geneid | 391365 |
---|---|
ensemblid | ENSG00000138068.12 |
hgncid | 33433 |
symbol | SULT6B1 |
name | sulfotransferase family 6B member 1 |
refseq_nuc | NM_001367551.1 |
refseq_prot | NP_001354480.1 |
ensembl_nuc | ENST00000535679.6 |
ensembl_prot | ENSP00000444081.1 |
mane_status | MANE Select |
chr | chr2 |
start | 37167820 |
end | 37188670 |
strand | - |
ver | v1.2 |
region | chr2:37167820-37188670 |
region5000 | chr2:37162820-37193670 |
regionname0 | SULT6B1_chr2_37167820_37188670 |
regionname5000 | SULT6B1_chr2_37162820_37193670 |
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 | 303 | 169 | 60 | 43 | 46 | 9 | 9 | 38 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002 | 0/0 | 303 | 164 | 13 | 28 | 103 | 2 | 18 | 77 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0003 | 0/0 | 303 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0004 | 0/0 | 303 | 3 | 1 | 0 | 0 | 1 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0005 | 0/0 | 303 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0006 | 0/0 | 303 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0007 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0008 | 0/0 | 303 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0009 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0010 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0011 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0012 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0013 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
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 | 912 | 168 | 60 | 42 | 46 | 9 | 9 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0002 | 0/0 | 912 | 160 | 12 | 25 | 103 | 2 | 18 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0003 | 0/0 | 912 | 5 | 4 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0004 | 0/0 | 912 | 3 | 1 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0005 | 0/0 | 912 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0006 | 0/0 | 912 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0007 | 0/0 | 912 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0008 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0009 | 0/0 | 912 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0010 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0012 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0013 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0014 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0015 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0016 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
c0017 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 146 | 344 | 74 | 72 | 152 | 14 | 30 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
t0002 | 0/0 | 142 | 10 | 10 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
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 | 24 | 1 | 6 | 14 | 2 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0002 | 0/0 | 20 | 0 | 1 | 19 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0003 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0004 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0006 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0024 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
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 | 912 | 168 | 60 | 42 | 46 | 9 | 9 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0001c0015 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0002 | 0/0 | 912 | 160 | 12 | 25 | 103 | 2 | 18 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0009 | 0/0 | 912 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0012 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0013 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0003c0003 | 0/0 | 912 | 5 | 4 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0004c0004 | 0/0 | 912 | 3 | 1 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0005c0006 | 0/0 | 912 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0006c0005 | 0/0 | 912 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0007c0008 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0008c0007 | 0/0 | 912 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0009c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0010c0016 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0011c0014 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0012c0010 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0013c0017 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1057 | 158 | 50 | 42 | 46 | 9 | 9 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0001c0001t0002 | 0/0 | 1053 | 10 | 10 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0001c0015t0001 | 0/0 | 1057 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0002t0001 | 0/0 | 1057 | 160 | 12 | 25 | 103 | 2 | 18 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0009t0001 | 0/0 | 1057 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0012t0001 | 0/0 | 1057 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0002c0013t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0003c0003t0001 | 0/0 | 1057 | 5 | 4 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0004c0004t0001 | 0/0 | 1057 | 3 | 1 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0005c0006t0001 | 0/0 | 1057 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0006c0005t0001 | 0/0 | 1057 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0007c0008t0001 | 0/0 | 1057 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0008c0007t0001 | 0/0 | 1057 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0009c0011t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0010c0016t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0011c0014t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0012c0010t0001 | 0/0 | 1057 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
a0013c0017t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | copy fasta | chr2 | 37162820 | 37193670 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 24 | 1 | 6 | 14 | 2 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0003 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0001c0015t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0002 | 0/0 | 20 | 0 | 1 | 19 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0009t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0012t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0002c0013t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0003c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0004c0004t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0004c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0005c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0005c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0006c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0006c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0007c0008t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0008c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0008c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0009c0011t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0010c0016t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0011c0014t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0012c0010t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
a0013c0017t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0212 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00099 | hp2 | a0006 | c0005 | t0001 | g0114 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00280 | hp2 | a0004 | c0004 | t0001 | g0024 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0104 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01069 | hp2 | a0002 | c0009 | t0001 | g0033 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01071 | hp2 | a0002 | c0009 | t0001 | g0033 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01243 | hp1 | a0001 | c0015 | t0001 | g0081 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01993 | hp1 | a0002 | c0012 | t0001 | g0178 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0106 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | CDX | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02257 | hp1 | a0007 | c0008 | t0001 | g0025 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02257 | hp2 | a0010 | c0016 | t0001 | g0093 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02280 | hp2 | a0013 | c0017 | t0001 | g0230 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02602 | hp1 | a0004 | c0004 | t0001 | g0047 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0103 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03098 | hp1 | a0002 | c0013 | t0001 | g0064 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03209 | hp1 | a0003 | c0003 | t0001 | g0059 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03669 | hp1 | a0008 | c0007 | t0001 | g0075 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0177 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03834 | hp1 | a0006 | c0005 | t0001 | g0113 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0119 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18906 | hp2 | a0011 | c0014 | t0001 | g0214 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18945 | hp2 | a0005 | c0006 | t0001 | g0126 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19007 | hp2 | a0012 | c0010 | t0001 | g0046 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19080 | hp2 | a0005 | c0006 | t0001 | g0123 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19240 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA20752 | hp1 | a0008 | c0007 | t0001 | g0220 | EUR | TSI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0210 | EUR | TSI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02109 | hp1 | a0009 | c0011 | t0001 | g0115 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA20300 | hp1 | a0007 | c0008 | t0001 | g0025 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA21309 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37167960
|
T | C | 1 | a0008 | 2 | HG03669.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.887A>G | p.Lys296Arg | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 917/1057 | 887/912 | 296/303 | chr2 | 37167960 | ||
chr2:37168029
|
A | G | 1 | a0005 | 2 | NA18945.hp2 NA19080.hp2 |
missense_variant | MODERATE | c.818T>C | p.Ile273Thr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 848/1057 | 818/912 | 273/303 | chr2 | 37168029 | ||
chr2:37171439
|
C | A | 2 | a0003a0013 | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
missense_variant | MODERATE | c.776G>T | p.Arg259Leu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/7 | 806/1057 | 776/912 | 259/303 | chr2 | 37171439 | ||
chr2:37175213
|
C | G | 2 | a0004a0011 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.543G>C | p.Arg181Ser | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/7 | 573/1057 | 543/912 | 181/303 | chr2 | 37175213 | ||
chr2:37179500
|
C | T | 1 | a0006 | 2 | HG00099.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.487G>A | p.Gly163Ser | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 517/1057 | 487/912 | 163/303 | chr2 | 37179500 | ||
chr2:37179502
|
T | C | 1 | a0007 | 2 | HG02257.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.485A>G | p.Tyr162Cys | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 515/1057 | 485/912 | 162/303 | chr2 | 37179502 | ||
chr2:37179518
|
