geneid | 5243 |
---|---|
ensemblid | ENSG00000085563.15 |
hgncid | 40 |
symbol | ABCB1 |
name | ATP binding cassette subfamily B member 1 |
refseq_nuc | NM_001348946.2 |
refseq_prot | NP_001335875.1 |
ensembl_nuc | ENST00000622132.5 |
ensembl_prot | ENSP00000478255.1 |
mane_status | MANE Select |
chr | chr7 |
start | 87503017 |
end | 87600884 |
strand | - |
ver | v1.2 |
region | chr7:87503017-87600884 |
region5000 | chr7:87498017-87605884 |
regionname0 | ABCB1_chr7_87503017_87600884 |
regionname5000 | ABCB1_chr7_87498017_87605884 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1280 | 212 | 78 | 40 | 69 | 10 | 15 | 40 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002 | 1/0 | 1280 | 74 | 4 | 12 | 38 | 4 | 15 | 29 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003 | 0/0 | 1280 | 35 | 0 | 7 | 26 | 0 | 2 | 23 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0004 | 0/0 | 1280 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0005 | 0/0 | 1280 | 4 | 0 | 2 | 2 | 0 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0006 | 0/0 | 1280 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0007 | 0/0 | 1280 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0008 | 0/0 | 1280 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0009 | 0/0 | 1280 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0010 | 0/0 | 1280 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0011 | 0/0 | 1280 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0012 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0013 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0014 | 0/1 | 1280 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0015 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0016 | 0/0 | 1280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0017 | 0/0 | 1280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0018 | 0/0 | 1280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0019 | 0/0 | 1280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0020 | 0/0 | 1280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3843 | 144 | 66 | 27 | 31 | 9 | 11 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0002 | 1/0 | 3843 | 66 | 3 | 10 | 37 | 4 | 11 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0003 | 0/0 | 3843 | 35 | 3 | 4 | 27 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0004 | 0/0 | 3843 | 34 | 0 | 6 | 26 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0005 | 0/0 | 3843 | 23 | 1 | 9 | 10 | 1 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0006 | 0/0 | 3843 | 7 | 6 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0007 | 0/0 | 3843 | 5 | 4 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0008 | 0/0 | 3843 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0009 | 0/0 | 3843 | 4 | 0 | 1 | 1 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0010 | 0/0 | 3843 | 3 | 0 | 1 | 0 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0011 | 0/0 | 3843 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0012 | 0/0 | 3843 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0013 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0014 | 0/0 | 3843 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0015 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0016 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0017 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0018 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0019 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0020 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0021 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0022 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0023 | 0/1 | 3843 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0024 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0025 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0026 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0027 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0028 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0029 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0030 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0031 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
c0032 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1363 | 214 | 51 | 45 | 88 | 8 | 21 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0002 | 0/0 | 1363 | 53 | 2 | 9 | 36 | 1 | 5 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0003 | 0/0 | 1363 | 17 | 5 | 6 | 2 | 1 | 3 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0004 | 0/0 | 1363 | 17 | 12 | 4 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0005 | 0/0 | 1363 | 12 | 1 | 0 | 10 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0006 | 0/0 | 1371 | 8 | 8 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0007 | 1/0 | 1363 | 6 | 0 | 3 | 0 | 2 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0008 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0009 | 0/0 | 1363 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0010 | 0/0 | 1363 | 2 | 1 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0011 | 0/0 | 1371 | 2 | 0 | 0 | 0 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0012 | 0/0 | 1363 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0013 | 0/0 | 1363 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0014 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0015 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0016 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0017 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0018 | 0/0 | 1363 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0019 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0020 | 0/0 | 1363 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0021 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
t0022 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3843 | 144 | 66 | 27 | 31 | 9 | 11 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0003 | 0/0 | 3843 | 35 | 3 | 4 | 27 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005 | 0/0 | 3843 | 23 | 1 | 9 | 10 | 1 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0006 | 0/0 | 3843 | 7 | 6 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0018 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0022 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0025 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0002 | 1/0 | 3843 | 66 | 3 | 10 | 37 | 4 | 11 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0009 | 0/0 | 3843 | 4 | 0 | 1 | 1 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0010 | 0/0 | 3843 | 3 | 0 | 1 | 0 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0024 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0004 | 0/0 | 3843 | 34 | 0 | 6 | 26 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0020 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0004c0007 | 0/0 | 3843 | 5 | 4 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0005c0008 | 0/0 | 3843 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0006c0012 | 0/0 | 3843 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0006c0017 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0007c0011 | 0/0 | 3843 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0008c0014 | 0/0 | 3843 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0009c0030 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0009c0031 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0010c0013 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0011c0027 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0012c0026 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0013c0019 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0014c0023 | 0/1 | 3843 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0015c0021 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0016c0028 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0017c0029 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0018c0016 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0019c0032 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0020c0015 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5205 | 88 | 38 | 16 | 23 | 5 | 6 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0002 | 0/0 | 5205 | 11 | 2 | 2 | 6 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0003 | 0/0 | 5205 | 12 | 3 | 4 | 2 | 1 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0004 | 0/0 | 5205 | 13 | 8 | 4 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0005 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0006 | 0/0 | 5213 | 6 | 6 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0007 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0008 | 0/0 | 5201 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0009 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0010 | 0/0 | 5205 | 2 | 1 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0011 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0015 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0018 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0019 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0021 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0001t0022 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0003t0001 | 0/0 | 5205 | 23 | 0 | 4 | 18 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0003t0002 | 0/0 | 5205 | 9 | 0 | 0 | 9 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0003t0006 | 0/0 | 5213 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0003t0009 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005t0001 | 0/0 | 5205 | 13 | 0 | 4 | 8 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005t0002 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005t0003 | 0/0 | 5205 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005t0005 | 0/0 | 5205 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005t0007 | 0/0 | 5205 | 4 | 0 | 3 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0005t0016 | 0/0 | 5201 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0006t0001 | 0/0 | 5205 | 2 | 1 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0006t0003 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0006t0004 | 0/0 | 5205 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0018t0017 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0022t0001 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0001c0025t0001 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0002t0001 | 0/0 | 5205 | 56 | 3 | 10 | 30 | 3 | 10 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0002t0002 | 0/0 | 5205 | 7 | 0 | 0 | 6 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0002t0007 | 1/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0002t0011 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0002t0013 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0009t0001 | 0/0 | 5205 | 2 | 0 | 1 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0009t0002 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0009t0013 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0010t0001 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0010t0002 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0010t0003 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0002c0024t0001 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0004t0001 | 0/0 | 5205 | 2 | 0 | 1 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0004t0002 | 0/0 | 5205 | 20 | 0 | 5 | 13 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0004t0005 | 0/0 | 5205 | 9 | 0 | 0 | 9 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0004t0012 | 0/0 | 5205 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0004t0020 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0003c0020t0001 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0004c0007t0001 | 0/0 | 5205 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0004c0007t0003 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0004c0007t0008 | 0/0 | 5201 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0005c0008t0001 | 0/0 | 5205 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0006c0012t0001 | 0/0 | 5205 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0006c0017t0002 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0007c0011t0001 | 0/0 | 5205 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0008c0014t0001 | 0/0 | 5205 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0009c0030t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0009c0031t0002 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0010c0013t0001 | 0/0 | 5205 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0011c0027t0001 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0012c0026t0014 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0013c0019t0009 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0014c0023t0001 | 0/1 | 5205 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0015c0021t0001 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0016c0028t0001 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0017c0029t0002 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0018c0016t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0019c0032t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
a0020c0015t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | copy fasta | chr7 | 87498017 | 87605884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0018g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0019g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0021g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0022g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0018t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0022t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0025t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0007g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0013g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0013g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0010t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0010t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0010t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0004t0020g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0020t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0007t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0007t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0007t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0007t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0008t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0008t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0008t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0006c0012t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0006c0012t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0006c0017t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0007c0011t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0007c0011t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0007c0011t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0008c0014t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0008c0014t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0009c0030t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0009c0031t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0010c0013t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0010c0013t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0011c0027t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0012c0026t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0013c0019t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0014c0023t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0015c0021t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0016c0028t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0017c0029t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0018c0016t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0019c0032t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0020c0015t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | GBR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00280 | hp2 | a0001 | c0005 | t0007 | g0076 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0078 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0330 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00423 | hp2 | a0003 | c0004 | t0005 | g0019 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00544 | hp2 | a0001 | c0003 | t0002 | g0245 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0319 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00597 | hp2 | a0001 | c0003 | t0002 | g0142 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00609 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00609 | hp2 | a0001 | c0003 | t0002 | g0255 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00639 | hp1 | a0004 | c0007 | t0001 | g0258 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00741 | hp1 | a0006 | c0012 | t0001 | g0273 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00741 | hp2 | a0002 | c0009 | t0001 | g0128 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01069 | hp2 | a0001 | c0005 | t0003 | g0002 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01070 | hp1 | a0001 | c0005 | t0007 | g0003 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01071 | hp1 | a0001 | c0005 | t0003 | g0002 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01071 | hp2 | a0001 | c0005 | t0007 | g0003 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01081 | hp2 | a0001 | c0005 | t0007 | g0079 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01106 | hp1 | a0006 | c0012 | t0001 | g0271 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0329 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01109 | hp1 | a0006 | c0017 | t0002 | g0272 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01169 | hp2 | a0001 | c0005 | t0001 | g0276 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01192 | hp1 | a0003 | c0004 | t0001 | g0071 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01255 | hp1 | a0008 | c0014 | t0001 | g0340 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01258 | hp2 | a0016 | c0028 | t0001 | g0147 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01261 | hp1 | a0002 | c0010 | t0001 | g0090 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01261 | hp2 | a0005 | c0008 | t0001 | g0187 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01358 | hp2 | a0003 | c0004 | t0002 | g0046 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01496 | hp1 | a0017 | c0029 | t0002 | g0130 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01496 | hp2 | a0003 | c0004 | t0002 | g0043 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0336 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0337 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01928 | hp1 | a0005 | c0008 | t0001 | g0199 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0223 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01952 | hp1 | a0003 | c0020 | t0001 | g0042 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01952 | hp2 | a0001 | c0003 | t0001 | g0222 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01978 | hp1 | a0003 | c0004 | t0002 | g0041 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01981 | hp1 | a0003 | c0004 | t0002 | g0045 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01981 | hp2 | a0001 | c0005 | t0001 | g0196 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01993 | hp2 | a0001 | c0001 | t0018 | g0281 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02015 | hp2 | a0001 | c0005 | t0001 | g0211 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02027 | hp2 | a0001 | c0005 | t0001 | g0293 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02040 | hp2 | a0001 | c0005 | t0001 | g0210 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02071 | hp1 | a0001 | c0003 | t0002 | g0228 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02129 | hp2 | a0003 | c0004 | t0002 | g0054 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02145 | hp1 | a0010 | c0013 | t0001 | g0262 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0230 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02155 | hp2 | a0003 | c0004 | t0002 | g0107 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02165 | hp2 | a0002 | c0002 | t0013 | g0141 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0332 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02572 | hp1 | a0004 | c0007 | t0003 | g0033 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02572 | hp2 | a0001 | c0005 | t0016 | g0096 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02615 | hp2 | a0001 | c0022 | t0001 | g0268 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02622 | hp2 | a0001 | c0006 | t0003 | g0023 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02647 | hp1 | a0004 | c0007 | t0001 | g0102 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02647 | hp2 | a0007 | c0011 | t0001 | g0092 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02698 | hp1 | a0001 | c0005 | t0001 | g0131 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02698 | hp2 | a0001 | c0025 | t0001 | g0122 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02717 | hp2 | a0001 | c0006 | t0001 | g0104 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02723 | hp1 | a0001 | c0018 | t0017 | g0039 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02886 | hp2 | a0004 | c0007 | t0008 | g0335 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02965 | hp2 | a0001 | c0006 | t0004 | g0009 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02970 | hp2 | a0015 | c0021 | t0001 | g0308 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03041 | hp1 | a0001 | c0006 | t0004 | g0328 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03098 | hp2 | a0012 | c0026 | t0014 | g0010 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03195 | hp1 | a0010 | c0013 | t0001 | g0189 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03209 | hp2 | a0001 | c0006 | t0004 | g0103 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03225 | hp2 | a0002 | c0024 | t0001 | g0184 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03239 | hp1 | a0008 | c0014 | t0001 | g0341 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03453 | hp1 | a0001 | c0003 | t0009 | g0113 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03491 | hp2 | a0001 | c0005 | t0005 | g0025 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03516 | hp1 | a0013 | c0019 | t0009 | g0237 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03540 | hp1 | a0001 | c0001 | t0021 | g0342 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03540 | hp2 | a0007 | c0011 | t0001 | g0094 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03654 | hp1 | a0003 | c0004 | t0002 | g0072 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03669 | hp1 | a0002 | c0002 | t0011 | g0162 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03688 | hp1 | a0001 | c0001 | t0011 | g0249 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03704 | hp1 | a0002 | c0010 | t0003 | g0030 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03834 | hp1 | a0003 | c0004 | t0002 | g0134 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0164 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03942 | hp2 | a0002 | c0009 | t0002 | g0177 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04184 | hp2 | a0011 | c0027 | t0001 | g0280 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04199 | hp2 | a0002 | c0010 | t0002 | g0070 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04228 | hp1 | a0001 | c0001 | t0015 | g0028 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04228 | hp2 | a0002 | c0009 | t0013 | g0277 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18612 | hp2 | a0009 | c0031 | t0002 | g0241 | EAS | CHB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18940 | hp1 | a0003 | c0004 | t0001 | g0044 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18941 | hp2 | a0002 | c0009 | t0001 | g0324 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18948 | hp1 | a0003 | c0004 | t0002 | g0174 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18948 | hp2 | a0001 | c0005 | t0001 | g0285 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18949 | hp1 | a0020 | c0015 | t0001 | g0080 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18952 | hp2 | a0003 | c0004 | t0005 | g0022 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18963 | hp2 | a0003 | c0004 | t0005 | g0015 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18964 | hp1 | a0003 | c0004 | t0002 | g0270 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18970 | hp2 | a0003 | c0004 | t0005 | g0012 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18971 | hp2 | a0003 | c0004 | t0002 | g0251 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18973 | hp1 | a0003 | c0004 | t0002 | g0064 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18977 | hp1 | a0003 | c0004 | t0002 | g0048 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18979 | hp1 | a0001 | c0005 | t0001 | g0286 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18979 | hp2 | a0003 | c0004 | t0020 | g0057 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18988 | hp1 | a0001 | c0005 | t0001 | g0304 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18988 | hp2 | a0003 | c0004 | t0005 | g0013 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18990 | hp1 | a0001 | c0003 | t0002 | g0243 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18990 | hp2 | a0003 | c0004 | t0005 | g0016 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18991 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18992 | hp1 | a0003 | c0004 | t0005 | g0014 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18994 | hp2 | a0003 | c0004 | t0002 | g0052 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18998 | hp1 | a0001 | c0005 | t0005 | g0021 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18998 | hp2 | a0001 | c0006 | t0001 | g0235 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19001 | hp1 | a0003 | c0004 | t0002 | g0075 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19003 | hp1 | a0003 | c0004 | t0005 | g0017 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19003 | hp2 | a0001 | c0005 | t0001 | g0126 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19004 | hp2 | a0001 | c0005 | t0001 | g0209 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19005 | hp2 | a0003 | c0004 | t0002 | g0067 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19010 | hp2 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19011 | hp1 | a0009 | c0030 | t0001 | g0242 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0338 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19056 | hp2 | a0003 | c0004 | t0002 | g0047 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19060 | hp1 | a0019 | c0032 | t0001 | g0110 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19063 | hp2 | a0003 | c0004 | t0002 | g0053 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19077 | hp1 | a0001 | c0005 | t0002 | g0300 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19082 | hp2 | a0003 | c0004 | t0005 | g0011 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19083 | hp1 | a0003 | c0004 | t0002 | g0050 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19088 | hp2 | a0003 | c0004 | t0012 | g0133 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19091 | hp1 | a0005 | c0008 | t0001 | g0215 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19091 | hp2 | a0018 | c0016 | t0001 | g0040 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0343 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | ASW | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ASW | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0121 | EUR | TSI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20805 | hp2 | a0001 | c0001 | t0010 | g0026 | EUR | TSI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | GIH | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0155 | SAS | GIH | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01123 | hp1 | a0001 | c0005 | t0001 | g0315 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01123 | hp2 | a0003 | c0004 | t0002 | g0069 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02109 | hp1 | a0004 | c0007 | t0008 | g0334 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02559 | hp2 | a0001 | c0003 | t0006 | g0062 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03471 | hp1 | a0001 | c0003 | t0006 | g0081 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG06807 | hp1 | a0007 | c0011 | t0001 | g0093 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18955 | hp1 | a0005 | c0008 | t0001 | g0217 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18955 | hp2 | a0003 | c0004 | t0012 | g0132 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0321 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA21309 | hp1 | a0001 | c0006 | t0004 | g0009 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA21309 | hp2 | a0001 | c0001 | t0019 | g0312 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
homoSapiens_chm13v2 | hp1 | a0014 | c0023 | t0001 | g0106 | REF | REF | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0007 | g0077 | REF | REF | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87504251
|
G | A | 1 | a0015 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3835C>T | p.Arg1279Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3971/5205 | 3835/3843 | 1279/1280 | chr7 | 87504251 | ||
