0109others(10): Show | 13 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1650-1322dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815910 | ||||||
chr2:43815910
|
G | GAA | 101 | a0001c0001t0003g0010a0001c0001t0003g0022a0001c0001t0003g0059others(98): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1650-1323_1650-132 others(6): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815910 | ||||||
chr2:43815910
|
G | GAAA | 15 | a0001c0001t0003g0129a0001c0001t0004g0019a0001c0001t0004g0060others(12): Show | 16 | HG00738.hp1 HG01261.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1650-1324_1650-132 others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815910 | ||||||
chr2:43815925
|
AAAG | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0103a0002c0002t0002g0104others(2): Show | 6 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650-1339_1650-133 others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815925 | ||||||
chr2:43815928
|
G | A | 1 | a0001c0001t0010g0030 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1650-1339C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815928 | ||||||
chr2:43815947
|
G | T | 1 | a0003c0003t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1650-1358C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815947 | ||||||
chr2:43815975
|
A | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0042others(10): Show | 15 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1650-1386T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815975 | ||||||
chr2:43815996
|
T | G | 56 | a0001c0001t0001g0119a0001c0001t0003g0159a0001c0001t0004g0019others(53): Show | 66 | HG00438.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1650-1407A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815996 | ||||||
chr2:43816094
|
A | T | 1 | a0001c0001t0010g0030 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1650-1505T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816094 | ||||||
chr2:43816139
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1650-1550A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816139 | ||||||
chr2:43816220
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1650-1631A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816220 | ||||||
chr2:43816254
|
G | A | 48 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0001g0205others(45): Show | 58 | HG00438.hp1 HG00733.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.1650-1665C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816254 | ||||||
chr2:43816313
|
A | T | 118 | a0001c0001t0001g0205a0001c0001t0003g0010a0001c0001t0003g0022others(115): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1650-1724T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816313 | ||||||
chr2:43816433
|
G | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0240 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1650-1844C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816433 | ||||||
chr2:43816433
|
GGA | G | 35 | a0001c0001t0001g0040a0001c0001t0001g0110a0002c0002t0002g0005others(32): Show | 39 | HG00438.hp1 HG00639.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1650-1846_1650-184 others(6): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816433 | ||||||
chr2:43816482
|
C | T | 3 | a0002c0002t0008g0148a0005c0005t0008g0044a0005c0005t0008g0045 | 3 | HG01884.hp1 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1650-1893G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816482 | ||||||
chr2:43816701
|
A | C | 6 | a0002c0002t0002g0003a0002c0002t0002g0009a0002c0002t0002g0103others(3): Show | 10 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-2112T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816701 | ||||||
chr2:43816755
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0001g0133others(1): Show | 5 | HG01192.hp2 HG01255.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650-2166A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816755 | ||||||
chr2:43816816
|
T | G | 1 | a0001c0001t0003g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1650-2227A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816816 | ||||||
chr2:43817097
|
C | T | 9 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(6): Show | 10 | HG00738.hp1 HG01261.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-2508G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817097 | ||||||
chr2:43817116
|
A | G | 126 | a0001c0001t0001g0040a0001c0001t0001g0068a0001c0001t0001g0188others(123): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1650-2527T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817116 | ||||||
chr2:43817327
|
A | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0242 | 3 | HG02155.hp1 NA18945.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1649+2588T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817327 | ||||||
chr2:43817454
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1649+2461G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817454 | ||||||
chr2:43817485
|
C | T | 8 | a0001c0001t0004g0019a0001c0001t0004g0096a0001c0001t0004g0153others(5): Show | 9 | HG00738.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1649+2430G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817485 | ||||||
chr2:43817541
|
C | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0003g0010others(102): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1649+2374G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817541 | ||||||
chr2:43817551
|
A | G | 4 | a0002c0002t0002g0130a0002c0002t0002g0131a0002c0002t0002g0158others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+2364T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817551 | ||||||
chr2:43817635
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1649+2280G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817635 | ||||||
chr2:43817636
|
G | A | 2 | a0001c0001t0004g0060a0001c0001t0004g0269 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1649+2279C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817636 | ||||||
chr2:43817638
|
G | A | 1 | a0002c0002t0002g0223 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1649+2277C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817638 | ||||||
chr2:43817647
|
C | T | 10 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(7): Show | 11 | HG00738.hp1 HG01261.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1649+2268G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817647 | ||||||
chr2:43817685
|
A | G | 14 | a0001c0001t0004g0019a0001c0001t0004g0060a0001c0001t0004g0096others(11): Show | 15 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1649+2230T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817685 | ||||||
chr2:43817700
|
A | G | 33 | a0001c0001t0001g0068a0001c0001t0010g0030a0002c0002t0002g0005others(30): Show | 39 | HG00438.hp1 HG00733.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1649+2215T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817700 | ||||||
chr2:43817728
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0165a0001c0001t0001g0169others(3): Show | 6 | HG01346.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1649+2187C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817728 | ||||||
chr2:43817746
|
C | A | 20 | a0001c0001t0001g0040a0001c0001t0001g0188a0001c0001t0001g0229others(17): Show | 21 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649+2169G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817746 | ||||||
chr2:43817757
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1649+2158T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817757 | ||||||
chr2:43817770
|
T | C | 16 | a0001c0001t0003g0129a0001c0001t0004g0019a0001c0001t0004g0060others(13): Show | 17 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1649+2145A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817770 | ||||||
chr2:43817791
|
T | A | 19 | a0001c0001t0003g0010a0001c0001t0003g0062a0001c0001t0003g0069others(16): Show | 21 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649+2124A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817791 | ||||||
chr2:43817866
|
C | T | 20 | a0001c0001t0001g0040a0001c0001t0001g0188a0001c0001t0001g0229others(17): Show | 21 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649+2049G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817866 | ||||||
chr2:43817996
|
C | T | 2 | a0001c0001t0005g0246a0001c0001t0005g0247 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1649+1919G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817996 | ||||||
