geneid | 950 |
---|---|
ensemblid | ENSG00000138760.11 |
hgncid | 1665 |
symbol | SCARB2 |
name | scavenger receptor class B member 2 |
refseq_nuc | NM_005506.4 |
refseq_prot | NP_005497.1 |
ensembl_nuc | ENST00000264896.8 |
ensembl_prot | ENSP00000264896.2 |
mane_status | MANE Select |
chr | chr4 |
start | 76158737 |
end | 76213824 |
strand | - |
ver | v1.2 |
region | chr4:76158737-76213824 |
region5000 | chr4:76153737-76218824 |
regionname0 | SCARB2_chr4_76158737_76213824 |
regionname5000 | SCARB2_chr4_76153737_76218824 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 478 | 363 | 83 | 62 | 163 | 15 | 38 | 127 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002 | 0/0 | 478 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0003 | 0/0 | 478 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0004 | 0/0 | 478 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0005 | 0/0 | 478 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0006 | 0/0 | 478 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0007 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0008 | 0/0 | 225 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0009 | 0/0 | 478 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1437 | 346 | 66 | 62 | 163 | 15 | 38 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0002 | 0/0 | 1437 | 16 | 16 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0003 | 0/0 | 1437 | 7 | 7 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0004 | 0/0 | 1437 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0005 | 0/0 | 1437 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0006 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0007 | 0/0 | 1437 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0008 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0009 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0011 | 0/0 | 1055 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
c0012 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3258 | 94 | 7 | 23 | 52 | 5 | 7 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0002 | 0/0 | 3258 | 84 | 19 | 10 | 44 | 2 | 9 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0003 | 0/0 | 3258 | 62 | 3 | 8 | 39 | 1 | 11 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0004 | 0/0 | 3258 | 30 | 9 | 4 | 14 | 1 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0005 | 0/1 | 3258 | 22 | 1 | 12 | 0 | 4 | 4 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0006 | 0/0 | 3258 | 20 | 18 | 1 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0007 | 0/0 | 3258 | 15 | 1 | 2 | 5 | 2 | 5 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0008 | 0/0 | 3258 | 15 | 15 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0009 | 0/0 | 3258 | 13 | 4 | 0 | 9 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0010 | 0/0 | 3258 | 5 | 0 | 0 | 5 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0011 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0012 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0013 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0014 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0015 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0016 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0017 | 0/0 | 3258 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0018 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0019 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0020 | 1/0 | 3258 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0021 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0022 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0023 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0024 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0025 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0026 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0027 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0028 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0029 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
t0030 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
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 | 9 | 0 | 4 | 4 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1437 | 346 | 66 | 62 | 163 | 15 | 38 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0002 | 0/0 | 1437 | 16 | 16 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0008 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003 | 0/0 | 1437 | 7 | 7 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0003c0006 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0003c0009 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0004c0004 | 0/0 | 1437 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0005c0005 | 0/0 | 1437 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0006c0007 | 0/0 | 1437 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0007c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0008c0011 | 0/0 | 1055 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0009c0012 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4694 | 93 | 7 | 23 | 52 | 4 | 7 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0002 | 0/0 | 4694 | 82 | 18 | 10 | 43 | 2 | 9 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0003 | 0/0 | 4694 | 62 | 3 | 8 | 39 | 1 | 11 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0004 | 0/0 | 4694 | 26 | 8 | 4 | 11 | 1 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0005 | 0/1 | 4694 | 22 | 1 | 12 | 0 | 4 | 4 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0006 | 0/0 | 4694 | 9 | 7 | 1 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0007 | 0/0 | 4694 | 10 | 1 | 2 | 0 | 2 | 5 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0008 | 0/0 | 4694 | 12 | 12 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0009 | 0/0 | 4694 | 11 | 2 | 0 | 9 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0010 | 0/0 | 4694 | 5 | 0 | 0 | 5 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0011 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0012 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0015 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0016 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0017 | 0/0 | 4694 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0018 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0020 | 1/0 | 4694 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0021 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0025 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0026 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0027 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0029 | 0/0 | 4694 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0001t0030 | 0/0 | 4694 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0002t0006 | 0/0 | 4694 | 10 | 10 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0002t0008 | 0/0 | 4694 | 3 | 3 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0002t0009 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0002t0023 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0001c0008t0012 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003t0004 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003t0006 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003t0014 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003t0019 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003t0022 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0002c0003t0024 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0003c0006t0013 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0003c0009t0028 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0004c0004t0004 | 0/0 | 4694 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0005c0005t0007 | 0/0 | 4694 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0006c0007t0007 | 0/0 | 4694 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0007c0010t0002 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0008c0011t0002 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
a0009c0012t0001 | 0/0 | 4694 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | copy fasta | chr4 | 76153737 | 76218824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0001 | 0/0 | 9 | 0 | 4 | 4 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0010g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0010g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0017g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0020g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0021g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0025g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0026g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0027g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0029g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0001t0030g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0002t0023g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0001c0008t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0014g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0022g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0002c0003t0024g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0003c0006t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0003c0006t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0003c0009t0028g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0004c0004t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0005c0005t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0005c0005t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0005c0005t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0006c0007t0007g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0007c0010t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0008c0011t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
a0009c0012t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0248 | EUR | GBR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0040 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00323 | hp1 | a0001 | c0001 | t0017 | g0068 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0232 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00438 | hp2 | a0006 | c0007 | t0007 | g0030 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00621 | hp2 | a0006 | c0007 | t0007 | g0030 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0236 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00673 | hp2 | a0001 | c0001 | t0009 | g0209 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0229 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01175 | hp1 | a0001 | c0001 | t0029 | g0220 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0122 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01257 | hp2 | a0001 | c0001 | t0030 | g0309 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0258 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0233 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0256 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01516 | hp2 | a0001 | c0001 | t0007 | g0164 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0165 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01884 | hp2 | a0001 | c0002 | t0006 | g0178 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01891 | hp1 | a0003 | c0009 | t0028 | g0240 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0191 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02083 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02129 | hp2 | a0001 | c0001 | t0027 | g0300 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0183 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02280 | hp2 | a0002 | c0003 | t0004 | g0241 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02451 | hp1 | a0001 | c0002 | t0006 | g0032 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02572 | hp1 | a0001 | c0001 | t0016 | g0025 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0190 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02615 | hp2 | a0003 | c0006 | t0013 | g0181 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02630 | hp2 | a0001 | c0002 | t0006 | g0184 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0187 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0213 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0163 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02809 | hp2 | a0002 | c0003 | t0014 | g0242 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02818 | hp1 | a0002 | c0003 | t0019 | g0093 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0182 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02896 | hp1 | a0001 | c0002 | t0008 | g0031 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02897 | hp2 | a0001 | c0002 | t0008 | g0031 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0107 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0188 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0108 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0230 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03041 | hp1 | a0002 | c0003 | t0014 | g0294 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03041 | hp2 | a0001 | c0002 | t0006 | g0177 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0186 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03098 | hp2 | a0001 | c0001 | t0025 | g0244 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03130 | hp1 | a0002 | c0003 | t0006 | g0189 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03139 | hp2 | a0001 | c0002 | t0023 | g0179 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03209 | hp1 | a0001 | c0001 | t0015 | g0094 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0202 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03453 | hp2 | a0001 | c0008 | t0012 | g0197 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03516 | hp1 | a0001 | c0001 | t0021 | g0200 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0198 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03540 | hp2 | a0002 | c0003 | t0024 | g0216 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0113 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0056 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0041 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04199 | hp2 | a0001 | c0001 | t0007 | g0088 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04204 | hp1 | a0001 | c0001 | t0007 | g0055 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0231 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0205 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18906 | hp2 | a0001 | c0002 | t0009 | g0175 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18939 | hp1 | a0004 | c0004 | t0004 | g0015 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18941 | hp1 | a0004 | c0004 | t0004 | g0015 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18948 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18949 | hp1 | a0005 | c0005 | t0007 | g0160 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18949 | hp2 | a0001 | c0001 | t0018 | g0136 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18950 | hp2 | a0005 | c0005 | t0007 | g0161 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18962 | hp2 | a0001 | c0001 | t0009 | g0211 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18965 | hp1 | a0001 | c0001 | t0026 | g0266 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18966 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18970 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18974 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18978 | hp1 | a0008 | c0011 | t0002 | g0284 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18979 | hp2 | a0005 | c0005 | t0007 | g0159 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18994 | hp2 | a0001 | c0001 | t0009 | g0210 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18995 | hp2 | a0001 | c0001 | t0009 | g0212 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA18999 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19004 | hp2 | a0004 | c0004 | t0004 | g0015 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19010 | hp1 | a0001 | c0001 | t0010 | g0129 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19043 | hp2 | a0001 | c0002 | t0006 | g0174 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0215 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19078 | hp1 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19087 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA19240 | hp2 | a0001 | c0002 | t0006 | g0185 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0033 | AFR | ASW | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20129 | hp2 | a0001 | c0002 | t0006 | g0032 | AFR | ASW | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0020 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0250 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20805 | hp2 | a0009 | c0012 | t0001 | g0092 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG02559 | hp2 | a0001 | c0002 | t0009 | g0176 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03471 | hp1 | a0007 | c0010 | t0002 | g0218 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG03471 | hp2 | a0001 | c0002 | t0008 | g0173 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA20300 | hp2 | a0003 | c0006 | t0013 | g0180 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA21309 | hp1 | a0002 | c0003 | t0022 | g0214 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0234 | REF | REF | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0020 | g0207 | REF | REF | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76158737
|
T | C | 1 | a0001 | 1 | HG02572.hp1 | splice_region_variant | LOW | c.*2976A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | chr4 | 76158737 | ||||||
chr4:76163238
|
C | T | 1 | a0004 | 3 | NA18939.hp1 NA18941.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.1385G>A | p.Gly462Glu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/12 | 1666/4694 | 1385/1437 | 462/478 | chr4 | 76163238 | ||
chr4:76163311
|
T | G | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1312A>C | p.Ile438Leu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/12 | 1593/4694 | 1312/1437 | 438/478 | chr4 | 76163311 | ||
chr4:76166279
|
T | C | 1 | a0006 | 2 | HG00438.hp2 HG00621.hp2 |
missense_variant | MODERATE | c.1210A>G | p.Met404Val | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/12 | 1491/4694 | 1210/1437 | 404/478 | chr4 | 76166279 | ||
chr4:76168404
|
C | T | 1 | a0002 | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.1186G>A | p.Val396Ile | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/12 | 1467/4694 | 1186/1437 | 396/478 | chr4 | 76168404 | ||
chr4:76172721
|
TTGCCCAG others(4076): Show |
T | 1 | a0008 | 1 | NA18978.hp1 | exon_loss_variant | HIGH | c.613-276_994+1422de others(1): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/12 | chr4 | 76172721 | ||||||
chr4:76179654
|
T | C | 1 | a0009 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.475A>G | p.Met159Val | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/12 | 756/4694 | 475/1437 | 159/478 | chr4 | 76179654 | ||
chr4:76179699
|
T | A | 1 | a0005 | 3 | NA18949.hp1 NA18950.hp2 NA18979.hp2 |