chr7:87504335
|
C | T | 1 | a0005 | 4 | HG01261.hp2 HG01928.hp1 NA18955.hp1 others(1): Show |
missense_variant | MODERATE | c.3751G>A | p.Val1251Ile | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3887/5205 | 3751/3843 | 1251/1280 | chr7 | 87504335 | ||
chr7:87504389
|
G | A | 1 | a0014 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.3697C>T | p.Arg1233Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3833/5205 | 3697/3843 | 1233/1280 | chr7 | 87504389 | ||
chr7:87509343
|
A | T | 1 | a0004 | 5 | HG00639.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
missense_variant | MODERATE | c.3421T>A | p.Ser1141Thr | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3557/5205 | 3421/3843 | 1141/1280 | chr7 | 87509343 | ||
chr7:87509442
|
A | G | 1 | a0012 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3322T>C | p.Trp1108Arg | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3458/5205 | 3322/3843 | 1108/1280 | chr7 | 87509442 | ||
chr7:87509444
|
T | G | 1 | a0016 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.3320A>C | p.Gln1107Pro | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3456/5205 | 3320/3843 | 1107/1280 | chr7 | 87509444 | ||
chr7:87515251
|
C | T | 1 | a0010 | 2 | HG02145.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.3262G>A | p.Asp1088Asn | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/28 | 3398/5205 | 3262/3843 | 1088/1280 | chr7 | 87515251 | ||
chr7:87519444
|
T | G | 1 | a0017 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2809A>C | p.Ile937Leu | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/28 | 2945/5205 | 2809/3843 | 937/1280 | chr7 | 87519444 | ||
chr7:87531302
|
A | C | 13 | a0001a0004a0005others(10): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
missense_variant | MODERATE | c.2677T>G | p.Ser893Ala | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/28 | 2813/5205 | 2677/3843 | 893/1280 | chr7 | 87531302 | ||
chr7:87531302
|
A | T | 2 | a0003a0018 | 36 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(33): Show |
missense_variant | MODERATE | c.2677T>A | p.Ser893Thr | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/28 | 2813/5205 | 2677/3843 | 893/1280 | chr7 | 87531302 | ||
chr7:87531358
|
A | G | 1 | a0013 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2621T>C | p.Val874Ala | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/28 | 2757/5205 | 2621/3843 | 874/1280 | chr7 | 87531358 | ||
chr7:87539281
|
G | C | 1 | a0009 | 2 | NA18612.hp2 NA19011.hp1 |
missense_variant | MODERATE | c.2384C>G | p.Ser795Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/28 | 2520/5205 | 2384/3843 | 795/1280 | chr7 | 87539281 | ||
chr7:87544882
|
G | A | 1 | a0012 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2005C>T | p.Arg669Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/28 | 2141/5205 | 2005/3843 | 669/1280 | chr7 | 87544882 | ||
chr7:87545988
|
G | A | 1 | a0011 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1762C>T | p.Arg588Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/28 | 1898/5205 | 1762/3843 | 588/1280 | chr7 | 87545988 | ||
chr7:87550493
|
C | T | 1 | a0006 | 3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
missense_variant | MODERATE | c.1199G>A | p.Ser400Asn | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/28 | 1335/5205 | 1199/3843 | 400/1280 | chr7 | 87550493 | ||
chr7:87561309
|
T | C | 1 | a0007 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.781A>G | p.Ile261Val | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/28 | 917/5205 | 781/3843 | 261/1280 | chr7 | 87561309 | ||
chr7:87570185
|
C | T | 1 | a0018 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.325G>A | p.Glu109Lys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/28 | 461/5205 | 325/3843 | 109/1280 | chr7 | 87570185 | ||
chr7:87585654
|
C | A | 1 | a0019 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.144G>T | p.Lys48Asn | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/28 | 280/5205 | 144/3843 | 48/1280 | chr7 | 87585654 | ||
chr7:87600124
|
T | C | 1 | a0008 | 2 | HG01255.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.61A>G | p.Asn21Asp | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/28 | 197/5205 | 61/3843 | 21/1280 | chr7 | 87600124 | ||
chr7:87600136
|
A | G | 1 | a0020 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.49T>C | p.Phe17Leu | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/28 | 185/5205 | 49/3843 | 17/1280 | chr7 | 87600136 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87504258
|
T | C | 1 | a0001c0022 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.3828A>G | p.Gly1276Gly | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3964/5205 | 3828/3843 | 1276/1280 | chr7 | 87504258 | ||
chr7:87509329
|
A | G | 21 | a0001c0001a0001c0003a0001c0018others(18): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
synonymous_variant | LOW | c.3435T>C | p.Ile1145Ile | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3571/5205 | 3435/3843 | 1145/1280 | chr7 | 87509329 | ||
chr7:87541369
|
T | C | 1 | a0001c0025 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.2307A>G | p.Thr769Thr | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/28 | 2443/5205 | 2307/3843 | 769/1280 | chr7 | 87541369 | ||
chr7:87549411
|
C | G | 1 | a0001c0018 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1662G>C | p.Leu554Leu | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/28 | 1798/5205 | 1662/3843 | 554/1280 | chr7 | 87549411 | ||
chr7:87550285
|
A | G | 20 | a0001c0001a0001c0005a0001c0018others(17): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
synonymous_variant | LOW | c.1236T>C | p.Gly412Gly | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/28 | 1372/5205 | 1236/3843 | 412/1280 | chr7 | 87550285 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87503314
|
C | G | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*929G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 929 | chr7 | 87503314 | |||||
chr7:87503509
|
C | G | 1 | a0001c0001t0018 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*734G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 734 | chr7 | 87503509 | |||||
chr7:87503600
|
C | T | 27 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(24): Show | 98 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*643G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 643 | chr7 | 87503600 | |||||
chr7:87503888
|
A | G | 1 | a0003c0004t0012 | 2 | NA18955.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*355T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 355 | chr7 | 87503888 | |||||
chr7:87503991
|
T | G | 3 | a0001c0001t0009a0001c0003t0009a0013c0019t0009 | 3 | HG03195.hp2 HG03453.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 252 | chr7 | 87503991 | |||||
chr7:87504050
|
T | C | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(17): Show | 88 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*193A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 193 | chr7 | 87504050 | |||||
chr7:87504070
|
A | ATGTCTCT others(1): Show |
7 | a0001c0001t0006a0001c0001t0011a0001c0001t0015others(4): Show | 13 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*165_*172dupGAGAGA others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 172 | chr7 | 87504070 | |||||
chr7:87504097
|
C | T | 4 | a0001c0001t0008a0001c0005t0016a0004c0007t0008others(1): Show | 7 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 146 | chr7 | 87504097 | |||||
chr7:87504154
|
T | A | 3 | a0001c0001t0004a0001c0001t0010a0001c0006t0004 | 19 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*89A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 89 | chr7 | 87504154 | |||||
chr7:87504160
|
TGTAA | T | 3 | a0001c0001t0008a0001c0005t0016a0004c0007t0008 | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*79_*82delTTAC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 79 | chr7 | 87504160 | |||||
chr7:87504173
|
T | C | 1 | a0003c0004t0020 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 70 | chr7 | 87504173 | |||||
chr7:87504222
|
A | G | 3 | a0001c0001t0006a0001c0001t0021a0001c0003t0006 | 9 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*21T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 21 | chr7 | 87504222 | |||||
chr7:87600185
|
T | C | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(65): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
5_prime_UTR_variant | MODIFIER | c.-1A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/28 | 1 | chr7 | 87600185 | |||||
chr7:87600791
|
T | C | 2 | a0001c0001t0021a0001c0001t0022 | 2 | HG03540.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-43A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/28 | 607 | chr7 | 87600791 | |||||
chr7:87600877
|
A | G | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(8): Show | 33 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-129T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/28 | 693 | chr7 | 87600877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87504535
|
A | G | 25 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0179others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.3637-86T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504535 | ||||||
chr7:87504536
|
T | C | 33 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0111others(30): Show | 33 | HG00639.hp2 HG00738.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.3637-87A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504536 | ||||||
chr7:87504547
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3637-98C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504547 | ||||||
chr7:87504568
|
G | A | 3 | a0001c0006t0001g0235a0002c0002t0001g0005a0002c0002t0001g0160 | 4 | NA18970.hp1 NA18982.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.3637-119C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504568 | ||||||
chr7:87504580
|
G | A | 1 | a0001c0001t0010g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3637-131C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504580 | ||||||
chr7:87504584
|
A | G | 4 | a0001c0001t0001g0266a0001c0001t0009g0267a0001c0022t0001g0268others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3637-135T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504584 | ||||||
chr7:87504601
|
T | C | 4 | a0001c0001t0001g0297a0001c0001t0001g0299a0001c0001t0019g0312others(1): Show | 4 | HG02895.hp2 HG02897.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3637-152A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504601 | ||||||
chr7:87504601
|
T | G | 2 | a0001c0001t0001g0065a0001c0018t0017g0039 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3637-152A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504601 | ||||||
chr7:87504616
|
T | C | 10 | a0001c0001t0001g0084a0001c0001t0002g0338a0001c0001t0002g0339others(7): Show | 10 | HG01243.hp2 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.3637-167A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504616 | ||||||
chr7:87504617
|
A | G | 2 | a0001c0001t0001g0292a0001c0003t0001g0164 | 2 | HG01928.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3637-168T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504617 | ||||||
chr7:87504631
|
C | A | 31 | a0001c0001t0001g0117a0001c0001t0001g0191a0001c0001t0001g0193others(28): Show | 32 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.3637-182G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504631 | ||||||
chr7:87504661
|
T | C | 1 | a0001c0001t0004g0330 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3637-212A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504661 | ||||||
chr7:87504666
|
T | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0091a0002c0002t0002g0121others(1): Show | 4 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3637-217A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504666 | ||||||
chr7:87504669
|
G | T | 3 | a0001c0001t0001g0091a0002c0002t0002g0121a0017c0029t0002g0130 | 3 | HG00735.hp1 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3637-220C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504669 | ||||||
chr7:87504673
|
T | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0201others(3): Show | 6 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3637-224A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504673 | ||||||
chr7:87504677
|
T | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0091others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3637-228A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504677 | ||||||
chr7:87504808
|
G | GA | 19 | a0001c0001t0001g0283a0001c0001t0001g0287a0001c0001t0001g0288others(16): Show | 19 | HG01175.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.3637-360dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504808 | ||||||
chr7:87504808
|
GA | G | 19 | a0001c0001t0001g0007a0001c0001t0001g0065a0001c0001t0001g0250others(16): Show | 21 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.3637-360delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504808 | ||||||
chr7:87504819
|
A | AT | 11 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0068others(8): Show | 11 | HG02258.hp1 HG02895.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.3637-371_3637-370i others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504819 | ||||||
chr7:87504819
|
A | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0065a0001c0001t0001g0250others(11): Show | 16 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.3637-370T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504819 | ||||||
chr7:87504978
|
T | A | 1 | a0003c0004t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3637-529A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504978 | ||||||
chr7:87505017
|
G | A | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3637-568C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505017 | ||||||
chr7:87505219
|
C | G | 34 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3636+678G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505219 | ||||||
chr7:87505243
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3636+654C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505243 | ||||||
chr7:87505504
|
T | C | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3636+393A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505504 | ||||||
chr7:87505639
|
T | C | 1 | a0020c0015t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3636+258A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505639 | ||||||
chr7:87505869
|
T | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3636+28A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505869 | ||||||
chr7:87506164
|
A | G | 5 | a0001c0001t0003g0037a0001c0001t0008g0097a0001c0001t0008g0098others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3490-121T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506164 | ||||||
chr7:87506550
|
AT | A | 8 | a0001c0001t0004g0100a0001c0001t0005g0034a0004c0007t0001g0102others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-508delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506550 | ||||||
chr7:87506553
|
A | T | 8 | a0001c0001t0004g0100a0001c0001t0005g0034a0004c0007t0001g0102others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-510T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506553 | ||||||
chr7:87506554
|
A | T | 8 | a0001c0001t0004g0100a0001c0001t0005g0034a0004c0007t0001g0102others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-511T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506554 | ||||||
chr7:87506557
|
T | A | 8 | a0001c0001t0004g0100a0001c0001t0005g0034a0004c0007t0001g0102others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-514A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506557 | ||||||
chr7:87506867
|
C | T | 3 | a0001c0001t0004g0100a0001c0001t0005g0034a0012c0026t0014g0010 | 3 | HG02280.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3490-824G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506867 | ||||||
chr7:87507016
|
T | C | 8 | a0001c0001t0004g0100a0001c0001t0005g0034a0004c0007t0001g0102others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-973A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507016 | ||||||
chr7:87507261
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3490-1218G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507261 | ||||||
chr7:87507355
|
T | C | 14 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0088others(11): Show | 14 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3490-1312A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507355 | ||||||
chr7:87507392
|
G | A | 8 | a0001c0001t0004g0100a0001c0001t0005g0034a0004c0007t0001g0102others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-1349C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507392 | ||||||
chr7:87507441
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3490-1398G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507441 | ||||||
chr7:87507699
|
C | T | 70 | a0001c0001t0001g0008a0001c0001t0001g0060a0001c0001t0001g0091others(67): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.3489+1576G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507699 | ||||||
chr7:87507702
|
C | T | 196 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0056others(193): Show | 198 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.3489+1573G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507702 | ||||||
chr7:87507995
|
AG | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0060a0001c0001t0001g0091others(67): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.3489+1279delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507995 | ||||||
chr7:87508142
|
T | G | 8 | a0001c0001t0001g0065a0001c0001t0001g0250a0001c0001t0003g0036others(5): Show | 8 | HG01081.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3489+1133A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508142 | ||||||
chr7:87508145
|
G | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0060a0001c0001t0001g0091others(67): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.3489+1130C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508145 | ||||||
chr7:87508162
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0001g0316a0001c0001t0001g0317others(1): Show | 4 | HG01516.hp2 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.3489+1113C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508162 | ||||||
chr7:87508446
|
T | C | 1 | a0002c0002t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3489+829A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508446 | ||||||
chr7:87508734
|
A | G | 1 | a0002c0002t0001g0154 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3489+541T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508734 | ||||||
chr7:87508870
|
A | G | 341 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(338): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.3489+405T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508870 | ||||||
chr7:87508911
|
G | C | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3489+364C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508911 | ||||||
chr7:87509193
|
G | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3489+82C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87509193 | ||||||
chr7:87509195
|
G | A | 240 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(237): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.3489+80C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87509195 | ||||||
chr7:87509216
|
A | C | 106 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(103): Show | 106 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3489+59T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87509216 | ||||||
chr7:87509638
|
A | G | 7 | a0001c0001t0005g0034a0004c0007t0001g0102a0004c0007t0001g0258others(4): Show | 7 | HG00639.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3283-157T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87509638 | ||||||
chr7:87509681
|
T | C | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3283-200A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87509681 | ||||||
chr7:87510000
|
A | G | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(113): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.3283-519T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510000 | ||||||
chr7:87510141
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3283-660A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510141 | ||||||
chr7:87510737
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3283-1256A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510737 | ||||||
chr7:87510804
|
A | C | 1 | a0001c0001t0002g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3283-1323T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510804 | ||||||
chr7:87510856
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3283-1375C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510856 | ||||||
chr7:87510859
|
G | A | 8 | a0001c0001t0001g0065a0001c0001t0001g0250a0001c0001t0003g0036others(5): Show | 8 | HG01081.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3283-1378C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510859 | ||||||
chr7:87511027
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0190a0001c0001t0001g0208 | 3 | HG02056.hp2 HG02080.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.3283-1546G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511027 | ||||||
chr7:87511395
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3283-1914C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511395 | ||||||
chr7:87511435
|
T | C | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3283-1954A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511435 | ||||||
chr7:87511465
|
T | C | 1 | a0002c0002t0001g0154 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3283-1984A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511465 | ||||||
chr7:87511492
|
A | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0123others(49): Show | 54 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.3283-2011T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511492 | ||||||
chr7:87511512
|
A | T | 1 | a0020c0015t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3283-2031T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511512 | ||||||
chr7:87511823
|
G | C | 2 | a0001c0003t0006g0062a0001c0003t0009g0113 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3283-2342C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511823 | ||||||
chr7:87511858
|
G | C | 113 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0001g0087others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3283-2377C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511858 | ||||||
chr7:87512181
|
A | C | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.3283-2700T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512181 | ||||||
chr7:87512182
|
A | C | 2 | a0001c0001t0019g0312a0003c0004t0002g0270 | 2 | NA18964.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3283-2701T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512182 | ||||||
chr7:87512190
|
A | T | 1 | a0001c0001t0008g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3283-2709T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512190 | ||||||
chr7:87512190
|
AT | A | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(120): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.3283-2710delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512190 | ||||||
chr7:87512236
|
T | G | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3283-2755A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512236 | ||||||
chr7:87512354
|
G | A | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3283-2873C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512354 | ||||||
chr7:87512435
|
C | T | 110 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(107): Show | 110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.3282+2796G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512435 | ||||||
chr7:87512498
|
T | C | 255 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(252): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3282+2733A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512498 | ||||||
chr7:87512556
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3282+2675G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512556 | ||||||
chr7:87512636
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3282+2595T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512636 | ||||||
chr7:87512673
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0031 | 2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.3282+2558C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512673 | ||||||
chr7:87512769
|
T | G | 1 | a0001c0001t0002g0138 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3282+2462A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512769 | ||||||
chr7:87512868
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3282+2363C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512868 | ||||||
chr7:87512895
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3282+2336G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512895 | ||||||
chr7:87512939
|
A | C | 1 | a0003c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3282+2292T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512939 | ||||||
chr7:87513133
|
G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3282+2098C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513133 | ||||||
chr7:87513158
|
G | T | 8 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0088others(5): Show | 8 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3282+2073C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513158 | ||||||
chr7:87513243
|
C | CCTTTT | 256 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(253): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.3282+1987_3282+198 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513243 | ||||||
chr7:87513510
|
G | C | 4 | a0003c0004t0005g0013a0003c0004t0005g0014a0003c0004t0005g0016others(1): Show | 4 | NA18988.hp2 NA18990.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.3282+1721C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513510 | ||||||
chr7:87513658
|
G | A | 1 | a0004c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3282+1573C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513658 | ||||||
chr7:87513837
|
T | C | 103 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(100): Show | 103 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.3282+1394A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513837 | ||||||
chr7:87513932
|
G | A | 1 | a0003c0004t0005g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3282+1299C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513932 | ||||||
chr7:87513939
|
T | A | 8 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0088others(5): Show | 8 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3282+1292A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513939 | ||||||
chr7:87513959
|
T | C | 122 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(119): Show | 122 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.3282+1272A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513959 | ||||||
chr7:87514006
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3282+1225T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514006 | ||||||
chr7:87514188
|
C | T | 120 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(117): Show | 120 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.3282+1043G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514188 | ||||||
chr7:87514225
|
T | C | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3282+1006A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514225 | ||||||
chr7:87514425
|
T | G | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3282+806A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514425 | ||||||
chr7:87514707
|
T | C | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3282+524A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514707 | ||||||
chr7:87514877
|
C | G | 3 | a0001c0003t0001g0164a0001c0003t0001g0319a0001c0003t0002g0255 | 3 | HG00558.hp2 HG00609.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3282+354G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514877 | ||||||
chr7:87515097
|
G | C | 53 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0068others(50): Show | 53 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.3282+134C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87515097 | ||||||
chr7:87515500
|
G | C | 117 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(114): Show | 117 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.3085-72C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515500 | ||||||
chr7:87515543
|
C | T | 1 | a0004c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3085-115G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515543 | ||||||
chr7:87515701
|
G | A | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3085-273C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515701 | ||||||
chr7:87515817
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0305 | 3 | HG01515.hp1 HG01517.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.3085-389C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515817 | ||||||