chr2:43818145
|
A | T | 4 | a0002c0002t0002g0147a0002c0002t0002g0150a0002c0002t0002g0157others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+1770T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818145 | ||||||
chr2:43818260
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1649+1655T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818260 | ||||||
chr2:43818263
|
G | A | 21 | a0001c0001t0001g0040a0001c0001t0001g0188a0001c0001t0001g0229others(18): Show | 22 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649+1652C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818263 | ||||||
chr2:43818273
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1649+1642T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818273 | ||||||
chr2:43818423
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1649+1492C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818423 | ||||||
chr2:43818485
|
G | C | 1 | a0002c0002t0002g0024 | 2 | HG01081.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1649+1430C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818485 | ||||||
chr2:43818487
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0115a0001c0001t0001g0122 | 3 | NA18942.hp2 NA18959.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1649+1428C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818487 | ||||||
chr2:43818607
|
A | G | 2 | a0001c0001t0003g0022a0001c0001t0003g0240 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1649+1308T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818607 | ||||||
chr2:43818708
|
G | C | 1 | a0013c0014t0002g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1649+1207C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818708 | ||||||
chr2:43818793
|
G | A | 31 | a0001c0001t0003g0010a0001c0001t0003g0022a0001c0001t0003g0061others(28): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1649+1122C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818793 | ||||||
chr2:43818828
|
G | A | 1 | a0001c0001t0003g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1649+1087C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818828 | ||||||
chr2:43818933
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1649+982C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818933 | ||||||
chr2:43818935
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1649+980T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818935 | ||||||
chr2:43819087
|
C | A | 23 | a0001c0001t0003g0010a0001c0001t0003g0022a0001c0001t0003g0061others(20): Show | 26 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1649+828G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819087 | ||||||
chr2:43819179
|
G | A | 3 | a0001c0001t0007g0239a0001c0001t0011g0273a0001c0001t0011g0274 | 3 | HG03490.hp2 HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1649+736C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819179 | ||||||
chr2:43819446
|
T | C | 90 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0003g0010others(87): Show | 100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1649+469A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819446 | ||||||
chr2:43819481
|
CT | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0139a0001c0001t0003g0010others(56): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1649+433delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819481 | ||||||
chr2:43819530
|
T | G | 3 | a0002c0002t0002g0027a0002c0002t0002g0196a0004c0004t0002g0266 | 4 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+385A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819530 | ||||||
chr2:43819630
|
A | G | 1 | a0002c0002t0002g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1649+285T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819630 | ||||||
chr2:43819634
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1649+281C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819634 | ||||||
chr2:43819698
|
G | A | 3 | a0002c0002t0002g0028a0002c0002t0002g0198a0002c0002t0002g0223 | 4 | HG02155.hp2 NA18952.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+217C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819698 | ||||||
chr2:43819773
|
C | T | 1 | a0001c0001t0010g0030 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1649+142G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819773 | ||||||
chr2:43820208
|
T | A | 7 | a0002c0002t0002g0142a0002c0002t0002g0190a0002c0002t0002g0200others(4): Show | 7 | HG00741.hp2 HG01192.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464-108A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820208 | ||||||
chr2:43820283
|
A | G | 4 | a0001c0001t0007g0109a0001c0001t0007g0154a0001c0001t0007g0160others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-183T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820283 | ||||||
chr2:43820319
|
C | T | 4 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0172others(1): Show | 4 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-219G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820319 | ||||||
chr2:43820376
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1464-276T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820376 | ||||||
chr2:43820391
|
C | T | 97 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0003g0010others(94): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1464-291G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820391 | ||||||
chr2:43820469
|
TAATGTTA | T | 3 | a0002c0002t0002g0027a0002c0002t0002g0196a0004c0004t0002g0266 | 4 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-376_1464-370d others(9): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820469 | ||||||
chr2:43820512
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1464-412G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820512 | ||||||
chr2:43820551
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1464-451C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820551 | ||||||
chr2:43820616
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1464-516A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820616 | ||||||
chr2:43820789
|
G | A | 4 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0172others(1): Show | 4 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-689C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820789 | ||||||
chr2:43820813
|
C | T | 1 | a0007c0007t0001g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1464-713G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820813 | ||||||
chr2:43820835
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1464-735C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820835 | ||||||
chr2:43820838
|
G | C | 2 | a0002c0002t0002g0055a0002c0002t0002g0056 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1464-738C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820838 | ||||||
chr2:43820842
|
T | A | 1 | a0002c0002t0002g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1464-742A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820842 | ||||||
chr2:43821005
|
CTT | C | 4 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0172others(1): Show | 4 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-907_1464-906d others(4): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821005 | ||||||
chr2:43821056
|
T | A | 1 | a0009c0018t0004g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1464-956A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821056 | ||||||
chr2:43821111
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1464-1011C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821111 | ||||||
chr2:43821203
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0132a0001c0001t0001g0235 | 3 | HG01123.hp1 HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1464-1103T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821203 | ||||||
chr2:43821207
|
C | T | 26 | a0001c0001t0001g0068a0002c0002t0002g0005a0002c0002t0002g0024others(23): Show | 31 | HG00733.hp2 HG01081.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1464-1107G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821207 | ||||||
chr2:43821407
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1464-1307G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821407 | ||||||
chr2:43821447
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0192a0001c0001t0001g0193others(4): Show | 8 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1464-1347C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821447 | ||||||