G | C | 1 | a0010 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.469C>G | p.Pro157Ala | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 499/1057 | 469/912 | 157/303 | chr2 | 37179518 | ||
chr2:37179537
|
C | G | 6 | a0002a0004a0005others(3): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
missense_variant | MODERATE | c.450G>C | p.Leu150Phe | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 480/1057 | 450/912 | 150/303 | chr2 | 37179537 | ||
chr2:37179568
|
C | T | 1 | a0009 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.419G>A | p.Arg140Gln | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 449/1057 | 419/912 | 140/303 | chr2 | 37179568 | ||
chr2:37187405
|
T | C | 1 | a0004 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.262A>G | p.Lys88Glu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/7 | 292/1057 | 262/912 | 88/303 | chr2 | 37187405 | ||
chr2:37187443
|
A | T | 1 | a0004 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.224T>A | p.Val75Asp | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/7 | 254/1057 | 224/912 | 75/303 | chr2 | 37187443 | ||
chr2:37188460
|
C | T | 1 | a0004 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.181G>A | p.Ala61Thr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/7 | 211/1057 | 181/912 | 61/303 | chr2 | 37188460 | ||
chr2:37188523
|
A | C | 1 | a0012 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.118T>G | p.Cys40Gly | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/7 | 148/1057 | 118/912 | 40/303 | chr2 | 37188523 | ||
chr2:37188607
|
C | A | 1 | a0013 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.34G>T | p.Asp12Tyr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/7 | 64/1057 | 34/912 | 12/303 | chr2 | 37188607 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37167962
|
C | T | 1 | a0002c0013 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.885G>A | p.Leu295Leu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 915/1057 | 885/912 | 295/303 | chr2 | 37167962 | ||
chr2:37171483
|
C | T | 1 | a0002c0012 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.732G>A | p.Ala244Ala | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/7 | 762/1057 | 732/912 | 244/303 | chr2 | 37171483 | ||
chr2:37171585
|
C | T | 1 | a0001c0015 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.630G>A | p.Leu210Leu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/7 | 660/1057 | 630/912 | 210/303 | chr2 | 37171585 | ||
chr2:37179501
|
A | G | 10 | a0002c0002a0002c0009a0002c0012others(7): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
synonymous_variant | LOW | c.486T>C | p.Tyr162Tyr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 516/1057 | 486/912 | 162/303 | chr2 | 37179501 | ||
chr2:37183440
|
G | A | 1 | a0002c0009 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.387C>T | p.Phe129Phe | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/7 | 417/1057 | 387/912 | 129/303 | chr2 | 37183440 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37167836
|
TTTAA | T | 1 | a0001c0001t0002 | 10 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*95_*98delTTAA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 95 | chr2 | 37167836 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37168124
|
T | A | 1 | a0002c0002t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.782-59A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168124 | ||||||
chr2:37168174
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.782-109C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168174 | ||||||
chr2:37168217
|
T | C | 7 | a0001c0001t0001g0071a0002c0002t0001g0026a0002c0002t0001g0060others(4): Show | 9 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-152A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168217 | ||||||
chr2:37168246
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.782-181C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168246 | ||||||
chr2:37168287
|
G | A | 7 | a0001c0001t0001g0071a0002c0002t0001g0026a0002c0002t0001g0060others(4): Show | 9 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-222C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168287 | ||||||
chr2:37168400
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.782-335G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168400 | ||||||
chr2:37168426
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.782-361T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168426 | ||||||
chr2:37168445
|
T | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(136): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.782-380A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168445 | ||||||
chr2:37168495
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(36): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.782-430C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168495 | ||||||
chr2:37168881
|
G | A | 64 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(61): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.782-816C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168881 | ||||||
chr2:37168892
|
C | T | 63 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-827G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168892 | ||||||
chr2:37168911
|
G | A | 7 | a0001c0001t0001g0082a0002c0013t0001g0064a0003c0003t0001g0059others(4): Show | 7 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-846C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168911 | ||||||
chr2:37168912
|
A | T | 7 | a0001c0001t0001g0082a0002c0013t0001g0064a0003c0003t0001g0059others(4): Show | 7 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-847T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168912 | ||||||
chr2:37168959
|
A | G | 1 | a0002c0002t0001g0190 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.782-894T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168959 | ||||||
chr2:37168964
|
G | C | 1 | a0002c0002t0001g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.782-899C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168964 | ||||||
chr2:37168993
|
G | A | 1 | a0002c0002t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.782-928C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168993 | ||||||
chr2:37169006
|
G | A | 63 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-941C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169006 | ||||||
chr2:37169025
|
G | A | 63 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-960C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169025 | ||||||
chr2:37169173
|
A | G | 63 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-1108T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169173 | ||||||
chr2:37169210
|
T | C | 63 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-1145A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169210 | ||||||
chr2:37169218
|
G | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.782-1153C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169218 | ||||||
chr2:37169219
|
A | T | 1 | a0002c0002t0001g0195 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.782-1154T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169219 | ||||||
chr2:37169361
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.782-1296G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169361 | ||||||
chr2:37169370
|
T | C | 11 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0109others(8): Show | 15 | HG00639.hp1 HG01433.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.782-1305A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169370 | ||||||
chr2:37169465
|
T | C | 63 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-1400A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169465 | ||||||
chr2:37169494
|
T | G | 1 | a0002c0002t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.782-1429A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169494 | ||||||
chr2:37169520
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.782-1455C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169520 | ||||||
chr2:37169605
|
C | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.782-1540G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169605 | ||||||
chr2:37169605
|
C | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0088others(2): Show | 9 | HG00639.hp2 HG01175.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-1540G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169605 | ||||||
chr2:37169615
|
A | G | 8 | a0001c0001t0001g0082a0001c0001t0002g0226a0002c0013t0001g0064others(5): Show | 8 | HG00738.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.782-1550T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169615 | ||||||
chr2:37169637
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(72): Show | 126 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.782-1572G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169637 | ||||||
chr2:37169638
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.782-1573C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169638 | ||||||
chr2:37169654
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.782-1589G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169654 | ||||||
chr2:37169681
|
G | C | 1 | a0002c0002t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.782-1616C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169681 | ||||||
chr2:37169700
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(71): Show | 125 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.782-1635G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169700 | ||||||
chr2:37169744
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.782-1679G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169744 | ||||||
chr2:37169778
|
C | A | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+1656G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169778 | ||||||
chr2:37169783
|
A | G | 64 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(61): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.781+1651T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169783 | ||||||
chr2:37169806
|
G | GT | 4 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0108others(1): Show | 4 | HG02970.hp2 HG02976.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+1627dupA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169806 | ||||||
chr2:37170038
|
A | T | 2 | a0002c0002t0001g0018a0002c0002t0001g0184 | 4 | NA18939.hp1 NA19005.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+1396T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170038 | ||||||
chr2:37170049
|
C | T | 3 | a0002c0002t0001g0173a0002c0002t0001g0213a0002c0002t0001g0227 | 3 | NA18983.hp2 NA19082.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.781+1385G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170049 | ||||||
chr2:37170100
|
T | G | 1 | a0013c0017t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781+1334A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170100 | ||||||
chr2:37170170
|
T | C | 1 | a0007c0008t0001g0025 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.781+1264A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170170 | ||||||
chr2:37170231
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.781+1203G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170231 | ||||||
chr2:37170271
|
A | G | 1 | a0002c0002t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.781+1163T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170271 | ||||||