chr7:87515831
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3085-403T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515831 | ||||||
chr7:87516018
|
C | T | 1 | a0002c0002t0001g0321 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3084+491G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516018 | ||||||
chr7:87516108
|
T | C | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3084+401A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516108 | ||||||
chr7:87516119
|
G | A | 2 | a0001c0003t0006g0062a0001c0003t0009g0113 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3084+390C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516119 | ||||||
chr7:87516167
|
G | A | 100 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.3084+342C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516167 | ||||||
chr7:87516231
|
G | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3084+278C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516231 | ||||||
chr7:87516493
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | NA18960.hp1 NA19011.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3084+16C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516493 | ||||||
chr7:87516728
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2928-63G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516728 | ||||||
chr7:87516731
|
C | CT | 12 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0208others(9): Show | 12 | HG00544.hp1 HG01358.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2928-67dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTT | 31 | a0001c0003t0001g0109a0001c0003t0001g0161a0001c0003t0001g0164others(28): Show | 31 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2928-70_2928-67dup others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTT | 8 | a0001c0001t0008g0098a0001c0003t0001g0135a0001c0003t0001g0157others(5): Show | 8 | HG02083.hp1 HG02135.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2928-71_2928-67dup others(5): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT | 7 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2928-73_2928-67dup others(7): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0010g0035a0003c0004t0002g0054a0003c0004t0002g0134 | 3 | HG02129.hp2 HG03834.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2928-83_2928-67dup others(17): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT others(11): Show |
29 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0073others(26): Show | 29 | HG00639.hp2 HG01496.hp2 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.2928-84_2928-67dup others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT others(12): Show |
23 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0001g0074others(20): Show | 23 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.2928-85_2928-67dup others(19): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT others(13): Show |
9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0022t0001g0268others(6): Show | 9 | HG00639.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2928-86_2928-67dup others(20): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT others(14): Show |
2 | a0003c0004t0005g0019a0010c0013t0001g0262 | 2 | HG00423.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2928-87_2928-67dup others(21): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
C | CTTTTTTT others(17): Show |
1 | a0003c0004t0005g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2928-67_2928-66ins others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516731
|
CTT | C | 51 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2928-68_2928-67del others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | ||||||
chr7:87516922
|
G | A | 1 | a0014c0023t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2928-257C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516922 | ||||||
chr7:87516956
|
C | T | 1 | a0001c0003t0002g0229 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2928-291G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516956 | ||||||
chr7:87516965
|
G | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2928-300C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516965 | ||||||
chr7:87517326
|
A | G | 1 | a0003c0004t0012g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2928-661T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517326 | ||||||
chr7:87517364
|
T | TTC | 60 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(57): Show | 60 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2928-701_2928-700d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517364 | ||||||
chr7:87517513
|
GATCCACT others(7): Show |
G | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2928-862_2928-849d others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517513 | ||||||
chr7:87517606
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2928-941C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517606 | ||||||
chr7:87517688
|
G | C | 1 | a0004c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2928-1023C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517688 | ||||||
chr7:87517831
|
T | A | 55 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2928-1166A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517831 | ||||||
chr7:87517832
|
GT | G | 55 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2928-1168delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517832 | ||||||
chr7:87518241
|
A | G | 2 | a0002c0002t0001g0129a0002c0002t0001g0156 | 2 | HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2927+1085T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518241 | ||||||
chr7:87518303
|
T | C | 1 | a0004c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2927+1023A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518303 | ||||||
chr7:87518450
|
T | C | 1 | a0001c0001t0003g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2927+876A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518450 | ||||||
chr7:87518539
|
T | G | 1 | a0001c0001t0001g0260 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2927+787A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518539 | ||||||
chr7:87518658
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2927+668A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518658 | ||||||
chr7:87518887
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2927+439T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518887 | ||||||
chr7:87518949
|
G | T | 60 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(57): Show | 60 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.2927+377C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518949 | ||||||
chr7:87518975
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2927+351A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518975 | ||||||
chr7:87519012
|
C | T | 55 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2927+314G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87519012 | ||||||
chr7:87519081
|
C | T | 1 | a0002c0002t0001g0322 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2927+245G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87519081 | ||||||
chr7:87519171
|
T | C | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2927+155A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87519171 | ||||||
chr7:87519596
|
G | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787-130C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519596 | ||||||
chr7:87519622
|
G | A | 4 | a0001c0003t0001g0222a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01952.hp2 HG02148.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787-156C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519622 | ||||||
chr7:87519920
|
AC | A | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2787-455delG | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519920 | ||||||
chr7:87519922
|
T | A | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2787-456A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519922 | ||||||
chr7:87520008
|
G | A | 1 | a0001c0005t0005g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2787-542C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87520008 | ||||||
chr7:87520217
|
A | AT | 55 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2786+558dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87520217 | ||||||
chr7:87520606
|
C | T | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.2786+170G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87520606 | ||||||
chr7:87521167
|
C | T | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2686-291G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521167 | ||||||
chr7:87521288
|
C | T | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-412G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521288 | ||||||
chr7:87521407
|
G | T | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2686-531C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521407 | ||||||
chr7:87521417
|
G | A | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2686-541C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521417 | ||||||
chr7:87521458
|
G | A | 115 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(112): Show | 115 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2686-582C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521458 | ||||||
chr7:87521570
|
A | G | 1 | a0001c0001t0019g0312 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2686-694T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521570 | ||||||
chr7:87521621
|
G | A | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-745C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521621 | ||||||
chr7:87521667
|
G | A | 1 | a0001c0003t0002g0255 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2686-791C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521667 | ||||||
chr7:87521774
|
T | C | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(153): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.2686-898A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521774 | ||||||
chr7:87521901
|
C | T | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2686-1025G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521901 | ||||||
chr7:87522067
|
G | A | 3 | a0002c0002t0001g0155a0002c0002t0001g0163a0002c0002t0001g0168 | 3 | HG01167.hp2 HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2686-1191C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522067 | ||||||
chr7:87522090
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2686-1214G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522090 | ||||||
chr7:87522208
|
C | G | 172 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(169): Show | 172 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.2686-1332G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522208 | ||||||
chr7:87522342
|
C | T | 155 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(152): Show | 155 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.2686-1466G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522342 | ||||||
chr7:87522368
|
G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2686-1492C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522368 | ||||||
chr7:87522477
|
C | T | 6 | a0001c0001t0007g0078a0001c0005t0001g0131a0001c0005t0001g0276others(3): Show | 7 | HG00280.hp2 HG00323.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2686-1601G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522477 | ||||||
chr7:87522530
|
G | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2686-1654C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522530 | ||||||
chr7:87522729
|
A | G | 53 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2686-1853T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522729 | ||||||
chr7:87522748
|
CT | C | 5 | a0001c0001t0001g0084a0001c0001t0004g0049a0001c0005t0002g0300others(2): Show | 5 | HG01243.hp2 HG03209.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-1873delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522748 | ||||||
chr7:87522756
|
TA | T | 51 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0068others(48): Show | 51 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.2686-1881delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522756 | ||||||
chr7:87522757
|
A | T | 53 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0256others(50): Show | 53 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.2686-1881T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522757 | ||||||
chr7:87522787
|
A | G | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-1911T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522787 | ||||||
chr7:87523022
|
T | C | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2686-2146A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523022 | ||||||
chr7:87523127
|
G | T | 1 | a0003c0004t0002g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2686-2251C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523127 | ||||||
chr7:87523195
|
G | A | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-2319C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523195 | ||||||
chr7:87523214
|
G | A | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-2338C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523214 | ||||||
chr7:87523258
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2686-2382T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523258 | ||||||
chr7:87523307
|
T | A | 50 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2686-2431A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523307 | ||||||
chr7:87523311
|
G | A | 1 | a0001c0003t0001g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2686-2435C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523311 | ||||||
chr7:87523339
|
A | G | 1 | a0001c0006t0004g0009 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2686-2463T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523339 | ||||||
chr7:87523474
|
C | A | 100 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2686-2598G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523474 | ||||||
chr7:87523551
|
G | A | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2686-2675C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523551 | ||||||
chr7:87523563
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2686-2687T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523563 | ||||||
chr7:87523570
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG01516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2686-2694G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523570 | ||||||
chr7:87523711
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2686-2835G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523711 | ||||||
chr7:87523782
|
C | T | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2686-2906G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523782 | ||||||
chr7:87523789
|
C | A | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2686-2913G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523789 | ||||||
chr7:87523790
|
G | A | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2686-2914C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523790 | ||||||
chr7:87523821
|
T | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-2945A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523821 | ||||||
chr7:87523844
|
G | A | 100 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2686-2968C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523844 | ||||||
chr7:87523863
|
A | G | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2686-2987T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523863 | ||||||
chr7:87523900
|
C | T | 53 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2686-3024G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523900 | ||||||
chr7:87524191
|
AAC | A | 5 | a0002c0002t0001g0005a0002c0002t0001g0149a0002c0002t0001g0160others(2): Show | 6 | NA18970.hp1 NA18973.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.2686-3317_2686-331 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524191 | ||||||
chr7:87524269
|
A | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-3393T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524269 | ||||||
chr7:87524379
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2686-3503A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524379 | ||||||
chr7:87524555
|
AG | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(81): Show | 90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2686-3680delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524555 | ||||||
chr7:87524599
|
G | C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2686-3723C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524599 | ||||||
chr7:87524701
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2686-3825C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524701 | ||||||
chr7:87524819
|
C | G | 1 | a0001c0003t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2686-3943G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524819 | ||||||
chr7:87524836
|
T | C | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686-3960A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524836 | ||||||
chr7:87525041
|
GT | G | 100 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2686-4166delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525041 | ||||||
chr7:87525330
|
A | G | 50 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2686-4454T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525330 | ||||||
chr7:87525438
|
A | G | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2686-4562T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525438 | ||||||
chr7:87525696
|
G | A | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686-4820C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525696 | ||||||
chr7:87526043
|
T | A | 7 | a0002c0002t0001g0148a0002c0002t0001g0169a0002c0002t0001g0326others(4): Show | 7 | NA18941.hp2 NA18949.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.2686-5167A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526043 | ||||||
chr7:87526164
|
C | CT | 55 | a0001c0001t0001g0087a0001c0001t0001g0179a0001c0001t0001g0180others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2685+5129dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526164 | ||||||
chr7:87526164
|
CT | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0101others(20): Show | 26 | HG00280.hp1 HG00323.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.2685+5129delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526164 | ||||||
chr7:87526240
|
T | C | 1 | a0001c0003t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2685+5054A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526240 | ||||||
chr7:87526279
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(81): Show | 90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2685+5015C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526279 | ||||||
chr7:87526461
|
G | A | 1 | a0003c0004t0002g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2685+4833C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526461 | ||||||
chr7:87526618
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685+4676T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526618 | ||||||
chr7:87526666
|
A | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2685+4628T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526666 | ||||||
chr7:87526688
|
G | A | 2 | a0001c0001t0001g0318a0004c0007t0001g0102 | 2 | HG02647.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2685+4606C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526688 | ||||||
chr7:87526693
|
T | C | 4 | a0003c0004t0005g0013a0003c0004t0005g0014a0003c0004t0005g0016others(1): Show | 4 | NA18988.hp2 NA18990.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685+4601A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526693 | ||||||
chr7:87526720
|
C | A | 3 | a0001c0001t0001g0084a0001c0001t0004g0049a0001c0001t0005g0034 | 3 | HG01243.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2685+4574G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526720 | ||||||
chr7:87526875
|
G | T | 17 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(14): Show | 17 | HG00738.hp2 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2685+4419C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526875 | ||||||
chr7:87526985
|
G | A | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2685+4309C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526985 | ||||||
chr7:87527063
|
A | T | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2685+4231T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527063 | ||||||
chr7:87527098
|
C | T | 1 | a0001c0001t0018g0281 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2685+4196G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527098 | ||||||
chr7:87527131
|
T | C | 1 | a0002c0010t0003g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2685+4163A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527131 | ||||||
chr7:87527198
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2685+4096C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527198 | ||||||
chr7:87527215
|
T | C | 1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2685+4079A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527215 | ||||||
chr7:87527240
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2685+4054G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527240 | ||||||
chr7:87527326
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2685+3968A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527326 | ||||||
chr7:87527445
|
A | G | 1 | a0002c0002t0011g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2685+3849T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527445 | ||||||
chr7:87527733
|
T | C | 2 | a0001c0001t0001g0206a0001c0005t0003g0002 | 3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2685+3561A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527733 | ||||||
chr7:87527735
|
G | A | 171 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(168): Show | 171 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.2685+3559C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527735 | ||||||
chr7:87527904
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2685+3390A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527904 | ||||||
chr7:87527978
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0004g0049a0002c0002t0001g0137 | 3 | HG01243.hp2 HG02056.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2685+3316G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527978 | ||||||
chr7:87528076
|
G | C | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2685+3218C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528076 | ||||||
chr7:87528150
|
C | G | 100 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2685+3144G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528150 | ||||||
chr7:87528181
|
G | C | 1 | a0001c0005t0001g0126 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2685+3113C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528181 | ||||||
chr7:87528267
|
A | C | 267 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(264): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.2685+3027T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528267 | ||||||
chr7:87528284
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2685+3010C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528284 | ||||||
chr7:87528313
|
T | C | 53 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0125others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2685+2981A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528313 | ||||||
chr7:87528328
|
T | A | 56 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0125others(53): Show | 56 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.2685+2966A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528328 | ||||||
chr7:87528390
|
C | T | 100 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2685+2904G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528390 | ||||||
chr7:87528439
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2685+2855T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528439 | ||||||
chr7:87528869
|
G | T | 267 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(264): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.2685+2425C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528869 | ||||||
chr7:87529084
|
A | T | 1 | a0001c0003t0002g0227 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2685+2210T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529084 | ||||||
chr7:87529596
|
T | C | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2685+1698A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529596 | ||||||
chr7:87529736
|
T | G | 1 | a0001c0003t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2685+1558A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529736 | ||||||
chr7:87529934
|
G | A | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2685+1360C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529934 | ||||||
chr7:87530012
|
G | T | 4 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0146others(1): Show | 4 | HG00408.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685+1282C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530012 | ||||||
chr7:87530203
|
A | C | 3 | a0001c0001t0004g0182a0001c0001t0004g0259a0001c0001t0004g0264 | 3 | HG02109.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2685+1091T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530203 | ||||||
chr7:87530570
|
G | A | 3 | a0001c0003t0001g0164a0001c0003t0001g0319a0001c0003t0002g0255 | 3 | HG00558.hp2 HG00609.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2685+724C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530570 | ||||||
chr7:87530757
|
A | G | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2685+537T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530757 | ||||||
chr7:87530790
|
A | AAAGAAAG others(1): Show |
26 | a0001c0001t0001g0203a0001c0001t0004g0100a0002c0002t0001g0004others(23): Show | 27 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.2685+496_2685+503d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | ||||||
chr7:87530790
|
A | AAAGAAAG others(9): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2685+488_2685+503d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | ||||||
chr7:87530790
|
A | C | 1 | a0002c0009t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2685+504T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | ||||||
chr7:87530790
|
AAAGAAAG others(1): Show |
A | 13 | a0001c0001t0001g0084a0001c0001t0001g0186a0001c0001t0019g0312others(10): Show | 13 | HG00609.hp2 HG01243.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2685+496_2685+503d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | ||||||
chr7:87530790
|
AAAGAAAG others(9): Show |
A | 5 | a0001c0001t0001g0181a0001c0001t0008g0055a0001c0003t0001g0109others(2): Show | 5 | HG01952.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685+488_2685+503d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | ||||||
chr7:87530790
|
AAAGAAAG others(17): Show |
A | 2 | a0003c0004t0002g0069a0003c0004t0002g0072 | 2 | HG01123.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2685+480_2685+503d others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | ||||||
chr7:87530796
|
A | AGCAAGAA others(1): Show |
5 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0003g0029others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685+497_2685+498i others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530796 | ||||||
chr7:87530804
|
A | C | 3 | a0001c0001t0003g0024a0001c0001t0003g0031a0001c0001t0010g0026 | 3 | HG00280.hp1 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2685+490T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530804 | ||||||
chr7:87530818
|
AAAGCAAG others(5): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2685+464_2685+475d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530818 | ||||||
chr7:87530818
|
AAAGCAAG others(13): Show |
A | 1 | a0003c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2685+456_2685+475d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530818 | ||||||
chr7:87530822
|
CAAGAAAG others(13): Show |
C | 55 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(52): Show | 55 | HG00423.hp2 HG01358.hp2 HG01496.hp2 others(52): Show |
intron_variant | MODIFIER | c.2685+452_2685+471d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530822 | ||||||
chr7:87530822
|
CAAGAAAG others(17): Show |
C | 49 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2685+448_2685+471d others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530822 | ||||||
chr7:87530826
|
AAAGCAAG others(5): Show |
A | 1 | a0003c0004t0002g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2685+456_2685+467d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530826 | ||||||
chr7:87530830
|
C | CAAGA | 6 | a0001c0001t0001g0065a0001c0001t0004g0049a0001c0001t0004g0182others(3): Show | 6 | HG01081.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685+460_2685+463d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | ||||||
chr7:87530830
|
CAAGAAAG others(5): Show |