chr2:43821452
|
C | T | 15 | a0001c0001t0003g0159a0001c0001t0003g0181a0001c0001t0004g0019others(12): Show | 16 | HG00738.hp1 HG01261.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1463+1345G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821452 | ||||||
chr2:43821476
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0169a0003c0003t0001g0262 | 3 | HG01346.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1463+1321C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821476 | ||||||
chr2:43821531
|
C | G | 11 | a0002c0002t0002g0041a0002c0002t0002g0142a0002c0002t0002g0150others(8): Show | 11 | HG00741.hp2 HG01192.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1463+1266G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821531 | ||||||
chr2:43821541
|
T | C | 6 | a0001c0001t0007g0241a0002c0002t0002g0043a0002c0002t0002g0080others(3): Show | 6 | HG02622.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1463+1256A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821541 | ||||||
chr2:43821787
|
C | G | 5 | a0002c0002t0002g0043a0002c0002t0002g0080a0002c0002t0002g0170others(2): Show | 5 | HG02622.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463+1010G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821787 | ||||||
chr2:43821981
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1463+816C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821981 | ||||||
chr2:43822390
|
C | G | 1 | a0004c0004t0002g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1463+407G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822390 | ||||||
chr2:43822476
|
A | AGCC | 13 | a0001c0001t0001g0047a0001c0001t0001g0063a0001c0001t0001g0086others(10): Show | 13 | HG01175.hp1 HG01175.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1463+320_1463+321i others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822476 | ||||||
chr2:43822476
|
AG | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0156others(8): Show | 11 | HG01346.hp1 HG01346.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1463+320delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822476 | ||||||
chr2:43822477
|
G | GC | 7 | a0001c0001t0001g0224a0002c0002t0002g0093a0002c0002t0002g0208others(4): Show | 7 | HG01243.hp1 HG01993.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(3): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | ||||||
chr2:43822477
|
G | GCC | 7 | a0001c0001t0001g0117a0001c0001t0003g0059a0001c0001t0003g0245others(4): Show | 7 | HG02886.hp2 HG03139.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(4): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | ||||||
chr2:43822477
|
G | GCCCCCCC others(3): Show |
1 | a0002c0002t0002g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1463+319_1463+320i others(12): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | ||||||
chr2:43822477
|
G | GCCGC | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0004g0269others(3): Show | 7 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(6): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | ||||||
chr2:43822477
|
G | GCCGCCC | 2 | a0001c0001t0003g0010a0002c0002t0002g0009 | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | ||||||
chr2:43822478
|
G | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 284 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1463+319C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822478 | ||||||
chr2:43822478
|
GC | G | 19 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0084others(16): Show | 21 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1463+318delG | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822478 | ||||||
chr2:43822479
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1463+318G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822479 | ||||||
chr2:43822479
|
C | CG | 46 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0072others(43): Show | 54 | HG00738.hp2 HG01106.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1463+317_1463+318i others(3): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822479 | ||||||
chr2:43822510
|
T | G | 7 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0003g0102others(4): Show | 7 | HG00738.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463+287A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822510 | ||||||
chr2:43822579
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1463+218T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822579 | ||||||
chr2:43822599
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1463+198C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822599 | ||||||
chr2:43822656
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0134 | 5 | HG00735.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1463+141G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822656 | ||||||
chr2:43822733
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0146others(11): Show | 15 | HG00323.hp1 HG00738.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1463+64G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822733 | ||||||
chr2:43822768
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1463+29C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822768 | ||||||
chr2:43823202
|
G | A | 2 | a0001c0001t0003g0010a0002c0002t0002g0009 | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-267C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823202 | ||||||
chr2:43823415
|
C | G | 1 | a0001c0001t0001g0039 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1325-480G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823415 | ||||||
chr2:43823432
|
T | C | 1 | a0002c0002t0002g0041 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1324+481A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823432 | ||||||
chr2:43823526
|
G | A | 6 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0003g0240others(3): Show | 7 | HG01109.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1324+387C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823526 | ||||||
chr2:43823548
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(117): Show | 154 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1324+365G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823548 | ||||||
chr2:43823569
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1324+344T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823569 | ||||||
chr2:43823671
|
C | G | 8 | a0001c0001t0001g0094a0001c0001t0001g0156a0001c0001t0003g0151others(5): Show | 8 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+242G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823671 | ||||||
chr2:43823749
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(107): Show | 144 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.1324+164C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823749 | ||||||
chr2:43823823
|
C | A | 1 | a0001c0001t0003g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+90G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823823 | ||||||
chr2:43823832
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0003g0151a0001c0001t0003g0152others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324+81C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823832 | ||||||
chr2:43823840
|
T | A | 2 | a0002c0002t0002g0029a0002c0002t0002g0237 | 3 | HG00733.hp2 HG01934.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1324+73A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823840 | ||||||
chr2:43824148
|
T | C | 5 | a0005c0005t0002g0036a0005c0005t0002g0037a0005c0005t0008g0038others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119-30A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 8/12 | chr2 | 43824148 | ||||||
chr2:43824434
|
T | TA | 3 | a0001c0001t0001g0026a0001c0001t0001g0097a0001c0001t0001g0144 | 4 | NA18950.hp2 NA18991.hp1 NA18993.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.905-3dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824434 | ||||||
chr2:43824558
|
T | A | 1 | a0001c0001t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.905-126A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824558 | ||||||
chr2:43824559
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.905-127C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824559 | ||||||
chr2:43824560
|
C | G | 1 | a0001c0001t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.905-128G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824560 | ||||||
chr2:43824751
|
