geneid | 25830 |
---|---|
ensemblid | ENSG00000130540.14 |
hgncid | 14903 |
symbol | SULT4A1 |
name | sulfotransferase family 4A member 1 |
refseq_nuc | NM_014351.4 |
refseq_prot | NP_055166.1 |
ensembl_nuc | ENST00000330884.9 |
ensembl_prot | ENSP00000332565.4 |
mane_status | MANE Select |
chr | chr22 |
start | 43824509 |
end | 43862513 |
strand | - |
ver | v1.2 |
region | chr22:43824509-43862513 |
region5000 | chr22:43819509-43867513 |
regionname0 | SULT4A1_chr22_43824509_43862513 |
regionname5000 | SULT4A1_chr22_43819509_43867513 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 284 | 384 | 91 | 70 | 164 | 18 | 39 | 122 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0002 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0003 | 0/0 | 284 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 855 | 383 | 90 | 70 | 164 | 18 | 39 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
c0002 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
c0003 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
c0004 | 0/0 | 855 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1622 | 99 | 5 | 8 | 68 | 3 | 15 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0002 | 0/0 | 1634 | 96 | 3 | 17 | 65 | 1 | 10 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0003 | 0/0 | 1634 | 60 | 22 | 14 | 10 | 6 | 8 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0004 | 0/1 | 1628 | 29 | 8 | 11 | 1 | 5 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0005 | 1/0 | 1624 | 27 | 9 | 10 | 3 | 1 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0006 | 0/0 | 1628 | 26 | 21 | 3 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0007 | 0/0 | 1634 | 7 | 0 | 0 | 7 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0008 | 0/0 | 1628 | 7 | 7 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0009 | 0/0 | 1628 | 6 | 2 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0010 | 0/0 | 1624 | 3 | 3 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0011 | 0/0 | 1640 | 2 | 1 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0012 | 0/0 | 1634 | 2 | 1 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0013 | 0/0 | 1628 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0014 | 0/0 | 1628 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0015 | 0/0 | 1628 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0016 | 0/0 | 1622 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0017 | 0/0 | 1622 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0018 | 0/0 | 1652 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0019 | 0/0 | 1646 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0020 | 0/0 | 1634 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0021 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0022 | 0/0 | 1628 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0023 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0024 | 0/0 | 1622 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0025 | 0/0 | 1622 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0026 | 0/0 | 1616 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0027 | 0/0 | 1616 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0028 | 0/0 | 1646 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
t0029 | 0/0 | 1628 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 17 | 1 | 3 | 13 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0002 | 0/0 | 15 | 0 | 5 | 10 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0003 | 0/1 | 10 | 0 | 4 | 1 | 3 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0004 | 0/0 | 7 | 2 | 1 | 3 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0007 | 0/0 | 6 | 0 | 1 | 0 | 1 | 4 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0008 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0015 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 855 | 383 | 90 | 70 | 164 | 18 | 39 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0003 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0002c0002 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0003c0004 | 0/0 | 855 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2476 | 99 | 5 | 8 | 68 | 3 | 15 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0002 | 0/0 | 2488 | 96 | 3 | 17 | 65 | 1 | 10 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0003 | 0/0 | 2488 | 59 | 22 | 14 | 10 | 6 | 7 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0004 | 0/1 | 2482 | 29 | 8 | 11 | 1 | 5 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0005 | 1/0 | 2478 | 26 | 8 | 10 | 3 | 1 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0006 | 0/0 | 2482 | 26 | 21 | 3 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0007 | 0/0 | 2488 | 7 | 0 | 0 | 7 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0008 | 0/0 | 2482 | 7 | 7 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0009 | 0/0 | 2482 | 6 | 2 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0010 | 0/0 | 2478 | 3 | 3 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0011 | 0/0 | 2494 | 2 | 1 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0012 | 0/0 | 2488 | 2 | 1 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0013 | 0/0 | 2482 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0014 | 0/0 | 2482 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0015 | 0/0 | 2482 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0016 | 0/0 | 2476 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0017 | 0/0 | 2476 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0018 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0019 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0021 | 0/0 | 2492 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0022 | 0/0 | 2482 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0023 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0024 | 0/0 | 2476 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0025 | 0/0 | 2476 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0026 | 0/0 | 2470 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0027 | 0/0 | 2470 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0028 | 0/0 | 2500 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0001t0029 | 0/0 | 2482 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0001c0003t0005 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0002c0002t0020 | 0/0 | 2488 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
a0003c0004t0003 | 0/0 | 2488 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | copy fasta | chr22 | 43819509 | 43867513 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 1 | 3 | 13 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0004 | 0/0 | 7 | 2 | 1 | 3 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0002 | 0/0 | 15 | 0 | 5 | 10 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 1 | 0 | 1 | 4 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0015 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0003 | 0/1 | 10 | 0 | 4 | 1 | 3 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0008 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0007g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0008g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0009g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0009g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0011g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0012g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0013g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0013g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0015g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0016g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0016g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0017g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0017g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0019g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0021g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0022g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0023g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0024g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0025g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0026g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0027g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0028g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0001t0029g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0001c0003t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0002c0002t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
a0003c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0003 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0090 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00438 | hp1 | a0001 | c0001 | t0009 | g0027 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00597 | hp1 | a0001 | c0001 | t0024 | g0170 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00621 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00733 | hp2 | a0001 | c0001 | t0027 | g0216 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01069 | hp1 | a0001 | c0001 | t0013 | g0085 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01099 | hp2 | a0001 | c0001 | t0016 | g0182 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01106 | hp2 | a0001 | c0001 | t0016 | g0183 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0123 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01175 | hp1 | a0001 | c0001 | t0013 | g0084 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0108 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0069 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01261 | hp2 | a0001 | c0001 | t0026 | g0215 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0126 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0128 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0003 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0116 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0034 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0003 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0091 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02040 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0132 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0140 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02056 | hp2 | a0001 | c0001 | t0017 | g0200 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02074 | hp1 | a0001 | c0001 | t0017 | g0194 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0135 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0107 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0119 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02647 | hp1 | a0001 | c0001 | t0019 | g0045 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02818 | hp2 | a0002 | c0002 | t0020 | g0048 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0268 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0110 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0044 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0111 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0129 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0137 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0113 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0118 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0032 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04115 | hp2 | a0003 | c0004 | t0003 | g0078 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04204 | hp1 | a0001 | c0001 | t0028 | g0217 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0071 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18943 | hp2 | a0001 | c0001 | t0025 | g0153 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18944 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18947 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18957 | hp2 | a0001 | c0001 | t0011 | g0047 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18961 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18984 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19030 | hp1 | a0001 | c0001 | t0014 | g0130 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0131 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19058 | hp1 | a0001 | c0001 | t0023 | g0199 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19087 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0143 | AFR | ASW | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | ASW | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0061 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0072 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0097 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02109 | hp2 | a0001 | c0001 | t0021 | g0083 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02486 | hp1 | a0001 | c0001 | t0022 | g0088 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG02559 | hp2 | a0001 | c0003 | t0005 | g0103 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0003 | REF | REF | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0105 | REF | REF | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43829188
|
G | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.614C>T | p.Thr205Met | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/7 | 745/2478 | 614/855 | 205/284 | chr22 | 43829188 | ||
chr22:43833672
|
C | T | 1 | a0002 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.571G>A | p.Val191Met | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/7 | 702/2478 | 571/855 | 191/284 | chr22 | 43833672 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43829073
|
C | T | 1 | a0001c0003 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.729G>A | p.Leu243Leu | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/7 | 860/2478 | 729/855 | 243/284 | chr22 | 43829073 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43824789
|
C | T | 1 | a0001c0001t0007 | 7 | NA18944.hp2 NA18947.hp1 NA18983.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1212 | chr22 | 43824789 | |||||
chr22:43824793
|
C | A | 10 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(7): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1208G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1208 | chr22 | 43824793 | |||||
chr22:43824984
|
C | G | 2 | a0001c0001t0004a0001c0001t0027 | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1017G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1017 | chr22 | 43824984 | |||||
chr22:43824986
|
C | T | 1 | a0001c0001t0024 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1015 | chr22 | 43824986 | |||||
chr22:43825066
|
G | C | 3 | a0001c0001t0014a0001c0001t0015a0001c0001t0021 | 5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*935C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 935 | chr22 | 43825066 | |||||
chr22:43825097
|
G | A | 1 | a0001c0001t0025 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 904 | chr22 | 43825097 | |||||
chr22:43825207
|