chr2:37170327
|
T | C | 64 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(61): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.781+1107A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170327 | ||||||
chr2:37170340
|
A | G | 64 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(61): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.781+1094T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170340 | ||||||
chr2:37170452
|
G | T | 1 | a0002c0002t0001g0121 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.781+982C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170452 | ||||||
chr2:37170473
|
A | G | 1 | a0009c0011t0001g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.781+961T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170473 | ||||||
chr2:37170473
|
A | T | 62 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(59): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.781+961T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170473 | ||||||
chr2:37170550
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(33): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.781+884G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170550 | ||||||
chr2:37170586
|
T | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(58): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.781+848A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170586 | ||||||
chr2:37170635
|
G | A | 61 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(58): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.781+799C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170635 | ||||||
chr2:37170667
|
A | G | 62 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(59): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.781+767T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170667 | ||||||
chr2:37170737
|
C | CA | 16 | a0001c0001t0001g0101a0001c0001t0001g0221a0001c0001t0001g0225others(13): Show | 20 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.781+696dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | ||||||
chr2:37170737
|
CA | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.781+696delT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | ||||||
chr2:37170737
|
CAA | C | 15 | a0001c0001t0001g0035a0001c0001t0001g0089a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.781+695_781+696del others(2): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | ||||||
chr2:37170737
|
CAAA | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0036others(26): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.781+694_781+696del others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | ||||||
chr2:37170914
|
G | A | 56 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(53): Show | 75 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.781+520C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170914 | ||||||
chr2:37170945
|
A | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(31): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.781+489T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170945 | ||||||
chr2:37171002
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.781+432C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171002 | ||||||
chr2:37171093
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.781+341T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171093 | ||||||
chr2:37171111
|
C | T | 3 | a0002c0002t0001g0110a0002c0002t0001g0143a0002c0002t0001g0189 | 3 | NA18979.hp1 NA18985.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.781+323G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171111 | ||||||
chr2:37171130
|
C | G | 1 | a0002c0002t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.781+304G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171130 | ||||||
chr2:37171226
|
C | T | 1 | a0002c0002t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.781+208G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171226 | ||||||
chr2:37171345
|
C | G | 1 | a0001c0001t0001g0007 | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+89G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171345 | ||||||
chr2:37171603
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.625-13A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37171603 | ||||||
chr2:37171618
|
T | C | 1 | a0002c0002t0001g0207 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.625-28A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37171618 | ||||||
chr2:37172013
|
A | C | 2 | a0002c0002t0001g0043a0002c0002t0001g0203 | 3 | NA18966.hp1 NA18969.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.625-423T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172013 | ||||||
chr2:37172041
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(7): Show | 20 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-451T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172041 | ||||||
chr2:37172050
|
AT | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.625-461delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172050 | ||||||
chr2:37172050
|
ATT | A | 20 | a0001c0001t0001g0169a0002c0002t0001g0009a0002c0002t0001g0010others(17): Show | 30 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.625-462_625-461del others(2): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172050 | ||||||
chr2:37172073
|
G | C | 1 | a0002c0002t0001g0125 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.625-483C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172073 | ||||||
chr2:37172115
|
A | G | 49 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0150others(46): Show | 66 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.625-525T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172115 | ||||||
chr2:37172137
|
A | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-547T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172137 | ||||||
chr2:37172179
|
T | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-589A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172179 | ||||||
chr2:37172208
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.625-618T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172208 | ||||||
chr2:37172251
|
T | G | 4 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0001g0105others(1): Show | 4 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-661A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172251 | ||||||
chr2:37172484
|
T | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0022others(24): Show | 39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.625-894A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172484 | ||||||
chr2:37172513
|
CT | C | 9 | a0001c0001t0001g0083a0001c0001t0001g0107a0002c0002t0001g0118others(6): Show | 9 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-924delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172513 | ||||||
chr2:37172593
|
C | T | 2 | a0002c0002t0001g0016a0002c0002t0001g0179 | 4 | HG00639.hp1 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1003G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172593 | ||||||
chr2:37172624
|
C | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG00323.hp1 HG01081.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.625-1034G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172624 | ||||||
chr2:37172662
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(13): Show | 27 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.625-1072G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172662 | ||||||
chr2:37172664
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(7): Show | 20 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-1074G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172664 | ||||||
chr2:37172668
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.625-1078A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172668 | ||||||
chr2:37172707
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1117G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172707 | ||||||
chr2:37172755
|
G | A | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1165C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172755 | ||||||
chr2:37172778
|
G | T | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.625-1188C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172778 | ||||||
chr2:37172787
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1197G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172787 | ||||||
chr2:37172823
|
C | CTTGT | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(174): Show | 285 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.625-1237_625-1234d others(6): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172823 | ||||||
chr2:37172823
|
C | CTTGTTTG others(1): Show |
7 | a0002c0002t0001g0026a0002c0002t0001g0060a0002c0002t0001g0061others(4): Show | 8 | HG00099.hp1 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.625-1241_625-1234d others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172823 | ||||||
chr2:37172876
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.625-1286C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172876 | ||||||
chr2:37172962
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.625-1372G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172962 | ||||||
chr2:37173010
|
A | G | 10 | a0002c0002t0001g0112a0002c0002t0001g0135a0003c0003t0001g0059others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1420T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173010 | ||||||
chr2:37173035
|
T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0077others(2): Show | 7 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.625-1445A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173035 | ||||||
chr2:37173081
|
G | C | 1 | a0010c0016t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.625-1491C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173081 | ||||||
chr2:37173179
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1589A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173179 | ||||||
chr2:37173306
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.625-1716A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173306 | ||||||
chr2:37173376
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1756A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173376 | ||||||
chr2:37173392
|
C | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1740G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173392 | ||||||
chr2:37173420
|
G | A | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1712C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173420 | ||||||
chr2:37173551
|
C | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(41): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.624+1581G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173551 | ||||||
chr2:37173721
|
C | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1411G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173721 | ||||||
chr2:37173730
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1402A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173730 | ||||||
chr2:37173758
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1374G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173758 | ||||||
chr2:37173805
|
TCCTTTGC others(17): Show |
T | 1 | a0002c0002t0001g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.624+1303_624+1326d others(26): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173805 | ||||||