A | T | 24 | a0001c0001t0001g0094a0001c0001t0001g0156a0001c0001t0001g0165others(21): Show | 24 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.904+138T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824751 | ||||||
chr2:43825027
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.775-9T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825027 | ||||||
chr2:43825028
|
C | A | 2 | a0001c0001t0003g0245a0002c0002t0002g0003 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-10G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825028 | ||||||
chr2:43825063
|
C | A | 10 | a0001c0001t0001g0094a0001c0001t0001g0156a0001c0001t0001g0244others(7): Show | 10 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.775-45G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825063 | ||||||
chr2:43825064
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0189 | 2 | NA18979.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.775-46C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825064 | ||||||
chr2:43825277
|
C | T | 13 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0003g0240others(10): Show | 14 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.775-259G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825277 | ||||||
chr2:43825359
|
G | A | 4 | a0001c0001t0001g0226a0001c0001t0003g0240a0001c0001t0007g0241others(1): Show | 5 | HG01109.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-341C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825359 | ||||||
chr2:43825405
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.775-387A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825405 | ||||||
chr2:43825601
|
G | T | 3 | a0002c0002t0002g0190a0002c0002t0002g0200a0002c0002t0002g0201 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.775-583C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825601 | ||||||
chr2:43825604
|
GTTA | G | 19 | a0001c0001t0001g0042a0002c0002t0002g0142a0003c0003t0001g0253others(16): Show | 20 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-589_775-587del others(3): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825604 | ||||||
chr2:43825607
|
A | G | 3 | a0001c0001t0003g0129a0002c0002t0002g0130a0002c0002t0002g0131 | 3 | HG02717.hp1 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.775-589T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825607 | ||||||
chr2:43825639
|
A | C | 20 | a0001c0001t0001g0094a0001c0001t0001g0156a0001c0001t0001g0169others(17): Show | 20 | HG01346.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.775-621T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825639 | ||||||
chr2:43825649
|
G | T | 1 | a0001c0001t0003g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.775-631C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825649 | ||||||
chr2:43825694
|
C | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(125): Show | 161 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.775-676G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825694 | ||||||
chr2:43825732
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.774+650C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825732 | ||||||
chr2:43825752
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.774+630C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825752 | ||||||
chr2:43825763
|
C | T | 1 | a0001c0013t0001g0211 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.774+619G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825763 | ||||||
chr2:43825869
|
A | G | 2 | a0003c0003t0001g0262a0003c0003t0006g0031 | 3 | HG03098.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.774+513T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825869 | ||||||
chr2:43825951
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(77): Show | 108 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.774+431C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825951 | ||||||
chr2:43826106
|
G | C | 3 | a0002c0002t0002g0190a0002c0002t0002g0200a0002c0002t0002g0201 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.774+276C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826106 | ||||||
chr2:43826166
|
C | CT | 9 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0244others(6): Show | 9 | HG00099.hp1 HG01361.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+215dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826166 | ||||||
chr2:43826184
|
G | T | 1 | a0002c0002t0002g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.774+198C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826184 | ||||||
chr2:43826216
|
A | G | 5 | a0005c0005t0002g0036a0005c0005t0002g0037a0005c0005t0008g0038others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+166T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826216 | ||||||
chr2:43826309
|
A | T | 6 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0003g0102others(3): Show | 6 | HG00738.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+73T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826309 | ||||||
chr2:43826622
|
A | G | 1 | a0002c0002t0002g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.635-101T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826622 | ||||||
chr2:43826638
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.635-117C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826638 | ||||||
chr2:43826791
|
G | A | 1 | a0001c0001t0005g0076 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.635-270C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826791 | ||||||
chr2:43826800
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.635-279T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826800 | ||||||
chr2:43826809
|
T | C | 5 | a0005c0005t0002g0036a0005c0005t0002g0037a0005c0005t0008g0038others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-288A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826809 | ||||||
chr2:43826984
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(86): Show | 120 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.635-463C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826984 | ||||||
chr2:43826985
|
C | T | 1 | a0002c0002t0002g0208 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.635-464G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826985 | ||||||
chr2:43827050
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.635-529G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827050 | ||||||
chr2:43827052
|
C | T | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.635-531G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827052 | ||||||
chr2:43827053
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.635-532C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827053 | ||||||
chr2:43827054
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0003g0151a0001c0001t0003g0152others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-533C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827054 | ||||||
chr2:43827127
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.635-606G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827127 | ||||||
chr2:43827245
|
A | C | 1 | a0001c0001t0003g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.635-724T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827245 | ||||||
chr2:43827279
|
C | T | 2 | a0001c0001t0006g0145a0002c0002t0002g0238 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.634+704G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827279 | ||||||
chr2:43827298
|
C | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(86): Show | 120 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.634+685G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827298 | ||||||
chr2:43827325
|
C | CA | 37 | a0001c0001t0001g0040a0001c0001t0001g0094a0001c0001t0001g0101others(34): Show | 38 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.634+657dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827325 | ||||||
chr2:43827325
|
C | CAA | 21 | a0001c0001t0001g0042a0001c0001t0001g0068a0002c0002t0002g0142others(18): Show | 22 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.634+656_634+657dup others(2): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827325 | ||||||
chr2:43827325
|
CA | C | 6 | a0001c0001t0001g0165a0006c0006t0001g0166a0006c0006t0006g0161others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+657delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827325 | ||||||
chr2:43827343
|
G | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 122 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.634+640C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827343 | ||||||