G | A | 1 | a0001c0001t0012 | 2 | HG01243.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 794 | chr22 | 43825207 | |||||
chr22:43825231
|
C | A | 1 | a0001c0001t0010 | 3 | HG02055.hp2 HG02976.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*770G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 770 | chr22 | 43825231 | |||||
chr22:43825312
|
C | T | 1 | a0001c0001t0014 | 2 | NA19030.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 689 | chr22 | 43825312 | |||||
chr22:43825367
|
A | G | 11 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(8): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*634T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 634 | chr22 | 43825367 | |||||
chr22:43825382
|
A | G | 1 | a0001c0001t0016 | 2 | HG01099.hp2 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*619T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 619 | chr22 | 43825382 | |||||
chr22:43825608
|
T | C | 1 | a0001c0001t0008 | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 393 | chr22 | 43825608 | |||||
chr22:43825685
|
C | CAATA | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*312_*315dupTATT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 315 | chr22 | 43825685 | |||||
chr22:43825836
|
G | A | 1 | a0002c0002t0020 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 165 | chr22 | 43825836 | |||||
chr22:43862403
|
C | T | 1 | a0001c0001t0013 | 2 | HG01069.hp1 HG01175.hp1 |
5_prime_UTR_variant | MODIFIER | c.-21G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 21 | chr22 | 43862403 | |||||
chr22:43862424
|
A | AGCCCGCA others(3): Show |
1 | a0001c0001t0021 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52_-43dupGCGTGCGG others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 43 | chr22 | 43862424 | |||||
chr22:43862431
|
A | ACGCGCC | 5 | a0001c0001t0003a0001c0001t0007a0001c0001t0012others(2): Show | 70 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-50dupGGCGCG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | |||||
chr22:43862431
|
A | ACGCGCCC others(5): Show |
1 | a0001c0001t0011 | 2 | HG03209.hp1 NA18957.hp2 |
5_prime_UTR_variant | MODIFIER | c.-61_-50dupGGCGCGGG others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | |||||
chr22:43862431
|
A | ACGCGCCC others(11): Show |
1 | a0001c0001t0019 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67_-50dupGGCGCGGG others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | |||||
chr22:43862431
|
A | ACGCGCCC others(17): Show |
1 | a0001c0001t0018 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-73_-50dupGGCGCGGG others(16): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | |||||
chr22:43862431
|
ACGCGCC | A | 6 | a0001c0001t0001a0001c0001t0016a0001c0001t0017others(3): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-50delGGCGCG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | |||||
chr22:43862431
|
ACGCGCCC others(5): Show |
A | 2 | a0001c0001t0026a0001c0001t0027 | 2 | HG00733.hp2 HG01261.hp2 |
5_prime_UTR_variant | MODIFIER | c.-61_-50delGGCGCGGG others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | |||||
chr22:43862459
|
G | A | 1 | a0001c0001t0029 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 77 | chr22 | 43862459 | |||||
chr22:43862459
|
G | GCCCGCA | 1 | a0001c0001t0002 | 96 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
5_prime_UTR_variant | MODIFIER | c.-78_-77insTGCGGG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 78 | chr22 | 43862459 | |||||
chr22:43862459
|
G | GCCCGCGC others(11): Show |
1 | a0001c0001t0028 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78_-77insTGCGGGCG others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 78 | chr22 | 43862459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43826244
|
G | T | 7 | a0001c0001t0005g0031a0001c0001t0005g0110a0001c0001t0005g0114others(4): Show | 8 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-131C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826244 | ||||||
chr22:43826357
|
A | T | 1 | a0001c0001t0004g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.743-244T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826357 | ||||||
chr22:43826465
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(86): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.743-352G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826465 | ||||||
chr22:43826487
|
T | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0037others(30): Show | 54 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.743-374A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826487 | ||||||
chr22:43826536
|
A | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.743-423T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826536 | ||||||
chr22:43826559
|
C | T | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.743-446G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826559 | ||||||
chr22:43826834
|
G | T | 1 | a0001c0001t0002g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.743-721C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826834 | ||||||
chr22:43826864
|
C | T | 4 | a0001c0001t0002g0042a0001c0001t0002g0230a0001c0001t0002g0232others(1): Show | 5 | HG02293.hp2 HG02738.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-751G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826864 | ||||||
chr22:43826927
|
A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(142): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.743-814T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826927 | ||||||
chr22:43826960
|
G | A | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.743-847C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826960 | ||||||
chr22:43827140
|
C | A | 2 | a0001c0001t0001g0171a0001c0001t0024g0170 | 2 | HG00597.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.743-1027G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827140 | ||||||
chr22:43827185
|
T | C | 5 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0015g0107others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-1072A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827185 | ||||||
chr22:43827186
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(76): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.743-1073A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827186 | ||||||
chr22:43827328
|
C | T | 5 | a0001c0001t0004g0011a0001c0001t0004g0094a0001c0001t0004g0095others(2): Show | 8 | HG02257.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-1215G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827328 | ||||||
chr22:43827335
|
T | C | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.743-1222A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827335 | ||||||
chr22:43827342
|
T | C | 1 | a0001c0001t0002g0250 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.743-1229A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827342 | ||||||
chr22:43827359
|
T | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0187a0001c0001t0001g0189others(1): Show | 5 | HG01255.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-1246A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827359 | ||||||
chr22:43827381
|
GAAAAATT others(39): Show |
G | 1 | a0001c0001t0023g0199 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.743-1314_743-1269d others(48): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827381 | ||||||
chr22:43827755
|
C | CCA | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(69): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.742+1303_742+1304d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | ||||||
chr22:43827755
|
C | CCACA | 71 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0001g0163others(68): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.742+1301_742+1304d others(6): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | ||||||
chr22:43827755
|
C | CCACACA | 56 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0240others(53): Show | 83 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.742+1299_742+1304d others(8): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | ||||||
chr22:43827755
|
C | CCACACAC others(1): Show |
16 | a0001c0001t0002g0218a0001c0001t0003g0016a0001c0001t0003g0026others(13): Show | 19 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+1297_742+1304d others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | ||||||
chr22:43827755
|
C | CCACACAC others(3): Show |
5 | a0001c0001t0003g0072a0001c0001t0003g0077a0001c0001t0003g0081others(2): Show | 5 | HG01081.hp1 HG01256.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+1295_742+1304d others(12): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | ||||||
chr22:43827755
|
C | CCACACAC others(5): Show |
1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.742+1293_742+1304d others(14): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | ||||||
chr22:43827810
|
G | C | 1 | a0001c0001t0014g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.742+1250C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827810 | ||||||
chr22:43828003
|
G | A | 12 | a0001c0001t0006g0133a0001c0001t0006g0136a0001c0001t0006g0137others(9): Show | 15 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.742+1057C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828003 | ||||||
chr22:43828144
|
C | T | 1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.742+916G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828144 | ||||||
chr22:43828191
|
G | A | 5 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(2): Show | 9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+869C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828191 | ||||||
chr22:43828366
|
G | A | 2 | a0001c0001t0016g0182a0001c0001t0016g0183 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.742+694C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828366 | ||||||
chr22:43828519
|
C | T | 5 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0015g0107others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+541G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828519 | ||||||
chr22:43828608
|
G | A | 1 | a0001c0001t0006g0034 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.742+452C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828608 | ||||||
chr22:43828631
|
C | A | 1 | a0001c0001t0002g0241 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.742+429G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828631 | ||||||
chr22:43828701
|
T | C | 2 | a0001c0001t0006g0008a0001c0001t0006g0138 | 6 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+359A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828701 | ||||||
chr22:43828845
|
C | T | 12 | a0001c0001t0006g0133a0001c0001t0006g0136a0001c0001t0006g0137others(9): Show | 15 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.742+215G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828845 | ||||||
chr22:43828862
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.742+198C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828862 | ||||||
chr22:43828976
|
C | G | 19 | a0001c0001t0004g0003a0001c0001t0004g0029a0001c0001t0004g0090others(16): Show | 33 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.742+84G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828976 | ||||||
chr22:43829037
|
G | A | 5 | a0001c0001t0006g0035a0001c0001t0006g0128a0001c0001t0006g0144others(2): Show | 6 | HG01433.hp2 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+23C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43829037 | ||||||
chr22:43829337
|
TTGTCCAG others(13): Show |
T | 1 | a0001c0001t0023g0199 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.604-159_604-140del others(20): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829337 | ||||||
chr22:43829580
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.604-382A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829580 | ||||||
chr22:43829764
|
A | G | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.604-566T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829764 | ||||||
chr22:43829914
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(205): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.604-716C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829914 | ||||||
chr22:43829919
|
A | C | 3 | a0001c0001t0006g0030a0001c0001t0006g0112a0001c0001t0006g0113 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-721T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829919 | ||||||
chr22:43829966
|
T | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.604-768A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829966 | ||||||
chr22:43829978
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(74): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.604-780C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829978 | ||||||
chr22:43829993
|
C | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(248): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.604-795G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829993 | ||||||
chr22:43830007
|
C | A | 1 | a0001c0001t0003g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.604-809G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830007 | ||||||
chr22:43830008
|
G | A | 63 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(60): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.604-810C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830008 | ||||||
chr22:43830346
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.604-1148C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830346 | ||||||
chr22:43830386
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.604-1188G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830386 | ||||||
chr22:43830552
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.604-1354C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830552 | ||||||
chr22:43830598
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.604-1400G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830598 | ||||||
chr22:43830722
|
G | C | 1 | a0001c0001t0002g0265 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.604-1524C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830722 | ||||||
chr22:43830768
|
C | T | 1 | a0001c0001t0028g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.604-1570G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830768 | ||||||
chr22:43830782
|
G | A | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.604-1584C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830782 | ||||||
chr22:43831010
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.604-1812G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831010 | ||||||
chr22:43831107
|
C | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.604-1909G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831107 | ||||||
chr22:43831126
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.604-1928G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831126 | ||||||
