geneid | 7368 |
---|---|
ensemblid | ENSG00000174607.11 |
hgncid | 12555 |
symbol | UGT8 |
name | UDP glycosyltransferase 8 |
refseq_nuc | NM_001128174.3 |
refseq_prot | NP_001121646.2 |
ensembl_nuc | ENST00000310836.11 |
ensembl_prot | ENSP00000311648.6 |
mane_status | MANE Select |
chr | chr4 |
start | 114598807 |
end | 114678225 |
strand | + |
ver | v1.2 |
region | chr4:114598807-114678225 |
region5000 | chr4:114593807-114683225 |
regionname0 | UGT8_chr4_114598807_114678225 |
regionname5000 | UGT8_chr4_114593807_114683225 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 541 | 233 | 81 | 48 | 72 | 12 | 19 | 51 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0002 | 0/0 | 541 | 36 | 0 | 4 | 26 | 2 | 4 | 15 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0003 | 0/0 | 541 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0004 | 1/0 | 541 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0005 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0006 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0007 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0008 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1626 | 214 | 77 | 42 | 65 | 11 | 18 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0002 | 0/0 | 1626 | 36 | 0 | 4 | 26 | 2 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0003 | 0/0 | 1626 | 11 | 0 | 3 | 7 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0004 | 0/0 | 1626 | 4 | 0 | 4 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0005 | 1/0 | 1626 | 3 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0006 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0007 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0008 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0009 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0010 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0011 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0012 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0013 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0014 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
c0015 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2108 | 106 | 20 | 25 | 44 | 6 | 10 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0002 | 0/0 | 2108 | 68 | 4 | 12 | 38 | 5 | 9 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0003 | 1/0 | 2108 | 30 | 23 | 6 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0004 | 0/0 | 2110 | 13 | 11 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0005 | 0/0 | 2110 | 12 | 0 | 3 | 8 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0006 | 0/0 | 2108 | 10 | 9 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0007 | 0/0 | 2114 | 7 | 0 | 0 | 7 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0008 | 0/0 | 2108 | 6 | 0 | 2 | 0 | 2 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0009 | 0/0 | 2108 | 6 | 6 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0010 | 0/0 | 2106 | 4 | 3 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0011 | 0/0 | 2108 | 3 | 3 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0012 | 0/0 | 2108 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0013 | 0/0 | 2108 | 2 | 0 | 0 | 0 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0014 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0015 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0016 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0017 | 0/0 | 2110 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0018 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0019 | 0/0 | 2108 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0020 | 0/0 | 2108 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0021 | 0/0 | 2106 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0022 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0023 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
t0024 | 0/0 | 2108 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1626 | 214 | 77 | 42 | 65 | 11 | 18 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0003 | 0/0 | 1626 | 11 | 0 | 3 | 7 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0006 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0007 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0011 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0013 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0014 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0015 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0002c0002 | 0/0 | 1626 | 36 | 0 | 4 | 26 | 2 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0003c0004 | 0/0 | 1626 | 4 | 0 | 4 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0004c0005 | 1/0 | 1626 | 3 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0005c0009 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0006c0010 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0007c0012 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0008c0008 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3733 | 99 | 19 | 20 | 44 | 6 | 9 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0002 | 0/0 | 3733 | 32 | 4 | 8 | 13 | 3 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0003 | 0/0 | 3733 | 24 | 19 | 5 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0004 | 0/0 | 3735 | 12 | 10 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0005 | 0/0 | 3735 | 3 | 0 | 1 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0006 | 0/0 | 3733 | 9 | 8 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0007 | 0/0 | 3739 | 6 | 0 | 0 | 6 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0008 | 0/0 | 3733 | 6 | 0 | 2 | 0 | 2 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0009 | 0/0 | 3733 | 6 | 6 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0010 | 0/0 | 3731 | 4 | 3 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0011 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0012 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0013 | 0/0 | 3733 | 2 | 0 | 0 | 0 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0015 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0016 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0020 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0022 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0023 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0001t0024 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0003t0001 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0003t0005 | 0/0 | 3735 | 9 | 0 | 2 | 6 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0003t0007 | 0/0 | 3739 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0006t0003 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0007t0014 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0007t0019 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0011t0001 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0013t0003 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0014t0018 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0001c0015t0021 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0002c0002t0002 | 0/0 | 3733 | 35 | 0 | 4 | 25 | 2 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0002c0002t0017 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0003c0004t0001 | 0/0 | 3733 | 4 | 0 | 4 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0004c0005t0003 | 1/0 | 3733 | 3 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0005c0009t0004 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0006c0010t0002 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0007c0012t0006 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