chr2:43827345
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(88): Show | 122 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.634+638C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827345 | ||||||
chr2:43827379
|
C | T | 1 | a0002c0002t0002g0055 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.634+604G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827379 | ||||||
chr2:43827400
|
T | C | 2 | a0001c0001t0001g0244a0002c0009t0002g0035 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+583A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827400 | ||||||
chr2:43827617
|
A | G | 2 | a0001c0001t0003g0245a0002c0002t0002g0003 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+366T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827617 | ||||||
chr2:43827655
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.634+328G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827655 | ||||||
chr2:43827799
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.634+184G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827799 | ||||||
chr2:43827830
|
A | G | 2 | a0001c0001t0001g0244a0002c0009t0002g0035 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+153T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827830 | ||||||
chr2:43827852
|
G | A | 18 | a0002c0002t0002g0142a0003c0003t0001g0253a0003c0003t0001g0254others(15): Show | 19 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.634+131C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827852 | ||||||
chr2:43827902
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.634+81C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827902 | ||||||
chr2:43828248
|
C | T | 34 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0001g0250others(31): Show | 35 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.502-133G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828248 | ||||||
chr2:43828307
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 134 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.502-192C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828307 | ||||||
chr2:43828371
|
C | T | 19 | a0001c0001t0001g0042a0002c0002t0002g0142a0003c0003t0001g0253others(16): Show | 20 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-256G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828371 | ||||||
chr2:43828388
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(159): Show | 198 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.502-273A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828388 | ||||||
chr2:43828404
|
G | A | 2 | a0001c0001t0003g0240a0001c0001t0010g0030 | 3 | HG01109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.502-289C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828404 | ||||||
chr2:43828472
|
C | CA | 26 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0003g0069others(23): Show | 28 | HG00738.hp1 HG00741.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.502-358dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | ||||||
chr2:43828472
|
CA | C | 14 | a0001c0001t0001g0156a0001c0001t0001g0178a0001c0001t0001g0244others(11): Show | 14 | HG01243.hp1 HG01346.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.502-358delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | ||||||
chr2:43828472
|
CAA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 134 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.502-359_502-358del others(2): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | ||||||
chr2:43828472
|
CAAAAAAA | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0250a0001c0001t0001g0251others(5): Show | 9 | HG01074.hp1 HG01109.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-364_502-358del others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | ||||||
chr2:43828472
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0005g0246a0002c0002t0002g0170a0002c0002t0002g0171others(3): Show | 6 | HG00642.hp2 HG01099.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-365_502-358del others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | ||||||
chr2:43828490
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | NA18945.hp1 NA18973.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.502-375T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828490 | ||||||
chr2:43828510
|
A | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(143): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-395T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828510 | ||||||
chr2:43828592
|
G | A | 1 | a0002c0002t0002g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502-477C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828592 | ||||||
chr2:43828731
|
C | T | 1 | a0004c0004t0002g0267 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.502-616G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828731 | ||||||
chr2:43828732
|
G | T | 1 | a0002c0002t0002g0130 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.502-617C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828732 | ||||||
chr2:43828738
|
G | C | 2 | a0002c0002t0002g0029a0002c0002t0002g0237 | 3 | HG00733.hp2 HG01934.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.502-623C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828738 | ||||||
chr2:43828783
|
C | T | 21 | a0001c0001t0001g0042a0001c0001t0001g0244a0002c0002t0002g0142others(18): Show | 22 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.502-668G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828783 | ||||||
chr2:43828858
|
C | CG | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(141): Show | 179 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.502-744dupC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828858 | ||||||
chr2:43828870
|
C | T | 45 | a0001c0001t0001g0156a0001c0001t0001g0165a0001c0001t0001g0169others(42): Show | 46 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.502-755G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828870 | ||||||
chr2:43828885
|
A | G | 4 | a0001c0001t0005g0073a0001c0001t0005g0074a0001c0001t0005g0076others(1): Show | 4 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-770T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828885 | ||||||
chr2:43828910
|
AG | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(105): Show | 142 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.502-796delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828910 | ||||||
chr2:43828952
|
G | A | 2 | a0001c0001t0003g0245a0002c0002t0002g0003 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-837C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828952 | ||||||
chr2:43828960
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.502-845C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828960 | ||||||
chr2:43828970
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502-855T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828970 | ||||||
chr2:43828972
|
AT | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0070a0006c0006t0001g0166 | 3 | HG02083.hp2 HG03225.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.502-858delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828972 | ||||||
chr2:43828973
|
T | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(106): Show | 144 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.502-858A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828973 | ||||||
chr2:43828976
|
T | A | 1 | a0006c0006t0001g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.502-861A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828976 | ||||||
chr2:43828991
|
CAAATA | C | 5 | a0001c0001t0003g0010a0002c0002t0002g0009a0002c0002t0002g0043others(2): Show | 7 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.502-881_502-877del others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828991 | ||||||
chr2:43829009
|
A | T | 19 | a0001c0001t0001g0042a0002c0002t0002g0142a0003c0003t0001g0253others(16): Show | 20 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-894T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829009 | ||||||
chr2:43829118
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.502-1003G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829118 | ||||||
chr2:43829183
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(143): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1068A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829183 | ||||||
chr2:43829184