chr22:43831145
|
C | T | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.604-1947G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831145 | ||||||
chr22:43831181
|
AG | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(74): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.604-1984delC | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831181 | ||||||
chr22:43831186
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.604-1988C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831186 | ||||||
chr22:43831226
|
A | G | 1 | a0001c0001t0006g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.604-2028T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831226 | ||||||
chr22:43831252
|
T | C | 1 | a0001c0001t0004g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-2054A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831252 | ||||||
chr22:43831288
|
C | CGGCAGCT others(17): Show |
1 | a0001c0001t0002g0236 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.604-2091_604-2090i others(26): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831288 | ||||||
chr22:43831288
|
C | CGGCAGCT others(16): Show |
59 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(56): Show | 94 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.604-2113_604-2091d others(25): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831288 | ||||||
chr22:43831288
|
C | CGGCAGCT others(39): Show |
1 | a0001c0001t0002g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.604-2091_604-2090i others(48): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831288 | ||||||
chr22:43831468
|
T | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+2172A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831468 | ||||||
chr22:43831482
|
A | C | 3 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0004g0100 | 3 | HG01175.hp2 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.603+2158T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831482 | ||||||
chr22:43831493
|
C | T | 4 | a0001c0001t0003g0016a0001c0001t0003g0026a0001c0001t0003g0080others(1): Show | 7 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.603+2147G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831493 | ||||||
chr22:43831520
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+2120C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831520 | ||||||
chr22:43831564
|
G | A | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603+2076C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831564 | ||||||
chr22:43831589
|
C | T | 1 | a0001c0001t0006g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.603+2051G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831589 | ||||||
chr22:43831590
|
G | A | 2 | a0001c0001t0006g0128a0001c0001t0006g0145 | 2 | HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.603+2050C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831590 | ||||||
chr22:43831676
|
A | G | 118 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(115): Show | 179 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.603+1964T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831676 | ||||||
chr22:43831708
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0202 | 4 | HG00544.hp1 HG02132.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+1932G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831708 | ||||||
chr22:43831772
|
C | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0009g0027 | 12 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.603+1868G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831772 | ||||||
chr22:43831906
|
G | GAC | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+1732_603+1733d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831906 | ||||||
chr22:43831925
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.603+1715T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831925 | ||||||
chr22:43831996
|
C | T | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.603+1644G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831996 | ||||||
chr22:43832110
|
G | A | 3 | a0001c0001t0006g0035a0001c0001t0006g0145a0001c0001t0006g0146 | 4 | HG03209.hp2 HG06807.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+1530C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832110 | ||||||
chr22:43832131
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.603+1509C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832131 | ||||||
chr22:43832196
|
T | G | 2 | a0001c0001t0003g0022a0001c0001t0003g0050 | 3 | HG01109.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.603+1444A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832196 | ||||||
chr22:43832235
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.603+1405A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832235 | ||||||
chr22:43832304
|
C | T | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603+1336G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832304 | ||||||
chr22:43832321
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.603+1319G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832321 | ||||||
chr22:43832389
|
C | T | 3 | a0001c0001t0006g0030a0001c0001t0006g0112a0001c0001t0006g0113 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+1251G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832389 | ||||||
chr22:43832441
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.603+1199C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832441 | ||||||
chr22:43832447
|
G | C | 1 | a0001c0001t0005g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.603+1193C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832447 | ||||||
chr22:43832487
|
G | A | 59 | a0001c0001t0001g0179a0001c0001t0002g0002a0001c0001t0002g0007others(56): Show | 92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.603+1153C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832487 | ||||||
chr22:43832530
|
G | A | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.603+1110C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832530 | ||||||
chr22:43832567
|
C | T | 1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.603+1073G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832567 | ||||||
chr22:43832700
|
C | T | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.603+940G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832700 | ||||||
chr22:43832819
|
C | T | 1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.603+821G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832819 | ||||||
chr22:43832963
|
G | C | 63 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(60): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.603+677C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832963 | ||||||
chr22:43833034
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0167 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.603+606G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833034 | ||||||
chr22:43833081
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.603+559C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833081 | ||||||
chr22:43833272
|
C | A | 3 | a0001c0001t0006g0030a0001c0001t0006g0112a0001c0001t0006g0113 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+368G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833272 | ||||||
chr22:43833283
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.603+357G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833283 | ||||||
chr22:43833293
|
G | A | 1 | a0001c0001t0002g0246 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.603+347C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833293 | ||||||
chr22:43833332
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.603+308A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833332 | ||||||
chr22:43833352
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.603+288G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833352 | ||||||
chr22:43833612
|
G | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(247): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.603+28C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833612 | ||||||
chr22:43833613
|
G | A | 1 | a0001c0001t0023g0199 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.603+27C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833613 | ||||||
chr22:43833614
|
A | G | 1 | a0001c0001t0023g0199 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.603+26T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833614 | ||||||
chr22:43833626
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.603+14G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833626 | ||||||
chr22:43833628
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+12C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833628 | ||||||
chr22:43833765
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509-31G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43833765 | ||||||
chr22:43833846
|
G | A | 1 | a0001c0001t0002g0232 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.509-112C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43833846 | ||||||
chr22:43833913
|
G | A | 63 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(60): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.509-179C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43833913 | ||||||
chr22:43834002
|
G | A | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.509-268C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834002 | ||||||
chr22:43834025
|
C | T | 1 | a0001c0001t0002g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.509-291G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834025 | ||||||
chr22:43834249
|
A | G | 1 | a0001c0001t0006g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509-515T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834249 | ||||||
chr22:43834263
|
G | T | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(64): Show | 96 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.509-529C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834263 | ||||||
chr22:43834285
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-551C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834285 | ||||||
chr22:43834292
|
TGCTTCCC others(49): Show |
T | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.509-614_509-559del others(56): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834292 | ||||||
chr22:43834303
|
CCCCCACC others(20): Show |
C | 1 | a0001c0001t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-596_509-570del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834303 | ||||||
chr22:43834310
|
C | T | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.509-576G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834310 | ||||||
chr22:43834320
|
TGCTTCCC others(21): Show |
T | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(78): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.509-614_509-587del others(28): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834320 | ||||||
chr22:43834331
|
CCCCCACC others(20): Show |
C | 1 | a0001c0001t0001g0180 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.509-624_509-598del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834331 | ||||||
chr22:43834334
|
CCACCGCG others(497): Show |
C | 57 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(54): Show | 82 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.509-1104_509-601de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834334 | ||||||
chr22:43834342
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-608C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834342 | ||||||
chr22:43834343
|
CCCTGAGC others(20): Show |
C | 1 | a0001c0001t0001g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.509-636_509-610del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834343 | ||||||
chr22:43834348
|
A | T | 1 | a0001c0001t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-614T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834348 | ||||||
chr22:43834348
|
AGCTTCCC others(525): Show |
A | 2 | a0001c0001t0003g0026a0001c0001t0006g0133 | 3 | HG00099.hp1 HG01496.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.509-1146_509-615de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834348 | ||||||
chr22:43834356
|
G | A | 2 | a0001c0001t0003g0070a0001c0001t0022g0088 | 2 | HG02486.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.509-622C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834356 | ||||||
chr22:43834362
|
CCACCGCG others(357): Show |
C | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-992_509-629del | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834362 | ||||||
chr22:43834362
|
CCACCGCG others(637): Show |
C | 1 | a0001c0001t0003g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.509-1272_509-629de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834362 | ||||||
chr22:43834369
|
GGCCCTGA others(441): Show |
G | 1 | a0001c0001t0005g0089 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.509-1083_509-636de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834369 | ||||||
chr22:43834370
|
G | T | 5 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-636C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834370 | ||||||
chr22:43834376
|
A | T | 5 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-642T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834376 | ||||||
chr22:43834397
|
T | G | 5 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-663A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834397 | ||||||
chr22:43834398
|
G | T | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-664C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834398 | ||||||
chr22:43834404
|
A | T | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-670T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834404 | ||||||
chr22:43834411
|
C | G | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-677G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834411 | ||||||
chr22:43834411
|
C | T | 60 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(57): Show | 95 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.509-677G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834411 | ||||||
chr22:43834414
|
A | G | 5 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-680T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834414 | ||||||
chr22:43834415
|
G | C | 5 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-681C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834415 | ||||||
chr22:43834418
|
A | C | 5 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-684T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834418 | ||||||
chr22:43834426
|
G | T | 5 | a0001c0001t0001g0150a0001c0001t0008g0012a0001c0001t0008g0132others(2): Show | 8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-692C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834426 | ||||||