missense_variant | MODERATE | c.430A>T | p.Ile144Leu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/12 | 711/4694 | 430/1437 | 144/478 | chr4 | 76179699 | ||
chr4:76181015
|
C | T | 1 | a0003 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.362G>A | p.Arg121Gln | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/12 | 643/4694 | 362/1437 | 121/478 | chr4 | 76181015 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76195736
|
C | G | 1 | a0001c0008 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.246G>C | p.Arg82Arg | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/12 | 527/4694 | 246/1437 | 82/478 | chr4 | 76195736 | ||
chr4:76213496
|
C | G | 2 | a0001c0002a0003c0006 | 18 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
synonymous_variant | LOW | c.48G>C | p.Leu16Leu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 329/4694 | 48/1437 | 16/478 | chr4 | 76213496 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76158925
|
T | G | 1 | a0001c0001t0021 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2788A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2788 | chr4 | 76158925 | |||||
chr4:76158944
|
G | A | 1 | a0001c0001t0011 | 2 | HG02970.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2769C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2769 | chr4 | 76158944 | |||||
chr4:76159229
|
T | C | 1 | a0001c0001t0029 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2484A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2484 | chr4 | 76159229 | |||||
chr4:76159242
|
G | A | 1 | a0001c0001t0027 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2471 | chr4 | 76159242 | |||||
chr4:76159325
|
G | A | 2 | a0003c0006t0013a0003c0009t0028 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2388C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2388 | chr4 | 76159325 | |||||
chr4:76159504
|
G | A | 4 | a0002c0003t0014a0002c0003t0019a0002c0003t0022others(1): Show | 5 | HG02809.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2209C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2209 | chr4 | 76159504 | |||||
chr4:76159646
|
C | T | 16 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(13): Show | 124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2067G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2067 | chr4 | 76159646 | |||||
chr4:76159678
|
T | C | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(18): Show | 144 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2035A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2035 | chr4 | 76159678 | |||||
chr4:76159754
|
A | G | 1 | a0001c0001t0015 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1959 | chr4 | 76159754 | |||||
chr4:76159854
|
A | G | 1 | a0001c0001t0018 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1859T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1859 | chr4 | 76159854 | |||||
chr4:76159933
|
T | A | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(15): Show | 126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1780A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1780 | chr4 | 76159933 | |||||
chr4:76160575
|
T | C | 1 | a0001c0001t0026 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1138A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1138 | chr4 | 76160575 | |||||
chr4:76160612
|
G | A | 3 | a0001c0001t0009a0001c0001t0010a0001c0002t0009 | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1101C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1101 | chr4 | 76160612 | |||||
chr4:76160624
|
T | A | 1 | a0001c0001t0017 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1089A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1089 | chr4 | 76160624 | |||||
chr4:76160661
|
G | C | 16 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(13): Show | 124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1052C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1052 | chr4 | 76160661 | |||||
chr4:76160683
|
G | A | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | 344 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*1030C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1030 | chr4 | 76160683 | |||||
chr4:76160684
|
C | A | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | 344 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*1029G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1029 | chr4 | 76160684 | |||||
chr4:76160932
|
A | G | 1 | a0001c0001t0025 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*781T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 781 | chr4 | 76160932 | |||||
chr4:76161120
|
T | C | 2 | a0001c0001t0029a0001c0002t0023 | 2 | HG01175.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*593A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 593 | chr4 | 76161120 | |||||
chr4:76161250
|
G | A | 3 | a0001c0001t0009a0001c0001t0010a0001c0002t0009 | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*463C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 463 | chr4 | 76161250 | |||||
chr4:76161596
|
C | T | 3 | a0001c0001t0009a0001c0001t0010a0001c0002t0009 | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*117G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 117 | chr4 | 76161596 | |||||
chr4:76161646
|
G | C | 3 | a0001c0001t0009a0001c0001t0010a0001c0002t0009 | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*67C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 67 | chr4 | 76161646 | |||||
chr4:76213554
|
G | A | 1 | a0001c0001t0030 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 11 | chr4 | 76213554 | |||||
chr4:76213633
|
C | T | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(10): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 90 | chr4 | 76213633 | |||||
chr4:76213675
|
G | C | 1 | a0002c0003t0024 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 132 | chr4 | 76213675 | |||||
chr4:76213717
|
G | A | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(11): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-174C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 174 | chr4 | 76213717 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76161794
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1399-43C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161794 | ||||||
chr4:76161917
|
TCAG | T | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.1399-169_1399-167d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161917 | ||||||
chr4:76161929
|
A | T | 64 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(61): Show | 80 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1399-178T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161929 | ||||||
chr4:76161956
|
C | T | 1 | a0001c0001t0005g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1399-205G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161956 | ||||||
chr4:76161957
|
T | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1399-206A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161957 | ||||||
chr4:76161971
|
C | A | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-220G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161971 | ||||||
chr4:76162031
|
G | A | 4 | a0001c0001t0005g0035a0001c0001t0005g0234a0001c0001t0007g0164others(1): Show | 5 | HG00738.hp1 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1399-280C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162031 | ||||||
chr4:76162161
|
C | T | 1 | a0001c0001t0005g0039 | 2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1399-410G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162161 | ||||||
chr4:76162197
|
G | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1399-446C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162197 | ||||||
chr4:76162226
|
G | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(30): Show | 37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1399-475C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162226 | ||||||
chr4:76162416
|
T | TA | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1399-666dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162416 | ||||||
chr4:76162481
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1399-730G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162481 | ||||||
chr4:76162601
|
T | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(91): Show | 124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1398+624A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162601 | ||||||
chr4:76162648
|
C | T | 2 | a0001c0001t0003g0050a0001c0001t0004g0016 | 4 | HG00558.hp1 HG02071.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+577G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162648 | ||||||
chr4:76162846
|
G | A | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1398+379C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162846 | ||||||
chr4:76163436
|
T | C | 61 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(58): Show | 77 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1240-53A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163436 | ||||||
chr4:76163498
|
C | A | 1 | a0001c0001t0003g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1240-115G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163498 | ||||||
chr4:76163714
|
C | T | 8 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(5): Show | 9 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240-331G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163714 | ||||||
chr4:76163720
|
G | A | 8 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(5): Show | 9 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240-337C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163720 | ||||||
chr4:76163819
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1240-436C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163819 | ||||||
chr4:76164013
|
A | G | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-630T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164013 | ||||||
chr4:76164221
|
C | T | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-838G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164221 | ||||||
chr4:76164250
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(274): Show | 345 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.1240-867T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164250 | ||||||
chr4:76164284
|
G | C | 1 | a0001c0001t0005g0236 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1240-901C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164284 | ||||||
chr4:76164480
|
C | G | 94 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(91): Show | 124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1240-1097G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164480 | ||||||
chr4:76164498
|
G | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1240-1115C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164498 | ||||||
chr4:76164504
|
G | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(30): Show | 37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240-1121C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164504 | ||||||
chr4:76164550
|
G | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-1167C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164550 | ||||||
chr4:76164576
|
C | A | 172 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(169): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.1240-1193G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164576 | ||||||
chr4:76164637
|
GA | G | 95 | a0001c0001t0002g0249a0001c0001t0003g0001a0001c0001t0003g0006others(92): Show | 125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1240-1255delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164637 | ||||||
chr4:76164691
|
C | A | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-1308G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164691 | ||||||
chr4:76164722
|
G | C | 1 | a0001c0001t0008g0205 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1240-1339C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164722 | ||||||
chr4:76164767
|
G | C | 96 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(93): Show | 126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.1240-1384C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164767 | ||||||
chr4:76164791
|
C | CA | 98 | a0001c0001t0001g0087a0001c0001t0002g0245a0001c0001t0002g0259others(95): Show | 128 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1240-1409dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164791 | ||||||
chr4:76164857
|
A | G | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+1393T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164857 | ||||||
chr4:76165253
|
G | A | 1 | a0001c0001t0002g0304 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1239+997C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165253 | ||||||
chr4:76165274
|
T | C | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1239+976A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165274 | ||||||
chr4:76165281
|
A | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+969T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165281 | ||||||
chr4:76165298
|
T | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+952A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165298 | ||||||
chr4:76165322
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1239+928A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165322 | ||||||
chr4:76165433
|
T | G | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+817A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165433 | ||||||
chr4:76165495
|
T | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+755A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165495 | ||||||
chr4:76165688
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1239+562C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165688 | ||||||
chr4:76165763
|
G | GT | 73 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0152others(70): Show | 100 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.1239+486dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165763 | ||||||
chr4:76165763
|
G | GTT | 7 | a0001c0001t0003g0073a0001c0001t0003g0076a0001c0001t0003g0081others(4): Show | 7 | HG00673.hp1 HG01934.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+485_1239+486d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165763 | ||||||
chr4:76165858
|
A | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+392T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165858 | ||||||
chr4:76165859
|
T | C | 3 | a0001c0001t0012g0191a0001c0008t0012g0197a0003c0006t0013g0180 | 3 | HG02055.hp2 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1239+391A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165859 | ||||||
chr4:76166025
|
A | G | 1 | a0001c0001t0006g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1239+225T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76166025 | ||||||
chr4:76166113
|
A | G | 1 | a0001c0001t0003g0023 | 2 | NA18986.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1239+137T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76166113 | ||||||
chr4:76166236
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1239+14C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76166236 | ||||||
chr4:76166551
|
G | T | 114 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(111): Show | 139 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1188-250C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166551 | ||||||
chr4:76166560
|
G | C | 1 | a0001c0001t0008g0012 | 3 | HG01891.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1188-259C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166560 | ||||||
chr4:76166653
|
GAGCCAAC others(5): Show |
G | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-364_1188-353d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166653 | ||||||
chr4:76166834
|
T | C | 2 | a0001c0001t0002g0245a0001c0001t0025g0244 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1188-533A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166834 | ||||||
chr4:76166844
|
C | G | 39 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(36): Show | 42 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1188-543G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166844 | ||||||
chr4:76166913
|
C | T | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-612G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166913 | ||||||
chr4:76167014
|
A | G | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-713T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167014 | ||||||
chr4:76167089
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1188-788A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167089 | ||||||
chr4:76167252
|
C | T | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-951G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167252 | ||||||
chr4:76167409
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1187+994A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167409 | ||||||
chr4:76167498
|
C | T | 40 | a0001c0001t0001g0124a0001c0001t0003g0106a0001c0001t0003g0109others(37): Show | 43 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1187+905G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167498 | ||||||
chr4:76167610
|
C | T | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+793G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167610 | ||||||
chr4:76167672
|
T | TC | 25 | a0001c0001t0001g0029a0001c0001t0001g0091a0001c0001t0001g0096others(22): Show | 28 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1187+730dupG | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167672 | ||||||
chr4:76167672
|
TC | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(152): Show | 212 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1187+730delG | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167672 | ||||||
chr4:76167681
|
C | G | 23 | a0001c0001t0004g0048a0001c0001t0004g0223a0001c0001t0004g0239others(20): Show | 25 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1187+722G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167681 | ||||||
chr4:76167682
|
C | G | 7 | a0001c0001t0002g0265a0001c0001t0003g0106a0001c0001t0003g0109others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187+721G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167682 | ||||||
chr4:76167682
|
CG | C | 24 | a0001c0001t0004g0048a0001c0001t0004g0223a0001c0001t0004g0239others(21): Show | 26 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1187+720delC | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167682 | ||||||
chr4:76167682
|
CGCT | C | 7 | a0001c0002t0006g0177a0002c0003t0004g0241a0002c0003t0006g0189others(4): Show | 7 | HG02280.hp2 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187+718_1187+720d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167682 | ||||||
chr4:76167683
|
G | C | 9 | a0001c0001t0002g0265a0001c0001t0003g0106a0001c0001t0003g0109others(6): Show | 10 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1187+720C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167683 | ||||||
chr4:76167684
|