a0008c0008t0001 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | copy fasta | chr4 | 114593807 | 114683225 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0008g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0008g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0009g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0010g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0011g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0012g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0015g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0020g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0022g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0023g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0001t0024g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0003t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0006t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0006t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0007t0014g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0007t0019g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0013t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0014t0018g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0001c0015t0021g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0002c0002t0017g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0003c0004t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0003c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0003c0004t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0004c0005t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0004c0005t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0004c0005t0003g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0005c0009t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0006c0010t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0007c0012t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
a0008c0008t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0002 | g0232 | EUR | GBR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00140 | hp2 | a0001 | c0001 | t0008 | g0012 | EUR | GBR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00280 | hp2 | a0001 | c0003 | t0005 | g0191 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00423 | hp1 | a0001 | c0003 | t0005 | g0183 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0256 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0146 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00733 | hp2 | a0003 | c0004 | t0001 | g0007 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00738 | hp2 | a0001 | c0006 | t0003 | g0234 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00741 | hp1 | a0003 | c0004 | t0001 | g0007 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01109 | hp2 | a0001 | c0015 | t0021 | g0165 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0225 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01257 | hp2 | a0001 | c0007 | t0019 | g0254 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01361 | hp2 | a0001 | c0001 | t0020 | g0121 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0170 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0169 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01928 | hp1 | a0001 | c0003 | t0005 | g0194 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01928 | hp2 | a0003 | c0004 | t0001 | g0094 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01981 | hp1 | a0001 | c0003 | t0005 | g0185 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG01981 | hp2 | a0003 | c0004 | t0001 | g0046 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0192 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02074 | hp2 | a0001 | c0003 | t0005 | g0197 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02602 | hp2 | a0001 | c0001 | t0008 | g0175 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02615 | hp1 | a0001 | c0001 | t0023 | g0210 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02723 | hp1 | a0004 | c0005 | t0003 | g0236 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02738 | hp1 | a0001 | c0011 | t0001 | g0047 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0205 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0203 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0223 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0224 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02976 | hp1 | a0008 | c0008 | t0001 | g0096 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03017 | hp2 | a0001 | c0001 | t0024 | g0127 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03098 | hp2 | a0004 | c0005 | t0003 | g0237 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03195 | hp2 | a0001 | c0013 | t0003 | g0212 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0202 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03225 | hp2 | a0007 | c0012 | t0006 | g0152 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03540 | hp1 | a0001 | c0007 | t0014 | g0255 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03669 | hp1 | a0001 | c0001 | t0013 | g0051 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03704 | hp2 | a0006 | c0010 | t0002 | g0023 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0176 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03710 | hp2 | a0001 | c0001 | t0013 | g0003 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0153 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0138 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0163 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18957 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18992 | hp1 | a0001 | c0003 | t0005 | g0041 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18999 | hp1 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19043 | hp1 | a0001 | c0001 | t0015 | g0231 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19054 | hp2 | a0001 | c0003 | t0007 | g0187 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19063 | hp1 | a0001 | c0003 | t0005 | g0198 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19064 | hp1 | a0001 | c0003 | t0005 | g0195 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19075 | hp1 | a0002 | c0002 | t0017 | g0134 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19077 | hp1 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19086 | hp2 | a0001 | c0003 | t0005 | g0184 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19240 | hp1 | a0001 | c0006 | t0003 | g0240 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20129 | hp1 | a0001 | c0014 | t0018 | g0168 | AFR | ASW | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20129 | hp2 | a0001 | c0001 | t0016 | g0227 | AFR | ASW | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0145 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20805 | hp2 | a0001 | c0001 | t0008 | g0012 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0209 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0206 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG03471 | hp2 | a0005 | c0009 | t0004 | g0235 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA21309 | hp1 | a0001 | c0001 | t0022 | g0119 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0208 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0097 | REF | REF | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0003 | g0238 | REF | REF | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:114623334