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.502-1069A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829184 | ||||||
chr2:43829240
|
C | T | 13 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0003g0102others(10): Show | 13 | HG00738.hp2 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-1125G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829240 | ||||||
chr2:43829305
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(143): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1190G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829305 | ||||||
chr2:43829350
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502-1235T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829350 | ||||||
chr2:43829402
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 151 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.502-1287T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829402 | ||||||
chr2:43829451
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(166): Show | 208 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.502-1336C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829451 | ||||||
chr2:43829539
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(143): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1424A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829539 | ||||||
chr2:43829661
|
A | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(143): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1546T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829661 | ||||||
chr2:43829674
|
CA | C | 6 | a0001c0001t0001g0156a0001c0001t0003g0151a0001c0001t0003g0152others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-1560delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829674 | ||||||
chr2:43829717
|
A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(143): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1602T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829717 | ||||||
chr2:43829843
|
G | T | 2 | a0001c0001t0004g0179a0001c0010t0004g0197 | 2 | HG02132.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.502-1728C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829843 | ||||||
chr2:43829854
|
T | C | 33 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0001g0250others(30): Show | 34 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.502-1739A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829854 | ||||||
chr2:43829883
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.502-1768G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829883 | ||||||
chr2:43829887
|
C | T | 15 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0003g0149others(12): Show | 15 | HG01346.hp2 HG02109.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.502-1772G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829887 | ||||||
chr2:43829888
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502-1773G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829888 | ||||||
chr2:43829891
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(106): Show | 144 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.502-1776T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829891 | ||||||
chr2:43829963
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(161): Show | 201 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.501+1806C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829963 | ||||||
chr2:43830079
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(99): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.501+1690C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830079 | ||||||
chr2:43830270
|
C | G | 33 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0001g0250others(30): Show | 34 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.501+1499G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830270 | ||||||
chr2:43830431
|
A | C | 21 | a0001c0001t0003g0129a0002c0002t0002g0130a0002c0002t0002g0131others(18): Show | 22 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+1338T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830431 | ||||||
chr2:43830615
|
G | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18993.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.501+1154C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830615 | ||||||
chr2:43830624
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18993.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.501+1145G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830624 | ||||||
chr2:43830625
|
G | A | 1 | a0002c0002t0002g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+1144C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830625 | ||||||
chr2:43830686
|
TCTC | T | 18 | a0002c0002t0002g0142a0003c0003t0001g0253a0003c0003t0001g0254others(15): Show | 19 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.501+1080_501+1082d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830686 | ||||||
chr2:43830738
|
T | C | 40 | a0001c0001t0001g0156a0001c0001t0001g0165a0001c0001t0001g0169others(37): Show | 41 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.501+1031A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830738 | ||||||
chr2:43830928
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(99): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.501+841T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830928 | ||||||
chr2:43830955
|
A | G | 3 | a0002c0002t0002g0190a0002c0002t0002g0200a0002c0002t0002g0201 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.501+814T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830955 | ||||||
chr2:43830980
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0002c0002t0002g0128 | 4 | HG01891.hp2 HG02698.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+789T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830980 | ||||||
chr2:43831062
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0129a0002c0002t0002g0130others(19): Show | 23 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.501+707C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831062 | ||||||
chr2:43831080
|
G | T | 2 | a0002c0002t0002g0130a0002c0002t0002g0131 | 2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.501+689C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831080 | ||||||
chr2:43831092
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501+677T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831092 | ||||||
chr2:43831234
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.501+535C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831234 | ||||||
chr2:43831331
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(140): Show | 179 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.501+438A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831331 | ||||||
chr2:43831369
|
C | T | 3 | a0001c0001t0003g0010a0002c0002t0002g0009a0002c0002t0002g0043 | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+400G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831369 | ||||||
chr2:43831439
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.501+330G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831439 | ||||||
chr2:43831599
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.501+170G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831599 | ||||||
chr2:43831628
|
G | A | 2 | a0001c0001t0001g0165a0006c0006t0001g0166 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.501+141C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831628 | ||||||
chr2:43831700
|
A | G | 1 | a0002c0002t0002g0198 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.501+69T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831700 | ||||||
chr2:43831758
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501+11C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831758 | ||||||
chr2:43831906
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-39C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 3/12 | chr2 | 43831906 | ||||||
chr2:43831920
|
G | T | 1 | a0002c0002t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.402+27C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 3/12 | chr2 | 43831920 | ||||||
chr2:43832277
|
C | A | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-194G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832277 | ||||||
chr2:43832288
|
G | T | 2 | a0003c0003t0001g0253a0004c0004t0002g0252 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.266-205C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832288 | ||||||
chr2:43832299
|