C | T | 30 | a0001c0001t0002g0265a0001c0001t0003g0106a0001c0001t0003g0109others(27): Show | 33 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1187+719G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167684 | ||||||
chr4:76167685
|
T | C | 1 | a0002c0003t0014g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1187+718A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167685 | ||||||
chr4:76167705
|
C | T | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+698G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167705 | ||||||
chr4:76167706
|
A | T | 2 | a0001c0001t0005g0233a0001c0001t0007g0057 | 2 | HG01358.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1187+697T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167706 | ||||||
chr4:76167767
|
C | T | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+636G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167767 | ||||||
chr4:76167768
|
G | A | 14 | a0001c0001t0002g0303a0001c0001t0004g0223a0001c0001t0004g0243others(11): Show | 15 | HG00408.hp2 HG01109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1187+635C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167768 | ||||||
chr4:76167792
|
T | C | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+611A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167792 | ||||||
chr4:76167930
|
T | C | 4 | a0001c0001t0003g0109a0001c0001t0004g0038a0001c0002t0006g0177others(1): Show | 5 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1187+473A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167930 | ||||||
chr4:76167971
|
A | G | 3 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0004g0295 | 3 | HG00423.hp2 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1187+432T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167971 | ||||||
chr4:76168158
|
G | C | 88 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(85): Show | 118 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1187+245C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168158 | ||||||
chr4:76168322
|
G | C | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+81C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168322 | ||||||
chr4:76168346
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187+57G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168346 | ||||||
chr4:76168351
|
C | T | 3 | a0001c0001t0003g0018a0001c0001t0003g0072a0001c0001t0003g0086 | 4 | HG03490.hp1 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187+52G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168351 | ||||||
chr4:76168775
|
C | G | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1114-299G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76168775 | ||||||
chr4:76168927
|
G | A | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-451C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76168927 | ||||||
chr4:76168934
|
G | A | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-458C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76168934 | ||||||
chr4:76169012
|
C | T | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-536G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169012 | ||||||
chr4:76169212
|
T | C | 95 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(92): Show | 125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1113+655A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169212 | ||||||
chr4:76169287
|
G | A | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+580C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169287 | ||||||
chr4:76169296
|
T | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1113+571A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169296 | ||||||
chr4:76169317
|
T | TAC | 6 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0002g0287others(3): Show | 6 | HG01257.hp2 HG03831.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+548_1113+549d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169317 | ||||||
chr4:76169317
|
T | TACAC | 66 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(63): Show | 78 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1113+546_1113+549d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169317 | ||||||
chr4:76169325
|
C | G | 1 | a0001c0001t0004g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1113+542G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169325 | ||||||
chr4:76169335
|
C | T | 74 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(71): Show | 96 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1113+532G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169335 | ||||||
chr4:76169341
|
C | CACACACA | 8 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(9): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | ||||||
chr4:76169341
|
C | CACACACA others(11): Show |
1 | a0001c0001t0006g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1113+525_1113+526i others(20): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | ||||||
chr4:76169341
|
C | CACACACA others(9): Show |
26 | a0001c0001t0003g0006a0001c0001t0003g0050a0001c0001t0003g0051others(23): Show | 32 | HG00558.hp1 HG00673.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(18): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | ||||||
chr4:76169341
|
C | CACACACA others(7): Show |
46 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0009others(43): Show | 66 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(16): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | ||||||
chr4:76169341
|
C | CACACACA others(5): Show |
5 | a0001c0001t0003g0008a0001c0001t0003g0022a0001c0001t0003g0024others(2): Show | 9 | HG01099.hp2 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | ||||||
chr4:76169341
|
C | CACACACA others(3): Show |
7 | a0001c0001t0003g0167a0001c0001t0004g0296a0001c0001t0004g0298others(4): Show | 7 | HG00558.hp2 HG02129.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | ||||||
chr4:76169342
|
G | A | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+525C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169342 | ||||||
chr4:76169476
|
T | G | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1113+391A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169476 | ||||||
chr4:76169692
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1113+175A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169692 | ||||||
chr4:76169853
|
A | T | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+14T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169853 | ||||||
chr4:76170033
|
AAGCTG | A | 95 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(92): Show | 125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.995-53_995-49delCA others(3): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170033 | ||||||
chr4:76170096
|
A | G | 1 | a0001c0001t0002g0291 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.995-111T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170096 | ||||||
chr4:76170437
|
G | A | 95 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(92): Show | 125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.995-452C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170437 | ||||||
chr4:76170440
|
G | A | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.995-455C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170440 | ||||||
chr4:76170463
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.995-478G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170463 | ||||||
chr4:76170508
|
C | T | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-523G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170508 | ||||||
chr4:76170528
|
A | T | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.995-543T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170528 | ||||||
chr4:76170529
|
T | A | 2 | a0001c0001t0029g0220a0001c0002t0023g0179 | 2 | HG01175.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.995-544A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170529 | ||||||
chr4:76170533
|
T | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0002g0217others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-548A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170533 | ||||||
chr4:76170540
|
T | TTTTTG | 3 | a0001c0001t0021g0200a0001c0001t0029g0220a0001c0002t0023g0179 | 3 | HG01175.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.995-560_995-556dup others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170540 | ||||||
chr4:76170671
|
C | T | 21 | a0001c0001t0004g0048a0001c0001t0004g0223a0001c0001t0004g0243others(18): Show | 23 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.995-686G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170671 | ||||||
chr4:76170714
|
T | C | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-729A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170714 | ||||||
chr4:76170845
|
G | A | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-860C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170845 | ||||||
chr4:76170945
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0287 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.995-961_995-960ins others(13): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | ||||||
chr4:76170945
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.995-961_995-960ins others(17): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | ||||||
chr4:76170945
|
AAT | A | 64 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(61): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.995-962_995-961del others(2): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | ||||||
chr4:76170945
|
AATAT | A | 2 | a0001c0001t0001g0104a0001c0001t0002g0042 | 3 | HG03195.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.995-964_995-961del others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | ||||||
chr4:76170945
|
AATATAT | A | 66 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0052others(63): Show | 81 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.995-966_995-961del others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | ||||||
chr4:76170945
|
AATATATA others(1): Show |
A | 105 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0002g0217others(102): Show | 141 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.995-968_995-961del others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | ||||||
chr4:76170971
|
T | A | 6 | a0001c0001t0001g0149a0001c0001t0002g0287a0001c0001t0006g0199others(3): Show | 6 | HG01175.hp1 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-986A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76170971
|
T | TATATATA others(3): Show |
37 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0058others(34): Show | 43 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.995-987_995-986ins others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76170971
|
T | TATATATA others(5): Show |
10 | a0001c0001t0001g0010a0001c0001t0001g0060a0001c0001t0001g0117others(7): Show | 12 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.995-987_995-986ins others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76170971
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0139 | 2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.995-987_995-986ins others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76170971
|
T | TATATATA others(9): Show |
15 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(12): Show | 19 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.995-987_995-986ins others(16): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76170971
|
T | TATATATA others(11): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0134 | 2 | HG00597.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.995-987_995-986ins others(18): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76170971
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0162 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.995-987_995-986ins others(24): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | ||||||
chr4:76171268
|
C | G | 7 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0014g0242others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1283G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171268 | ||||||
chr4:76171323
|
C | A | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1338G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171323 | ||||||
chr4:76171345
|
C | T | 3 | a0003c0006t0013g0180a0003c0006t0013g0181a0003c0009t0028g0240 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.995-1360G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171345 | ||||||
chr4:76171519
|
A | T | 2 | a0001c0001t0003g0007a0004c0004t0004g0015 | 6 | HG04184.hp1 NA18939.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1534T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171519 | ||||||
chr4:76171549
|
G | A | 1 | a0001c0001t0007g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.995-1564C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171549 | ||||||
chr4:76171549
|
GT | G | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1565delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171549 | ||||||
chr4:76171703
|
CA | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1719delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171703 | ||||||
chr4:76171706
|
C | A | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1721G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171706 | ||||||
chr4:76171755
|
TG | T | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1771delC | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171755 | ||||||
chr4:76171863
|
T | C | 1 | a0001c0001t0008g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.995-1878A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171863 | ||||||
chr4:76171967
|
AGT | A | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1984_995-1983d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171967 | ||||||
chr4:76171975
|
T | G | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1990A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171975 | ||||||
chr4:76171985
|
C | T | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-2000G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171985 | ||||||
chr4:76172004
|
C | CTATA | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-2023_995-2020d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172004 | ||||||
chr4:76172200
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.994+1944C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172200 | ||||||
chr4:76172200
|
GTA | G | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.994+1942_994+1943d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172200 | ||||||
chr4:76172202
|
A | G | 1 | a0001c0001t0002g0044 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.994+1942T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172202 | ||||||
chr4:76172204
|
ATATATAT others(1): Show |
A | 9 | a0001c0001t0012g0191a0001c0008t0012g0197a0002c0003t0004g0241others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+1932_994+1939d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172204 | ||||||
chr4:76172209
|
T | C | 86 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(83): Show | 116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.994+1935A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172209 | ||||||
chr4:76172679
|
CT | C | 83 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(80): Show | 105 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.994+1464delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172679 | ||||||
chr4:76172679
|
CTT | C | 87 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(84): Show | 117 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.994+1463_994+1464d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172679 | ||||||
chr4:76172752
|
C | T | 1 | a0001c0001t0001g0027 | 2 | NA18964.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.994+1392G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172752 | ||||||
chr4:76172779
|
A | G | 2 | a0001c0001t0029g0220a0001c0002t0023g0179 | 2 | HG01175.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.994+1365T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172779 | ||||||
chr4:76172799
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.994+1345C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172799 | ||||||
chr4:76172905
|
A | G | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.994+1239T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172905 | ||||||
chr4:76173053
|
CA | C | 2 | a0001c0001t0003g0022a0001c0001t0004g0228 | 3 | HG01099.hp2 HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.994+1090delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173053 | ||||||
chr4:76173220
|
C | G | 1 | a0001c0001t0005g0036 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.994+924G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173220 | ||||||
chr4:76173328
|
CT | C | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.994+815delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173328 | ||||||
chr4:76173328
|
CTT | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(143): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.994+814_994+815del others(2): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173328 | ||||||
chr4:76173328
|
CTTT | C | 77 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(74): Show | 106 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.994+813_994+815del others(3): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173328 | ||||||
chr4:76173329
|
T | G | 1 | a0001c0001t0008g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.994+815A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173329 | ||||||
chr4:76173388
|
C | T | 82 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(79): Show | 104 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.994+756G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173388 | ||||||
chr4:76173425
|
G | A | 1 | a0001c0001t0003g0070 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.994+719C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173425 | ||||||
chr4:76173580
|
C | T | 1 | a0001c0001t0008g0012 | 3 | HG01891.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.994+564G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173580 | ||||||
chr4:76173627
|
C | T | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.994+517G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173627 | ||||||
chr4:76173678
|
T | G | 148 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(145): Show | 194 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.994+466A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173678 | ||||||
chr4:76173686
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.994+458G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173686 | ||||||
chr4:76173820
|
T | G | 1 | a0001c0001t0003g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.994+324A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173820 | ||||||
chr4:76173864
|
T | C | 2 | a0001c0001t0005g0229a0001c0001t0005g0232 | 2 | HG00323.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.994+280A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173864 | ||||||
chr4:76173882