chr22:43834453
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.509-719C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834453 | ||||||
chr22:43834454
|
T | G | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-720A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834454 | ||||||
chr22:43834468
|
GCGCCCCC others(21): Show |
G | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(107): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.509-762_509-735del others(28): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834468 | ||||||
chr22:43834471
|
CCCCCACC others(20): Show |
C | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-764_509-738del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834471 | ||||||
chr22:43834474
|
CCACCGCG others(77): Show |
C | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-824_509-741del others(84): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834474 | ||||||
chr22:43834482
|
G | T | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-748C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834482 | ||||||
chr22:43834488
|
A | T | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-754T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834488 | ||||||
chr22:43834488
|
AGCTTCCC others(385): Show |
A | 31 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(28): Show | 47 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.509-1146_509-755de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834488 | ||||||
chr22:43834488
|
AGCTTCCC others(413): Show |
A | 6 | a0001c0001t0002g0237a0001c0001t0002g0267a0001c0001t0008g0012others(3): Show | 9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-1174_509-755de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834488 | ||||||
chr22:43834496
|
A | G | 4 | a0001c0001t0002g0223a0001c0001t0002g0234a0001c0001t0004g0099others(1): Show | 4 | HG01192.hp2 HG02486.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-762T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834496 | ||||||
chr22:43834496
|
ACGCCCCC others(273): Show |
A | 21 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(18): Show | 35 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.509-1042_509-763de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834496 | ||||||
chr22:43834499
|
CCCCCACC others(384): Show |
C | 2 | a0001c0001t0002g0223a0001c0001t0002g0234 | 2 | HG02738.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.509-1156_509-766de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834499 | ||||||
chr22:43834502
|
CCACCGCG others(329): Show |
C | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-1104_509-769de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834502 | ||||||
chr22:43834516
|
AGCTTCCC others(385): Show |
A | 33 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(30): Show | 45 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.509-1174_509-783de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834516 | ||||||
chr22:43834527
|
CCCCCACC others(272): Show |
C | 1 | a0001c0001t0004g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.509-1072_509-794de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834527 | ||||||
chr22:43834583
|
CCCCCACC others(48): Show |
C | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-904_509-850del others(55): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834583 | ||||||
chr22:43834600
|
TGCTTCCC others(49): Show |
T | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(72): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.509-922_509-867del others(56): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834600 | ||||||
chr22:43834600
|
TGCTTCCC others(245): Show |
T | 5 | a0001c0001t0006g0008a0001c0001t0006g0138a0001c0001t0006g0147others(2): Show | 9 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-1118_509-867de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834600 | ||||||
chr22:43834600
|
TGCTTCCC others(329): Show |
T | 2 | a0001c0001t0006g0127a0001c0001t0006g0139 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.509-1202_509-867de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834600 | ||||||
chr22:43834611
|
CCCCCACC others(48): Show |
C | 2 | a0001c0001t0001g0162a0001c0001t0001g0175 | 2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.509-932_509-878del others(55): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834611 | ||||||
chr22:43834622
|
T | G | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-888A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834622 | ||||||
chr22:43834628
|
T | A | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-894A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834628 | ||||||
chr22:43834628
|
TGCTTCCC others(21): Show |
T | 1 | a0001c0001t0010g0143 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.509-922_509-895del others(28): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834628 | ||||||
chr22:43834650
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-916C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834650 | ||||||
chr22:43834656
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-922T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834656 | ||||||
chr22:43834705
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.509-971A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834705 | ||||||
chr22:43834719
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-985G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834719 | ||||||
chr22:43834723
|
C | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(74): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.509-989G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834723 | ||||||
chr22:43834734
|
T | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(91): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.509-1000A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834734 | ||||||
chr22:43834758
|
C | T | 1 | a0001c0001t0005g0032 | 2 | HG01074.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.509-1024G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834758 | ||||||
chr22:43834762
|
T | G | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-1028A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834762 | ||||||
chr22:43834796
|
AGCTTCCC others(105): Show |
A | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-1174_509-1063d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834796 | ||||||
chr22:43834832
|
G | A | 1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509-1098C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834832 | ||||||
chr22:43834838
|
ACACCGCG others(245): Show |
A | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-1356_509-1105d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834838 | ||||||
chr22:43834845
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.509-1111C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834845 | ||||||
chr22:43834860
|
G | A | 52 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(49): Show | 77 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.509-1126C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834860 | ||||||
chr22:43834874
|
T | G | 6 | a0001c0001t0006g0008a0001c0001t0006g0138a0001c0001t0006g0147others(3): Show | 10 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1140A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834874 | ||||||
chr22:43834880
|
T | A | 6 | a0001c0001t0006g0008a0001c0001t0006g0138a0001c0001t0006g0147others(3): Show | 10 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1146A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834880 | ||||||
chr22:43834880
|
TGCTTCCC others(49): Show |
T | 1 | a0001c0001t0001g0165 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.509-1202_509-1147d others(58): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834880 | ||||||
chr22:43834888
|
G | A | 1 | a0001c0001t0003g0026 | 2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.509-1154C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834888 | ||||||
chr22:43834894
|
CCACCGCG others(105): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.509-1272_509-1161d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834894 | ||||||
chr22:43834900
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0003g0063 | 3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.509-1166G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834900 | ||||||
chr22:43834902
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(152): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.509-1168A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834902 | ||||||
chr22:43834908
|
T | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(152): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.509-1174A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834908 | ||||||
chr22:43834908
|
TGCTTCCC others(21): Show |
T | 39 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(36): Show | 59 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.509-1202_509-1175d others(30): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834908 | ||||||
chr22:43834930
|
G | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(134): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.509-1196C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834930 | ||||||
chr22:43834936
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(134): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.509-1202T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834936 | ||||||
chr22:43834943
|
C | T | 3 | a0001c0001t0003g0015a0001c0001t0003g0059a0001c0001t0003g0075 | 5 | HG00323.hp2 HG01081.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1209G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834943 | ||||||
chr22:43834945
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.509-1211G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834945 | ||||||
chr22:43835002
|
A | G | 1 | a0001c0001t0002g0237 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.509-1268T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835002 | ||||||
chr22:43835003
|
C | G | 60 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(57): Show | 86 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.509-1269G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835003 | ||||||
chr22:43835006
|
A | C | 2 | a0001c0001t0002g0237a0001c0001t0006g0106 | 2 | HG03041.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.509-1272T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835006 | ||||||
chr22:43835006
|
ACACCGCG others(77): Show |
A | 60 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(57): Show | 86 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.509-1356_509-1273d others(86): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835006 | ||||||
chr22:43835014
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.509-1280C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835014 | ||||||
chr22:43835020
|
T | A | 5 | a0001c0001t0001g0174a0001c0001t0008g0012a0001c0001t0008g0132others(2): Show | 8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-1286A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835020 | ||||||
chr22:43835042
|
T | G | 5 | a0001c0001t0003g0070a0001c0001t0008g0012a0001c0001t0008g0132others(2): Show | 8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-1308A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835042 | ||||||
chr22:43835048
|
T | A | 5 | a0001c0001t0003g0070a0001c0001t0008g0012a0001c0001t0008g0132others(2): Show | 8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-1314A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835048 | ||||||
chr22:43835051
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0036others(41): Show | 55 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.509-1317A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835051 | ||||||
chr22:43835069
|
G | T | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1335C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835069 | ||||||
chr22:43835069
|
GGCCCTGA others(21): Show |
G | 1 | a0001c0001t0004g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509-1363_509-1336d others(30): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835069 | ||||||
chr22:43835086
|
G | A | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1352C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835086 | ||||||
chr22:43835087
|
C | G | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1353G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835087 | ||||||
chr22:43835090
|
C | A | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1356G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835090 | ||||||
chr22:43835115
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.509-1381C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835115 | ||||||
chr22:43835118
|
ACACCGCA others(21): Show |
A | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.509-1412_509-1385d others(30): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835118 | ||||||
chr22:43835152
|
C | G | 3 | a0001c0001t0002g0018a0001c0001t0002g0246a0001c0001t0002g0258 | 5 | NA18612.hp1 NA18952.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1418G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835152 | ||||||
chr22:43835443
|
A | G | 7 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(4): Show | 11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-1709T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835443 | ||||||
chr22:43835505
|
C | T | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-1771G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835505 | ||||||
chr22:43835929
|
G | A | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.509-2195C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835929 | ||||||
chr22:43835963
|
C | T | 1 | a0001c0001t0006g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509-2229G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835963 | ||||||
chr22:43836068
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.509-2334G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836068 | ||||||
chr22:43836089
|
C | T | 2 | a0001c0001t0003g0024a0001c0001t0003g0060 | 3 | HG03688.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.509-2355G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836089 | ||||||
chr22:43836133
|
C | T | 2 | a0001c0001t0006g0127a0001c0001t0006g0139 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.509-2399G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836133 | ||||||
chr22:43836136
|
T | C | 66 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(63): Show | 95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.509-2402A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836136 | ||||||
chr22:43836153
|
CACTGCAG others(119): Show |