C | 27 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(24): Show | 27 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.2685+452_2685+463d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | ||||||
chr7:87530830
|
CAAGAAAG others(9): Show |
C | 1 | a0002c0002t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2685+448_2685+463d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | ||||||
chr7:87530830
|
CAAGAAAG others(13): Show |
C | 3 | a0007c0011t0001g0092a0007c0011t0001g0093a0007c0011t0001g0094 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2685+444_2685+463d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | ||||||
chr7:87530830
|
CAAGAAAG others(17): Show |
C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2685+440_2685+463d others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | ||||||
chr7:87530834
|
AAAGC | A | 8 | a0001c0003t0001g0135a0001c0003t0001g0224a0001c0003t0001g0225others(5): Show | 8 | HG00639.hp1 HG02083.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2685+456_2685+459d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530834 | ||||||
chr7:87530838
|
C | A | 16 | a0001c0001t0001g0065a0001c0001t0001g0193a0001c0001t0001g0213others(13): Show | 17 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.2685+456G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGA | 12 | a0001c0001t0001g0119a0001c0001t0001g0191a0001c0001t0003g0024others(9): Show | 15 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.2685+452_2685+455d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(1): Show |
29 | a0001c0001t0001g0060a0001c0001t0001g0091a0001c0001t0001g0116others(26): Show | 29 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.2685+448_2685+455d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(5): Show |
13 | a0001c0001t0001g0008a0001c0001t0001g0185a0001c0001t0001g0192others(10): Show | 14 | HG00280.hp2 HG00738.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2685+444_2685+455d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(9): Show |
7 | a0001c0001t0001g0118a0001c0001t0001g0214a0001c0001t0002g0274others(4): Show | 7 | HG00323.hp1 HG00642.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2685+440_2685+455d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(13): Show |
4 | a0001c0001t0001g0108a0001c0001t0001g0205a0001c0001t0001g0250others(1): Show | 4 | HG01261.hp2 HG03098.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685+436_2685+455d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(5): Show |
13 | a0002c0002t0001g0136a0002c0002t0001g0137a0002c0002t0001g0143others(10): Show | 13 | HG00558.hp1 HG01257.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.2685+455_2685+456i others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(9): Show |
8 | a0001c0001t0001g0112a0001c0001t0002g0338a0001c0005t0003g0002others(5): Show | 10 | HG00544.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2685+455_2685+456i others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(13): Show |
4 | a0001c0001t0001g0111a0001c0001t0001g0206a0002c0002t0001g0105others(1): Show | 4 | HG01433.hp2 HG03490.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2685+455_2685+456i others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(17): Show |
1 | a0002c0002t0001g0160 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2685+455_2685+456i others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(13): Show |
1 | a0001c0001t0001g0314 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2685+455_2685+456i others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
C | CAAGAAAG others(21): Show |
1 | a0001c0001t0002g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2685+455_2685+456i others(30): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530838
|
CAAGA | C | 9 | a0001c0003t0006g0062a0001c0003t0006g0081a0001c0003t0009g0113others(6): Show | 9 | HG00741.hp2 HG01167.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2685+452_2685+455d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | ||||||
chr7:87530842
|
A | AAAGC | 15 | a0001c0006t0004g0103a0002c0002t0001g0148a0002c0002t0001g0168others(12): Show | 15 | HG01192.hp2 HG01258.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.2685+451_2685+452i others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530842 | ||||||
chr7:87530846
|
A | C | 1 | a0001c0006t0004g0328 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2685+448T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530846 | ||||||
chr7:87530850
|
A | C | 1 | a0002c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2685+444T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530850 | ||||||
chr7:87530889
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2685+405T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530889 | ||||||
chr7:87531245
|
A | G | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2685+49T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87531245 | ||||||
chr7:87531733
|
T | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2482-236A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87531733 | ||||||
chr7:87531983
|
A | T | 1 | a0001c0003t0002g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2482-486T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87531983 | ||||||
chr7:87531992
|
G | A | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2482-495C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87531992 | ||||||
chr7:87532204
|
T | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2482-707A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532204 | ||||||
chr7:87532267
|
T | C | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-770A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532267 | ||||||
chr7:87532480
|
C | T | 2 | a0005c0008t0001g0215a0005c0008t0001g0217 | 2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2482-983G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532480 | ||||||
chr7:87532561
|
A | T | 1 | a0002c0002t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2482-1064T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532561 | ||||||
chr7:87532716
|
C | T | 1 | a0002c0002t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2482-1219G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532716 | ||||||
chr7:87532751
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2482-1254A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532751 | ||||||
chr7:87532928
|
C | G | 1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2482-1431G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532928 | ||||||
chr7:87532967
|
G | A | 8 | a0003c0004t0001g0044a0003c0004t0002g0041a0003c0004t0002g0043others(5): Show | 8 | HG01358.hp2 HG01496.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2482-1470C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532967 | ||||||
chr7:87532986
|
C | A | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2482-1489G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532986 | ||||||
chr7:87533012
|
A | G | 1 | a0001c0003t0001g0234 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2482-1515T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533012 | ||||||
chr7:87533025
|
A | G | 103 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(100): Show | 103 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2482-1528T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533025 | ||||||
chr7:87533514
|
C | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-2017G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533514 | ||||||
chr7:87533571
|
T | C | 5 | a0002c0002t0001g0127a0002c0002t0001g0136a0002c0002t0001g0165others(2): Show | 5 | HG00558.hp1 HG02015.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.2482-2074A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533571 | ||||||
chr7:87533700
|
T | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2482-2203A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533700 | ||||||
chr7:87533733
|
C | T | 257 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(254): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2482-2236G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533733 | ||||||
chr7:87533809
|
T | C | 8 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(5): Show | 9 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-2312A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533809 | ||||||
chr7:87533847
|
T | C | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-2350A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533847 | ||||||
chr7:87533964
|
G | C | 1 | a0002c0002t0001g0171 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2482-2467C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533964 | ||||||
chr7:87534004
|
C | T | 3 | a0007c0011t0001g0092a0007c0011t0001g0093a0007c0011t0001g0094 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2481+2454G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534004 | ||||||
chr7:87534007
|
C | A | 1 | a0001c0003t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2481+2451G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534007 | ||||||
chr7:87534297
|
T | C | 2 | a0001c0003t0001g0233a0001c0003t0002g0227 | 2 | NA18977.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2481+2161A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534297 | ||||||
chr7:87534411
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0260a0001c0001t0001g0306 | 3 | HG02145.hp2 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2481+2047A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534411 | ||||||
chr7:87534434
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2481+2024C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534434 | ||||||
chr7:87534913
|
T | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2481+1545A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534913 | ||||||
chr7:87534915
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+1543A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534915 | ||||||
chr7:87534917
|
T | TA | 35 | a0001c0001t0001g0091a0001c0001t0001g0118a0001c0001t0001g0188others(32): Show | 35 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2481+1540dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534917
|
T | TAA | 47 | a0001c0001t0001g0087a0001c0001t0001g0123a0001c0001t0001g0125others(44): Show | 47 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2481+1539_2481+154 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534917
|
T | TAAA | 9 | a0001c0001t0001g0284a0001c0001t0001g0288a0001c0001t0001g0291others(6): Show | 9 | HG01123.hp1 HG01346.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.2481+1538_2481+154 others(7): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534917
|
T | TAAAAA | 72 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(69): Show | 72 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2481+1536_2481+154 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534917
|
T | TAAAAAA | 20 | a0001c0001t0006g0066a0001c0001t0008g0055a0001c0003t0001g0135others(17): Show | 20 | HG00423.hp2 HG01123.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.2481+1535_2481+154 others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534917
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2481+1530_2481+154 others(15): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534917
|
TA | T | 9 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(6): Show | 10 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2481+1540delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | ||||||
chr7:87534926
|
A | AAC | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(3): Show | 6 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2481+1531_2481+153 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534926 | ||||||
chr7:87534945
|
A | AT | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(74): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2481+1512dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534945 | ||||||
chr7:87534945
|
A | ATT | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(4): Show | 7 | HG00408.hp2 HG00597.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.2481+1511_2481+151 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534945 | ||||||
chr7:87534954
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2481+1504A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534954 | ||||||
chr7:87535015
|
A | G | 5 | a0002c0002t0001g0153a0002c0002t0001g0158a0002c0002t0001g0275others(2): Show | 5 | HG02071.hp2 NA18964.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2481+1443T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535015 | ||||||
chr7:87535033
|
A | C | 3 | a0006c0012t0001g0271a0006c0012t0001g0273a0006c0017t0002g0272 | 3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2481+1425T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535033 | ||||||
chr7:87535167
|
G | A | 50 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2481+1291C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535167 | ||||||
chr7:87535261
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2481+1197A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535261 | ||||||
chr7:87535312
|
T | C | 6 | a0001c0001t0001g0051a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2481+1146A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535312 | ||||||
chr7:87535338
|
A | AT | 83 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0060others(80): Show | 87 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2481+1119dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535338 | ||||||
chr7:87535338
|
A | ATT | 100 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0068others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2481+1118_2481+111 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535338 | ||||||
chr7:87535338
|
AT | A | 26 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0099others(23): Show | 29 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2481+1119delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535338 | ||||||
chr7:87535387
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2481+1071A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535387 | ||||||
chr7:87535440
|
C | A | 103 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(100): Show | 103 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2481+1018G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535440 | ||||||
chr7:87535520
|
G | GA | 165 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(162): Show | 165 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.2481+937_2481+938i others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535520 | ||||||
chr7:87535539
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2481+919G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535539 | ||||||
chr7:87535576
|
T | A | 257 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(254): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2481+882A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535576 | ||||||
chr7:87535654
|
C | T | 1 | a0006c0017t0002g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2481+804G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535654 | ||||||
chr7:87535670
|
A | G | 165 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(162): Show | 165 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.2481+788T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535670 | ||||||
chr7:87535735
|
G | A | 1 | a0001c0001t0010g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2481+723C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535735 | ||||||
chr7:87535838
|
C | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2481+620G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535838 | ||||||
chr7:87536090
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2481+368A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536090 | ||||||
chr7:87536095
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2481+363G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536095 | ||||||
chr7:87536316
|
G | A | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2481+142C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536316 | ||||||
chr7:87536372
|
C | T | 1 | a0004c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2481+86G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536372 | ||||||
chr7:87536385
|
G | T | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+73C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536385 | ||||||
chr7:87536418
|
G | A | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+40C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536418 | ||||||
chr7:87536434
|
C | T | 50 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2481+24G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536434 | ||||||
chr7:87536915
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2398-374C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87536915 | ||||||
chr7:87536966
|
T | C | 2 | a0001c0003t0002g0244a0001c0003t0002g0245 | 2 | HG00544.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2398-425A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87536966 | ||||||
chr7:87537031
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2398-490C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537031 | ||||||
chr7:87537133
|
G | A | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2398-592C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537133 | ||||||
chr7:87537442
|
G | T | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2398-901C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537442 | ||||||
chr7:87537504
|
G | A | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2398-963C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537504 | ||||||
chr7:87537552
|
T | C | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2398-1011A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537552 | ||||||
chr7:87537665
|
T | C | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2398-1124A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537665 | ||||||
chr7:87537688
|
C | T | 62 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(59): Show | 62 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(59): Show |
intron_variant | MODIFIER | c.2398-1147G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537688 | ||||||
chr7:87537956
|
T | G | 3 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0010g0026 | 4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+1312A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537956 | ||||||
chr7:87537980
|
C | T | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2397+1288G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537980 | ||||||
chr7:87538393
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2397+875A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538393 | ||||||
chr7:87538586
|
C | T | 1 | a0001c0003t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2397+682G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538586 | ||||||
chr7:87538711
|
C | T | 62 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(59): Show | 62 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(59): Show |
intron_variant | MODIFIER | c.2397+557G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538711 | ||||||
chr7:87538715
|
T | C | 1 | a0001c0003t0002g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2397+553A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538715 | ||||||
chr7:87538769
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2397+499A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538769 | ||||||
chr7:87538912
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2397+356G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538912 | ||||||
chr7:87539139
|
C | T | 6 | a0003c0004t0002g0047a0003c0004t0002g0050a0003c0004t0002g0054others(3): Show | 6 | HG02129.hp2 NA18955.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2397+129G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87539139 | ||||||
chr7:87539140
|
G | A | 1 | a0001c0003t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2397+128C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87539140 | ||||||
chr7:87539212
|
A | G | 4 | a0001c0001t0002g0216a0001c0001t0002g0274a0005c0008t0001g0187others(1): Show | 4 | HG00738.hp1 HG01261.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+56T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87539212 | ||||||
chr7:87539433
|
C | T | 336 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(333): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2320-88G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87539433 | ||||||
chr7:87539721
|
C | T | 64 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(61): Show | 64 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.2320-376G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87539721 | ||||||
chr7:87539876
|
G | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2320-531C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87539876 | ||||||
chr7:87540040
|
C | T | 32 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0284others(29): Show | 32 | HG00140.hp1 HG00423.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.2320-695G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540040 | ||||||
chr7:87540079
|
A | T | 2 | a0009c0030t0001g0242a0009c0031t0002g0241 | 2 | NA18612.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2320-734T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540079 | ||||||
chr7:87540106
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2320-761A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540106 | ||||||
chr7:87540148
|
T | C | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2320-803A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540148 | ||||||
chr7:87540353
|
T | C | 52 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2319+1004A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540353 | ||||||
chr7:87540386
|
A | C | 2 | a0002c0002t0001g0004a0002c0002t0001g0173 | 3 | HG01070.hp2 HG01515.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2319+971T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540386 | ||||||
chr7:87540504
|
G | T | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2319+853C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540504 | ||||||
chr7:87540567
|
A | G | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2319+790T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540567 | ||||||
chr7:87540701
|
C | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0060others(81): Show | 90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2319+656G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540701 | ||||||
chr7:87540847
|
A | G | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2319+510T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540847 | ||||||
chr7:87541189
|
A | G | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2319+168T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87541189 | ||||||
chr7:87541491
|
T | C | 1 | a0002c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2212-27A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87541491 | ||||||
chr7:87541576
|
C | T | 1 | a0002c0002t0001g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2212-112G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87541576 | ||||||
chr7:87541836
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(151): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2212-372A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87541836 | ||||||
chr7:87542037
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2212-573A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542037 | ||||||
chr7:87542067
|
G | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(151): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2212-603C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542067 | ||||||
chr7:87542211
|
T | C | 50 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2212-747A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542211 | ||||||
chr7:87542343
|
T | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(209): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.2212-879A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542343 | ||||||
chr7:87542363
|
A | G | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2212-899T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542363 | ||||||
chr7:87542387
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2212-923A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542387 | ||||||
chr7:87542544
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2212-1080G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542544 | ||||||
chr7:87542571
|
C | T | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2212-1107G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542571 | ||||||
chr7:87542575
|
T | C | 1 | a0002c0002t0001g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2212-1111A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542575 | ||||||
chr7:87542658
|
CT | C | 157 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(154): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2212-1195delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542658 | ||||||
chr7:87542737
|
A | G | 336 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(333): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2212-1273T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542737 | ||||||
chr7:87542816
|
T | C | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+1313A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542816 | ||||||
chr7:87542820
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(151): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2211+1309A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542820 | ||||||
chr7:87543073
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(151): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2211+1056A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543073 | ||||||
chr7:87543105
|
C | A | 2 | a0001c0005t0001g0210a0001c0005t0001g0211 | 2 | HG02015.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.2211+1024G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543105 | ||||||
chr7:87543175
|
T | A | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2211+954A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543175 | ||||||
chr7:87543180
|
G | C | 1 | a0002c0002t0001g0275 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2211+949C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543180 | ||||||
chr7:87543249
|
G | A | 9 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2211+880C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543249 | ||||||
chr7:87543272
|
C | G | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2211+857G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543272 | ||||||
chr7:87543282
|
C | T | 67 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(64): Show | 67 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(64): Show |
intron_variant | MODIFIER | c.2211+847G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543282 | ||||||
chr7:87543340
|
G | A | 1 | a0003c0004t0001g0044 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211+789C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543340 | ||||||
chr7:87543535
|
C | T | 1 | a0001c0005t0001g0329 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2211+594G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543535 | ||||||
chr7:87543565
|
C | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(151): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2211+564G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543565 | ||||||
chr7:87543583
|
T | C | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2211+546A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543583 | ||||||
chr7:87543776
|
A | T | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+353T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543776 | ||||||
chr7:87543786
|
A | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0316a0001c0001t0001g0317others(2): Show | 5 | HG01123.hp1 HG01516.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+343T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543786 | ||||||
chr7:87543800
|
A | G | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2211+329T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543800 | ||||||
chr7:87544351
|
A | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(151): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2065-76T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544351 | ||||||
chr7:87544489
|
A | T | 1 | a0003c0004t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2065-214T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544489 | ||||||
chr7:87544576
|
T | G | 4 | a0001c0001t0006g0059a0001c0001t0006g0061a0001c0001t0006g0238others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+247A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544576 | ||||||
chr7:87544741
|
C | T | 2 | a0003c0004t0005g0011a0003c0004t0005g0012 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2064+82G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544741 | ||||||
chr7:87544750
|
T | C | 217 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(214): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2064+73A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544750 | ||||||