chr2:37173824
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0048others(6): Show | 19 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+1308G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173824 | ||||||
chr2:37174021
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.624+1111C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174021 | ||||||
chr2:37174033
|
C | T | 1 | a0003c0003t0001g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.624+1099G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174033 | ||||||
chr2:37174071
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.624+1061G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174071 | ||||||
chr2:37174092
|
C | A | 110 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(107): Show | 169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.624+1040G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174092 | ||||||
chr2:37174163
|
C | G | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0221others(3): Show | 6 | HG01106.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+969G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174163 | ||||||
chr2:37174227
|
CT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(111): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.624+904delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174227 | ||||||
chr2:37174227
|
CTT | C | 83 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0027others(80): Show | 133 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.624+903_624+904del others(2): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174227 | ||||||
chr2:37174227
|
CTTT | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0001g0100others(14): Show | 21 | HG00639.hp1 HG01106.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+902_624+904del others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174227 | ||||||
chr2:37174283
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0057 | 8 | HG01074.hp1 HG01099.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+849C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174283 | ||||||
chr2:37174380
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+752T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174380 | ||||||
chr2:37174456
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+676A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174456 | ||||||
chr2:37174465
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.624+667A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174465 | ||||||
chr2:37174529
|
A | G | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.624+603T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174529 | ||||||
chr2:37174538
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.624+594G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174538 | ||||||
chr2:37174738
|
T | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+394A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174738 | ||||||
chr2:37174793
|
A | ATAACT | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.624+338_624+339ins others(5): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174793 | ||||||
chr2:37174881
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(181): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.624+251T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174881 | ||||||
chr2:37174885
|
A | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+247T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174885 | ||||||
chr2:37174895
|
G | A | 1 | a0002c0002t0001g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.624+237C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174895 | ||||||
chr2:37174950
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.624+182A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174950 | ||||||
chr2:37174996
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+136G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174996 | ||||||
chr2:37175012
|
A | G | 1 | a0002c0002t0001g0031 | 2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.624+120T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175012 | ||||||
chr2:37175082
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+50G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175082 | ||||||
chr2:37175089
|
G | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+43C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175089 | ||||||
chr2:37175094
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.624+38G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175094 | ||||||
chr2:37175127
|
C | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(42): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
splice_region_variant&intron_variant | LOW | c.624+5G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175127 | ||||||
chr2:37175230
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(42): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
splice_region_variant&intron_variant | LOW | c.530-4T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175230 | ||||||
chr2:37175391
|
A | G | 1 | a0002c0002t0001g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.530-165T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175391 | ||||||
chr2:37175519
|
A | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-293T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175519 | ||||||
chr2:37175549
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-323A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175549 | ||||||
chr2:37175625
|
G | C | 1 | a0002c0002t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.530-399C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175625 | ||||||
chr2:37175659
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-433T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175659 | ||||||
chr2:37175730
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(181): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.530-504T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175730 | ||||||
chr2:37175752
|
C | T | 1 | a0002c0009t0001g0033 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.530-526G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175752 | ||||||
chr2:37175753
|
A | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-527T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175753 | ||||||
chr2:37175771
|
G | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-545C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175771 | ||||||
chr2:37175812
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.530-586T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175812 | ||||||
chr2:37175956
|
C | A | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-730G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175956 | ||||||
chr2:37176101
|
G | A | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-875C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176101 | ||||||
chr2:37176102
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-876A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176102 | ||||||
chr2:37176114
|
G | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-888C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176114 | ||||||
chr2:37176260
|
C | CT | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.530-1035dupA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176260 | ||||||
chr2:37176260
|
C | CTT | 15 | a0001c0001t0001g0058a0001c0001t0001g0073a0001c0001t0001g0095others(12): Show | 15 | HG01934.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.530-1036_530-1035d others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176260 | ||||||
chr2:37176356
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0162 | 3 | NA18974.hp1 NA18983.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.530-1130C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176356 | ||||||
chr2:37176356
|
G | C | 2 | a0002c0002t0001g0060a0002c0002t0001g0061 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.530-1130C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176356 | ||||||
chr2:37176394
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.530-1168C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176394 | ||||||
chr2:37176443
|
A | G | 6 | a0002c0002t0001g0026a0002c0002t0001g0060a0002c0002t0001g0061others(3): Show | 7 | HG02886.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-1217T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176443 | ||||||
chr2:37176491
|
T | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0022others(24): Show | 39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.530-1265A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176491 | ||||||
chr2:37176556
|
G | A | 1 | a0002c0013t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.530-1330C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176556 | ||||||
chr2:37176676
|
C | T | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.530-1450G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176676 | ||||||
chr2:37176694
|
C | T | 1 | a0002c0002t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.530-1468G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176694 | ||||||
chr2:37176872
|
T | C | 3 | a0002c0002t0001g0026a0002c0002t0001g0062a0002c0002t0001g0063 | 4 | HG02922.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-1646A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176872 | ||||||
chr2:37176936
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-1710T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176936 | ||||||
chr2:37176971
|
G | A | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.530-1745C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176971 | ||||||
chr2:37177028
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.530-1802C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177028 | ||||||
chr2:37177151
|
CTCA | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0022others(24): Show | 39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.530-1928_530-1926d others(5): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177151 | ||||||
chr2:37177155
|
T | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 6 | HG00323.hp1 HG01081.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-1929A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177155 | ||||||
chr2:37177184
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(43): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.530-1958G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177184 | ||||||
chr2:37177226
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-2000G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177226 | ||||||
chr2:37177284
|
G | A | 1 | a0002c0002t0001g0198 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.530-2058C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177284 | ||||||
chr2:37177345
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2113T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177345 | ||||||
chr2:37177368
|
T | C | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2090A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177368 | ||||||
chr2:37177371
|
C | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2087G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177371 | ||||||
chr2:37177409
|