C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.509-2545_509-2420d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836153 | ||||||
chr22:43836159
|
A | G | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2425T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836159 | ||||||
chr22:43836173
|
C | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(183): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.509-2439G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836173 | ||||||
chr22:43836178
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(183): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.509-2444A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836178 | ||||||
chr22:43836194
|
C | A | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2460G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836194 | ||||||
chr22:43836195
|
G | A | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.509-2461C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836195 | ||||||
chr22:43836195
|
G | C | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2461C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836195 | ||||||
chr22:43836222
|
C | T | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2488G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836222 | ||||||
chr22:43836257
|
G | C | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2523C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836257 | ||||||
chr22:43836285
|
A | G | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.509-2551T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836285 | ||||||
chr22:43836341
|
C | T | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2526G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836341 | ||||||
chr22:43836349
|
A | T | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.508+2518T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836349 | ||||||
chr22:43836383
|
C | G | 13 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(10): Show | 16 | HG01069.hp1 HG01175.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+2484G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836383 | ||||||
chr22:43836388
|
T | C | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2479A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836388 | ||||||
chr22:43836397
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0036others(42): Show | 56 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.508+2470G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836397 | ||||||
chr22:43836404
|
A | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.508+2463T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836404 | ||||||
chr22:43836405
|
C | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.508+2462G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836405 | ||||||
chr22:43836413
|
G | A | 1 | a0001c0001t0006g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.508+2454C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836413 | ||||||
chr22:43836425
|
C | T | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2442G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836425 | ||||||
chr22:43836440
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.508+2427C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836440 | ||||||
chr22:43836446
|
A | C | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2421T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836446 | ||||||
chr22:43836447
|
C | A | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2420G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836447 | ||||||
chr22:43836467
|
T | C | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2400A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836467 | ||||||
chr22:43836488
|
C | A | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2379G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836488 | ||||||
chr22:43836489
|
A | C | 11 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(8): Show | 14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2378T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836489 | ||||||
chr22:43836514
|
CCTACACA others(77): Show |
C | 66 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(63): Show | 95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.508+2269_508+2352d others(86): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836514 | ||||||
chr22:43836613
|
C | G | 66 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(63): Show | 95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.508+2254G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836613 | ||||||
chr22:43836635
|
T | G | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(64): Show | 96 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.508+2232A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836635 | ||||||
chr22:43836800
|
A | T | 6 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0012others(3): Show | 9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+2067T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836800 | ||||||
chr22:43836854
|
G | A | 2 | a0001c0001t0003g0062a0001c0001t0003g0074 | 2 | HG01109.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.508+2013C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836854 | ||||||
chr22:43837007
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(176): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.508+1860C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837007 | ||||||
chr22:43837164
|
T | G | 16 | a0001c0001t0005g0031a0001c0001t0005g0110a0001c0001t0005g0114others(13): Show | 18 | HG01069.hp1 HG01175.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.508+1703A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837164 | ||||||
chr22:43837169
|
G | A | 1 | a0001c0001t0006g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.508+1698C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837169 | ||||||
chr22:43837200
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.508+1667C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837200 | ||||||
chr22:43837495
|
G | C | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.508+1372C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837495 | ||||||
chr22:43837546
|
A | G | 30 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(27): Show | 50 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.508+1321T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837546 | ||||||
chr22:43837560
|
G | C | 1 | a0001c0001t0002g0246 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.508+1307C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837560 | ||||||
chr22:43838143
|
C | T | 1 | a0001c0001t0008g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508+724G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838143 | ||||||
chr22:43838159
|
G | A | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.508+708C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838159 | ||||||
chr22:43838167
|
G | A | 8 | a0001c0001t0006g0008a0001c0001t0006g0112a0001c0001t0006g0127others(5): Show | 12 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.508+700C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838167 | ||||||
chr22:43838203
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(262): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.508+664T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838203 | ||||||
chr22:43838265
|
C | T | 1 | a0001c0001t0006g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.508+602G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838265 | ||||||
chr22:43838406
|
G | A | 1 | a0001c0001t0006g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.508+461C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838406 | ||||||
chr22:43838446
|
G | C | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+421C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838446 | ||||||
chr22:43838504
|
T | C | 2 | a0001c0001t0003g0022a0001c0001t0003g0050 | 3 | HG01109.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.508+363A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838504 | ||||||
chr22:43838619
|
G | A | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508+248C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838619 | ||||||
chr22:43838848
|
G | T | 1 | a0001c0001t0002g0043 | 2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.508+19C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838848 | ||||||
chr22:43839053
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.382-60G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839053 | ||||||
chr22:43839106
|
G | C | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-113C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839106 | ||||||
chr22:43839321
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-328G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839321 | ||||||
chr22:43839566
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.381+379G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839566 | ||||||
chr22:43839815
|
G | A | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.381+130C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839815 | ||||||
chr22:43839895
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.381+50G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839895 | ||||||
chr22:43840123
|
G | C | 1 | a0001c0001t0005g0121 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.301-98C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840123 | ||||||
chr22:43840125
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.301-100C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840125 | ||||||
chr22:43840159
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.301-134C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840159 | ||||||
chr22:43840261
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-236C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840261 | ||||||
chr22:43840288
|
G | A | 7 | a0001c0001t0001g0036a0001c0001t0001g0156a0001c0001t0001g0162others(4): Show | 8 | NA18940.hp1 NA18950.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-263C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840288 | ||||||
chr22:43840382
|
G | A | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.301-357C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840382 | ||||||
chr22:43840527
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.301-502C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840527 | ||||||
chr22:43840540
|
G | T | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.301-515C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840540 | ||||||
chr22:43840561
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.301-536C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840561 | ||||||
chr22:43840580
|
G | A | 4 | a0001c0001t0003g0016a0001c0001t0003g0026a0001c0001t0003g0080others(1): Show | 7 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-555C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840580 | ||||||
chr22:43840601
|
G | A | 6 | a0001c0001t0006g0133a0001c0001t0006g0136a0001c0001t0006g0137others(3): Show | 9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-576C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840601 | ||||||
chr22:43840753
|
C | G | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-728G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840753 | ||||||
chr22:43840805
|
C | T | 2 | a0001c0001t0003g0022a0001c0001t0003g0050 | 3 | HG01109.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.301-780G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840805 | ||||||
chr22:43840920
|
GC | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0037others(29): Show | 53 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.300+881delG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840920 | ||||||
chr22:43840936
|
G | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.300+866C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840936 | ||||||
chr22:43840984
|
C | T | 67 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(64): Show | 102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.300+818G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840984 | ||||||
chr22:43841029
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.300+773T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841029 | ||||||
chr22:43841084
|
C | T | 5 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0015g0107others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+718G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841084 | ||||||
chr22:43841101
|
C | A | 1 | a0001c0001t0005g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.300+701G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841101 | ||||||
chr22:43841102
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.300+700C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841102 | ||||||
chr22:43841160
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.300+642C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841160 | ||||||
chr22:43841371
|
C | T | 1 | a0001c0001t0002g0257 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.300+431G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841371 | ||||||
chr22:43841447
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.300+355A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841447 | ||||||
chr22:43841522
|
C | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.300+280G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841522 | ||||||
chr22:43841580
|
C | T | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.300+222G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841580 | ||||||
chr22:43841752
|
T | C | 1 | a0001c0001t0011g0047 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.300+50A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841752 | ||||||
chr22:43842218
|
G | A | 5 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(2): Show | 9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-286C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842218 | ||||||
chr22:43842290
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.170-358C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842290 | ||||||
chr22:43842296
|
A | T | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-364T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842296 | ||||||
chr22:43842386
|
G | A | 10 | a0001c0001t0005g0031a0001c0001t0005g0110a0001c0001t0005g0114others(7): Show | 12 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-454C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842386 | ||||||
chr22:43842416
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-484G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842416 | ||||||
chr22:43842425
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | NA18974.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.170-493C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842425 | ||||||