chr7:87545068
|
A | G | 1 | a0001c0003t0002g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1888-69T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545068 | ||||||
chr7:87545074
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0004g0330others(1): Show | 4 | HG00323.hp2 HG01106.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1888-75C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545074 | ||||||
chr7:87545094
|
T | C | 1 | a0003c0004t0005g0019 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1888-95A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545094 | ||||||
chr7:87545144
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0008a0001c0001t0001g0305 | 3 | HG01515.hp1 HG01517.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1888-155_1888-146d others(12): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545144 | ||||||
chr7:87545188
|
C | T | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(148): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1888-189G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545188 | ||||||
chr7:87545261
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1888-262G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545261 | ||||||
chr7:87545265
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1888-266G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545265 | ||||||
chr7:87545293
|
A | G | 1 | a0001c0001t0019g0312 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1888-294T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545293 | ||||||
chr7:87545477
|
C | T | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1887+386G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545477 | ||||||
chr7:87545478
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1887+385C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545478 | ||||||
chr7:87545603
|
A | G | 1 | a0003c0004t0002g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1887+260T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545603 | ||||||
chr7:87546277
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1726-253G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546277 | ||||||
chr7:87546288
|
A | G | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1726-264T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546288 | ||||||
chr7:87546303
|
C | T | 2 | a0001c0001t0006g0058a0001c0001t0006g0066 | 2 | HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1726-279G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546303 | ||||||
chr7:87546310
|
C | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(125): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1726-286G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546310 | ||||||
chr7:87546311
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1726-287C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546311 | ||||||
chr7:87546311
|
G | T | 1 | a0001c0001t0011g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1726-287C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546311 | ||||||
chr7:87546474
|
G | A | 11 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0001others(8): Show | 12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-450C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546474 | ||||||
chr7:87546488
|
G | A | 143 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(140): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1726-464C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546488 | ||||||
chr7:87546562
|
A | T | 2 | a0001c0001t0004g0049a0001c0018t0017g0039 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1726-538T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546562 | ||||||
chr7:87546594
|
AG | A | 142 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(139): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1726-571delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546594 | ||||||
chr7:87546691
|
A | G | 1 | a0002c0002t0002g0150 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1726-667T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546691 | ||||||
chr7:87546699
|
T | C | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-675A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546699 | ||||||
chr7:87546720
|
C | G | 2 | a0002c0002t0001g0320a0002c0002t0001g0321 | 2 | HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1726-696G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546720 | ||||||
chr7:87546765
|
A | G | 1 | a0001c0003t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1726-741T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546765 | ||||||
chr7:87546832
|
A | G | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1726-808T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546832 | ||||||
chr7:87547097
|
T | C | 1 | a0002c0024t0001g0184 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1726-1073A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547097 | ||||||
chr7:87547114
|
C | T | 2 | a0001c0001t0019g0312a0002c0010t0001g0090 | 2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1726-1090G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547114 | ||||||
chr7:87547132
|
C | G | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1726-1108G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547132 | ||||||
chr7:87547147
|
A | G | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1726-1123T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547147 | ||||||
chr7:87547155
|
C | T | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1726-1131G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547155 | ||||||
chr7:87547321
|
A | G | 4 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0088others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-1297T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547321 | ||||||
chr7:87547579
|
A | G | 5 | a0001c0001t0001g0198a0001c0001t0001g0239a0001c0005t0001g0196others(2): Show | 5 | HG01928.hp1 HG01981.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-1555T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547579 | ||||||
chr7:87547691
|
G | A | 2 | a0006c0012t0001g0271a0006c0012t0001g0273 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1725+1657C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547691 | ||||||
chr7:87547735
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1725+1613G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547735 | ||||||
chr7:87547805
|
T | C | 51 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(48): Show | 51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1725+1543A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547805 | ||||||
chr7:87547838
|
G | A | 49 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1725+1510C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547838 | ||||||
chr7:87547850
|
C | CA | 155 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(152): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1725+1497dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547850 | ||||||
chr7:87547850
|
C | CAA | 59 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0074others(56): Show | 59 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1725+1496_1725+149 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547850 | ||||||
chr7:87547850
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1725+1488_1725+149 others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547850 | ||||||
chr7:87547885
|
G | A | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1725+1463C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547885 | ||||||
chr7:87548035
|
T | A | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+1313A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548035 | ||||||
chr7:87548040
|
T | A | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1725+1308A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548040 | ||||||
chr7:87548101
|
G | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1725+1247C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548101 | ||||||
chr7:87548117
|
G | GAGGGGAG others(13): Show |
12 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0001others(9): Show | 13 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725+1211_1725+123 others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548117 | ||||||
chr7:87548137
|
A | AAGGGG | 11 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(8): Show | 11 | HG01123.hp1 HG01981.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1725+1210_1725+121 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | ||||||
chr7:87548137
|
A | AAGGGGAG others(18): Show |
1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1725+1210_1725+121 others(29): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | ||||||
chr7:87548137
|
A | AAGGGGAG others(13): Show |
7 | a0001c0001t0001g0051a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1725+1210_1725+121 others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | ||||||
chr7:87548137
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1725+1211T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | ||||||
chr7:87548142
|
A | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1725+1206T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548142 | ||||||
chr7:87548147
|
G | A | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1725+1201C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548147 | ||||||
chr7:87548147
|
GAGGGAAG others(28): Show |
G | 1 | a0002c0002t0001g0246 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1725+1166_1725+120 others(39): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548147 | ||||||
chr7:87548152
|
A | AAGGGG | 3 | a0001c0001t0002g0240a0001c0005t0001g0315a0003c0004t0002g0045 | 3 | HG01123.hp1 HG01981.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1725+1195_1725+119 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548152 | ||||||
chr7:87548152
|
A | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1725+1196T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548152 | ||||||
chr7:87548162
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(112): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1725+1186C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548162 | ||||||
chr7:87548162
|
GAGGGAAA others(13): Show |
G | 127 | a0001c0001t0001g0051a0001c0001t0001g0256a0001c0001t0001g0257others(124): Show | 130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1725+1166_1725+118 others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548162 | ||||||
chr7:87548164
|
GGGAAA | G | 30 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(27): Show | 30 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1725+1179_1725+118 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548164 | ||||||
chr7:87548167
|
A | AAGGGAAG others(3): Show |
53 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1725+1180_1725+118 others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548167 | ||||||
chr7:87548167
|
A | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(112): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1725+1181T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548167 | ||||||
chr7:87548169
|
A | G | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(166): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1725+1179T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548169 | ||||||
chr7:87548182
|
A | G | 198 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(195): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1725+1166T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548182 | ||||||
chr7:87548187
|
A | G | 1 | a0003c0004t0012g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1725+1161T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548187 | ||||||
chr7:87548197
|
A | G | 51 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(48): Show | 51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1725+1151T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548197 | ||||||
chr7:87548260
|
G | A | 1 | a0002c0002t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1725+1088C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548260 | ||||||
chr7:87548349
|
A | G | 1 | a0001c0005t0003g0002 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1725+999T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548349 | ||||||
chr7:87548675
|
G | A | 1 | a0001c0003t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1725+673C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548675 | ||||||
chr7:87548739
|
C | T | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1725+609G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548739 | ||||||
chr7:87548740
|
G | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1725+608C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548740 | ||||||
chr7:87548827
|
G | C | 1 | a0003c0004t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1725+521C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548827 | ||||||
chr7:87548899
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1725+449G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548899 | ||||||
chr7:87548900
|
G | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1725+448C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548900 | ||||||
chr7:87548927
|
A | C | 1 | a0001c0003t0002g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1725+421T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548927 | ||||||
chr7:87548963
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1725+385A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548963 | ||||||
chr7:87549212
|
C | A | 5 | a0001c0001t0019g0312a0002c0010t0001g0090a0004c0007t0008g0334others(2): Show | 5 | HG01261.hp1 HG02109.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+136G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87549212 | ||||||
chr7:87549310
|
C | T | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1725+38G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87549310 | ||||||
chr7:87549571
|
A | C | 2 | a0002c0002t0002g0121a0017c0029t0002g0130 | 2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1555-53T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549571 | ||||||
chr7:87549761
|
C | T | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1554+90G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549761 | ||||||
chr7:87549770
|
G | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(121): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1554+81C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549770 | ||||||
chr7:87549827
|
A | G | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1554+24T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549827 | ||||||
chr7:87550127
|
G | A | 21 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(18): Show | 21 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1350+44C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/27 | chr7 | 87550127 | ||||||
chr7:87550130
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1350+41A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/27 | chr7 | 87550130 | ||||||
chr7:87550154
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0004g0049 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1350+17G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/27 | chr7 | 87550154 | ||||||
chr7:87550300
|
C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.1225-4G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/27 | chr7 | 87550300 | ||||||
chr7:87550358
|
A | T | 1 | a0001c0003t0002g0252 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1225-62T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/27 | chr7 | 87550358 | ||||||
chr7:87550379
|
T | C | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1225-83A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/27 | chr7 | 87550379 | ||||||
chr7:87550619
|
A | C | 3 | a0001c0003t0001g0109a0001c0003t0001g0223a0001c0003t0002g0228 | 3 | HG01934.hp1 HG02071.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1114-41T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 10/27 | chr7 | 87550619 | ||||||
chr7:87550882
|
C | T | 221 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(218): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1000-44G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87550882 | ||||||
chr7:87550976
|
A | G | 1 | a0001c0001t0019g0312 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1000-138T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87550976 | ||||||
chr7:87551000
|
A | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000-162T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551000 | ||||||
chr7:87551189
|
T | A | 4 | a0002c0002t0001g0322a0002c0002t0001g0323a0002c0002t0001g0325others(1): Show | 4 | NA19001.hp2 NA19074.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-351A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551189 | ||||||
chr7:87551244
|
T | G | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1000-406A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551244 | ||||||
chr7:87551313
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1000-475T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551313 | ||||||
chr7:87551356
|
G | A | 1 | a0004c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1000-518C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551356 | ||||||
chr7:87551362
|
A | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(220): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1000-524T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551362 | ||||||
chr7:87551422
|
T | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000-584A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551422 | ||||||
chr7:87551499
|
A | T | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-661T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551499 | ||||||
chr7:87551650
|
C | T | 3 | a0002c0002t0001g0143a0002c0002t0001g0246a0002c0002t0002g0140 | 3 | HG03704.hp2 NA18946.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1000-812G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551650 | ||||||
chr7:87551659
|
T | C | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1000-821A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551659 | ||||||
chr7:87551659
|
TA | T | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(121): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1000-822delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551659 | ||||||
chr7:87551716
|
T | C | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000-878A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551716 | ||||||
chr7:87551859
|
C | T | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1000-1021G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551859 | ||||||
chr7:87551895
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1000-1057C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551895 | ||||||
chr7:87552102
|
C | A | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1000-1264G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552102 | ||||||
chr7:87552329
|
T | C | 3 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021 | 3 | NA18998.hp1 NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.999+1432A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552329 | ||||||
chr7:87552332
|
A | G | 1 | a0001c0003t0002g0227 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.999+1429T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552332 | ||||||
chr7:87552382
|
C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.999+1379G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552382 | ||||||
chr7:87552492
|
C | T | 4 | a0001c0003t0006g0062a0001c0003t0006g0081a0001c0003t0009g0113others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+1269G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552492 | ||||||
chr7:87552533
|
G | T | 221 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(218): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.999+1228C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552533 | ||||||
chr7:87552629
|
C | T | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.999+1132G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552629 | ||||||
chr7:87552647
|
T | TA | 11 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0001others(8): Show | 12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.999+1113dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552647 | ||||||
chr7:87552653
|
A | T | 5 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+1108T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552653 | ||||||
chr7:87552711
|
G | GA | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(135): Show | 143 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.999+1049dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552711 | ||||||
chr7:87552711
|
G | GAA | 79 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(76): Show | 80 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.999+1048_999+1049d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552711 | ||||||
chr7:87552721
|
G | A | 221 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(218): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.999+1040C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552721 | ||||||
chr7:87552941
|
G | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.999+820C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552941 | ||||||
chr7:87552976
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.999+785G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552976 | ||||||
chr7:87553056
|
A | G | 2 | a0001c0006t0001g0104a0001c0006t0004g0103 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.999+705T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553056 | ||||||
chr7:87553108
|
AT | A | 9 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(6): Show | 10 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+652delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553108 | ||||||
chr7:87553151
|
G | A | 2 | a0001c0003t0001g0222a0001c0003t0001g0230 | 2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.999+610C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553151 | ||||||
chr7:87553202
|
G | C | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.999+559C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553202 | ||||||
chr7:87553211
|
C | T | 1 | a0001c0001t0019g0312 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.999+550G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553211 | ||||||
chr7:87553212
|
G | A | 2 | a0009c0030t0001g0242a0009c0031t0002g0241 | 2 | NA18612.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.999+549C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553212 | ||||||
chr7:87553247
|
A | C | 11 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0001others(8): Show | 12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.999+514T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553247 | ||||||
chr7:87553317
|
C | CT | 51 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(48): Show | 52 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.999+443dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553317 | ||||||
chr7:87553317
|
C | CTT | 8 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0032others(5): Show | 8 | HG02055.hp1 HG02886.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+442_999+443dup others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553317 | ||||||
chr7:87553317
|
CT | C | 9 | a0001c0001t0001g0084a0001c0001t0004g0049a0001c0001t0005g0034others(6): Show | 9 | HG01243.hp2 HG01517.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+443delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553317 | ||||||
chr7:87553339
|
T | TTTTGAGA others(3): Show |
1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.999+421_999+422ins others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553339 | ||||||
chr7:87553381
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.999+380G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553381 | ||||||
chr7:87553407
|
G | A | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.999+354C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553407 | ||||||
chr7:87553413
|
C | T | 1 | a0003c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.999+348G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553413 | ||||||
chr7:87553463
|
G | T | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.999+298C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553463 | ||||||
chr7:87553482
|
G | A | 1 | a0001c0003t0001g0234 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.999+279C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553482 | ||||||
chr7:87553524
|
G | C | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+237C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553524 | ||||||
chr7:87553555
|
C | T | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.999+206G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553555 | ||||||
chr7:87553566
|
T | C | 221 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(218): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.999+195A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553566 | ||||||
chr7:87553571
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.999+190G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553571 | ||||||
chr7:87553599
|
T | G | 11 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0001others(8): Show | 12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.999+162A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553599 | ||||||
chr7:87553626
|
T | C | 1 | a0002c0002t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.999+135A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553626 | ||||||
chr7:87554038
|
T | C | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(121): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.828-106A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554038 | ||||||
chr7:87554085
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.828-153A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554085 | ||||||
chr7:87554090
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.828-158G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554090 | ||||||
chr7:87554152
|
T | C | 4 | a0002c0002t0001g0322a0002c0002t0001g0323a0002c0002t0001g0325others(1): Show | 4 | NA19001.hp2 NA19074.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.828-220A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554152 | ||||||
chr7:87554304
|
T | C | 2 | a0003c0004t0002g0107a0003c0004t0020g0057 | 2 | HG02155.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.828-372A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554304 | ||||||
chr7:87554336
|
T | TA | 242 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(239): Show | 249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.828-405dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554336 | ||||||
chr7:87554336
|
T | TAA | 8 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0004g0049others(5): Show | 8 | HG00140.hp2 HG01243.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.828-406_828-405dup others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554336 | ||||||
chr7:87554467
|
T | C | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.828-535A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554467 | ||||||
chr7:87554526
|
A | T | 1 | a0001c0003t0001g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.828-594T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554526 | ||||||
chr7:87554547
|
A | G | 11 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0001others(8): Show | 12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.828-615T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554547 | ||||||
chr7:87554682
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.828-750G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554682 | ||||||
chr7:87554685
|
C | T | 2 | a0001c0001t0019g0312a0002c0010t0001g0090 | 2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.828-753G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554685 | ||||||
chr7:87554866
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.828-934G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554866 | ||||||
chr7:87554921
|
C | A | 1 | a0007c0011t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.828-989G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554921 | ||||||
chr7:87555055
|
C | T | 1 | a0002c0002t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.828-1123G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555055 | ||||||
chr7:87555107
|
C | A | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.828-1175G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555107 | ||||||
chr7:87555263
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.828-1331C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555263 | ||||||
chr7:87555333
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.828-1401G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555333 | ||||||
chr7:87555408
|
T | G | 2 | a0003c0004t0002g0053a0003c0004t0002g0067 | 2 | NA19005.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.828-1476A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555408 | ||||||
chr7:87555559
|