|
G | A | 1 | a0008 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.454G>A | p.Gly152Arg | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 624/3733 | 454/1626 | 152/541 | chr4 | 114623334 | ||
chr4:114623440
|
G | A | 1 | a0005 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.560G>A | p.Arg187His | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 730/3733 | 560/1626 | 187/541 | chr4 | 114623440 | ||
chr4:114623540
|
G | C | 1 | a0006 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.660G>C | p.Gln220His | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 830/3733 | 660/1626 | 220/541 | chr4 | 114623540 | ||
chr4:114623557
|
C | T | 2 | a0002a0006 | 37 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(34): Show |
missense_variant | MODERATE | c.677C>T | p.Pro226Leu | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 847/3733 | 677/1626 | 226/541 | chr4 | 114623557 | ||
chr4:114668146
|
A | G | 7 | a0001a0002a0003others(4): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
missense_variant | MODERATE | c.1104A>G | p.Ile368Met | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/6 | 1274/3733 | 1104/1626 | 368/541 | chr4 | 114668146 | ||
chr4:114668285
|
A | G | 1 | a0003 | 4 | HG00733.hp2 HG00741.hp1 HG01928.hp2 others(1): Show |
missense_variant | MODERATE | c.1243A>G | p.Lys415Glu | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/6 | 1413/3733 | 1243/1626 | 415/541 | chr4 | 114668285 | ||
chr4:114676026
|
A | G | 1 | a0007 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1364A>G | p.Asn455Ser | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1534/3733 | 1364/1626 | 455/541 | chr4 | 114676026 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:114623408
|
C | T | 1 | a0001c0015 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.528C>T | p.Tyr176Tyr | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 698/3733 | 528/1626 | 176/541 | chr4 | 114623408 | ||
chr4:114623498
|
G | T | 1 | a0001c0007 | 2 | HG01257.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.618G>T | p.Gly206Gly | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 788/3733 | 618/1626 | 206/541 | chr4 | 114623498 | ||
chr4:114623558
|
A | G | 13 | a0001c0001a0001c0003a0001c0007others(10): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
synonymous_variant | LOW | c.678A>G | p.Pro226Pro | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 848/3733 | 678/1626 | 226/541 | chr4 | 114623558 | ||
chr4:114623615
|
C | T | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.735C>T | p.Asp245Asp | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 905/3733 | 735/1626 | 245/541 | chr4 | 114623615 | ||
chr4:114623621
|
A | G | 1 | a0001c0003 | 11 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(8): Show |
synonymous_variant | LOW | c.741A>G | p.Ala247Ala | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 911/3733 | 741/1626 | 247/541 | chr4 | 114623621 | ||
chr4:114665716
|
C | T | 1 | a0001c0013 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1002C>T | p.Asn334Asn | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/6 | 1172/3733 | 1002/1626 | 334/541 | chr4 | 114665716 | ||
chr4:114676270
|
T | C | 1 | a0001c0011 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1608T>C | p.His536His | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1778/3733 | 1608/1626 | 536/541 | chr4 | 114676270 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:114598933
|
C | T | 1 | a0001c0001t0024 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/6 | 23948 | chr4 | 114598933 | |||||
chr4:114598947
|
A | G | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(23): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
5_prime_UTR_variant | MODIFIER | c.-30A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/6 | 23934 | chr4 | 114598947 | |||||
chr4:114676297
|
C | T | 2 | a0001c0001t0009a0001c0001t0023 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 9 | chr4 | 114676297 | |||||
chr4:114676590
|
G | A | 2 | a0001c0001t0011a0001c0001t0012 | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*302G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 302 | chr4 | 114676590 | |||||
chr4:114676639
|
GTA | G | 1 | a0001c0001t0010 | 4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*353_*354delAT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 353 | INFO_REALIGN_3_PRIME | chr4 | 114676639 | ||||
chr4:114676641
|
A | ATG | 5 | a0001c0001t0004a0001c0001t0005a0001c0003t0005others(2): Show | 26 | HG00280.hp2 HG00423.hp1 HG01255.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376dupGT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 377 | INFO_REALIGN_3_PRIME | chr4 | 114676641 | ||||
chr4:114676641
|
ATG | A | 4 | a0001c0001t0015a0001c0001t0016a0001c0001t0022others(1): Show | 4 | HG01109.hp2 NA19043.hp1 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376delGT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 375 | INFO_REALIGN_3_PRIME | chr4 | 114676641 | ||||
chr4:114676665
|
T | TTGTGTG | 2 | a0001c0001t0007a0001c0003t0007 | 7 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*391_*396dupGTGTGT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 397 | INFO_REALIGN_3_PRIME | chr4 | 114676665 | ||||
chr4:114676797
|
A | C | 1 | a0001c0001t0020 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*509A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 509 | chr4 | 114676797 | |||||
chr4:114676799
|
G | A | 2 | a0001c0001t0006a0007c0012t0006 | 10 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*511G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 511 | chr4 | 114676799 | |||||
chr4:114676939
|
T | C | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(9): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*651T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 651 | chr4 | 114676939 | |||||
chr4:114677109
|
A | G | 1 | a0001c0015t0021 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 821 | chr4 | 114677109 | |||||
chr4:114677165
|
C | T | 1 | a0001c0001t0013 | 2 | HG03669.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*877C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 877 | chr4 | 114677165 | |||||
chr4:114677248
|
G | A | 1 | a0001c0007t0019 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 960 | chr4 | 114677248 | |||||
chr4:114677304
|
T | G | 2 | a0001c0007t0014a0001c0007t0019 | 2 | HG01257.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1016T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1016 | chr4 | 114677304 | |||||
chr4:114677421
|
G | A | 2 | a0001c0007t0014a0001c0007t0019 | 2 | HG01257.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1133G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1133 | chr4 | 114677421 | |||||