chr22:43842443
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0192a0001c0001t0001g0205 | 4 | HG00099.hp2 HG00140.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-511A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842443 | ||||||
chr22:43842525
|
T | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(131): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.170-593A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842525 | ||||||
chr22:43842568
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.170-636G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842568 | ||||||
chr22:43842641
|
C | A | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-709G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842641 | ||||||
chr22:43842924
|
G | C | 1 | a0001c0001t0004g0092 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.170-992C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842924 | ||||||
chr22:43842948
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.170-1016G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842948 | ||||||
chr22:43842975
|
A | ATC | 56 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0037others(53): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.170-1045_170-1044d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTC | 60 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0039others(57): Show | 74 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.170-1047_170-1044d others(6): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTC | 19 | a0001c0001t0001g0036a0001c0001t0001g0162a0001c0001t0001g0177others(16): Show | 29 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-1049_170-1044d others(8): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(1): Show |
20 | a0001c0001t0002g0229a0001c0001t0003g0006a0001c0001t0003g0023others(17): Show | 28 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.170-1051_170-1044d others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(3): Show |
4 | a0001c0001t0003g0064a0001c0001t0003g0082a0001c0001t0009g0086others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-1053_170-1044d others(12): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(5): Show |
36 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0015others(33): Show | 56 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.170-1055_170-1044d others(14): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(7): Show |
3 | a0001c0001t0003g0058a0001c0001t0003g0080a0001c0001t0018g0044 | 3 | HG02738.hp1 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.170-1057_170-1044d others(16): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(9): Show |
2 | a0001c0001t0003g0061a0001c0001t0012g0069 | 2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.170-1059_170-1044d others(18): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(11): Show |
2 | a0001c0001t0003g0049a0001c0001t0003g0056 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.170-1061_170-1044d others(20): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43842975
|
A | ATCTCTCT others(13): Show |
1 | a0001c0001t0003g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.170-1063_170-1044d others(22): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | ||||||
chr22:43843094
|
G | A | 1 | a0001c0001t0005g0033 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.170-1162C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843094 | ||||||
chr22:43843177
|
G | A | 7 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(4): Show | 11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-1245C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843177 | ||||||
chr22:43843197
|
T | C | 1 | a0001c0001t0013g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.170-1265A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843197 | ||||||
chr22:43843212
|
C | T | 1 | a0002c0002t0020g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.170-1280G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843212 | ||||||
chr22:43843311
|
A | G | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.170-1379T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843311 | ||||||
chr22:43843316
|
A | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-1384T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843316 | ||||||
chr22:43843415
|
C | A | 1 | a0001c0001t0005g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.170-1483G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843415 | ||||||
chr22:43843619
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(248): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.170-1687A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843619 | ||||||
chr22:43843690
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.170-1758C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843690 | ||||||
chr22:43843721
|
C | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0156a0001c0001t0001g0162others(4): Show | 8 | NA18940.hp1 NA18950.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-1789G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843721 | ||||||
chr22:43843870
|
G | T | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-1938C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843870 | ||||||
chr22:43843982
|
G | A | 2 | a0001c0001t0004g0093a0001c0001t0004g0101 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.170-2050C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843982 | ||||||
chr22:43844188
|
T | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0184 | 2 | NA18940.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.170-2256A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844188 | ||||||
chr22:43844282
|
T | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0015others(52): Show | 79 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.170-2350A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844282 | ||||||
chr22:43844334
|
G | A | 2 | a0001c0001t0004g0011a0001c0001t0004g0102 | 5 | HG02257.hp1 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-2402C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844334 | ||||||
chr22:43844342
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.170-2410G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844342 | ||||||
chr22:43844425
|
G | C | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-2493C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844425 | ||||||
chr22:43844547
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.170-2615T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844547 | ||||||
chr22:43844685
|
C | T | 2 | a0001c0001t0006g0008a0001c0001t0006g0138 | 6 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-2753G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844685 | ||||||
chr22:43844805
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(248): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.170-2873G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844805 | ||||||
chr22:43844831
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.170-2899G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844831 | ||||||
chr22:43844832
|
G | A | 1 | a0001c0001t0006g0133 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.170-2900C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844832 | ||||||
chr22:43844879
|
A | G | 2 | a0001c0001t0003g0067a0001c0001t0003g0068 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.170-2947T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844879 | ||||||
chr22:43844983
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-3051G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844983 | ||||||
chr22:43845095
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(262): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.170-3163A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845095 | ||||||
chr22:43845230
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.170-3298C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845230 | ||||||
chr22:43845396
|
T | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-3464A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845396 | ||||||
chr22:43845405
|
C | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0036others(43): Show | 57 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.170-3473G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845405 | ||||||
chr22:43845509
|
G | A | 7 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(4): Show | 11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-3577C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845509 | ||||||
chr22:43845521
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-3589C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845521 | ||||||
chr22:43845550
|
CT | C | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-3619delA | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845550 | ||||||
chr22:43845562
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0036others(43): Show | 57 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.170-3630C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845562 | ||||||
chr22:43845599
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.170-3667G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845599 | ||||||
chr22:43845646
|
G | T | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-3714C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845646 | ||||||
chr22:43845689
|
G | A | 1 | a0001c0001t0003g0054 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-3757C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845689 | ||||||
chr22:43845693
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-3761G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845693 | ||||||
chr22:43845694
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.170-3762C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845694 | ||||||
chr22:43845719
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.170-3787C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845719 | ||||||
chr22:43845759
|
A | G | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.170-3827T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845759 | ||||||
chr22:43845780
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0003g0063 | 3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.170-3848A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845780 | ||||||
chr22:43845938
|
C | T | 14 | a0001c0001t0005g0031a0001c0001t0005g0104a0001c0001t0005g0110others(11): Show | 16 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-4006G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845938 | ||||||
chr22:43846187
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(248): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.170-4255G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846187 | ||||||
chr22:43846222
|
C | T | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-4290G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846222 | ||||||
chr22:43846311
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.170-4379G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846311 | ||||||
chr22:43846396
|
G | T | 1 | a0001c0001t0004g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.170-4464C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846396 | ||||||
chr22:43846807
|
G | C | 4 | a0001c0001t0008g0012a0001c0001t0008g0132a0001c0001t0008g0134others(1): Show | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-4875C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846807 | ||||||
chr22:43847212
|
C | T | 1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.170-5280G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847212 | ||||||
chr22:43847590
|
T | C | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-5658A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847590 | ||||||
chr22:43847704
|
G | A | 2 | a0001c0001t0003g0053a0001c0001t0003g0054 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.170-5772C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847704 | ||||||
chr22:43847799
|
G | A | 5 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0001t0015g0107others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-5867C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847799 | ||||||
chr22:43847809
|
G | A | 7 | a0001c0001t0006g0133a0001c0001t0006g0136a0001c0001t0006g0137others(4): Show | 10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-5877C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847809 | ||||||
chr22:43847894
|
C | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(233): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.170-5962G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847894 | ||||||
chr22:43848119
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(74): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.170-6187C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848119 | ||||||
chr22:43848149
|
C | T | 1 | a0001c0001t0022g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.170-6217G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848149 | ||||||
chr22:43848226
|
A | G | 49 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(46): Show | 74 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.170-6294T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848226 | ||||||
chr22:43848253
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.170-6321C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848253 | ||||||
chr22:43848403
|
C | G | 1 | a0001c0001t0002g0040 | 2 | NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.170-6471G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848403 | ||||||
chr22:43848422
|
C | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(233): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.170-6490G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848422 | ||||||
chr22:43848580
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.170-6648G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848580 | ||||||
chr22:43848719
|
G | A | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-6787C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848719 | ||||||
chr22:43848741
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(248): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.170-6809T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848741 | ||||||
chr22:43849106
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-7174G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849106 | ||||||
chr22:43849107
|
C | T | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-7175G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849107 | ||||||
chr22:43849129
|
G | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-7197C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849129 | ||||||
chr22:43849201