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.994+262A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173882 | ||||||
chr4:76173895
|
A | G | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.994+249T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173895 | ||||||
chr4:76173950
|
T | C | 1 | a0001c0001t0004g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.994+194A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173950 | ||||||
chr4:76173990
|
A | G | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.994+154T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173990 | ||||||
chr4:76174062
|
C | T | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.994+82G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76174062 | ||||||
chr4:76174096
|
C | G | 5 | a0002c0003t0014g0242a0002c0003t0014g0294a0002c0003t0019g0093others(2): Show | 5 | HG02809.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+48G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76174096 | ||||||
chr4:76174118
|
A | G | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.994+26T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76174118 | ||||||
chr4:76174421
|
C | T | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.825-108G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174421 | ||||||
chr4:76174436
|
G | A | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.825-123C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174436 | ||||||
chr4:76174504
|
G | A | 2 | a0001c0001t0006g0192a0001c0001t0006g0204 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.825-191C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174504 | ||||||
chr4:76174629
|
T | A | 1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.825-316A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174629 | ||||||
chr4:76174637
|
T | C | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.825-324A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174637 | ||||||
chr4:76174787
|
C | T | 13 | a0001c0001t0003g0019a0001c0001t0003g0054a0001c0001t0003g0064others(10): Show | 14 | HG00597.hp1 HG03834.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.825-474G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174787 | ||||||
chr4:76174803
|
C | A | 8 | a0001c0001t0004g0223a0001c0001t0004g0243a0001c0001t0004g0246others(5): Show | 9 | HG01109.hp2 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.825-490G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174803 | ||||||
chr4:76174870
|
A | T | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.825-557T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174870 | ||||||
chr4:76174965
|
G | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(30): Show | 37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.825-652C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174965 | ||||||
chr4:76175004
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.825-691G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175004 | ||||||
chr4:76175067
|
A | G | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.824+724T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175067 | ||||||
chr4:76175073
|
G | GT | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.824+717dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175073 | ||||||
chr4:76175366
|
A | G | 96 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(93): Show | 126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.824+425T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175366 | ||||||
chr4:76175453
|
G | T | 155 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(152): Show | 201 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.824+338C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175453 | ||||||
chr4:76175533
|
G | A | 6 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.824+258C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175533 | ||||||
chr4:76175576
|
C | A | 1 | a0001c0001t0021g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.824+215G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175576 | ||||||
chr4:76175578
|
A | G | 1 | a0001c0001t0012g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.824+213T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175578 | ||||||
chr4:76175624
|
T | C | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.824+167A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175624 | ||||||
chr4:76175690
|
C | T | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.824+101G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175690 | ||||||
chr4:76175984
|
T | C | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.705-74A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76175984 | ||||||
chr4:76176036
|
C | T | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.705-126G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176036 | ||||||
chr4:76176093
|
C | A | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.705-183G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176093 | ||||||
chr4:76176132
|
G | A | 1 | a0005c0005t0007g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-222C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176132 | ||||||
chr4:76176134
|
G | A | 1 | a0005c0005t0007g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-224C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176134 | ||||||
chr4:76176136
|
T | C | 1 | a0005c0005t0007g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-226A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176136 | ||||||
chr4:76176137
|
T | A | 1 | a0005c0005t0007g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-227A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176137 | ||||||
chr4:76176138
|
T | C | 1 | a0005c0005t0007g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-228A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176138 | ||||||
chr4:76176139
|
G | A | 1 | a0005c0005t0007g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-229C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176139 | ||||||
chr4:76176183
|
C | T | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.704+254G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176183 | ||||||
chr4:76176220
|
A | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(67): Show | 82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.704+217T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176220 | ||||||
chr4:76176421
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.704+16T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176421 | ||||||
chr4:76176605
|
T | C | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-77A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76176605 | ||||||
chr4:76176798
|
G | A | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-270C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76176798 | ||||||
chr4:76176987
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.613-459A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76176987 | ||||||
chr4:76177021
|
CT | C | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-494delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177021 | ||||||
chr4:76177278
|
T | A | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-750A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177278 | ||||||
chr4:76177445
|
A | G | 1 | a0001c0001t0002g0275 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.613-917T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177445 | ||||||
chr4:76177676
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.613-1148G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177676 | ||||||
chr4:76177713
|
G | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.613-1185C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177713 | ||||||
chr4:76177785
|
T | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.613-1257A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177785 | ||||||
chr4:76177832
|
C | T | 1 | a0001c0001t0006g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.613-1304G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177832 | ||||||
chr4:76178019
|
G | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.613-1491C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178019 | ||||||
chr4:76178077
|
C | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+1440G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178077 | ||||||
chr4:76178175
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.612+1342A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178175 | ||||||
chr4:76178231
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(67): Show | 82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.612+1286T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178231 | ||||||
chr4:76178493
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.612+1024A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178493 | ||||||
chr4:76178508
|
A | C | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.612+1009T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178508 | ||||||
chr4:76178520
|
C | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+997G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178520 | ||||||
chr4:76178591
|
C | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+926G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178591 | ||||||
chr4:76178602
|
A | G | 2 | a0001c0002t0009g0175a0001c0002t0009g0176 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.612+915T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178602 | ||||||
chr4:76178638
|
A | G | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.612+879T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178638 | ||||||
chr4:76178666
|
A | C | 4 | a0001c0001t0005g0035a0001c0001t0005g0234a0001c0001t0007g0164others(1): Show | 5 | HG00738.hp1 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.612+851T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178666 | ||||||
chr4:76178746
|
A | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+771T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178746 | ||||||
chr4:76178966
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.612+551A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178966 | ||||||
chr4:76179028
|
G | GGTTTTT | 5 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0001t0001g0117others(2): Show | 6 | HG01106.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+483_612+488dup others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179028 | ||||||
chr4:76179028
|
GGTTTTT | G | 13 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(10): Show | 19 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.612+483_612+488del others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179028 | ||||||
chr4:76179047
|
GTTTTTGT others(1): Show |
G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+462_612+469del others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179047 | ||||||
chr4:76179047
|
GTTTTTGT others(4): Show |
G | 1 | a0001c0001t0004g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.612+459_612+469del others(11): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179047 | ||||||
chr4:76179053
|
GTTTTT | G | 94 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(91): Show | 124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.612+459_612+463del others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179053 | ||||||
chr4:76179054
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.612+463A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179054 | ||||||
chr4:76179059
|
T | G | 4 | a0001c0001t0001g0110a0001c0001t0002g0013a0001c0001t0002g0037others(1): Show | 7 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+458A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179059 | ||||||
chr4:76179119
|
T | C | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.612+398A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179119 | ||||||
chr4:76179290
|
A | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+227T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179290 | ||||||
chr4:76179440
|
CAA | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 6 | NA18964.hp2 NA18971.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+75_612+76delTT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179440 | ||||||
chr4:76179748
|
A | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.424-43T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76179748 | ||||||
chr4:76179915
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(67): Show | 82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.424-210A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76179915 | ||||||
chr4:76180062
|
G | A | 91 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0001others(88): Show | 121 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.424-357C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180062 | ||||||
chr4:76180084
|
T | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.424-379A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180084 | ||||||
chr4:76180225
|
A | C | 77 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(74): Show | 99 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.424-520T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180225 | ||||||
chr4:76180484
|
C | G | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.423+470G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180484 | ||||||
chr4:76180512
|
T | G | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.423+442A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180512 | ||||||
chr4:76180595
|
T | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.423+359A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180595 | ||||||
chr4:76180705
|
C | T | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.423+249G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180705 | ||||||
chr4:76180773
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.423+181T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180773 | ||||||
chr4:76180819
|
G | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.423+135C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180819 | ||||||
chr4:76180853
|
C | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.423+101G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180853 | ||||||
chr4:76181270
|
G | A | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-169C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181270 | ||||||
chr4:76181321
|
C | A | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276-220G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181321 | ||||||
chr4:76181373
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276-272C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181373 | ||||||
chr4:76181386
|
G | A | 1 | a0001c0001t0003g0021 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.276-285C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181386 | ||||||
chr4:76182001
|
T | C | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.276-900A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182001 | ||||||
chr4:76182043
|
C | CAAAATTT others(6): Show |
84 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(81): Show | 113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.276-955_276-943dup others(13): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182043 | ||||||
chr4:76182311
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.276-1210A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182311 | ||||||
chr4:76182376
|
T | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-1275A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182376 | ||||||
chr4:76182469
|
T | C | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-1368A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182469 | ||||||
chr4:76182510
|
G | A | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276-1409C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182510 | ||||||
chr4:76182536
|
G | C | 1 | a0002c0003t0024g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.276-1435C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182536 | ||||||
chr4:76182655
|
G | A | 58 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(55): Show | 85 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.276-1554C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182655 | ||||||
chr4:76182705
|
T | C | 1 | a0001c0001t0002g0292 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.276-1604A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182705 | ||||||
chr4:76182776
|
G | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-1675C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182776 | ||||||
chr4:76182935
|
C | CAT | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-1836_276-1835d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182935 | ||||||
chr4:76182999
|
T | C | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-1898A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182999 | ||||||
chr4:76183124
|
T | C | 60 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(57): Show | 76 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.276-2023A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183124 | ||||||
chr4:76183356
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.276-2255C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183356 | ||||||
chr4:76183376
|
T | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-2275A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183376 | ||||||
chr4:76183571
|
T | TA | 4 | a0001c0001t0001g0069a0001c0001t0001g0098a0001c0001t0002g0260others(1): Show | 4 | HG01361.hp1 HG01496.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-2471dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183571 | ||||||
chr4:76183731
|
G | C | 2 | a0001c0001t0003g0050a0001c0001t0004g0016 | 4 | HG00558.hp1 HG02071.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-2630C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183731 | ||||||
chr4:76183776
|
T | A | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.276-2675A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183776 | ||||||
chr4:76183790
|
C | T | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-2689G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183790 | ||||||
chr4:76184021
|
G | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-2920C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184021 | ||||||
chr4:76184163
|
C | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3062G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184163 | ||||||
chr4:76184251
|
A | C | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-3150T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184251 | ||||||
chr4:76184269
|
C | T | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.276-3168G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184269 | ||||||
chr4:76184463
|
C | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3362G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184463 | ||||||
chr4:76184472
|
C | T | 1 | a0002c0003t0024g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.276-3371G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184472 | ||||||