C | A | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+2049G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177409 | ||||||
chr2:37177411
|
CA | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(154): Show | 257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.529+2046delT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177411 | ||||||
chr2:37177411
|
CAA | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0101others(24): Show | 35 | HG00738.hp2 HG01106.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.529+2045_529+2046d others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177411 | ||||||
chr2:37177430
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2028T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177430 | ||||||
chr2:37177447
|
A | G | 1 | a0002c0002t0001g0182 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.529+2011T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177447 | ||||||
chr2:37177448
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2010T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177448 | ||||||
chr2:37177450
|
A | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2008T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177450 | ||||||
chr2:37177457
|
A | AATACAGC | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(108): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.529+1994_529+2000d others(9): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177457 | ||||||
chr2:37177556
|
G | A | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1902C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177556 | ||||||
chr2:37177571
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0022others(24): Show | 39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.529+1887T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177571 | ||||||
chr2:37177591
|
A | T | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1867T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177591 | ||||||
chr2:37177703
|
A | G | 1 | a0002c0002t0001g0181 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.529+1755T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177703 | ||||||
chr2:37177717
|
C | G | 1 | a0002c0013t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.529+1741G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177717 | ||||||
chr2:37177860
|
T | A | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1598A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177860 | ||||||
chr2:37177944
|
C | G | 3 | a0004c0004t0001g0024a0004c0004t0001g0047a0011c0014t0001g0214 | 4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1514G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177944 | ||||||
chr2:37177979
|
T | A | 1 | a0003c0003t0001g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.529+1479A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177979 | ||||||
chr2:37178065
|
G | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0022others(25): Show | 40 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.529+1393C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178065 | ||||||
chr2:37178148
|
A | C | 2 | a0002c0002t0001g0042a0002c0002t0001g0204 | 3 | HG00642.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.529+1310T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178148 | ||||||
chr2:37178250
|
T | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(43): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.529+1208A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178250 | ||||||
chr2:37178290
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.529+1168A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178290 | ||||||
chr2:37178306
|
C | T | 1 | a0012c0010t0001g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.529+1152G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178306 | ||||||
chr2:37178354
|
G | C | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+1104C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178354 | ||||||
chr2:37178388
|
A | G | 45 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(42): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.529+1070T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178388 | ||||||
chr2:37178450
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.529+1008C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178450 | ||||||
chr2:37178481
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.529+977G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178481 | ||||||
chr2:37178512
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.529+946T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178512 | ||||||
chr2:37178545
|
T | A | 1 | a0002c0013t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.529+913A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178545 | ||||||
chr2:37178614
|
AT | A | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+843delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178614 | ||||||
chr2:37178637
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0221others(1): Show | 4 | HG01106.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+821G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178637 | ||||||
chr2:37178714
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+744T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178714 | ||||||
chr2:37178768
|
G | T | 1 | a0002c0002t0001g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.529+690C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178768 | ||||||
chr2:37178953
|
T | TTTTG | 108 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(105): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.529+501_529+504dup others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178953 | ||||||
chr2:37178953
|
TTTTG | T | 3 | a0002c0002t0001g0016a0002c0002t0001g0179a0002c0012t0001g0178 | 5 | HG00639.hp1 HG01433.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+501_529+504del others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178953 | ||||||
chr2:37178977
|
T | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0098others(13): Show | 24 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.529+481A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178977 | ||||||
chr2:37179000
|
C | T | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.529+458G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179000 | ||||||
chr2:37179019
|
C | T | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+439G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179019 | ||||||
chr2:37179040
|
T | C | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+418A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179040 | ||||||
chr2:37179119
|
A | T | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+339T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179119 | ||||||
chr2:37179131
|
T | C | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529+327A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179131 | ||||||
chr2:37179141
|
G | A | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+317C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179141 | ||||||
chr2:37179144
|
G | C | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.529+314C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179144 | ||||||
chr2:37179160
|
G | A | 1 | a0002c0002t0001g0200 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.529+298C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179160 | ||||||
chr2:37179173
|
C | T | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529+285G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179173 | ||||||
chr2:37179174
|
A | G | 115 | a0001c0001t0001g0095a0002c0002t0001g0002a0002c0002t0001g0004others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.529+284T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179174 | ||||||
chr2:37179204
|
C | T | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529+254G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179204 | ||||||
chr2:37179225
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.529+233A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179225 | ||||||
chr2:37179271
|
T | C | 2 | a0003c0003t0001g0059a0013c0017t0001g0230 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.529+187A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179271 | ||||||
chr2:37179276
|
C | T | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+182G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179276 | ||||||
chr2:37179618
|
T | C | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.403-34A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179618 | ||||||
chr2:37179622
|
T | C | 1 | a0002c0002t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.403-38A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179622 | ||||||
chr2:37179657
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.403-73A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179657 | ||||||
chr2:37179664
|
A | G | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.403-80T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179664 | ||||||
chr2:37179666
|
G | C | 1 | a0003c0003t0001g0106 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-82C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179666 | ||||||
chr2:37179682
|
C | T | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-98G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179682 | ||||||
chr2:37179689
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0057 | 8 | HG01074.hp1 HG01099.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.403-105C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179689 | ||||||
chr2:37179723
|
A | G | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.403-139T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179723 | ||||||
chr2:37179795
|
G | T | 3 | a0002c0002t0001g0210a0002c0002t0001g0211a0002c0002t0001g0212 | 3 | HG00099.hp1 HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.403-211C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179795 | ||||||
chr2:37179893
|
T | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.403-309A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179893 | ||||||
chr2:37179947
|
A | T | 1 | a0011c0014t0001g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.403-363T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179947 | ||||||
chr2:37179961
|
A | G | 3 | a0003c0003t0001g0104a0003c0003t0001g0105a0003c0003t0001g0106 | 3 | HG00738.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.403-377T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179961 | ||||||
chr2:37180035
|
A | G | 115 | a0001c0001t0001g0150a0002c0002t0001g0002a0002c0002t0001g0004others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-451T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180035 | ||||||
chr2:37180078
|
A | C | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-494T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180078 | ||||||
chr2:37180079
|
G | T | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-495C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180079 | ||||||
chr2:37180080
|
T | G | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-496A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180080 | ||||||
chr2:37180109
|
A | C | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-525T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180109 | ||||||
chr2:37180160
|