G | A | 11 | a0001c0001t0001g0165a0001c0001t0001g0244a0001c0001t0003g0149others(8): Show | 11 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-216C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832299 | ||||||
chr2:43832355
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.266-272C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832355 | ||||||
chr2:43832964
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(140): Show | 181 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.266-881A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832964 | ||||||
chr2:43832982
|
G | A | 2 | a0003c0003t0001g0262a0003c0003t0006g0031 | 3 | HG03098.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.266-899C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832982 | ||||||
chr2:43833090
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0165a0002c0002t0002g0140others(3): Show | 7 | HG01192.hp1 HG02145.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-1007C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833090 | ||||||
chr2:43833363
|
A | ATAT | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(35): Show | 41 | HG00323.hp1 HG00673.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.266-1283_266-1281d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
A | ATATTAT | 14 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0057others(11): Show | 16 | HG00438.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.266-1286_266-1281d others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
A | ATATTATT others(2): Show |
11 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(8): Show | 11 | HG00099.hp2 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-1289_266-1281d others(11): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
ATAT | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.266-1283_266-1281d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
ATATTAT | A | 17 | a0001c0001t0001g0042a0001c0001t0001g0121a0001c0001t0001g0122others(14): Show | 18 | HG00735.hp2 HG00741.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.266-1286_266-1281d others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
ATATTATT others(2): Show |
A | 5 | a0003c0003t0001g0263a0003c0003t0001g0264a0003c0003t0003g0265others(2): Show | 5 | HG00438.hp1 HG01943.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1289_266-1281d others(11): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
ATATTATT others(5): Show |
A | 1 | a0001c0001t0001g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.266-1292_266-1281d others(14): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833363
|
ATATTATT others(17): Show |
A | 2 | a0001c0001t0003g0245a0002c0002t0002g0003 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1304_266-1281d others(26): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | ||||||
chr2:43833452
|
G | C | 1 | a0001c0001t0001g0039 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.266-1369C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833452 | ||||||
chr2:43833469
|
A | C | 5 | a0002c0002t0002g0170a0002c0002t0002g0171a0002c0002t0002g0172others(2): Show | 5 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1386T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833469 | ||||||
chr2:43833531
|
G | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(140): Show | 181 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.266-1448C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833531 | ||||||
chr2:43833693
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(99): Show | 136 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.266-1610A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833693 | ||||||
chr2:43833710
|
A | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(99): Show | 136 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.266-1627T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833710 | ||||||
chr2:43833744
|
G | A | 4 | a0001c0001t0003g0010a0002c0002t0002g0009a0002c0002t0002g0043others(1): Show | 6 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-1661C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833744 | ||||||
chr2:43833770
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(140): Show | 181 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.266-1687A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833770 | ||||||
chr2:43833935
|
C | T | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-1852G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833935 | ||||||
chr2:43833982
|
C | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.266-1899G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833982 | ||||||
chr2:43834114
|
G | C | 6 | a0001c0001t0004g0167a0006c0006t0006g0161a0006c0006t0006g0162others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-2031C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834114 | ||||||
chr2:43834178
|
G | A | 2 | a0001c0001t0001g0235a0002c0002t0002g0236 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.266-2095C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834178 | ||||||
chr2:43834214
|
T | A | 1 | a0002c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.266-2131A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834214 | ||||||
chr2:43834243
|
T | C | 1 | a0004c0004t0002g0268 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.266-2160A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834243 | ||||||
chr2:43834296
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0003g0245a0002c0002t0002g0003 | 6 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-2213G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834296 | ||||||
chr2:43834326
|
A | G | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-2243T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834326 | ||||||
chr2:43834370
|
G | A | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-2287C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834370 | ||||||
chr2:43834466
|
T | C | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-2383A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834466 | ||||||
chr2:43834500
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0003g0126 | 2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.266-2417C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834500 | ||||||
chr2:43834570
|
T | G | 1 | a0002c0002t0002g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.266-2487A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834570 | ||||||
chr2:43834855
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.266-2772G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834855 | ||||||
chr2:43834892
|
C | T | 1 | a0002c0002t0002g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.266-2809G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834892 | ||||||
chr2:43835062
|
C | T | 4 | a0006c0006t0006g0161a0006c0006t0006g0162a0006c0006t0006g0163others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+2772G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835062 | ||||||
chr2:43835147
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 180 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.265+2687G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835147 | ||||||
chr2:43835237
|
ACATTGGC others(20): Show |
A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(145): Show | 186 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.265+2570_265+2596d others(29): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835237 | ||||||
chr2:43835293
|
TG | T | 17 | a0001c0001t0001g0156a0001c0001t0003g0129a0001c0001t0003g0149others(14): Show | 17 | HG01346.hp2 HG02109.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.265+2540delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835293 | ||||||
chr2:43835298
|
G | A | 5 | a0002c0002t0002g0170a0002c0002t0002g0171a0002c0002t0002g0172others(2): Show | 5 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+2536C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835298 | ||||||
chr2:43835375
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.265+2459T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835375 | ||||||
chr2:43835443
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.265+2391G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835443 | ||||||
chr2:43835645
|
G | A | 3 | a0002c0002t0002g0029a0002c0002t0002g0237a0002c0002t0002g0238 | 4 | HG00733.hp2 HG01934.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+2189C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835645 | ||||||