chr4:76184491
|
C | T | 1 | a0001c0001t0009g0208 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.276-3390G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184491 | ||||||
chr4:76184547
|
T | G | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-3446A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184547 | ||||||
chr4:76184605
|
A | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.276-3504T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184605 | ||||||
chr4:76184613
|
A | T | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-3512T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184613 | ||||||
chr4:76184642
|
C | T | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-3541G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184642 | ||||||
chr4:76184758
|
A | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3657T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184758 | ||||||
chr4:76184785
|
CA | C | 110 | a0001c0001t0001g0091a0001c0001t0001g0142a0001c0001t0003g0001others(107): Show | 146 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.276-3685delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184785 | ||||||
chr4:76184785
|
CAA | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3686_276-3685d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184785 | ||||||
chr4:76184797
|
A | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3696T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184797 | ||||||
chr4:76184798
|
A | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3697T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184798 | ||||||
chr4:76184799
|
A | T | 157 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(154): Show | 204 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.276-3698T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184799 | ||||||
chr4:76184893
|
A | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3792T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184893 | ||||||
chr4:76184962
|
T | A | 7 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0002g0277others(4): Show | 8 | NA18943.hp1 NA18962.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-3861A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184962 | ||||||
chr4:76184984
|
G | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3883C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184984 | ||||||
chr4:76185068
|
T | C | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3967A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185068 | ||||||
chr4:76185209
|
G | A | 93 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.276-4108C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185209 | ||||||
chr4:76185332
|
G | C | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-4231C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185332 | ||||||
chr4:76185426
|
C | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-4325G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185426 | ||||||
chr4:76185607
|
T | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 6 | NA18964.hp2 NA18971.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-4506A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185607 | ||||||
chr4:76185659
|
G | A | 60 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(57): Show | 76 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.276-4558C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185659 | ||||||
chr4:76185717
|
T | A | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-4616A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185717 | ||||||
chr4:76185721
|
G | A | 2 | a0001c0001t0005g0233a0001c0001t0007g0057 | 2 | HG01358.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.276-4620C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185721 | ||||||
chr4:76185915
|
G | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-4814C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185915 | ||||||
chr4:76186139
|
C | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.276-5038G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186139 | ||||||
chr4:76186250
|
G | A | 2 | a0001c0002t0009g0175a0001c0002t0009g0176 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.276-5149C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186250 | ||||||
chr4:76186409
|
G | A | 107 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(104): Show | 143 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.276-5308C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186409 | ||||||
chr4:76186415
|
G | A | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.276-5314C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186415 | ||||||
chr4:76186521
|
G | A | 6 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-5420C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186521 | ||||||
chr4:76187005
|
T | TA | 7 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-5905dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187005 | ||||||
chr4:76187107
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.276-6006A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187107 | ||||||
chr4:76187153
|
C | T | 170 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(167): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-6052G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187153 | ||||||
chr4:76187436
|
G | A | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-6335C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187436 | ||||||
chr4:76187515
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.276-6414T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187515 | ||||||
chr4:76187530
|
C | G | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.276-6429G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187530 | ||||||
chr4:76187560
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01070.hp1 HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.276-6459A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187560 | ||||||
chr4:76187614
|
T | C | 3 | a0001c0001t0003g0167a0001c0001t0004g0296a0001c0001t0004g0297 | 3 | HG02027.hp2 NA18747.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.276-6513A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187614 | ||||||
chr4:76187620
|
A | T | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-6519T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187620 | ||||||
chr4:76187641
|
T | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-6540A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187641 | ||||||
chr4:76187690
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-6589A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187690 | ||||||
chr4:76187799
|
A | C | 1 | a0001c0001t0002g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.276-6698T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187799 | ||||||
chr4:76187850
|
C | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-6749G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187850 | ||||||
chr4:76188080
|
C | T | 1 | a0001c0001t0005g0258 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.276-6979G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188080 | ||||||
chr4:76188128
|
T | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-7027A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188128 | ||||||
chr4:76188286
|
T | G | 1 | a0001c0001t0003g0006 | 3 | NA19002.hp2 NA19003.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.276-7185A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188286 | ||||||
chr4:76188365
|
AGACT | A | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.276-7268_276-7265d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188365 | ||||||
chr4:76188427
|
T | G | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7280A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188427 | ||||||
chr4:76188473
|
A | C | 1 | a0001c0001t0005g0039 | 2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.275+7234T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188473 | ||||||
chr4:76188490
|
GTTAGGCC others(1): Show |
G | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7209_275+7216d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188490 | ||||||
chr4:76188548
|
C | T | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7159G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188548 | ||||||
chr4:76188556
|
T | C | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7151A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188556 | ||||||
chr4:76188557
|
G | A | 61 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(58): Show | 77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.275+7150C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188557 | ||||||
chr4:76188704
|
T | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+7003A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188704 | ||||||
chr4:76188726
|
A | C | 80 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(77): Show | 109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+6981T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188726 | ||||||
chr4:76188852
|
A | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+6855T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188852 | ||||||
chr4:76188870
|
T | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0024 | 5 | NA18946.hp1 NA18981.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+6837A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188870 | ||||||
chr4:76188881
|
A | C | 3 | a0005c0005t0007g0159a0005c0005t0007g0160a0005c0005t0007g0161 | 3 | NA18949.hp1 NA18950.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.275+6826T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188881 | ||||||
chr4:76189010
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+6697G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189010 | ||||||
chr4:76189114
|
T | C | 62 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+6593A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189114 | ||||||
chr4:76189136
|
T | C | 7 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+6571A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189136 | ||||||
chr4:76189157
|
C | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+6550G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189157 | ||||||
chr4:76189158
|
C | A | 4 | a0001c0001t0002g0005a0001c0001t0002g0034a0001c0001t0002g0219others(1): Show | 8 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+6549G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189158 | ||||||
chr4:76189158
|
C | G | 192 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(189): Show | 243 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.275+6549G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189158 | ||||||
chr4:76189212
|
C | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(99): Show | 118 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.275+6495G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189212 | ||||||
chr4:76189238
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.275+6469C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189238 | ||||||
chr4:76189262
|
T | C | 2 | a0001c0001t0010g0011a0001c0001t0010g0129 | 4 | NA18970.hp1 NA18999.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+6445A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189262 | ||||||
chr4:76189427
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | NA18944.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.275+6280G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189427 | ||||||
chr4:76189470
|
T | C | 1 | a0001c0001t0005g0248 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.275+6237A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189470 | ||||||
chr4:76189474
|
C | CTGTTGT | 241 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(238): Show | 306 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.275+6227_275+6232d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | ||||||
chr4:76189474
|
C | CTGTTGTT others(2): Show |
17 | a0001c0001t0001g0027a0001c0001t0001g0131a0001c0001t0001g0132others(14): Show | 18 | HG00280.hp1 HG01515.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+6224_275+6232d others(11): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | ||||||
chr4:76189474
|
C | CTGTTGTT others(5): Show |
1 | a0001c0002t0006g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.275+6221_275+6232d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | ||||||
chr4:76189474
|
C | CTGTTGTT others(8): Show |
4 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0006g0206others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+6218_275+6232d others(17): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | ||||||
chr4:76189474
|
C | CTGTTGTT others(11): Show |
1 | a0001c0001t0004g0038 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.275+6215_275+6232d others(20): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | ||||||
chr4:76189474
|
CTGTTGT | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 6 | HG01106.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+6227_275+6232d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | ||||||
chr4:76189575
|
G | A | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0004g0270 | 3 | NA18974.hp1 NA19062.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.275+6132C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189575 | ||||||
chr4:76189658
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.275+6049C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189658 | ||||||
chr4:76189684
|
T | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+6023A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189684 | ||||||
chr4:76189806
|
T | C | 10 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(7): Show | 10 | HG01891.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.275+5901A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189806 | ||||||
chr4:76189814
|
C | G | 2 | a0001c0001t0007g0164a0001c0001t0007g0165 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.275+5893G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189814 | ||||||
chr4:76189863
|
C | T | 1 | a0001c0001t0018g0136 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.275+5844G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189863 | ||||||
chr4:76189864
|
G | A | 42 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(39): Show | 46 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.275+5843C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189864 | ||||||
chr4:76189876
|
C | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5831G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189876 | ||||||
chr4:76189879
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(111): Show | 136 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.275+5828G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189879 | ||||||
chr4:76189880
|
C | T | 7 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+5827G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189880 | ||||||
chr4:76189947
|
G | A | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.275+5760C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189947 | ||||||
chr4:76190008
|
ACTTT | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5695_275+5698d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190008 | ||||||
chr4:76190009
|
CT | C | 26 | a0001c0001t0001g0063a0001c0001t0001g0132a0001c0001t0001g0142others(23): Show | 33 | HG00673.hp2 HG01515.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.275+5697delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190009 | ||||||
chr4:76190011
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0002g0221 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.275+5696A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190011 | ||||||
chr4:76190136
|
G | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+5571C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190136 | ||||||
chr4:76190166
|
G | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5541C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190166 | ||||||
chr4:76190199
|
G | A | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.275+5508C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190199 | ||||||
chr4:76190238
|
A | G | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+5469T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190238 | ||||||
chr4:76190257
|
A | G | 274 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(271): Show | 342 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.275+5450T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190257 | ||||||
chr4:76190328
|
A | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+5379T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190328 | ||||||
chr4:76190365
|
T | G | 1 | a0001c0001t0004g0252 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.275+5342A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190365 | ||||||
chr4:76190523
|
C | T | 10 | a0001c0001t0001g0110a0001c0001t0002g0013a0001c0001t0002g0037others(7): Show | 13 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.275+5184G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190523 | ||||||
chr4:76190602
|
G | A | 61 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(58): Show | 77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.275+5105C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190602 | ||||||
chr4:76190610
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5097G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190610 | ||||||
chr4:76190645
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.275+5062G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190645 | ||||||
chr4:76190721
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+4986A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190721 | ||||||
chr4:76190738
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.275+4969G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190738 | ||||||
chr4:76190739
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0121a0001c0001t0002g0045 | 4 | NA18983.hp1 NA19012.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+4968C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190739 | ||||||
chr4:76190785
|
AAAAC | A | 15 | a0001c0001t0003g0021a0001c0001t0009g0004a0001c0001t0009g0033others(12): Show | 22 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.275+4918_275+4921d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190785 | ||||||
chr4:76190956
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.275+4751C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190956 | ||||||
chr4:76190982
|
C | A | 21 | a0001c0001t0004g0048a0001c0001t0004g0223a0001c0001t0004g0243others(18): Show | 23 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.275+4725G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190982 | ||||||
chr4:76191039
|
C | T | 1 | a0004c0004t0004g0015 | 3 | NA18939.hp1 NA18941.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.275+4668G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191039 | ||||||