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(232): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.170-7269A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849201 | ||||||
chr22:43849258
|
T | A | 1 | a0001c0001t0008g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.170-7326A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849258 | ||||||
chr22:43849299
|
G | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(249): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.170-7367C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849299 | ||||||
chr22:43849314
|
G | A | 2 | a0001c0001t0006g0127a0001c0001t0006g0139 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.170-7382C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849314 | ||||||
chr22:43849391
|
G | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(50): Show | 79 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.170-7459C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849391 | ||||||
chr22:43849509
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.170-7577G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849509 | ||||||
chr22:43849545
|
G | A | 1 | a0001c0001t0002g0246 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.170-7613C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849545 | ||||||
chr22:43849837
|
C | T | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-7905G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849837 | ||||||
chr22:43850227
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-8295T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850227 | ||||||
chr22:43850252
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-8320G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850252 | ||||||
chr22:43850562
|
C | T | 7 | a0001c0001t0006g0133a0001c0001t0006g0136a0001c0001t0006g0137others(4): Show | 10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-8630G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850562 | ||||||
chr22:43850596
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(262): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.170-8664A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850596 | ||||||
chr22:43850860
|
C | T | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.170-8928G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850860 | ||||||
chr22:43850877
|
C | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-8945G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850877 | ||||||
chr22:43850989
|
T | C | 2 | a0001c0001t0002g0256a0001c0001t0002g0260 | 2 | HG02135.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.170-9057A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850989 | ||||||
chr22:43851205
|
G | T | 7 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(4): Show | 11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-9273C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851205 | ||||||
chr22:43851208
|
G | C | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-9276C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851208 | ||||||
chr22:43851494
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.170-9562C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851494 | ||||||
chr22:43851624
|
G | A | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-9692C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851624 | ||||||
chr22:43851900
|
A | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-9968T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851900 | ||||||
chr22:43851905
|
T | C | 2 | a0001c0001t0009g0086a0001c0001t0009g0087 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.170-9973A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851905 | ||||||
chr22:43851908
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-9976C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851908 | ||||||
chr22:43851988
|
C | T | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.170-10056G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851988 | ||||||
chr22:43852137
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.169+10077G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852137 | ||||||
chr22:43852345
|
G | T | 1 | a0001c0001t0003g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.169+9869C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852345 | ||||||
chr22:43852348
|
G | GT | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(127): Show | 191 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.169+9865dupA | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852348 | ||||||
chr22:43852348
|
G | GTT | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0210others(6): Show | 14 | HG00280.hp1 HG00280.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+9864_169+9865d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852348 | ||||||
chr22:43852351
|
T | G | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.169+9863A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852351 | ||||||
chr22:43852391
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.169+9823G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852391 | ||||||
chr22:43852406
|
A | C | 1 | a0001c0001t0006g0133 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169+9808T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852406 | ||||||
chr22:43852597
|
C | T | 5 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(2): Show | 9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+9617G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852597 | ||||||
chr22:43852624
|
G | A | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+9590C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852624 | ||||||
chr22:43852637
|
C | T | 2 | a0001c0001t0002g0229a0001c0001t0002g0230 | 2 | NA19004.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.169+9577G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852637 | ||||||
chr22:43852663
|
T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 8 | HG02040.hp1 HG02071.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+9551A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852663 | ||||||
chr22:43852721
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(59): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+9493G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852721 | ||||||
chr22:43852747
|
G | C | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+9467C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852747 | ||||||
chr22:43852760
|
C | T | 2 | a0001c0001t0003g0024a0001c0001t0003g0060 | 3 | HG03688.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.169+9454G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852760 | ||||||
chr22:43852996
|
G | T | 2 | a0001c0001t0002g0224a0001c0001t0002g0255 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.169+9218C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852996 | ||||||
chr22:43852999
|
C | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0266a0001c0001t0002g0267 | 8 | HG00280.hp1 HG01261.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+9215G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852999 | ||||||
chr22:43853140
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.169+9074A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853140 | ||||||
chr22:43853222
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0003g0063 | 3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.169+8992G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853222 | ||||||
chr22:43853389
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+8825C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853389 | ||||||
chr22:43853397
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.169+8817C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853397 | ||||||
chr22:43853402
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.169+8812C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853402 | ||||||
chr22:43853477
|
C | T | 1 | a0001c0001t0005g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.169+8737G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853477 | ||||||
chr22:43853500
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169+8714G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853500 | ||||||
chr22:43853583
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+8631G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853583 | ||||||
chr22:43853593
|
C | G | 1 | a0001c0001t0005g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+8621G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853593 | ||||||
chr22:43853597
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+8617C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853597 | ||||||
chr22:43853819
|
A | C | 2 | a0001c0001t0003g0023a0001c0001t0003g0063 | 3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.169+8395T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853819 | ||||||
chr22:43853898
|
G | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+8316C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853898 | ||||||
chr22:43853971
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.169+8243C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853971 | ||||||
chr22:43853975
|
A | AG | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+8238dupC | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853975 | ||||||
chr22:43854021
|
G | A | 2 | a0001c0001t0014g0130a0001c0001t0014g0131 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169+8193C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854021 | ||||||
chr22:43854024
|
C | T | 1 | a0001c0001t0003g0062 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.169+8190G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854024 | ||||||
chr22:43854025
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(76): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.169+8189C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854025 | ||||||
chr22:43854129
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169+8085G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854129 | ||||||
chr22:43854138
|
A | G | 1 | a0001c0001t0006g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.169+8076T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854138 | ||||||
chr22:43854187
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+8027G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854187 | ||||||
chr22:43854267
|
C | T | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.169+7947G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854267 | ||||||
chr22:43854274
|
C | A | 2 | a0001c0001t0005g0114a0001c0001t0010g0143 | 2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169+7940G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854274 | ||||||
chr22:43854381
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(74): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.169+7833G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854381 | ||||||
chr22:43854616
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169+7598G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854616 | ||||||
chr22:43854641
|
G | A | 1 | a0001c0001t0002g0043 | 2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.169+7573C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854641 | ||||||
chr22:43854690
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(192): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.169+7524T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854690 | ||||||
chr22:43854750
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(75): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+7464G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854750 | ||||||
chr22:43854789
|
C | T | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.169+7425G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854789 | ||||||
chr22:43854801
|
C | T | 1 | a0001c0001t0017g0194 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.169+7413G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854801 | ||||||
chr22:43854939
|
G | A | 2 | a0001c0001t0016g0182a0001c0001t0016g0183 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.169+7275C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854939 | ||||||
chr22:43855073
|
G | T | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.169+7141C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855073 | ||||||
chr22:43855269
|
C | G | 12 | a0001c0001t0005g0031a0001c0001t0005g0110a0001c0001t0005g0114others(9): Show | 14 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+6945G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855269 | ||||||
chr22:43855309
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0036others(42): Show | 56 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.169+6905C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855309 | ||||||
chr22:43855446
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(59): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+6768C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855446 | ||||||
chr22:43855613
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(59): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+6601C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855613 | ||||||
chr22:43855711
|
T | A | 1 | a0001c0001t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.169+6503A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855711 | ||||||
chr22:43855711
|
T | G | 1 | a0001c0001t0009g0028 | 2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.169+6503A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855711 | ||||||
chr22:43855735
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.169+6479C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855735 | ||||||
chr22:43855768
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+6446G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855768 | ||||||
chr22:43855795
|
GC | G | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+6418delG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855795 | ||||||
chr22:43855802
|
C | T | 7 | a0001c0001t0006g0133a0001c0001t0006g0136a0001c0001t0006g0137others(4): Show | 10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+6412G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855802 | ||||||
chr22:43855911
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.169+6303G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855911 | ||||||
chr22:43855972
|
T | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+6242A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855972 | ||||||
chr22:43856090
|
A | C | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+6124T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856090 | ||||||
chr22:43856155
|
T | C | 1 | a0001c0001t0002g0250 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.169+6059A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856155 | ||||||