A | G | 1 | a0001c0001t0006g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.828-1627T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555559 | ||||||
chr7:87555602
|
A | G | 19 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(16): Show | 19 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.828-1670T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555602 | ||||||
chr7:87556257
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.828-2325A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556257 | ||||||
chr7:87556382
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.828-2450A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556382 | ||||||
chr7:87556578
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(119): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.828-2646C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556578 | ||||||
chr7:87556663
|
G | A | 27 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.828-2731C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556663 | ||||||
chr7:87556702
|
C | G | 51 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(48): Show | 51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.828-2770G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556702 | ||||||
chr7:87556836
|
T | C | 28 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.828-2904A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556836 | ||||||
chr7:87556977
|
A | G | 1 | a0002c0002t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.828-3045T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556977 | ||||||
chr7:87557350
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.828-3418G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87557350 | ||||||
chr7:87557432
|
A | G | 2 | a0002c0009t0001g0128a0016c0028t0001g0147 | 2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.828-3500T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87557432 | ||||||
chr7:87557873
|
T | A | 3 | a0006c0012t0001g0271a0006c0012t0001g0273a0006c0017t0002g0272 | 3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.827+3390A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87557873 | ||||||
chr7:87558180
|
C | T | 4 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0146others(1): Show | 4 | HG00408.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+3083G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558180 | ||||||
chr7:87558225
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.827+3038A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558225 | ||||||
chr7:87558406
|
G | A | 3 | a0007c0011t0001g0092a0007c0011t0001g0093a0007c0011t0001g0094 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.827+2857C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558406 | ||||||
chr7:87558443
|
T | C | 1 | a0003c0004t0012g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.827+2820A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558443 | ||||||
chr7:87558449
|
C | T | 1 | a0005c0008t0001g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.827+2814G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558449 | ||||||
chr7:87558467
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827+2796T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558467 | ||||||
chr7:87558497
|
A | C | 28 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.827+2766T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558497 | ||||||
chr7:87558651
|
A | G | 1 | a0001c0005t0001g0293 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.827+2612T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558651 | ||||||
chr7:87558679
|
T | C | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(121): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.827+2584A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558679 | ||||||
chr7:87558682
|
T | A | 2 | a0002c0002t0001g0336a0002c0002t0001g0337 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.827+2581A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558682 | ||||||
chr7:87558731
|
G | A | 9 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(6): Show | 10 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.827+2532C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558731 | ||||||
chr7:87558776
|
C | T | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.827+2487G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558776 | ||||||
chr7:87559093
|
T | G | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.827+2170A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559093 | ||||||
chr7:87559151
|
T | G | 52 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0125others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.827+2112A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559151 | ||||||
chr7:87559195
|
A | G | 1 | a0001c0001t0011g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.827+2068T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559195 | ||||||
chr7:87559241
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0031 | 2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.827+2022C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559241 | ||||||
chr7:87559282
|
G | C | 9 | a0001c0001t0001g0108a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00738.hp1 HG01261.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.827+1981C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559282 | ||||||
chr7:87559294
|
C | T | 28 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.827+1969G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559294 | ||||||
chr7:87559408
|
C | T | 6 | a0001c0001t0019g0312a0001c0018t0017g0039a0002c0010t0001g0090others(3): Show | 6 | HG01261.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.827+1855G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559408 | ||||||
chr7:87559423
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0208 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.827+1840G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559423 | ||||||
chr7:87559542
|
A | T | 2 | a0002c0002t0001g0143a0002c0002t0002g0140 | 2 | HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.827+1721T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559542 | ||||||
chr7:87559588
|
T | C | 1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.827+1675A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559588 | ||||||
chr7:87559622
|
T | C | 1 | a0001c0001t0007g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.827+1641A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559622 | ||||||
chr7:87559733
|
C | G | 28 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.827+1530G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559733 | ||||||
chr7:87559868
|
C | T | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.827+1395G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559868 | ||||||
chr7:87560157
|
T | C | 2 | a0001c0001t0001g0206a0001c0005t0003g0002 | 3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.827+1106A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560157 | ||||||
chr7:87560170
|
C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.827+1093G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560170 | ||||||
chr7:87560371
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827+892G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560371 | ||||||
chr7:87560401
|
T | C | 1 | a0003c0004t0002g0064 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.827+862A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560401 | ||||||
chr7:87560464
|
T | C | 1 | a0001c0001t0019g0312 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.827+799A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560464 | ||||||
chr7:87560489
|
A | G | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.827+774T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560489 | ||||||
chr7:87560522
|
T | C | 2 | a0003c0004t0002g0107a0003c0004t0020g0057 | 2 | HG02155.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.827+741A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560522 | ||||||
chr7:87560552
|
T | C | 3 | a0002c0002t0001g0165a0002c0002t0001g0178a0002c0002t0001g0212 | 3 | HG00558.hp1 NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.827+711A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560552 | ||||||
chr7:87560614
|
T | G | 268 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(265): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.827+649A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560614 | ||||||
chr7:87560770
|
A | G | 49 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.827+493T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560770 | ||||||
chr7:87561136
|
C | T | 27 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.827+127G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87561136 | ||||||
chr7:87561637
|
A | G | 45 | a0001c0003t0001g0109a0001c0003t0001g0161a0001c0003t0001g0164others(42): Show | 46 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.703-250T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561637 | ||||||
chr7:87561782
|
T | G | 2 | a0001c0005t0001g0131a0001c0005t0001g0276 | 2 | HG01169.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.703-395A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561782 | ||||||
chr7:87561838
|
T | C | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.703-451A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561838 | ||||||
chr7:87561928
|
G | A | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.703-541C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561928 | ||||||
chr7:87561930
|
G | A | 193 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(190): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.703-543C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561930 | ||||||
chr7:87561963
|
G | A | 5 | a0001c0003t0006g0081a0001c0003t0009g0113a0001c0006t0003g0023others(2): Show | 6 | HG02622.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-576C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561963 | ||||||
chr7:87562298
|
C | T | 1 | a0001c0003t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.703-911G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562298 | ||||||
chr7:87562343
|
A | G | 1 | a0003c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.703-956T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562343 | ||||||
chr7:87562353
|
C | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(126): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.703-966G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562353 | ||||||
chr7:87562406
|
T | G | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703-1019A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562406 | ||||||
chr7:87562463
|
A | G | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703-1076T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562463 | ||||||
chr7:87562532
|
A | G | 27 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.703-1145T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562532 | ||||||
chr7:87562570
|
TA | T | 4 | a0001c0001t0019g0312a0002c0010t0001g0090a0004c0007t0008g0334others(1): Show | 4 | HG01261.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1184delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562570 | ||||||
chr7:87562630
|
A | G | 5 | a0001c0001t0019g0312a0001c0018t0017g0039a0002c0010t0001g0090others(2): Show | 5 | HG01261.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-1243T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562630 | ||||||
chr7:87562763
|
G | GA | 28 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.703-1377dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562763 | ||||||
chr7:87562763
|
GA | G | 22 | a0001c0001t0001g0084a0001c0001t0001g0099a0001c0001t0001g0101others(19): Show | 22 | HG01243.hp2 HG01255.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.703-1377delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562763 | ||||||
chr7:87562930
|
C | G | 27 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.703-1543G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562930 | ||||||
chr7:87562941
|
A | G | 49 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0179others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.703-1554T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562941 | ||||||
chr7:87562959
|
C | T | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(121): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.703-1572G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562959 | ||||||
chr7:87562999
|
G | T | 4 | a0001c0001t0019g0312a0002c0010t0001g0090a0004c0007t0008g0334others(1): Show | 4 | HG01261.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1612C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562999 | ||||||
chr7:87563205
|
T | G | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703-1818A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563205 | ||||||
chr7:87563415
|
G | A | 222 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(219): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.703-2028C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563415 | ||||||
chr7:87563420
|
A | G | 2 | a0005c0008t0001g0215a0005c0008t0001g0217 | 2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.703-2033T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563420 | ||||||
chr7:87563665
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.703-2278G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563665 | ||||||
chr7:87563885
|
C | T | 26 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(23): Show | 26 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.702+2185G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563885 | ||||||
chr7:87563984
|
AG | A | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+2085delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563984 | ||||||
chr7:87564144
|
C | T | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.702+1926G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564144 | ||||||
chr7:87564281
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0091others(58): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.702+1789C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564281 | ||||||
chr7:87564286
|
A | G | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.702+1784T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564286 | ||||||
chr7:87564346
|
C | T | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.702+1724G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564346 | ||||||
chr7:87564484
|
A | G | 5 | a0001c0001t0005g0034a0001c0018t0017g0039a0002c0010t0001g0090others(2): Show | 5 | HG01261.hp1 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+1586T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564484 | ||||||
chr7:87564720
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+1350C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564720 | ||||||
chr7:87564789
|
G | A | 3 | a0002c0010t0001g0090a0004c0007t0008g0334a0004c0007t0008g0335 | 3 | HG01261.hp1 HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.702+1281C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564789 | ||||||
chr7:87564913
|
T | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.702+1157A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564913 | ||||||
chr7:87564923
|
A | G | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+1147T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564923 | ||||||
chr7:87565014
|
T | G | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.702+1056A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565014 | ||||||
chr7:87565078
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+992G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565078 | ||||||
chr7:87565494
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.702+576C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565494 | ||||||
chr7:87565567
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+503C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565567 | ||||||
chr7:87565640
|
T | TA | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+429dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565640 | ||||||
chr7:87565657
|
T | G | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.702+413A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565657 | ||||||
chr7:87565730
|
G | T | 1 | a0002c0002t0001g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.702+340C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565730 | ||||||
chr7:87565759
|
T | G | 2 | a0001c0001t0004g0100a0001c0001t0008g0098 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.702+311A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565759 | ||||||
chr7:87565790
|
C | T | 150 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0084others(147): Show | 153 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.702+280G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565790 | ||||||
chr7:87566016
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702+54C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87566016 | ||||||
chr7:87566026
|
G | A | 1 | a0004c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.702+44C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87566026 | ||||||
chr7:87566433
|
C | T | 1 | a0001c0005t0001g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.531-192G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566433 | ||||||
chr7:87566534
|
T | C | 124 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(121): Show | 127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.530+251A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566534 | ||||||
chr7:87566572
|
T | C | 13 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0111others(10): Show | 13 | HG00323.hp2 HG01081.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+213A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566572 | ||||||
chr7:87566580
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.530+205A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566580 | ||||||
chr7:87566646
|
G | A | 124 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(121): Show | 127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.530+139C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566646 | ||||||
chr7:87567297
|
T | C | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-321A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567297 | ||||||
chr7:87567743
|
C | T | 124 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(121): Show | 127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.339-767G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567743 | ||||||
chr7:87567789
|
T | C | 5 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-813A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567789 | ||||||
chr7:87567821
|
G | A | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.339-845C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567821 | ||||||
chr7:87567875
|
A | C | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.339-899T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567875 | ||||||
chr7:87567899
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339-923G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567899 | ||||||
chr7:87567904
|
C | T | 1 | a0003c0004t0002g0174 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.339-928G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567904 | ||||||
chr7:87567913
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.339-937A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567913 | ||||||
chr7:87567968
|
G | A | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.339-992C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567968 | ||||||
chr7:87568035
|
A | G | 196 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0084others(193): Show | 199 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.339-1059T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568035 | ||||||
chr7:87568221
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.339-1245G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568221 | ||||||
chr7:87568240
|
G | GACAATAA others(14): Show |
1 | a0002c0002t0001g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.339-1285_339-1265d others(23): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568240 | ||||||
chr7:87568242
|
C | CAAT | 59 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(56): Show | 61 | HG00423.hp2 HG01123.hp2 HG01175.hp1 others(58): Show |
intron_variant | MODIFIER | c.339-1269_339-1267d others(5): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | ||||||
chr7:87568242
|
C | CAATAAT | 3 | a0001c0001t0006g0061a0001c0018t0017g0039a0002c0010t0002g0070 | 3 | HG02258.hp1 HG02723.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.339-1272_339-1267d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | ||||||
chr7:87568242
|
C | CAATAATA others(17): Show |
114 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(111): Show | 117 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.339-1267_339-1266i others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | ||||||
chr7:87568242
|
C | CAATAATA others(20): Show |
6 | a0001c0003t0001g0222a0001c0006t0001g0104a0001c0006t0004g0103others(3): Show | 6 | HG01358.hp1 HG01952.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-1267_339-1266i others(29): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | ||||||
chr7:87568266
|
T | TAATAATA others(4): Show |
51 | a0001c0001t0001g0065a0001c0001t0001g0111a0001c0001t0001g0112others(48): Show | 51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(13): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | ||||||
chr7:87568266
|
T | TAATAATA others(7): Show |
4 | a0001c0001t0001g0250a0001c0001t0001g0309a0001c0001t0002g0083others(1): Show | 4 | HG01106.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | ||||||
chr7:87568266
|
T | TAATAATA others(10): Show |
5 | a0001c0001t0001g0060a0001c0001t0001g0260a0001c0001t0001g0289others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(19): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | ||||||
chr7:87568266
|
T | TAATAATA others(13): Show |
5 | a0001c0001t0001g0087a0001c0001t0003g0037a0001c0001t0004g0085others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | ||||||
chr7:87568266
|
T | TAATAATA others(16): Show |
2 | a0001c0001t0004g0086a0001c0001t0008g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.339-1291_339-1290i others(25): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | ||||||
chr7:87568266
|
T | TAATAATA others(19): Show |
1 | a0004c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.339-1291_339-1290i others(28): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | ||||||
chr7:87568267
|
A | AATAATAA others(7): Show |
1 | a0001c0001t0004g0330 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.339-1292_339-1291i others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568267 | ||||||
chr7:87568278
|
G | A | 121 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(118): Show | 124 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.339-1302C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568278 | ||||||
chr7:87568413
|
C | CA | 72 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(69): Show | 72 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.339-1438dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568413 | ||||||
chr7:87568433
|
A | C | 1 | a0001c0003t0001g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.339-1457T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568433 | ||||||
chr7:87568457
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0004g0006 | 4 | HG01175.hp1 HG01255.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-1481A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568457 | ||||||
chr7:87568695
|
A | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0005t0001g0126 | 3 | HG00621.hp1 NA18959.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.338+1477T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568695 | ||||||
chr7:87568913
|
T | C | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.338+1259A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568913 | ||||||
chr7:87569030
|
T | G | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.338+1142A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569030 | ||||||
chr7:87569051
|
G | A | 43 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(40): Show | 43 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.338+1121C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569051 | ||||||
chr7:87569063
|
C | T | 1 | a0002c0002t0002g0139 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.338+1109G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569063 | ||||||
chr7:87569143
|
G | A | 122 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(119): Show | 125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.338+1029C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569143 | ||||||
chr7:87569293
|
A | G | 1 | a0001c0003t0001g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.338+879T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569293 | ||||||
chr7:87569332
|
CA | C | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0091others(78): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.338+839delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569332 | ||||||
chr7:87569332
|
CAA | C | 78 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(75): Show | 79 | HG00280.hp1 HG00639.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.338+838_338+839del others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569332 | ||||||
chr7:87569332
|
CAAA | C | 177 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0084others(174): Show | 180 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.338+837_338+839del others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569332 | ||||||
chr7:87569580
|
T | TA | 10 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(7): Show | 11 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.338+591dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569580 | ||||||
chr7:87569728
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.338+444G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569728 | ||||||
chr7:87569866
|
G | A | 73 | a0001c0001t0002g0138a0001c0003t0001g0135a0001c0003t0001g0157others(70): Show | 75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.338+306C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569866 | ||||||
chr7:87569948
|
C | A | 120 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(117): Show | 123 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.338+224G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569948 | ||||||
chr7:87569949
|
T | A | 120 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(117): Show | 123 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.338+223A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569949 | ||||||
chr7:87569986
|
A | C | 2 | a0001c0006t0001g0104a0001c0006t0004g0103 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.338+186T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569986 | ||||||
chr7:87569987
|
C | A | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.338+185G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569987 | ||||||
chr7:87570049
|
T | C | 32 | a0001c0003t0001g0109a0001c0003t0001g0161a0001c0003t0001g0164others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.338+123A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87570049 | ||||||
chr7:87570096
|
A | C | 13 | a0001c0001t0004g0049a0003c0004t0002g0048a0003c0004t0002g0052others(10): Show | 13 | HG00423.hp2 HG03209.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.338+76T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87570096 | ||||||
chr7:87570248
|
C | A | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-25G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570248 | ||||||
chr7:87570299
|
A | G | 6 | a0001c0003t0002g0243a0001c0003t0002g0244a0001c0003t0002g0245others(3): Show | 6 | HG00544.hp2 HG00609.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-76T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570299 | ||||||
chr7:87570362
|
T | C | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287-139A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570362 | ||||||
chr7:87570648
|
A | G | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.287-425T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570648 | ||||||
chr7:87570899
|
A | G | 1 | a0001c0006t0004g0009 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.287-676T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570899 | ||||||
chr7:87571016
|
G | T | 2 | a0001c0001t0001g0206a0001c0005t0003g0002 | 3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.287-793C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571016 | ||||||
chr7:87571060
|
T | C | 1 | a0002c0009t0013g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.287-837A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571060 | ||||||
chr7:87571151
|
T | A | 271 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(268): Show | 275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.287-928A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571151 | ||||||
chr7:87571176