chr4:76191078
|
TAAC | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+4626_275+4628d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191078 | ||||||
chr4:76191291
|
A | G | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | NA18947.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.275+4416T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191291 | ||||||
chr4:76191295
|
A | T | 1 | a0001c0002t0006g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.275+4412T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191295 | ||||||
chr4:76191318
|
A | G | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+4389T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191318 | ||||||
chr4:76191404
|
C | CACCA | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+4302_275+4303i others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191404 | ||||||
chr4:76191487
|
T | C | 80 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(77): Show | 109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+4220A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191487 | ||||||
chr4:76191533
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+4174A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191533 | ||||||
chr4:76191552
|
C | T | 1 | a0002c0003t0024g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.275+4155G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191552 | ||||||
chr4:76191574
|
A | G | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275+4133T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191574 | ||||||
chr4:76191690
|
G | T | 1 | a0001c0001t0006g0215 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.275+4017C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191690 | ||||||
chr4:76191698
|
C | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(240): Show | 307 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.275+4009G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191698 | ||||||
chr4:76191731
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(66): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.275+3976G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191731 | ||||||
chr4:76191737
|
CCCCT | C | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+3966_275+3969d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191737 | ||||||
chr4:76191759
|
C | T | 239 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(236): Show | 303 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.275+3948G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191759 | ||||||
chr4:76191766
|
T | G | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275+3941A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191766 | ||||||
chr4:76191779
|
C | CT | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3927dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191779 | ||||||
chr4:76191848
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0002g0221 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.275+3859C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191848 | ||||||
chr4:76191855
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275+3852G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191855 | ||||||
chr4:76192197
|
G | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3510C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192197 | ||||||
chr4:76192218
|
G | T | 1 | a0001c0001t0008g0205 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.275+3489C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192218 | ||||||
chr4:76192250
|
A | T | 80 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(77): Show | 109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+3457T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192250 | ||||||
chr4:76192406
|
T | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3301A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192406 | ||||||
chr4:76192491
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.275+3216C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192491 | ||||||
chr4:76192526
|
T | C | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275+3181A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192526 | ||||||
chr4:76192628
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+3079C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192628 | ||||||
chr4:76192637
|
G | GA | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+3069dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192637 | ||||||
chr4:76192649
|
C | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3058G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192649 | ||||||
chr4:76192651
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.275+3056G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192651 | ||||||
chr4:76192654
|
T | C | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+3053A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192654 | ||||||
chr4:76192681
|
CA | C | 8 | a0001c0001t0004g0252a0002c0003t0004g0241a0002c0003t0006g0189others(5): Show | 8 | HG01069.hp1 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+3025delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192681 | ||||||
chr4:76192681
|
CAA | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3024_275+3025d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192681 | ||||||
chr4:76192765
|
A | T | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+2942T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192765 | ||||||
chr4:76193034
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0002g0259 | 2 | NA19058.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.275+2673G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193034 | ||||||
chr4:76193037
|
A | G | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+2670T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193037 | ||||||
chr4:76193100
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.275+2607G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193100 | ||||||
chr4:76193107
|
A | C | 1 | a0001c0001t0002g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.275+2600T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193107 | ||||||
chr4:76193120
|
A | C | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+2587T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193120 | ||||||
chr4:76193365
|
C | T | 9 | a0001c0001t0005g0230a0001c0001t0005g0231a0002c0003t0004g0241others(6): Show | 9 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.275+2342G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193365 | ||||||
chr4:76193412
|
G | T | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275+2295C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193412 | ||||||
chr4:76193595
|
T | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(30): Show | 37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.275+2112A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193595 | ||||||
chr4:76193731
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1976A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193731 | ||||||
chr4:76193783
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(66): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.275+1924G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193783 | ||||||
chr4:76193862
|
A | G | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1845T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193862 | ||||||
chr4:76193919
|
G | A | 1 | a0001c0001t0021g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.275+1788C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193919 | ||||||
chr4:76193998
|
G | A | 80 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(77): Show | 109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+1709C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193998 | ||||||
chr4:76194034
|
G | A | 1 | a0001c0001t0008g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.275+1673C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194034 | ||||||
chr4:76194037
|
G | C | 1 | a0001c0001t0008g0205 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.275+1670C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194037 | ||||||
chr4:76194050
|
G | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1657C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194050 | ||||||
chr4:76194113
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1594G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194113 | ||||||
chr4:76194296
|
C | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1411G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194296 | ||||||
chr4:76194346
|
C | T | 3 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0004g0295 | 3 | HG00423.hp2 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.275+1361G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194346 | ||||||
chr4:76194367
|
C | CATA | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+1339_275+1340i others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194367 | ||||||
chr4:76194400
|
T | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1307A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194400 | ||||||
chr4:76194410
|
G | T | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275+1297C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194410 | ||||||
chr4:76194474
|
A | AGGC | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1230_275+1232d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194474 | ||||||
chr4:76194494
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1213G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194494 | ||||||
chr4:76194521
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1186G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194521 | ||||||
chr4:76194696
|
C | A | 1 | a0001c0001t0006g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275+1011G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194696 | ||||||
chr4:76194696
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1011G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194696 | ||||||
chr4:76194749
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.275+958A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194749 | ||||||
chr4:76194793
|
C | G | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+914G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194793 | ||||||
chr4:76194815
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+892A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194815 | ||||||
chr4:76194831
|
C | A | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275+876G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194831 | ||||||
chr4:76194841
|
C | G | 1 | a0001c0001t0002g0303 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.275+866G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194841 | ||||||
chr4:76194842
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+865C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194842 | ||||||
chr4:76194918
|
C | G | 1 | a0001c0001t0012g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.275+789G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194918 | ||||||
chr4:76194942
|
G | C | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+765C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194942 | ||||||
chr4:76194964
|
G | C | 80 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(77): Show | 109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+743C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194964 | ||||||
chr4:76194965
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00642.hp2 HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.275+742G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194965 | ||||||
chr4:76194990
|
T | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+717A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194990 | ||||||
chr4:76195064
|
G | C | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | NA18947.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.275+643C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195064 | ||||||
chr4:76195091
|
A | G | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+616T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195091 | ||||||
chr4:76195186
|
T | C | 1 | a0003c0009t0028g0240 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.275+521A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195186 | ||||||
chr4:76195194
|
G | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+513C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195194 | ||||||
chr4:76195196
|
C | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+511G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195196 | ||||||
chr4:76195249
|
C | T | 21 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(18): Show | 27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+458G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195249 | ||||||
chr4:76195374
|
T | A | 1 | a0001c0001t0004g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.275+333A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195374 | ||||||
chr4:76195448
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.275+259T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195448 | ||||||
chr4:76195506
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+201C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195506 | ||||||
chr4:76195575
|
G | A | 6 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+132C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195575 | ||||||
chr4:76195871
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp2 | splice_region_variant&intron_variant | LOW | c.118-7T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195871 | ||||||
chr4:76195891
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-27G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195891 | ||||||
chr4:76195943
|
G | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.118-79C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195943 | ||||||
chr4:76195958
|
C | T | 1 | a0001c0001t0012g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-94G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195958 | ||||||
chr4:76196060
|
G | A | 1 | a0004c0004t0004g0015 | 3 | NA18939.hp1 NA18941.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.118-196C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196060 | ||||||
chr4:76196072
|
G | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.118-208C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196072 | ||||||
chr4:76196156
|
G | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(30): Show | 37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.118-292C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196156 | ||||||
chr4:76196308
|
G | A | 1 | a0002c0003t0019g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.118-444C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196308 | ||||||
chr4:76196318
|
A | T | 1 | a0001c0001t0003g0021 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.118-454T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196318 | ||||||
chr4:76196384
|
T | C | 3 | a0001c0001t0003g0106a0001c0001t0006g0206a0001c0002t0006g0174 | 3 | HG03195.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-520A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196384 | ||||||
chr4:76196421
|
A | C | 141 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(138): Show | 186 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.118-557T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196421 | ||||||
chr4:76196596
|
G | A | 77 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(74): Show | 106 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.118-732C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196596 | ||||||
chr4:76196774
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-910C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196774 | ||||||
chr4:76196913
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.118-1049C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196913 | ||||||
chr4:76196980
|
G | A | 2 | a0001c0001t0006g0206a0001c0002t0006g0174 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.118-1116C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196980 | ||||||
chr4:76196981
|
GT | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1118delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196981 | ||||||
chr4:76197083
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.118-1219G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197083 | ||||||
chr4:76197096
|
C | T | 4 | a0001c0001t0006g0199a0001c0001t0021g0200a0001c0001t0029g0220others(1): Show | 4 | HG01175.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-1232G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197096 | ||||||
chr4:76197102
|
T | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1238A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197102 | ||||||
chr4:76197132
|
T | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1268A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197132 | ||||||
chr4:76197214
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1350G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197214 | ||||||
chr4:76197302
|
T | G | 1 | a0001c0001t0002g0260 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-1438A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197302 | ||||||
chr4:76197340
|
G | T | 9 | a0001c0001t0009g0004a0001c0001t0009g0208a0001c0001t0009g0209others(6): Show | 14 | HG00673.hp2 HG02083.hp1 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-1476C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197340 | ||||||
chr4:76197344
|
C | A | 1 | a0001c0001t0008g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118-1480G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197344 | ||||||
chr4:76197344
|
C | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-1480G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197344 | ||||||
chr4:76197469
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0002g0259 | 2 | NA19058.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.118-1605C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197469 | ||||||
chr4:76197516
|
T | TCAAACTG others(6): Show |
7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1653_118-1652i others(15): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197516 | ||||||
chr4:76197518
|
G | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1654C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197518 | ||||||
chr4:76197578
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1714G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197578 | ||||||
chr4:76197586
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1722A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197586 | ||||||
chr4:76197630
|
C | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1766G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197630 | ||||||
chr4:76197766
|