chr22:43856184
|
T | C | 1 | a0001c0001t0005g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+6030A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856184 | ||||||
chr22:43856253
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.169+5961G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856253 | ||||||
chr22:43856266
|
G | GAAGA | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5944_169+5947d others(6): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856266 | ||||||
chr22:43856319
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.169+5895A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856319 | ||||||
chr22:43856522
|
A | C | 1 | a0001c0001t0008g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.169+5692T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856522 | ||||||
chr22:43856553
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.169+5661G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856553 | ||||||
chr22:43856594
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169+5620C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856594 | ||||||
chr22:43856683
|
C | A | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169+5531G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856683 | ||||||
chr22:43856797
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169+5417C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856797 | ||||||
chr22:43856945
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+5269G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856945 | ||||||
chr22:43857016
|
C | CTGATTA | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5192_169+5197d others(8): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857016 | ||||||
chr22:43857033
|
G | C | 1 | a0001c0001t0002g0043 | 2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.169+5181C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857033 | ||||||
chr22:43857209
|
C | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+5005G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857209 | ||||||
chr22:43857210
|
G | A | 2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.169+5004C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857210 | ||||||
chr22:43857234
|
G | A | 1 | a0001c0001t0005g0125 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.169+4980C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857234 | ||||||
chr22:43857370
|
CA | C | 30 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(27): Show | 37 | HG00597.hp2 HG00741.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.169+4843delT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857370 | ||||||
chr22:43857370
|
CAA | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(151): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.169+4842_169+4843d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857370 | ||||||
chr22:43857370
|
CAAA | C | 67 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0002g0224others(64): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.169+4841_169+4843d others(5): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857370 | ||||||
chr22:43857788
|
G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+4426C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857788 | ||||||
chr22:43857816
|
G | T | 1 | a0001c0001t0002g0252 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.169+4398C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857816 | ||||||
chr22:43857891
|
A | C | 1 | a0001c0001t0003g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169+4323T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857891 | ||||||
chr22:43857926
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.169+4288A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857926 | ||||||
chr22:43858003
|
T | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+4211A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858003 | ||||||
chr22:43858035
|
G | A | 7 | a0001c0001t0006g0008a0001c0001t0006g0127a0001c0001t0006g0138others(4): Show | 11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+4179C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858035 | ||||||
chr22:43858049
|
C | CA | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(118): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.169+4164dupT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858049 | ||||||
chr22:43858049
|
C | CAA | 53 | a0001c0001t0001g0038a0001c0001t0001g0152a0001c0001t0001g0188others(50): Show | 80 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.169+4163_169+4164d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858049 | ||||||
chr22:43858049
|
CA | C | 54 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(51): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+4164delT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858049 | ||||||
chr22:43858072
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.169+4142T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858072 | ||||||
chr22:43858084
|
A | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(59): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+4130T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858084 | ||||||
chr22:43858142
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(262): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.169+4072A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858142 | ||||||
chr22:43858147
|
T | C | 1 | a0001c0001t0002g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.169+4067A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858147 | ||||||
chr22:43858223
|
G | A | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.169+3991C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858223 | ||||||
chr22:43858479
|
G | A | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+3735C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858479 | ||||||
chr22:43858583
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.169+3631G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858583 | ||||||
chr22:43858605
|
T | C | 1 | a0001c0001t0010g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.169+3609A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858605 | ||||||
chr22:43858629
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0006g0034 | 3 | HG01516.hp1 HG01517.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.169+3585A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858629 | ||||||
chr22:43858649
|
C | T | 1 | a0001c0001t0029g0268 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.169+3565G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858649 | ||||||
chr22:43858719
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.169+3495G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858719 | ||||||
chr22:43858797
|
C | T | 13 | a0001c0001t0003g0014a0001c0001t0003g0022a0001c0001t0003g0049others(10): Show | 16 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.169+3417G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858797 | ||||||
chr22:43858804
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0212a0001c0001t0001g0213 | 4 | NA18940.hp2 NA18948.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3410C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858804 | ||||||
chr22:43859238
|
G | A | 3 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0264 | 3 | HG02523.hp1 NA18954.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.169+2976C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859238 | ||||||
chr22:43859296
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.169+2918C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859296 | ||||||
chr22:43859342
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0036others(42): Show | 56 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.169+2872G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859342 | ||||||
chr22:43859384
|
C | T | 1 | a0001c0001t0015g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.169+2830G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859384 | ||||||
chr22:43859441
|
G | A | 1 | a0001c0001t0025g0153 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.169+2773C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859441 | ||||||
chr22:43859452
|
C | T | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.169+2762G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859452 | ||||||
chr22:43859647
|
C | T | 1 | a0001c0001t0006g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.169+2567G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859647 | ||||||
chr22:43859673
|
A | G | 1 | a0001c0001t0025g0153 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.169+2541T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859673 | ||||||
chr22:43859767
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+2447C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859767 | ||||||
chr22:43859779
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.169+2435C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859779 | ||||||
chr22:43859829
|
T | G | 1 | a0001c0001t0006g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169+2385A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859829 | ||||||
chr22:43859838
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.169+2376T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859838 | ||||||
chr22:43859948
|
T | C | 61 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(58): Show | 96 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.169+2266A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859948 | ||||||
chr22:43859952
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(193): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.169+2262C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859952 | ||||||
chr22:43859984
|
G | C | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+2230C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859984 | ||||||
chr22:43860016
|
G | A | 2 | a0001c0001t0013g0084a0001c0001t0013g0085 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.169+2198C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860016 | ||||||
chr22:43860046
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+2168G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860046 | ||||||
chr22:43860071
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.169+2143A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860071 | ||||||
chr22:43860080
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169+2134T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860080 | ||||||
chr22:43860254
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.169+1960G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860254 | ||||||
chr22:43860324
|
G | GC | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(264): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.169+1889dupG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860324 | ||||||
chr22:43860352
|
A | G | 3 | a0001c0001t0005g0104a0001c0001t0005g0142a0001c0003t0005g0103 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+1862T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860352 | ||||||
chr22:43860428
|
G | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(52): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+1786C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860428 | ||||||
chr22:43860568
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.169+1646G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860568 | ||||||
chr22:43860587
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.169+1627G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860587 | ||||||
chr22:43860620
|
T | C | 1 | a0001c0001t0005g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.169+1594A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860620 | ||||||
chr22:43860701
|
CA | C | 63 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(60): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.169+1512delT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860701 | ||||||
chr22:43860847
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.169+1367T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860847 | ||||||
chr22:43861047
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.169+1167G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861047 | ||||||
chr22:43861171
|
C | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+1043G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861171 | ||||||
chr22:43861176
|
A | G | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.169+1038T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861176 | ||||||
chr22:43861364
|
T | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+850A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861364 | ||||||
chr22:43861547
|
A | G | 17 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0004g0029others(14): Show | 30 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.169+667T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861547 | ||||||
chr22:43861651
|
G | A | 1 | a0001c0001t0010g0143 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169+563C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861651 | ||||||
chr22:43861694
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0266a0001c0001t0002g0267 | 8 | HG00280.hp1 HG01261.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+520C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861694 | ||||||
chr22:43861713
|
C | G | 1 | a0001c0001t0005g0089 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169+501G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861713 | ||||||
chr22:43861882
|
C | A | 63 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(60): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.169+332G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861882 | ||||||
chr22:43861953
|
T | C | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+261A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861953 | ||||||
chr22:43862091
|
A | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+123T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862091 | ||||||
chr22:43862123
|
A | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+91T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862123 | ||||||
chr22:43862134
|
C | G | 56 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0014others(53): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+80G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862134 | ||||||
chr22:43862156
|
G | C | 67 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(64): Show | 103 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.169+58C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862156 | ||||||
chr22:43862196
|
G | A | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169+18C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862196 |