T | A | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(108): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.403-576A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180160 | ||||||
chr2:37180199
|
C | A | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-615G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180199 | ||||||
chr2:37180406
|
G | C | 1 | a0013c0017t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-822C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180406 | ||||||
chr2:37180487
|
G | C | 115 | a0001c0001t0001g0144a0002c0002t0001g0002a0002c0002t0001g0004others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-903C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180487 | ||||||
chr2:37180576
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.403-992G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180576 | ||||||
chr2:37180609
|
C | T | 1 | a0002c0002t0001g0041 | 2 | NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.403-1025G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180609 | ||||||
chr2:37180691
|
C | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0160 | 3 | NA19003.hp1 NA19056.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.403-1107G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180691 | ||||||
chr2:37180694
|
G | C | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(108): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.403-1110C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180694 | ||||||
chr2:37180715
|
T | C | 123 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0086others(120): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.403-1131A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180715 | ||||||
chr2:37180754
|
T | C | 1 | a0002c0002t0001g0130 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.403-1170A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180754 | ||||||
chr2:37180777
|
G | T | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-1193C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180777 | ||||||
chr2:37180815
|
C | T | 1 | a0002c0002t0001g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.403-1231G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180815 | ||||||
chr2:37180833
|
A | G | 115 | a0001c0001t0001g0144a0002c0002t0001g0002a0002c0002t0001g0004others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-1249T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180833 | ||||||
chr2:37180867
|
G | C | 113 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(110): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.403-1283C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180867 | ||||||
chr2:37180873
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-1289C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180873 | ||||||
chr2:37180988
|
A | G | 1 | a0002c0002t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.403-1404T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180988 | ||||||
chr2:37181000
|
T | C | 1 | a0002c0002t0001g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.403-1416A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181000 | ||||||
chr2:37181005
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.403-1421A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181005 | ||||||
chr2:37181086
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.403-1502T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181086 | ||||||
chr2:37181148
|
A | G | 1 | a0013c0017t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-1564T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181148 | ||||||
chr2:37181155
|
T | G | 112 | a0001c0001t0001g0144a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.403-1571A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181155 | ||||||
chr2:37181170
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(190): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.403-1586T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181170 | ||||||
chr2:37181247
|
C | T | 1 | a0002c0002t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.403-1663G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181247 | ||||||
chr2:37181345
|
T | C | 1 | a0002c0002t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.403-1761A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181345 | ||||||
chr2:37181405
|
C | T | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(108): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.403-1821G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181405 | ||||||
chr2:37181443
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(43): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.403-1859C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181443 | ||||||
chr2:37181461
|
A | G | 1 | a0002c0013t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.403-1877T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181461 | ||||||
chr2:37181504
|
C | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.403-1920G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181504 | ||||||
chr2:37181532
|
A | G | 110 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(107): Show | 169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.402+1893T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181532 | ||||||
chr2:37181554
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.402+1871T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181554 | ||||||
chr2:37181563
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1862T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181563 | ||||||
chr2:37181568
|
C | CG | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1856_402+1857i others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181568 | ||||||
chr2:37181569
|
A | G | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(109): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.402+1856T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181569 | ||||||
chr2:37181621
|
TC | T | 113 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(110): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.402+1803delG | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181621 | ||||||
chr2:37181627
|
C | T | 2 | a0002c0002t0001g0040a0002c0002t0001g0175 | 3 | NA19007.hp1 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.402+1798G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181627 | ||||||
chr2:37181631
|
T | C | 113 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(110): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.402+1794A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181631 | ||||||
chr2:37181681
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.402+1744G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181681 | ||||||
chr2:37181717
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1708T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181717 | ||||||
chr2:37181815
|
A | G | 45 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(42): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.402+1610T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181815 | ||||||
chr2:37181826
|
A | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0164a0001c0001t0001g0219others(2): Show | 5 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+1599T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181826 | ||||||
chr2:37182005
|
A | G | 112 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+1420T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182005 | ||||||
chr2:37182145
|
C | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0219a0001c0001t0001g0229others(1): Show | 4 | HG01074.hp2 HG01106.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+1280G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182145 | ||||||
chr2:37182167
|
C | T | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+1258G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182167 | ||||||
chr2:37182241
|
G | A | 112 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+1184C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182241 | ||||||
chr2:37182251
|
A | AACTATGC others(13): Show |
1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1173_402+1174i others(22): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182251 | ||||||
chr2:37182253
|
AT | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(64): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.402+1171delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182253 | ||||||
chr2:37182253
|
ATT | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG02647.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+1170_402+1171d others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182253 | ||||||
chr2:37182253
|
ATTT | A | 109 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(106): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.402+1169_402+1171d others(5): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182253 | ||||||
chr2:37182254
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1171A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182254 | ||||||
chr2:37182255
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1170A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182255 | ||||||
chr2:37182270
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1155A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182270 | ||||||
chr2:37182279
|
G | A | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+1146C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182279 | ||||||
chr2:37182285
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.402+1140C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182285 | ||||||
chr2:37182312
|
G | C | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.402+1113C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182312 | ||||||
chr2:37182314
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1111G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182314 | ||||||
chr2:37182315
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1110C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182315 | ||||||
chr2:37182336
|
G | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1089C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182336 | ||||||
chr2:37182339
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1086G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182339 | ||||||
chr2:37182341
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1084G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182341 | ||||||
chr2:37182343
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1082A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182343 | ||||||
chr2:37182356
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(43): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.402+1069G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182356 | ||||||
chr2:37182365
|
T | C | 112 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+1060A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182365 | ||||||
chr2:37182400
|
C | T | 1 | a0004c0004t0001g0024 | 2 | HG00280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1025G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182400 | ||||||
chr2:37182429
|
G | C | 112 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+996C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182429 | ||||||
chr2:37182549
|