T | A | 1 | a0001c0001t0004g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-1902A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197766 | ||||||
chr4:76197895
|
C | CT | 8 | a0001c0001t0008g0202a0002c0003t0004g0241a0002c0003t0006g0189others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2032dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197895 | ||||||
chr4:76197985
|
G | A | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-2121C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197985 | ||||||
chr4:76198054
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.118-2190C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198054 | ||||||
chr4:76198065
|
C | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0007others(76): Show | 108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.118-2201G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198065 | ||||||
chr4:76198143
|
T | C | 2 | a0001c0001t0003g0070a0001c0001t0003g0071 | 2 | NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.118-2279A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198143 | ||||||
chr4:76198293
|
T | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-2429A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198293 | ||||||
chr4:76198308
|
C | T | 1 | a0001c0001t0008g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118-2444G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198308 | ||||||
chr4:76198328
|
G | A | 1 | a0001c0002t0008g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-2464C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198328 | ||||||
chr4:76198348
|
G | A | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118-2484C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198348 | ||||||
chr4:76198365
|
A | G | 2 | a0001c0001t0007g0088a0001c0001t0007g0113 | 2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.118-2501T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198365 | ||||||
chr4:76198394
|
G | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0049others(60): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.118-2530C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198394 | ||||||
chr4:76198471
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0002g0269 | 2 | NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.118-2607A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198471 | ||||||
chr4:76198488
|
A | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-2624T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198488 | ||||||
chr4:76198581
|
C | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-2717G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198581 | ||||||
chr4:76198608
|
CCT | C | 13 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(10): Show | 19 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-2746_118-2745d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198608 | ||||||
chr4:76198631
|
A | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-2767T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198631 | ||||||
chr4:76198789
|
T | C | 7 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2925A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198789 | ||||||
chr4:76198821
|
C | A | 7 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2957G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198821 | ||||||
chr4:76198837
|
AGTGAGT | A | 3 | a0001c0002t0009g0175a0001c0002t0009g0176a0001c0008t0012g0197 | 3 | HG02559.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.118-2979_118-2974d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198837 | ||||||
chr4:76198837
|
AGTGAGTG others(1): Show |
A | 9 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(6): Show | 15 | HG00673.hp2 HG02083.hp1 NA18948.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-2981_118-2974d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198837 | ||||||
chr4:76198837
|
AGTGAGTG others(5): Show |
A | 1 | a0001c0001t0009g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.118-2985_118-2974d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198837 | ||||||
chr4:76198839
|
TGA | T | 6 | a0002c0003t0004g0241a0002c0003t0014g0242a0002c0003t0014g0294others(3): Show | 6 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-2977_118-2976d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198839 | ||||||
chr4:76198841
|
A | AGT | 26 | a0001c0001t0001g0052a0001c0001t0001g0087a0001c0001t0001g0096others(23): Show | 28 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.118-2979_118-2978d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | AGTGAGT | 3 | a0001c0001t0003g0109a0001c0002t0006g0177a0001c0002t0006g0178 | 3 | HG01884.hp2 HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118-2978_118-2977i others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | AGTGAGTG others(3): Show |
2 | a0001c0001t0006g0206a0001c0002t0006g0174 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.118-2978_118-2977i others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | AGTGT | 20 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0138others(17): Show | 26 | HG00609.hp1 HG01192.hp2 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-2981_118-2978d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | AGTGTGT | 38 | a0001c0001t0001g0025a0001c0001t0001g0049a0001c0001t0001g0067others(35): Show | 49 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.118-2983_118-2978d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | AGTGTGTG others(1): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0075a0001c0001t0001g0089others(9): Show | 13 | HG00423.hp1 HG01070.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-2985_118-2978d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0003g0167a0001c0001t0029g0220a0001c0002t0023g0179 | 3 | HG01175.hp1 HG03139.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.118-2987_118-2978d others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
A | T | 1 | a0002c0003t0006g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-2977T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
AGT | A | 59 | a0001c0001t0001g0135a0001c0001t0001g0157a0001c0001t0002g0272others(56): Show | 81 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.118-2979_118-2978d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
AGTGT | A | 4 | a0001c0001t0006g0192a0001c0001t0006g0204a0005c0005t0007g0160others(1): Show | 4 | HG03486.hp2 NA18949.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-2981_118-2978d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
AGTGTGT | A | 3 | a0001c0001t0003g0018a0001c0001t0003g0072a0001c0001t0003g0086 | 4 | HG03490.hp1 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2983_118-2978d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198841
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0003g0054 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118-2989_118-2978d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | ||||||
chr4:76198843
|
T | TGA | 2 | a0001c0001t0003g0007a0004c0004t0004g0015 | 6 | HG04184.hp1 NA18939.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-2980_118-2979i others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198843 | ||||||
chr4:76198873
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118-3009A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198873 | ||||||
chr4:76198882
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.118-3018C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198882 | ||||||
chr4:76198883
|
A | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3019T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198883 | ||||||
chr4:76199036
|
C | T | 4 | a0001c0001t0006g0199a0001c0001t0021g0200a0001c0001t0029g0220others(1): Show | 4 | HG01175.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-3172G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199036 | ||||||
chr4:76199216
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3352G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199216 | ||||||
chr4:76199252
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-3388G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199252 | ||||||
chr4:76199330
|
T | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3466A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199330 | ||||||
chr4:76199392
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3528G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199392 | ||||||
chr4:76199393
|
A | G | 13 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(10): Show | 19 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-3529T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199393 | ||||||
chr4:76199393
|
A | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3529T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199393 | ||||||
chr4:76199556
|
C | T | 1 | a0001c0002t0006g0182 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.118-3692G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199556 | ||||||
chr4:76199568
|
A | AT | 12 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(9): Show | 18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.118-3705dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199568 | ||||||
chr4:76199611
|
T | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3747A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199611 | ||||||
chr4:76199720
|
G | A | 20 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(17): Show | 26 | HG00673.hp2 HG02083.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-3856C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199720 | ||||||
chr4:76199745
|
G | A | 7 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0004g0038others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3881C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199745 | ||||||
chr4:76199762
|
C | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3898G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199762 | ||||||
chr4:76199863
|
G | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3999C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199863 | ||||||
chr4:76200050
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0002g0290 | 2 | HG01081.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.118-4186C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200050 | ||||||
chr4:76200056
|
T | C | 1 | a0001c0001t0008g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118-4192A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200056 | ||||||
chr4:76200193
|
A | G | 266 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(263): Show | 333 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.118-4329T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200193 | ||||||
chr4:76200343
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4479C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200343 | ||||||
chr4:76200349
|
A | G | 4 | a0001c0001t0003g0109a0001c0001t0004g0038a0001c0002t0006g0177others(1): Show | 5 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4485T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200349 | ||||||
chr4:76200411
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4547A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200411 | ||||||
chr4:76200735
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.118-4871T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200735 | ||||||
chr4:76200925
|
T | C | 2 | a0001c0001t0012g0191a0001c0008t0012g0197 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-5061A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200925 | ||||||
chr4:76200954
|
G | C | 20 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(17): Show | 26 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.118-5090C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200954 | ||||||
chr4:76200961
|
A | G | 2 | a0002c0003t0004g0241a0002c0003t0006g0189 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.118-5097T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200961 | ||||||
chr4:76201028
|
C | A | 4 | a0001c0001t0001g0067a0001c0001t0002g0046a0001c0001t0002g0291others(1): Show | 5 | HG02129.hp1 NA18947.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-5164G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201028 | ||||||
chr4:76201057
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5193G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201057 | ||||||
chr4:76201348
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5484A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201348 | ||||||
chr4:76201354
|
G | C | 14 | a0001c0001t0009g0004a0001c0001t0009g0033a0001c0001t0009g0208others(11): Show | 20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-5490C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201354 | ||||||
chr4:76201356
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5492C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201356 | ||||||
chr4:76201487
|
C | G | 6 | a0001c0001t0003g0019a0001c0001t0003g0054a0001c0001t0003g0073others(3): Show | 7 | NA18974.hp1 NA18977.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5623G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201487 | ||||||
chr4:76201539
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5675A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201539 | ||||||
chr4:76201785
|
T | C | 3 | a0001c0001t0003g0106a0001c0001t0006g0206a0001c0002t0006g0174 | 3 | HG03195.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-5921A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201785 | ||||||
chr4:76201864
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0005g0230a0001c0001t0005g0231 | 3 | HG02735.hp2 HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.118-6000T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201864 | ||||||
chr4:76201979
|
A | G | 3 | a0001c0001t0008g0195a0001c0001t0008g0196a0001c0002t0008g0173 | 3 | HG03130.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.118-6115T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201979 | ||||||
chr4:76202081
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0072 | 3 | HG03491.hp2 HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.118-6217T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202081 | ||||||
chr4:76202161
|
G | C | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-6297C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202161 | ||||||
chr4:76202355
|
G | A | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-6491C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202355 | ||||||
chr4:76202365
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-6501C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202365 | ||||||
chr4:76202551
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-6687C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202551 | ||||||
chr4:76202688
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-6824G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202688 | ||||||
chr4:76202785
|
G | C | 8 | a0001c0008t0012g0197a0002c0003t0004g0241a0002c0003t0006g0189others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-6921C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202785 | ||||||
chr4:76202891
|
C | T | 1 | a0001c0001t0004g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.118-7027G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202891 | ||||||
chr4:76203001
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118-7137G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203001 | ||||||
chr4:76203043
|
A | G | 307 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(304): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.118-7179T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203043 | ||||||
chr4:76203125
|
C | T | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7261G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203125 | ||||||
chr4:76203212
|
T | A | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7348A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203212 | ||||||
chr4:76203270
|
T | C | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7406A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203270 | ||||||
chr4:76203297
|
G | T | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7433C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203297 | ||||||
chr4:76203409
|
T | C | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7545A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203409 | ||||||
chr4:76203413
|
C | A | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7549G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203413 | ||||||
chr4:76203462
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7598G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203462 | ||||||
chr4:76203464
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7600G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203464 | ||||||
chr4:76203592
|
A | G | 70 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(67): Show | 97 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.118-7728T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203592 | ||||||
chr4:76203614
|
A | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7750T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203614 | ||||||
chr4:76203772
|
C | T | 3 | a0001c0001t0004g0038a0001c0002t0006g0177a0001c0002t0006g0178 | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-7908G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203772 | ||||||
chr4:76203788
|
A | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7924T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203788 | ||||||
chr4:76204159
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-8295A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204159 | ||||||
chr4:76204180
|
G | A | 1 | a0001c0001t0002g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.118-8316C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204180 | ||||||
chr4:76204181
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-8317G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204181 | ||||||
chr4:76204192
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-8328C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204192 | ||||||
chr4:76204359
|
C | G | 8 | a0001c0008t0012g0197a0002c0003t0004g0241a0002c0003t0006g0189others(5): Show | 8 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-8495G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204359 | ||||||
chr4:76204523
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-8659C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204523 | ||||||
chr4:76204598
|
G | A | 2 | a0001c0001t0006g0192a0001c0001t0006g0204 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.118-8734C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204598 | ||||||
chr4:76204725
|
C | A | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(222): Show | 284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.117+8702G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204725 | ||||||
chr4:76204890
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0002g0305 | 2 | HG02080.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.117+8537G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204890 | ||||||