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287-953T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571176 | ||||||
chr7:87571213
|
G | A | 123 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0003g0037others(120): Show | 126 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.287-990C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571213 | ||||||
chr7:87571322
|
A | G | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0307others(4): Show | 7 | HG01243.hp1 HG02486.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-1099T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571322 | ||||||
chr7:87571323
|
T | C | 122 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(119): Show | 125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.287-1100A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571323 | ||||||
chr7:87571418
|
G | C | 2 | a0001c0001t0001g0206a0001c0005t0003g0002 | 3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.287-1195C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571418 | ||||||
chr7:87571457
|
C | G | 271 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(268): Show | 275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.287-1234G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571457 | ||||||
chr7:87571499
|
T | C | 2 | a0001c0006t0001g0104a0001c0006t0004g0103 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.287-1276A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571499 | ||||||
chr7:87571526
|
C | T | 271 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(268): Show | 275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.287-1303G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571526 | ||||||
chr7:87571620
|
A | G | 6 | a0001c0003t0001g0218a0001c0003t0001g0219a0001c0003t0001g0220others(3): Show | 6 | HG00438.hp1 HG02135.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-1397T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571620 | ||||||
chr7:87571645
|
G | A | 1 | a0001c0001t0006g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-1422C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571645 | ||||||
chr7:87571675
|
C | G | 1 | a0019c0032t0001g0110 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.287-1452G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571675 | ||||||
chr7:87571742
|
A | G | 13 | a0001c0001t0004g0049a0003c0004t0002g0048a0003c0004t0002g0052others(10): Show | 13 | HG00423.hp2 HG03209.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-1519T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571742 | ||||||
chr7:87571753
|
C | T | 4 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0010g0026others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-1530G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571753 | ||||||
chr7:87571769
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.287-1546G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571769 | ||||||
chr7:87571770
|
C | T | 122 | a0001c0001t0001g0084a0001c0001t0002g0138a0001c0001t0004g0100others(119): Show | 125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.287-1547G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571770 | ||||||
chr7:87571871
|
C | G | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287-1648G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571871 | ||||||
chr7:87572064
|
T | C | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1841A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572064 | ||||||
chr7:87572166
|
G | C | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1943C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572166 | ||||||
chr7:87572178
|
T | TAG | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1956_287-1955i others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572178 | ||||||
chr7:87572179
|
T | A | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1956A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572179 | ||||||
chr7:87572180
|
T | G | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1957A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572180 | ||||||
chr7:87572410
|
G | A | 69 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-2187C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572410 | ||||||
chr7:87572436
|
T | C | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-2213A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572436 | ||||||
chr7:87572554
|
T | C | 9 | a0001c0001t0001g0108a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00738.hp1 HG01261.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.287-2331A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572554 | ||||||
chr7:87572582
|
A | G | 43 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(40): Show | 43 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.287-2359T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572582 | ||||||
chr7:87572771
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.287-2548T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572771 | ||||||
chr7:87573086
|
G | A | 190 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0084others(187): Show | 193 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.287-2863C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573086 | ||||||
chr7:87573228
|
T | C | 62 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0111others(59): Show | 62 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.287-3005A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573228 | ||||||
chr7:87573236
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.287-3013C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573236 | ||||||
chr7:87573299
|
C | T | 260 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(257): Show | 262 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.287-3076G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573299 | ||||||
chr7:87573308
|
G | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-3085C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573308 | ||||||
chr7:87573345
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.287-3122C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573345 | ||||||
chr7:87573484
|
T | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.287-3261A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573484 | ||||||
chr7:87573758
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.287-3535T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573758 | ||||||
chr7:87573890
|
C | CAA | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-3668_287-3667i others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573890 | ||||||
chr7:87573891
|
G | T | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-3668C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573891 | ||||||
chr7:87574188
|
A | G | 2 | a0001c0003t0006g0081a0001c0003t0009g0113 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.287-3965T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574188 | ||||||
chr7:87574289
|
T | C | 3 | a0001c0001t0001g0195a0004c0007t0008g0334a0004c0007t0008g0335 | 3 | HG02109.hp1 HG02886.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.287-4066A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574289 | ||||||
chr7:87574500
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.287-4277T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574500 | ||||||
chr7:87574524
|
C | T | 276 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(273): Show | 283 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(280): Show |
intron_variant | MODIFIER | c.287-4301G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574524 | ||||||
chr7:87574773
|
C | T | 1 | a0001c0006t0004g0009 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.287-4550G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574773 | ||||||
chr7:87574867
|
G | T | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-4644C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574867 | ||||||
chr7:87574963
|
C | T | 255 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(252): Show | 262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.287-4740G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574963 | ||||||
chr7:87575221
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0002g0082 | 3 | HG02040.hp1 HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.287-4998T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575221 | ||||||
chr7:87575294
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.287-5071G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575294 | ||||||
chr7:87575340
|
G | A | 1 | a0002c0024t0001g0184 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.287-5117C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575340 | ||||||
chr7:87575513
|
T | C | 1 | a0001c0005t0001g0329 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.287-5290A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575513 | ||||||
chr7:87575556
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-5333T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575556 | ||||||
chr7:87575589
|
C | T | 22 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0036others(19): Show | 22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.287-5366G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575589 | ||||||
chr7:87575743
|
T | C | 1 | a0008c0014t0001g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.287-5520A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575743 | ||||||
chr7:87575879
|
C | T | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5656G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575879 | ||||||
chr7:87575881
|
A | T | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5658T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575881 | ||||||
chr7:87576158
|
C | CT | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5936dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576158 | ||||||
chr7:87576163
|
T | A | 255 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(252): Show | 262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.287-5940A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576163 | ||||||
chr7:87576347
|
A | G | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.287-6124T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576347 | ||||||
chr7:87576361
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.287-6138A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576361 | ||||||
chr7:87576391
|
T | C | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.287-6168A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576391 | ||||||
chr7:87576410
|
AGT | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG01069.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.287-6189_287-6188d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576410 | ||||||
chr7:87576502
|
A | G | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-6279T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576502 | ||||||
chr7:87576947
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.287-6724C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576947 | ||||||
chr7:87576972
|
G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287-6749C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576972 | ||||||
chr7:87577123
|
A | G | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.287-6900T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577123 | ||||||
chr7:87577299
|
C | T | 2 | a0008c0014t0001g0340a0008c0014t0001g0341 | 2 | HG01255.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.287-7076G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577299 | ||||||
chr7:87577573
|
T | A | 2 | a0003c0004t0002g0043a0003c0004t0002g0046 | 2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.287-7350A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577573 | ||||||
chr7:87577592
|
T | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0124others(41): Show | 46 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.287-7369A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577592 | ||||||
chr7:87577639
|
C | T | 3 | a0006c0012t0001g0271a0006c0012t0001g0273a0006c0017t0002g0272 | 3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.287-7416G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577639 | ||||||
chr7:87577812
|
G | A | 183 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(180): Show | 187 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.287-7589C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577812 | ||||||
chr7:87577821
|
C | A | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.287-7598G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577821 | ||||||
chr7:87577892
|
T | C | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.286+7620A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577892 | ||||||
chr7:87577930
|
C | A | 1 | a0001c0001t0004g0330 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.286+7582G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577930 | ||||||
chr7:87578051
|
A | C | 1 | a0002c0002t0001g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.286+7461T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578051 | ||||||
chr7:87578132
|
G | T | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.286+7380C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578132 | ||||||
chr7:87578222
|
T | A | 1 | a0001c0003t0009g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286+7290A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578222 | ||||||
chr7:87578297
|
C | T | 16 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(13): Show | 16 | HG00738.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+7215G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578297 | ||||||
chr7:87578455
|
G | A | 22 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0036others(19): Show | 22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.286+7057C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578455 | ||||||
chr7:87578598
|
C | T | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+6914G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578598 | ||||||
chr7:87578659
|
T | C | 1 | a0001c0006t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.286+6853A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578659 | ||||||
chr7:87578692
|
CT | C | 257 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(254): Show | 264 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.286+6819delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578692 | ||||||
chr7:87578724
|
C | T | 1 | a0002c0002t0002g0175 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.286+6788G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578724 | ||||||
chr7:87578909
|
A | G | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+6603T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578909 | ||||||
chr7:87578939
|
T | C | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+6573A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578939 | ||||||
chr7:87579061
|
TA | T | 5 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+6450delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579061 | ||||||
chr7:87579065
|
T | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0124others(41): Show | 46 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.286+6447A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579065 | ||||||
chr7:87579172
|
G | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6340C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579172 | ||||||
chr7:87579239
|
C | T | 1 | a0003c0004t0002g0054 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.286+6273G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579239 | ||||||
chr7:87579363
|
T | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6149A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579363 | ||||||
chr7:87579390
|
G | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6122C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579390 | ||||||
chr7:87579488
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0331 | 2 | HG00408.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.286+6024A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579488 | ||||||
chr7:87579671
|
G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+5841C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579671 | ||||||
chr7:87579759
|
G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.286+5753C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579759 | ||||||
chr7:87579766
|
T | A | 22 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0036others(19): Show | 22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.286+5746A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579766 | ||||||
chr7:87579790
|
G | C | 1 | a0001c0001t0002g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.286+5722C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579790 | ||||||
chr7:87579834
|
G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+5678C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579834 | ||||||
chr7:87580056
|
T | C | 255 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(252): Show | 262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.286+5456A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580056 | ||||||
chr7:87580067
|
T | C | 1 | a0002c0002t0011g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.286+5445A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580067 | ||||||
chr7:87580103
|
A | C | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+5409T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580103 | ||||||
chr7:87580276
|
G | C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.286+5236C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580276 | ||||||
chr7:87580299
|
G | T | 1 | a0003c0004t0002g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.286+5213C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580299 | ||||||
chr7:87580440
|
A | G | 2 | a0002c0002t0001g0005a0002c0002t0001g0166 | 3 | NA18970.hp1 NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.286+5072T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580440 | ||||||
chr7:87580609
|
A | G | 1 | a0002c0002t0001g0136 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.286+4903T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580609 | ||||||
chr7:87580674
|
G | A | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+4838C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580674 | ||||||
chr7:87580685
|
C | T | 2 | a0003c0004t0005g0011a0003c0004t0005g0012 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.286+4827G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580685 | ||||||
chr7:87580820
|
A | G | 1 | a0002c0009t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.286+4692T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580820 | ||||||
chr7:87580863
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.286+4649C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580863 | ||||||
chr7:87580943
|
A | G | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+4569T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580943 | ||||||
chr7:87581271
|
T | C | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0004g0100others(1): Show | 4 | HG02280.hp2 HG03579.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+4241A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581271 | ||||||
chr7:87581381
|
G | C | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+4131C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581381 | ||||||
chr7:87581541
|
C | T | 4 | a0001c0005t0001g0209a0001c0005t0001g0285a0001c0005t0001g0286others(1): Show | 4 | NA18948.hp2 NA18979.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3971G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581541 | ||||||
chr7:87581658
|
C | A | 255 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(252): Show | 262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.286+3854G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581658 | ||||||
chr7:87581729
|
T | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+3783A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581729 | ||||||
chr7:87581750
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0250a0001c0001t0004g0330others(1): Show | 4 | HG00323.hp2 HG01081.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+3762A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581750 | ||||||
chr7:87581844
|
C | T | 4 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0010g0026others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+3668G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581844 | ||||||
chr7:87581866
|
G | C | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.286+3646C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581866 | ||||||
chr7:87582004
|
G | A | 1 | a0001c0001t0006g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.286+3508C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582004 | ||||||
chr7:87582091
|
G | A | 1 | a0001c0005t0002g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286+3421C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582091 | ||||||
chr7:87582170
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0111others(61): Show | 67 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+3342C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582170 | ||||||
chr7:87582171
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0031 | 2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.286+3341C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582171 | ||||||
chr7:87582277
|
T | C | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+3235A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582277 | ||||||
chr7:87582512
|
C | T | 4 | a0001c0005t0001g0131a0002c0002t0001g0332a0002c0002t0002g0121others(1): Show | 4 | HG01496.hp1 HG02280.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3000G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582512 | ||||||
chr7:87582598
|
T | C | 6 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0004g0182others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+2914A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582598 | ||||||
chr7:87582612
|
G | C | 1 | a0002c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.286+2900C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582612 | ||||||
chr7:87582619
|
T | C | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.286+2893A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582619 | ||||||
chr7:87582672
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.286+2840C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582672 | ||||||
chr7:87582948
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0004g0100 | 3 | HG02280.hp2 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.286+2564T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582948 | ||||||
chr7:87583068
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.286+2444C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583068 | ||||||
chr7:87583088
|
G | A | 3 | a0006c0012t0001g0271a0006c0012t0001g0273a0006c0017t0002g0272 | 3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.286+2424C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583088 | ||||||
chr7:87583145
|
G | A | 22 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0036others(19): Show | 22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.286+2367C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583145 | ||||||
chr7:87583273
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+2239T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583273 | ||||||
chr7:87583674
|
T | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0108others(68): Show | 74 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.286+1838A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583674 | ||||||
chr7:87583710
|
AGTTTACT others(8): Show |
A | 15 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(12): Show | 15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1787_286+1801d others(17): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583710 | ||||||
chr7:87583728
|
G | T | 15 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(12): Show | 15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1784C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583728 | ||||||
chr7:87583729
|
T | C | 15 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(12): Show | 15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1783A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583729 | ||||||
chr7:87583813
|
G | C | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+1699C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583813 | ||||||
chr7:87583916
|
A | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0111others(61): Show | 67 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+1596T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583916 | ||||||
chr7:87583937
|
C | T | 1 | a0001c0005t0005g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.286+1575G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583937 | ||||||
chr7:87583942
|
C | T | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+1570G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583942 | ||||||
chr7:87584048
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0250 | 2 | HG01081.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.286+1464C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584048 | ||||||
chr7:87584068
|
C | T | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+1444G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584068 | ||||||
chr7:87584562
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.286+950C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584562 | ||||||
chr7:87584585
|
C | T | 128 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(125): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.286+927G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584585 | ||||||
chr7:87584936
|
A | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0005t0001g0315 | 3 | HG01123.hp1 HG01516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.286+576T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584936 | ||||||
chr7:87584951
|
A | AC | 52 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(49): Show | 52 | HG01192.hp1 HG01358.hp2 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.286+560dupG | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584951 | ||||||
chr7:87584959
|
A | C | 127 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(124): Show | 128 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.286+553T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584959 | ||||||
chr7:87584961
|
A | C | 13 | a0001c0001t0001g0108a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 13 | HG01978.hp2 HG02027.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.286+551T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584961 | ||||||
chr7:87585076
|
C | T | 47 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063others(44): Show | 47 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.286+436G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585076 | ||||||
chr7:87585192
|
T | C | 15 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(12): Show | 15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+320A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585192 | ||||||
chr7:87585215
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+297G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585215 | ||||||
chr7:87585373
|
T | C | 10 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0003t0006g0081others(7): Show | 11 | HG01261.hp1 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+139A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585373 | ||||||
chr7:87585786
|
C | T | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.118-106G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87585786 | ||||||
chr7:87585798
|
A | C | 338 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(335): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.118-118T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87585798 | ||||||
chr7:87585988
|
G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.118-308C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87585988 | ||||||
chr7:87586279
|
G | A | 4 | a0001c0001t0002g0240a0001c0001t0002g0301a0001c0001t0002g0302others(1): Show | 4 | HG00423.hp1 NA18949.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-599C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586279 | ||||||
chr7:87586372
|
A | T | 1 | a0002c0024t0001g0184 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118-692T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586372 | ||||||
chr7:87586425
|
C | G | 1 | a0007c0011t0001g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.118-745G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586425 | ||||||
chr7:87586449
|
G | A | 3 | a0001c0003t0006g0081a0001c0003t0009g0113a0001c0006t0003g0023 | 3 | HG02622.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.118-769C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586449 | ||||||
chr7:87586834
|
G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(274): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.118-1154C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586834 | ||||||