chr4:114677554
|
T | C | 1 | a0001c0001t0023 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1266 | chr4 | 114677554 | |||||
chr4:114678003
|
T | G | 1 | a0001c0001t0008 | 6 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1715T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1715 | chr4 | 114678003 | |||||
chr4:114678046
|
A | G | 1 | a0001c0001t0016 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1758A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1758 | chr4 | 114678046 | |||||
chr4:114678116
|
T | C | 1 | a0001c0014t0018 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1828 | chr4 | 114678116 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:114599013
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(101): Show | 110 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+39G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599013 | ||||||
chr4:114599249
|
G | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(230): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-3+275G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599249 | ||||||
chr4:114599383
|
C | T | 1 | a0002c0002t0002g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3+409C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599383 | ||||||
chr4:114599430
|
C | G | 1 | a0001c0001t0015g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3+456C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599430 | ||||||
chr4:114599438
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-3+464C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599438 | ||||||
chr4:114599581
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-3+607A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599581 | ||||||
chr4:114599608
|
G | T | 1 | a0002c0002t0002g0230 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-3+634G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599608 | ||||||
chr4:114599615
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+641C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599615 | ||||||
chr4:114599675
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+701G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599675 | ||||||
chr4:114599833
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-3+859C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599833 | ||||||
chr4:114599884
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+910G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599884 | ||||||
chr4:114599943
|
C | T | 23 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(20): Show | 26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+969C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599943 | ||||||
chr4:114599954
|
C | T | 1 | a0001c0001t0005g0110 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-3+980C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599954 | ||||||
chr4:114599988
|
C | T | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+1014C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599988 | ||||||
chr4:114600413
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-3+1439G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600413 | ||||||
chr4:114600417
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-3+1443A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600417 | ||||||
chr4:114600442
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+1468C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600442 | ||||||
chr4:114600451
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-3+1477C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600451 | ||||||
chr4:114600640
|
A | C | 23 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(20): Show | 26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+1666A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600640 | ||||||
chr4:114600648
|
C | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(120): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-3+1674C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600648 | ||||||
chr4:114600811
|
T | C | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+1837T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600811 | ||||||
chr4:114600872
|
A | G | 1 | a0002c0002t0002g0177 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-3+1898A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600872 | ||||||
chr4:114600971
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-3+1997A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600971 | ||||||
chr4:114601150
|
G | A | 24 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(21): Show | 26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3+2176G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601150 | ||||||
chr4:114601232
|
G | T | 23 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(20): Show | 26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+2258G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601232 | ||||||
chr4:114601262
|
T | G | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+2288T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601262 | ||||||
chr4:114601589
|
TA | T | 28 | a0001c0001t0001g0108a0001c0001t0002g0006a0001c0001t0002g0009others(25): Show | 32 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+2624delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114601589 | |||||
chr4:114601744
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3+2770G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601744 | ||||||
chr4:114601829
|
G | GT | 26 | a0001c0001t0001g0107a0001c0001t0003g0005a0001c0001t0003g0016others(23): Show | 29 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.-3+2869dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114601829 | |||||
chr4:114601833
|
T | G | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3+2859T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601833 | ||||||
chr4:114602107
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-3+3133G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602107 | ||||||
chr4:114602153
|
T | C | 3 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0013t0003g0212 | 3 | HG02258.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-3+3179T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602153 | ||||||
chr4:114602254
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+3280C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602254 | ||||||
chr4:114602332
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(199): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-3+3358G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602332 | ||||||
chr4:114602529
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+3555A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602529 | ||||||
chr4:114602711
|
G | GAT | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+3739_-3+3740dup others(2): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114602711 | |||||
chr4:114602742
|
G | A | 23 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(20): Show | 26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+3768G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602742 | ||||||
chr4:114602786