chr4:76204905
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0002g0269 | 2 | NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.117+8522T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204905 | ||||||
chr4:76205068
|
G | A | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+8359C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205068 | ||||||
chr4:76205071
|
A | G | 5 | a0001c0001t0002g0014a0001c0001t0002g0265a0001c0001t0002g0267others(2): Show | 7 | NA18941.hp2 NA18965.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+8356T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205071 | ||||||
chr4:76205138
|
C | A | 1 | a0001c0002t0006g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.117+8289G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205138 | ||||||
chr4:76205172
|
T | C | 1 | a0003c0006t0013g0180 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+8255A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205172 | ||||||
chr4:76205187
|
G | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+8240C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205187 | ||||||
chr4:76205349
|
A | AAAAAT | 46 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(43): Show | 56 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.117+8073_117+8077d others(7): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205349 | ||||||
chr4:76205423
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.117+8004T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205423 | ||||||
chr4:76205784
|
C | T | 1 | a0001c0001t0003g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.117+7643G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205784 | ||||||
chr4:76205865
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.117+7562A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205865 | ||||||
chr4:76205875
|
C | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+7552G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205875 | ||||||
chr4:76205951
|
G | A | 45 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(42): Show | 55 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.117+7476C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205951 | ||||||
chr4:76206159
|
G | A | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+7268C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206159 | ||||||
chr4:76206230
|
G | T | 1 | a0001c0001t0005g0258 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.117+7197C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206230 | ||||||
chr4:76206391
|
A | G | 4 | a0001c0001t0004g0048a0003c0006t0013g0180a0003c0006t0013g0181others(1): Show | 5 | HG01891.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+7036T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206391 | ||||||
chr4:76206440
|
A | G | 1 | a0001c0001t0005g0229 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+6987T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206440 | ||||||
chr4:76206618
|
T | A | 46 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(43): Show | 56 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.117+6809A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206618 | ||||||
chr4:76206663
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6764C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206663 | ||||||
chr4:76206740
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6687G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206740 | ||||||
chr4:76206741
|
G | A | 1 | a0001c0001t0006g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.117+6686C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206741 | ||||||
chr4:76206822
|
G | C | 1 | a0001c0001t0009g0212 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.117+6605C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206822 | ||||||
chr4:76206873
|
A | G | 274 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(271): Show | 339 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.117+6554T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206873 | ||||||
chr4:76206967
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6460A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206967 | ||||||
chr4:76206995
|
T | A | 3 | a0001c0001t0003g0109a0001c0001t0029g0220a0001c0002t0023g0179 | 3 | HG01175.hp1 HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.117+6432A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206995 | ||||||
chr4:76207005
|
A | G | 1 | a0001c0001t0004g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.117+6422T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207005 | ||||||
chr4:76207068
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6359G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207068 | ||||||
chr4:76207100
|
G | C | 78 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(75): Show | 90 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.117+6327C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207100 | ||||||
chr4:76207287
|
A | G | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6140T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207287 | ||||||
chr4:76207481
|
C | T | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5946G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207481 | ||||||
chr4:76207495
|
T | C | 1 | a0001c0001t0002g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.117+5932A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207495 | ||||||
chr4:76207571
|
G | A | 34 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0096others(31): Show | 38 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.117+5856C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207571 | ||||||
chr4:76207734
|
C | T | 2 | a0001c0001t0003g0070a0001c0001t0003g0071 | 2 | NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.117+5693G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207734 | ||||||
chr4:76207758
|
T | C | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5669A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207758 | ||||||
chr4:76207941
|
G | A | 7 | a0002c0003t0004g0241a0002c0003t0006g0189a0002c0003t0014g0242others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5486C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207941 | ||||||
chr4:76207964
|
T | G | 21 | a0001c0001t0004g0048a0001c0001t0004g0223a0001c0001t0004g0243others(18): Show | 23 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+5463A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207964 | ||||||
chr4:76208119
|
T | G | 4 | a0001c0001t0003g0109a0001c0001t0029g0220a0001c0002t0023g0179others(1): Show | 4 | HG01175.hp1 HG02145.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+5308A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208119 | ||||||
chr4:76208237
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0002g0221 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.117+5190A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208237 | ||||||
chr4:76208392
|
C | T | 1 | a0001c0008t0012g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+5035G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208392 | ||||||
chr4:76208404
|
C | T | 7 | a0001c0001t0003g0109a0001c0001t0004g0038a0001c0001t0029g0220others(4): Show | 8 | HG01175.hp1 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+5023G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208404 | ||||||
chr4:76208415
|
C | G | 35 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0095others(32): Show | 39 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.117+5012G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208415 | ||||||
chr4:76208531
|
C | T | 2 | a0001c0002t0006g0177a0001c0002t0006g0178 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.117+4896G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208531 | ||||||
chr4:76208626
|
T | C | 17 | a0001c0001t0004g0048a0001c0001t0004g0223a0001c0001t0004g0243others(14): Show | 19 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.117+4801A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208626 | ||||||
chr4:76208659
|
T | C | 21 | a0001c0001t0002g0005a0001c0001t0002g0034a0001c0001t0002g0222others(18): Show | 27 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.117+4768A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208659 | ||||||
chr4:76208687
|
G | A | 79 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0087others(76): Show | 111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.117+4740C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208687 | ||||||
chr4:76208702
|
T | C | 1 | a0002c0003t0019g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117+4725A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208702 | ||||||
chr4:76208755
|
C | A | 264 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(261): Show | 328 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.117+4672G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208755 | ||||||
chr4:76208756
|
T | C | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.117+4671A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208756 | ||||||
chr4:76208809
|
G | A | 18 | a0001c0001t0002g0237a0001c0001t0003g0109a0001c0001t0004g0048others(15): Show | 21 | HG01175.hp1 HG02145.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+4618C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208809 | ||||||
chr4:76208823
|
T | C | 3 | a0001c0001t0006g0204a0001c0001t0021g0200a0003c0009t0028g0240 | 3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.117+4604A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208823 | ||||||
chr4:76209052
|
T | C | 9 | a0001c0001t0002g0005a0001c0001t0002g0034a0001c0001t0002g0222others(6): Show | 13 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+4375A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209052 | ||||||
chr4:76209101
|
C | T | 2 | a0001c0001t0004g0239a0003c0009t0028g0240 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.117+4326G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209101 | ||||||
chr4:76209132
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(65): Show | 83 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.117+4295C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209132 | ||||||
chr4:76209167
|
A | G | 81 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0095others(78): Show | 97 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.117+4260T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209167 | ||||||
chr4:76209188
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+4239C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209188 | ||||||
chr4:76209437
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0006g0206a0001c0001t0008g0195others(2): Show | 5 | HG03130.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+3990A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209437 | ||||||
chr4:76209493
|
C | T | 1 | a0001c0001t0007g0112 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.117+3934G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209493 | ||||||
chr4:76209505
|
A | C | 1 | a0001c0001t0002g0259 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.117+3922T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209505 | ||||||
chr4:76209553
|
G | C | 1 | a0001c0001t0004g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+3874C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209553 | ||||||
chr4:76209554
|
A | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 8 | HG01106.hp1 HG01123.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+3873T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209554 | ||||||
chr4:76209649
|
G | A | 10 | a0001c0001t0002g0245a0001c0001t0004g0038a0001c0001t0004g0239others(7): Show | 11 | HG01169.hp1 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+3778C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209649 | ||||||
chr4:76209781
|
T | C | 15 | a0001c0001t0002g0249a0001c0001t0002g0254a0001c0001t0002g0255others(12): Show | 18 | HG00140.hp2 HG00280.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+3646A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209781 | ||||||
chr4:76209916
|
T | C | 101 | a0001c0001t0001g0095a0001c0001t0001g0172a0001c0001t0002g0002others(98): Show | 126 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.117+3511A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209916 | ||||||
chr4:76209932
|
C | T | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+3495G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209932 | ||||||
chr4:76210095
|
A | C | 1 | a0001c0001t0006g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.117+3332T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210095 | ||||||
chr4:76210100
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.117+3327A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210100 | ||||||
chr4:76210141
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0026others(65): Show | 82 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.117+3286C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210141 | ||||||
chr4:76210251
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0003g0006a0001c0001t0003g0050 | 5 | NA18747.hp2 NA18994.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+3176C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210251 | ||||||
chr4:76210357
|
C | T | 1 | a0002c0003t0024g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.117+3070G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210357 | ||||||
chr4:76210917
|
T | C | 1 | a0001c0001t0005g0258 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.117+2510A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210917 | ||||||
chr4:76210919
|
G | A | 24 | a0001c0001t0002g0217a0001c0001t0002g0219a0001c0001t0006g0199others(21): Show | 28 | HG01175.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.117+2508C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210919 | ||||||
chr4:76210989
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.117+2438T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210989 | ||||||
chr4:76211207
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(251): Show | 315 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+2220A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211207 | ||||||
chr4:76211270
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.117+2157C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211270 | ||||||
chr4:76211271
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.117+2156T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211271 | ||||||
chr4:76211300
|
A | G | 1 | a0002c0003t0019g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117+2127T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211300 | ||||||
chr4:76211361
|
T | TAAGTA | 260 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(257): Show | 321 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.117+2065_117+2066i others(7): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211361 | ||||||
chr4:76211369
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+2058C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211369 | ||||||
chr4:76211398
|
T | A | 16 | a0001c0002t0006g0032a0001c0002t0006g0174a0001c0002t0006g0177others(13): Show | 18 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+2029A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211398 | ||||||
chr4:76211404
|
T | G | 76 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0014others(73): Show | 97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.117+2023A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211404 | ||||||
chr4:76211469
|
A | C | 1 | a0001c0001t0015g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+1958T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211469 | ||||||
chr4:76211481
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(174): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.117+1946G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211481 | ||||||
chr4:76211786
|
C | T | 1 | a0002c0003t0019g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117+1641G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211786 | ||||||
chr4:76211895
|
T | C | 62 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0014others(59): Show | 79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.117+1532A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211895 | ||||||
chr4:76211926
|
A | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(195): Show | 242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.117+1501T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211926 | ||||||
chr4:76212022
|
G | A | 14 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194others(11): Show | 18 | HG00673.hp2 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.117+1405C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212022 | ||||||
chr4:76212300
|
C | T | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.117+1127G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212300 | ||||||
chr4:76212426
|
G | A | 1 | a0001c0001t0012g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+1001C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212426 | ||||||
chr4:76212448
|
T | C | 1 | a0001c0001t0012g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+979A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212448 | ||||||
chr4:76212491
|
G | A | 1 | a0001c0001t0006g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.117+936C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212491 | ||||||
chr4:76212492
|
C | G | 1 | a0001c0001t0006g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.117+935G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212492 | ||||||
chr4:76212576
|
C | T | 1 | a0009c0012t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.117+851G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212576 | ||||||
chr4:76212630
|
T | C | 2 | a0001c0001t0002g0307a0001c0001t0004g0308 | 2 | NA18980.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.117+797A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212630 | ||||||
chr4:76212762
|
T | G | 1 | a0001c0001t0008g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117+665A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212762 | ||||||
chr4:76213058
|
TC | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0013others(111): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.117+368delG | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213058 | ||||||
chr4:76213130
|
TG | T | 55 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0052others(52): Show | 77 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.117+296delC | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213130 | ||||||
chr4:76213257
|
C | T | 1 | a0001c0001t0012g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+170G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213257 | ||||||
chr4:76213312
|
C | T | 4 | a0001c0001t0008g0187a0001c0001t0008g0188a0001c0001t0008g0190others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+115G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213312 |