G | C | 1 | a0003c0003t0001g0106 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.402+876C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182549 | ||||||
chr2:37182607
|
G | A | 112 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+818C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182607 | ||||||
chr2:37182658
|
A | G | 4 | a0002c0002t0001g0208a0002c0002t0001g0210a0002c0002t0001g0211others(1): Show | 4 | HG00099.hp1 HG00735.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+767T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182658 | ||||||
chr2:37182665
|
A | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+760T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182665 | ||||||
chr2:37182710
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+715G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182710 | ||||||
chr2:37182711
|
A | G | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+714T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182711 | ||||||
chr2:37182743
|
G | T | 45 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(42): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.402+682C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182743 | ||||||
chr2:37182873
|
T | C | 2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.402+552A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182873 | ||||||
chr2:37182894
|
A | G | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+531T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182894 | ||||||
chr2:37182899
|
C | T | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+526G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182899 | ||||||
chr2:37182914
|
T | G | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+511A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182914 | ||||||
chr2:37182972
|
G | C | 2 | a0002c0002t0001g0043a0002c0002t0001g0203 | 3 | NA18966.hp1 NA18969.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.402+453C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182972 | ||||||
chr2:37183088
|
A | C | 45 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(42): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.402+337T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183088 | ||||||
chr2:37183173
|
T | G | 115 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0216others(112): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.402+252A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183173 | ||||||
chr2:37183214
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.402+211A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183214 | ||||||
chr2:37183323
|
T | G | 1 | a0002c0002t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+102A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183323 | ||||||
chr2:37183372
|
T | G | 1 | a0010c0016t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.402+53A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183372 | ||||||
chr2:37183394
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.402+31G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183394 | ||||||
chr2:37183411
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+14C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183411 | ||||||
chr2:37183550
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-36C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183550 | ||||||
chr2:37183662
|
G | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-148C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183662 | ||||||
chr2:37183675
|
A | G | 4 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0001g0105others(1): Show | 4 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-161T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183675 | ||||||
chr2:37183720
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-206G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183720 | ||||||
chr2:37183721
|
G | A | 116 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0144others(113): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.313-207C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183721 | ||||||
chr2:37183743
|
A | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0216a0001c0001t0001g0217 | 5 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-229T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183743 | ||||||
chr2:37183812
|
T | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-298A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183812 | ||||||
chr2:37183820
|
T | G | 112 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.313-306A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183820 | ||||||
chr2:37183853
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(191): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.313-339A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183853 | ||||||
chr2:37183871
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0171 | 3 | HG00140.hp2 HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.313-357A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183871 | ||||||
chr2:37183913
|
C | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-399G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183913 | ||||||
chr2:37183933
|
T | C | 115 | a0001c0001t0001g0065a0001c0001t0001g0144a0002c0002t0001g0002others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.313-419A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183933 | ||||||
chr2:37183939
|
C | T | 45 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(42): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.313-425G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183939 | ||||||
chr2:37184009
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-495T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184009 | ||||||
chr2:37184079
|
T | A | 46 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(43): Show | 61 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.313-565A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184079 | ||||||
chr2:37184156
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-642T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184156 | ||||||
chr2:37184299
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.313-785G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184299 | ||||||
chr2:37184309
|
A | G | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-795T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184309 | ||||||
chr2:37184327
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-813C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184327 | ||||||
chr2:37184339
|
A | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0099others(7): Show | 12 | HG01106.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-825T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184339 | ||||||
chr2:37184454
|
T | C | 1 | a0001c0001t0001g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.313-940A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184454 | ||||||
chr2:37184594
|
T | C | 1 | a0002c0002t0001g0026 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.313-1080A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184594 | ||||||
chr2:37184622
|
G | T | 1 | a0013c0017t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.313-1108C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184622 | ||||||
chr2:37184637
|
C | G | 4 | a0002c0002t0001g0039a0002c0002t0001g0172a0002c0002t0001g0173others(1): Show | 5 | HG00621.hp1 NA18939.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.313-1123G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184637 | ||||||
chr2:37184647
|
A | G | 10 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0099others(7): Show | 12 | HG01106.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-1133T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184647 | ||||||
chr2:37184660
|
A | G | 115 | a0001c0001t0001g0065a0001c0001t0001g0144a0002c0002t0001g0002others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.313-1146T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184660 | ||||||
chr2:37184692
|
C | T | 2 | a0002c0002t0001g0134a0002c0002t0001g0136 | 2 | HG02486.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.313-1178G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184692 | ||||||
chr2:37184693
|
G | C | 2 | a0003c0003t0001g0059a0013c0017t0001g0230 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.313-1179C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184693 | ||||||
chr2:37184730
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1216C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184730 | ||||||
chr2:37184756
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1242G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184756 | ||||||
chr2:37184767
|
T | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1253A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184767 | ||||||
chr2:37184788
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1274G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184788 | ||||||
chr2:37184811
|
G | A | 3 | a0003c0003t0001g0104a0003c0003t0001g0105a0003c0003t0001g0106 | 3 | HG00738.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.313-1297C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184811 | ||||||
chr2:37184826
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1312G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184826 | ||||||
chr2:37184827
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.313-1313T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184827 | ||||||
chr2:37184830
|
T | TA | 8 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0219others(5): Show | 8 | HG01070.hp2 HG01074.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-1317dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184830 | ||||||
chr2:37184841
|
A | AC | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1328_313-1327i others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184841 | ||||||
chr2:37184844
|
C | A | 1 | a0013c0017t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.313-1330G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184844 | ||||||
chr2:37184889
|
A | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1375T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184889 | ||||||
chr2:37184910
|
G | A | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-1396C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184910 | ||||||
chr2:37185006
|
G | A | 115 | a0001c0001t0001g0065a0001c0001t0001g0144a0002c0002t0001g0002others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.313-1492C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185006 | ||||||
chr2:37185044
|
C | A | 1 | a0002c0002t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.313-1530G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185044 | ||||||
chr2:37185049
|
T | C | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-1535A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185049 | ||||||
chr2:37185057
|
A | AT | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1544dupA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185057 | ||||||
chr2:37185060
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.313-1546T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185060 | ||||||
chr2:37185186
|