chr7:87586900
|
AAG | A | 253 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056others(250): Show | 260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.118-1222_118-1221d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586900 | ||||||
chr7:87587106
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.118-1426G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587106 | ||||||
chr7:87587108
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-1428C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587108 | ||||||
chr7:87587249
|
T | C | 1 | a0001c0001t0019g0312 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118-1569A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587249 | ||||||
chr7:87587279
|
C | T | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.118-1599G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587279 | ||||||
chr7:87587351
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-1671G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587351 | ||||||
chr7:87587375
|
A | G | 4 | a0003c0004t0005g0013a0003c0004t0005g0014a0003c0004t0005g0016others(1): Show | 4 | NA18988.hp2 NA18990.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1695T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587375 | ||||||
chr7:87587431
|
A | C | 2 | a0001c0006t0001g0104a0001c0006t0004g0103 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.118-1751T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587431 | ||||||
chr7:87587471
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0208 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.118-1791G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587471 | ||||||
chr7:87587488
|
T | C | 1 | a0001c0003t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.118-1808A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587488 | ||||||
chr7:87587501
|
G | T | 61 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0111others(58): Show | 64 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.118-1821C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587501 | ||||||
chr7:87587507
|
A | G | 1 | a0002c0002t0001g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.118-1827T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587507 | ||||||
chr7:87587597
|
T | C | 1 | a0001c0003t0001g0231 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.118-1917A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587597 | ||||||
chr7:87587600
|
A | G | 3 | a0001c0003t0001g0231a0012c0026t0014g0010a0013c0019t0009g0237 | 3 | HG00438.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.118-1920T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587600 | ||||||
chr7:87587610
|
A | G | 4 | a0001c0003t0001g0231a0002c0002t0001g0129a0012c0026t0014g0010others(1): Show | 4 | HG00438.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1930T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587610 | ||||||
chr7:87587647
|
A | G | 6 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0310others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-1967T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587647 | ||||||
chr7:87587744
|
A | G | 10 | a0001c0001t0001g0188a0001c0001t0001g0265a0001c0001t0001g0266others(7): Show | 11 | HG00140.hp2 HG00621.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-2064T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587744 | ||||||
chr7:87587755
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.118-2075T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587755 | ||||||
chr7:87587770
|
G | A | 2 | a0001c0001t0004g0100a0001c0018t0017g0039 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.118-2090C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587770 | ||||||
chr7:87587832
|
A | G | 1 | a0002c0002t0001g0320 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.118-2152T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587832 | ||||||
chr7:87587845
|
A | G | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2165T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587845 | ||||||
chr7:87587849
|
T | C | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2169A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587849 | ||||||
chr7:87587854
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-2174C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587854 | ||||||
chr7:87587857
|
A | G | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2177T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587857 | ||||||
chr7:87587861
|
T | C | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2181A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587861 | ||||||
chr7:87587861
|
T | G | 1 | a0001c0001t0001g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118-2181A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587861 | ||||||
chr7:87587874
|
C | CA | 45 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(42): Show | 45 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.118-2195dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587874 | ||||||
chr7:87587874
|
C | CAA | 8 | a0001c0001t0006g0059a0001c0001t0008g0097a0001c0005t0016g0096others(5): Show | 8 | HG02055.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-2196_118-2195d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587874 | ||||||
chr7:87587874
|
CA | C | 153 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0101others(150): Show | 157 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-2195delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587874 | ||||||
chr7:87587899
|
T | C | 137 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(134): Show | 141 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.118-2219A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587899 | ||||||
chr7:87587929
|
A | T | 1 | a0002c0002t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.118-2249T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587929 | ||||||
chr7:87587947
|
CT | C | 132 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(129): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.118-2268delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587947 | ||||||
chr7:87588156
|
G | GT | 16 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0010g0035others(13): Show | 16 | HG00423.hp2 HG02572.hp1 NA18952.hp2 others(13): Show |
intron_variant | MODIFIER | c.118-2477dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588156 | ||||||
chr7:87588156
|
GT | G | 106 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0116others(103): Show | 110 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.118-2477delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588156 | ||||||
chr7:87588255
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.118-2575A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588255 | ||||||
chr7:87588340
|
C | T | 1 | a0011c0027t0001g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.118-2660G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588340 | ||||||
chr7:87588348
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-2668C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588348 | ||||||
chr7:87588431
|
G | T | 2 | a0003c0004t0002g0053a0003c0004t0002g0067 | 2 | NA19005.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.118-2751C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588431 | ||||||
chr7:87588514
|
G | A | 2 | a0007c0011t0001g0093a0007c0011t0001g0094 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.118-2834C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588514 | ||||||
chr7:87588646
|
A | G | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.118-2966T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588646 | ||||||
chr7:87588704
|
G | A | 1 | a0001c0006t0003g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-3024C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588704 | ||||||
chr7:87588807
|
A | G | 1 | a0005c0008t0001g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.118-3127T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588807 | ||||||
chr7:87588886
|
C | T | 14 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(11): Show | 14 | HG00423.hp2 NA18952.hp2 NA18963.hp2 others(11): Show |
intron_variant | MODIFIER | c.118-3206G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588886 | ||||||
chr7:87589031
|
A | G | 181 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(178): Show | 185 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.118-3351T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589031 | ||||||
chr7:87589059
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.118-3379G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589059 | ||||||
chr7:87589161
|
T | A | 1 | a0003c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.118-3481A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589161 | ||||||
chr7:87589191
|
G | A | 1 | a0003c0004t0002g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.118-3511C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589191 | ||||||
chr7:87589315
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.118-3635A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589315 | ||||||
chr7:87589423
|
C | T | 1 | a0002c0002t0002g0121 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.118-3743G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589423 | ||||||
chr7:87589491
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.118-3811T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589491 | ||||||
chr7:87589701
|
C | A | 5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0009g0267others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-4021G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589701 | ||||||
chr7:87589761
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0305 | 3 | HG01515.hp1 HG01517.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.118-4081C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589761 | ||||||
chr7:87589805
|
G | GAGAGAGA others(12): Show |
1 | a0001c0001t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-4126_118-4125i others(21): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGA | 28 | a0001c0001t0001g0119a0001c0001t0001g0180a0001c0001t0001g0239others(25): Show | 28 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.118-4127_118-4126d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGA | 21 | a0001c0001t0001g0250a0001c0001t0001g0306a0001c0001t0001g0307others(18): Show | 21 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.118-4129_118-4126d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGA | 16 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(13): Show | 16 | HG00323.hp2 HG00639.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.118-4131_118-4126d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(1): Show |
12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0314others(9): Show | 13 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-4133_118-4126d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(3): Show |
6 | a0001c0001t0003g0018a0001c0006t0001g0104a0001c0006t0004g0103others(3): Show | 6 | HG01123.hp2 HG02717.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-4135_118-4126d others(12): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(5): Show |
15 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0003g0020others(12): Show | 15 | HG00423.hp2 HG01192.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.118-4137_118-4126d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(7): Show |
4 | a0001c0001t0001g0051a0001c0001t0003g0036a0003c0004t0002g0075others(1): Show | 4 | HG02897.hp2 NA18952.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4139_118-4126d others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(9): Show |
15 | a0001c0001t0001g0056a0001c0001t0001g0181a0001c0001t0006g0058others(12): Show | 15 | HG01496.hp2 HG01952.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-4141_118-4126d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(11): Show |
13 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0073others(10): Show | 13 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-4143_118-4126d others(20): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(13): Show |
1 | a0001c0001t0004g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118-4145_118-4126d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(15): Show |
2 | a0001c0001t0005g0034a0012c0026t0014g0010 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.118-4147_118-4126d others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(19): Show |
2 | a0001c0001t0004g0089a0001c0001t0004g0100 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.118-4151_118-4126d others(28): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
G | GGAGAGAG others(23): Show |
1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.118-4155_118-4126d others(32): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
GGA | G | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0185others(1): Show | 4 | HG03041.hp2 HG03225.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4127_118-4126d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589805
|
GGAGA | G | 5 | a0001c0001t0001g0278a0001c0001t0001g0318a0001c0001t0004g0006others(2): Show | 6 | HG00735.hp2 HG01175.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-4129_118-4126d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | ||||||
chr7:87589836
|
G | GA | 9 | a0001c0001t0001g0269a0002c0002t0001g0173a0002c0002t0001g0176others(6): Show | 9 | HG01358.hp1 HG03831.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-4157_118-4156i others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | ||||||
chr7:87589836
|
G | GAGAGAGA others(4): Show |
1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-4157_118-4156i others(13): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | ||||||
chr7:87589836
|
G | GAGAGAGA others(6): Show |
1 | a0001c0001t0003g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-4157_118-4156i others(15): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | ||||||
chr7:87589836
|
G | GAGAGAGA others(8): Show |
5 | a0001c0001t0001g0065a0001c0001t0001g0087a0001c0001t0006g0066others(2): Show | 5 | HG01081.hp1 HG01358.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4157_118-4156i others(17): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | ||||||
chr7:87589836
|
G | GAGAGAGA others(10): Show |
2 | a0001c0001t0001g0068a0003c0004t0002g0067 | 2 | NA18906.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.118-4157_118-4156i others(19): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | ||||||
chr7:87589836
|
G | GAGAGAGA others(12): Show |
1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.118-4157_118-4156i others(21): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | ||||||
chr7:87589837
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118-4157C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589837 | ||||||
chr7:87589849
|
G | GGA | 7 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0005t0001g0315others(4): Show | 7 | HG01123.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4171_118-4170d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589849 | ||||||
chr7:87589849
|
G | GGAGAGA | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(1): Show | 4 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-4175_118-4170d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589849 | ||||||
chr7:87589853
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG00408.hp2 HG00597.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-4173T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589853 | ||||||
chr7:87589860
|
G | A | 2 | a0001c0001t0010g0035a0004c0007t0003g0033 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.118-4180C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589860 | ||||||
chr7:87590165
|
G | C | 108 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(105): Show | 112 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.118-4485C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87590165 | ||||||
chr7:87590519
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-4839T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87590519 | ||||||
chr7:87590633
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.118-4953G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87590633 | ||||||
chr7:87591018
|
T | C | 89 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(86): Show | 91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.117+4748A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591018 | ||||||
chr7:87591246
|
C | T | 105 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(102): Show | 109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.117+4520G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591246 | ||||||
chr7:87591255
|
A | G | 1 | a0001c0001t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+4511T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591255 | ||||||
chr7:87591390
|
C | T | 1 | a0004c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117+4376G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591390 | ||||||
chr7:87591398
|
A | C | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117+4368T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591398 | ||||||
chr7:87591466
|
C | T | 2 | a0001c0001t0010g0035a0004c0007t0003g0033 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.117+4300G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591466 | ||||||
chr7:87591499
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.117+4267C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591499 | ||||||
chr7:87591570
|
A | G | 178 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(175): Show | 182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.117+4196T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591570 | ||||||
chr7:87591575
|
C | T | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0278others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+4191G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591575 | ||||||
chr7:87591770
|
G | T | 1 | a0012c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.117+3996C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591770 | ||||||
chr7:87591900
|
A | G | 105 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(102): Show | 109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.117+3866T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591900 | ||||||
chr7:87591902
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.117+3864C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591902 | ||||||
chr7:87592306
|
T | C | 1 | a0004c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117+3460A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592306 | ||||||
chr7:87592362
|
C | T | 9 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0036others(6): Show | 9 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+3404G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592362 | ||||||
chr7:87592482
|
C | A | 23 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0018others(20): Show | 23 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.117+3284G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592482 | ||||||
chr7:87592859
|
CCTAAGA | C | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+2901_117+2906d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592859 | ||||||
chr7:87592928
|
C | CT | 7 | a0001c0001t0001g0073a0001c0001t0001g0108a0001c0003t0001g0109others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+2837dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592928 | ||||||
chr7:87592928
|
C | CTT | 35 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(32): Show | 35 | HG01081.hp1 HG01123.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.117+2836_117+2837d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592928 | ||||||
chr7:87592928
|
CT | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0084a0001c0001t0001g0087others(85): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.117+2837delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592928 | ||||||
chr7:87592962
|
C | G | 24 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0018others(21): Show | 24 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+2804G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592962 | ||||||
chr7:87593161
|
T | A | 35 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0001others(32): Show | 37 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.117+2605A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593161 | ||||||
chr7:87593232
|
T | C | 1 | a0001c0003t0001g0319 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.117+2534A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593232 | ||||||
chr7:87593365
|
TA | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+2400delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593365 | ||||||
chr7:87593440
|
T | C | 2 | a0001c0006t0001g0104a0001c0006t0004g0103 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.117+2326A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593440 | ||||||
chr7:87593557
|
T | C | 8 | a0002c0002t0001g0320a0002c0002t0001g0321a0002c0002t0001g0322others(5): Show | 8 | HG01975.hp1 NA18941.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+2209A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593557 | ||||||
chr7:87594212
|
C | A | 2 | a0001c0006t0004g0009a0001c0006t0004g0328 | 3 | HG02965.hp2 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.117+1554G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594212 | ||||||
chr7:87594312
|
G | C | 12 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(9): Show | 12 | HG00423.hp2 NA18952.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+1454C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594312 | ||||||
chr7:87594383
|
A | G | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+1383T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594383 | ||||||
chr7:87594423
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+1343G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594423 | ||||||
chr7:87594647
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+1119G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594647 | ||||||
chr7:87594715
|
G | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+1051C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594715 | ||||||
chr7:87594750
|
A | T | 1 | a0014c0023t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.117+1016T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594750 | ||||||
chr7:87594864
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.117+902G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594864 | ||||||
chr7:87594935
|
C | T | 46 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(43): Show | 46 | HG01081.hp1 HG01123.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.117+831G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594935 | ||||||
chr7:87595112
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+654G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595112 | ||||||
chr7:87595113
|
A | G | 36 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0001others(33): Show | 38 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.117+653T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595113 | ||||||
chr7:87595264
|
T | C | 2 | a0001c0001t0004g0330a0001c0005t0001g0329 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.117+502A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595264 | ||||||
chr7:87595348
|
C | A | 1 | a0001c0001t0001g0331 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.117+418G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595348 | ||||||
chr7:87595367
|
G | A | 9 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0036others(6): Show | 9 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+399C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595367 | ||||||
chr7:87595385
|
C | T | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117+381G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595385 | ||||||
chr7:87595456
|
C | A | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+310G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595456 | ||||||
chr7:87595632
|
C | G | 11 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(8): Show | 13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+134G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595632 | ||||||
chr7:87595730
|
G | A | 35 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0003g0001others(32): Show | 37 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.117+36C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595730 | ||||||
chr7:87595857
|
A | G | 1 | a0001c0005t0007g0076 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69-43T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87595857 | ||||||
chr7:87595965
|
C | A | 1 | a0001c0001t0010g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-151G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87595965 | ||||||
chr7:87595996
|
A | G | 1 | a0002c0002t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.69-182T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87595996 | ||||||
chr7:87596610
|
TG | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0004g0085others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.69-797delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87596610 | ||||||
chr7:87596847
|
G | C | 1 | a0003c0004t0002g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.69-1033C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87596847 | ||||||
chr7:87596992
|
A | C | 3 | a0007c0011t0001g0092a0007c0011t0001g0093a0007c0011t0001g0094 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.69-1178T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87596992 | ||||||
chr7:87597348
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69-1534T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87597348 | ||||||
chr7:87597374
|
A | G | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-1560T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87597374 | ||||||
chr7:87598040
|
C | A | 1 | a0001c0001t0002g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.68+2077G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598040 | ||||||
chr7:87598217
|
T | C | 1 | a0002c0002t0001g0332 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68+1900A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598217 | ||||||
chr7:87598327
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0004g0085others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+1790G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598327 | ||||||
chr7:87598428
|
A | G | 7 | a0003c0004t0001g0044a0003c0004t0002g0041a0003c0004t0002g0043others(4): Show | 7 | HG01358.hp2 HG01496.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+1689T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598428 | ||||||
chr7:87598544
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.68+1573T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598544 | ||||||
chr7:87598589
|
A | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68+1528T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598589 | ||||||
chr7:87598605
|
T | C | 1 | a0002c0002t0001g0333 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.68+1512A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598605 | ||||||
chr7:87598744
|
T | C | 2 | a0004c0007t0008g0334a0004c0007t0008g0335 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.68+1373A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598744 | ||||||
chr7:87598951
|
G | A | 2 | a0002c0002t0001g0336a0002c0002t0001g0337 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.68+1166C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598951 | ||||||
chr7:87599243
|
G | C | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+874C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599243 | ||||||
chr7:87599700
|
G | A | 3 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68+417C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599700 | ||||||
chr7:87599709
|
C | T | 12 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0027others(9): Show | 14 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.68+408G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599709 | ||||||
chr7:87599743
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.68+374T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599743 | ||||||
chr7:87599944
|
C | T | 1 | a0001c0003t0006g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+173G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599944 | ||||||
chr7:87600263
|
TC | T | 36 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060others(33): Show | 36 | HG01081.hp1 HG01123.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-74delG | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/27 | chr7 | 87600263 | ||||||
chr7:87600518
|
C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7+237G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/27 | chr7 | 87600518 | ||||||
chr7:87600615
|
G | T | 13 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0005t0005g0021others(10): Show | 13 | HG00423.hp2 HG03098.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+140C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/27 | chr7 | 87600615 |