chr2:43835732
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.265+2102G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835732 | ||||||
chr2:43835745
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.265+2089T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835745 | ||||||
chr2:43835757
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(124): Show | 161 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.265+2077C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835757 | ||||||
chr2:43835768
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.265+2066C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835768 | ||||||
chr2:43835811
|
T | C | 1 | a0001c0001t0007g0239 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.265+2023A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835811 | ||||||
chr2:43835912
|
G | A | 1 | a0002c0002t0002g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.265+1922C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835912 | ||||||
chr2:43835944
|
CT | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0138a0001c0001t0001g0139others(16): Show | 23 | HG01192.hp1 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.265+1889delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835944 | ||||||
chr2:43835959
|
G | C | 18 | a0003c0003t0001g0253a0003c0003t0001g0254a0003c0003t0001g0256others(15): Show | 19 | HG00438.hp1 HG00741.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+1875C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835959 | ||||||
chr2:43835960
|
A | T | 1 | a0002c0009t0002g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.265+1874T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835960 | ||||||
chr2:43836043
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+1791A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836043 | ||||||
chr2:43836061
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 180 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.265+1773G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836061 | ||||||
chr2:43836176
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+1658T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836176 | ||||||
chr2:43836188
|
G | A | 3 | a0001c0001t0003g0240a0001c0001t0007g0241a0001c0001t0010g0030 | 4 | HG01109.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1646C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836188 | ||||||
chr2:43836207
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+1627G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836207 | ||||||
chr2:43836214
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(145): Show | 186 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.265+1620A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836214 | ||||||
chr2:43836218
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(170): Show | 214 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.265+1616T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836218 | ||||||
chr2:43836221
|
A | G | 3 | a0005c0005t0002g0036a0005c0005t0002g0037a0005c0005t0008g0038 | 3 | HG01884.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.265+1613T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836221 | ||||||
chr2:43836231
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.265+1603C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836231 | ||||||
chr2:43836246
|
A | AT | 2 | a0001c0001t0003g0245a0002c0002t0002g0003 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1587dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836246 | ||||||
chr2:43836278
|
G | T | 5 | a0002c0002t0002g0170a0002c0002t0002g0171a0002c0002t0002g0172others(2): Show | 5 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1556C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836278 | ||||||
chr2:43836324
|
T | C | 1 | a0002c0002t0002g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.265+1510A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836324 | ||||||
chr2:43836440
|
G | C | 2 | a0001c0001t0003g0245a0002c0002t0002g0003 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1394C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836440 | ||||||
chr2:43836496
|
T | C | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1338A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836496 | ||||||
chr2:43836513
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+1321A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836513 | ||||||
chr2:43836548
|
A | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+1286T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836548 | ||||||
chr2:43836592
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 15 | HG01192.hp1 HG01243.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.265+1242G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836592 | ||||||
chr2:43836712
|
C | T | 3 | a0005c0005t0002g0036a0005c0005t0002g0037a0005c0005t0008g0038 | 3 | HG01884.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.265+1122G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836712 | ||||||
chr2:43836823
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 6 | HG00609.hp2 NA18962.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1011T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836823 | ||||||
chr2:43836923
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 180 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.265+911G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836923 | ||||||
chr2:43836958
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+876C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836958 | ||||||
chr2:43837033
|
A | ACG | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(100): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.265+800_265+801ins others(2): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837033 | ||||||
chr2:43837034
|
A | C | 20 | a0001c0001t0001g0143a0001c0001t0001g0156a0001c0001t0003g0149others(17): Show | 20 | HG00642.hp2 HG01099.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.265+800T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837034 | ||||||
chr2:43837035
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(100): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.265+799C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837035 | ||||||
chr2:43837035
|
G | GA | 6 | a0001c0001t0001g0143a0002c0002t0002g0170a0002c0002t0002g0171others(3): Show | 6 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+798dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837035 | ||||||
chr2:43837119
|
T | G | 1 | a0001c0001t0003g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265+715A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837119 | ||||||
chr2:43837120
|
CT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(128): Show | 168 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.265+713delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837120 | ||||||
chr2:43837212
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(131): Show | 169 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.265+622A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837212 | ||||||
chr2:43837309
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0003g0245a0002c0002t0002g0003 | 6 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+525A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837309 | ||||||
chr2:43837645
|
G | A | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+189C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837645 | ||||||
chr2:43838000
|
G | T | 2 | a0001c0001t0001g0040a0002c0002t0002g0041 | 2 | HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.144-45C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838000 | ||||||
chr2:43838060
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.144-105G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838060 | ||||||
chr2:43838193
|
C | A | 1 | a0001c0001t0004g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.144-238G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838193 | ||||||
chr2:43838291
|
G | T | 3 | a0005c0005t0002g0036a0005c0005t0002g0037a0005c0005t0008g0038 | 3 | HG01884.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.143+246C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838291 | ||||||
chr2:43838399
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.143+138G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838399 |