A | G | 5 | a0002c0002t0001g0026a0002c0002t0001g0060a0002c0002t0001g0061others(2): Show | 6 | HG02886.hp2 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-1672T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185186 | ||||||
chr2:37185352
|
C | T | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-1838G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185352 | ||||||
chr2:37185443
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312+1912C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185443 | ||||||
chr2:37185444
|
T | C | 114 | a0001c0001t0001g0065a0002c0002t0001g0002a0002c0002t0001g0004others(111): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.312+1911A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185444 | ||||||
chr2:37185459
|
G | C | 1 | a0002c0013t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.312+1896C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185459 | ||||||
chr2:37185464
|
C | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1891G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185464 | ||||||
chr2:37185517
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.312+1838C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185517 | ||||||
chr2:37185518
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.312+1837T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185518 | ||||||
chr2:37185537
|
C | T | 4 | a0001c0001t0002g0023a0001c0001t0002g0045a0001c0001t0002g0218others(1): Show | 7 | HG02055.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1818G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185537 | ||||||
chr2:37185543
|
C | G | 1 | a0002c0002t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.312+1812G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185543 | ||||||
chr2:37185583
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.312+1772A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185583 | ||||||
chr2:37185610
|
C | T | 1 | a0002c0002t0001g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.312+1745G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185610 | ||||||
chr2:37185717
|
C | CA | 29 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.312+1637dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185717
|
C | CAAAAAAA others(1): Show |
8 | a0002c0002t0001g0067a0002c0002t0001g0068a0002c0002t0001g0111others(5): Show | 8 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+1630_312+1637d others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185717
|
C | CAAAAAAA others(2): Show |
33 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0030others(30): Show | 45 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.312+1629_312+1637d others(11): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185717
|
C | CAAAAAAA others(3): Show |
4 | a0002c0002t0001g0010a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 7 | HG00621.hp2 HG01943.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+1628_312+1637d others(12): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185717
|
C | CAAAAAAA others(4): Show |
1 | a0002c0002t0001g0139 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.312+1627_312+1637d others(13): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185717
|
CAAAAAAA | C | 5 | a0002c0002t0001g0012a0002c0002t0001g0044a0002c0002t0001g0110others(2): Show | 9 | HG01975.hp1 HG01978.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1631_312+1637d others(9): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185717
|
CAAAAAAA others(1): Show |
C | 54 | a0001c0001t0001g0144a0002c0002t0001g0002a0002c0002t0001g0011others(51): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.312+1630_312+1637d others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | ||||||
chr2:37185727
|
A | AAAAAAAA others(1): Show |
6 | a0002c0002t0001g0026a0002c0002t0001g0060a0002c0002t0001g0061others(3): Show | 7 | HG02886.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1627_312+1628i others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185727 | ||||||
chr2:37185752
|
T | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1603A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185752 | ||||||
chr2:37185792
|
T | G | 113 | a0001c0001t0001g0065a0001c0001t0001g0144a0002c0002t0001g0002others(110): Show | 172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.312+1563A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185792 | ||||||
chr2:37185918
|
T | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1437A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185918 | ||||||
chr2:37185923
|
C | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1432G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185923 | ||||||
chr2:37185990
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1365T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185990 | ||||||
chr2:37186002
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(190): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.312+1353C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186002 | ||||||
chr2:37186099
|
C | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 85 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.312+1256G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186099 | ||||||
chr2:37186227
|
T | A | 113 | a0001c0001t0001g0065a0001c0001t0001g0144a0002c0002t0001g0002others(110): Show | 172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.312+1128A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186227 | ||||||
chr2:37186327
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG02622.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312+1028C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186327 | ||||||
chr2:37186384
|
A | C | 115 | a0001c0001t0001g0065a0001c0001t0001g0144a0002c0002t0001g0002others(112): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.312+971T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186384 | ||||||
chr2:37186526
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+829G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186526 | ||||||
chr2:37186532
|
G | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+823C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186532 | ||||||
chr2:37186569
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+786G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186569 | ||||||
chr2:37186611
|
G | C | 1 | a0003c0003t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+744C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186611 | ||||||
chr2:37186634
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+721T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186634 | ||||||
chr2:37186717
|
C | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(66): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.312+638G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186717 | ||||||
chr2:37186722
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+633G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186722 | ||||||
chr2:37186728
|
C | CA | 5 | a0002c0002t0001g0215a0003c0003t0001g0103a0003c0003t0001g0104others(2): Show | 5 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+626dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186728 | ||||||
chr2:37186759
|
A | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+596T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186759 | ||||||
chr2:37186770
|
C | G | 1 | a0002c0002t0001g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312+585G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186770 | ||||||
chr2:37186842
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+513C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186842 | ||||||
chr2:37186897
|
A | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+458T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186897 | ||||||
chr2:37186901
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+454C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186901 | ||||||
chr2:37186935
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+420G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186935 | ||||||
chr2:37186976
|
A | G | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+379T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186976 | ||||||
chr2:37187074
|
G | A | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+281C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187074 | ||||||
chr2:37187083
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+272C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187083 | ||||||
chr2:37187084
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.312+271C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187084 | ||||||
chr2:37187176
|
A | G | 6 | a0003c0003t0001g0059a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+179T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187176 | ||||||
chr2:37187180
|
T | C | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+175A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187180 | ||||||
chr2:37187288
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.312+67T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187288 | ||||||
chr2:37187334
|
T | G | 1 | a0001c0001t0002g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312+21A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187334 | ||||||
chr2:37187614
|
G | A | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.200-147C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187614 | ||||||
chr2:37187782
|
T | G | 1 | a0002c0002t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.200-315A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187782 | ||||||
chr2:37187805
|
A | T | 1 | a0002c0002t0001g0143 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.200-338T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187805 | ||||||
chr2:37187865
|
GA | G | 42 | a0001c0001t0001g0140a0001c0001t0002g0141a0001c0001t0002g0142others(39): Show | 57 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.200-399delT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187865 | ||||||
chr2:37188179
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199+263G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188179 | ||||||
chr2:37188191
|
C | A | 1 | a0001c0001t0002g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.199+251G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188191 | ||||||
chr2:37188206
|
C | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0047 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199+236G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188206 | ||||||
chr2:37188212
|
T | C | 5 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0001g0105others(2): Show | 5 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+230A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188212 | ||||||
chr2:37188267
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+175G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188267 | ||||||
chr2:37188290
|
A | T | 1 | a0002c0002t0001g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199+152T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188290 | ||||||
chr2:37188328
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.199+114T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188328 | ||||||
chr2:37188353
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0034others(152): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.199+89C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188353 |