|
T | A | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3+3812T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602786 | ||||||
chr4:114603052
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4078A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603052 | ||||||
chr4:114603054
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+4080A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603054 | ||||||
chr4:114603271
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-3+4297T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603271 | ||||||
chr4:114603489
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4515A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603489 | ||||||
chr4:114603665
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-3+4691G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603665 | ||||||
chr4:114603708
|
T | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0117a0001c0001t0002g0118others(2): Show | 6 | HG00741.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+4734T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603708 | ||||||
chr4:114603855
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+4881T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603855 | ||||||
chr4:114603918
|
G | C | 1 | a0001c0001t0002g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+4944G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603918 | ||||||
chr4:114603963
|
T | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4989T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603963 | ||||||
chr4:114603964
|
TA | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4992delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114603964 | |||||
chr4:114604196
|
C | G | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+5222C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604196 | ||||||
chr4:114604293
|
C | T | 3 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0013t0003g0212 | 3 | HG02258.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-3+5319C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604293 | ||||||
chr4:114604318
|
A | G | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5344A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604318 | ||||||
chr4:114604457
|
C | CT | 70 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(67): Show | 75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-3+5498dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114604457 | |||||
chr4:114604457
|
C | CTT | 44 | a0001c0001t0002g0120a0001c0001t0002g0172a0001c0001t0002g0173others(41): Show | 51 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+5497_-3+5498dup others(2): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114604457 | |||||
chr4:114604472
|
TC | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5503delC | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114604472 | |||||
chr4:114604473
|
C | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(228): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-3+5499C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604473 | ||||||
chr4:114604474
|
C | T | 30 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(27): Show | 33 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.-3+5500C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604474 | ||||||
chr4:114604545
|
G | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+5571G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604545 | ||||||
chr4:114604748
|
C | T | 1 | a0001c0001t0006g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-3+5774C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604748 | ||||||
chr4:114604769
|
A | G | 42 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0006g0135others(39): Show | 49 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+5795A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604769 | ||||||
chr4:114604887
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-3+5913T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604887 | ||||||
chr4:114604888
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-3+5914C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604888 | ||||||
chr4:114605205
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-3+6231A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114605205 | ||||||
chr4:114605540
|
A | G | 1 | a0001c0014t0018g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-3+6566A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114605540 | ||||||
chr4:114605935
|
A | C | 1 | a0001c0001t0002g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-3+6961A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114605935 | ||||||
chr4:114606104
|
C | A | 1 | a0002c0002t0002g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-3+7130C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606104 | ||||||
chr4:114606130
|
C | T | 24 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(21): Show | 26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3+7156C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606130 | ||||||
chr4:114606152
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-3+7178C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606152 | ||||||
chr4:114606327
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-3+7353A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606327 | ||||||
chr4:114606433
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+7459T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606433 | ||||||
chr4:114606734
|
A | T | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+7760A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606734 | ||||||
chr4:114606738
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-3+7764G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606738 | ||||||
chr4:114606826
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+7852T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606826 | ||||||
chr4:114607233
|
G | A | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+8259G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114607233 | ||||||
chr4:114607486
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-3+8512G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114607486 | ||||||
chr4:114607728
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+8754A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114607728 | ||||||
chr4:114608093
|
G | A | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+9119G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608093 | ||||||
chr4:114608098
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+9124T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608098 | ||||||
chr4:114608291
|
G | T | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+9317G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608291 | ||||||
chr4:114608520
|
C | A | 24 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(21): Show | 26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3+9546C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608520 | ||||||
chr4:114608561
|
A | C | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+9587A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608561 | ||||||
chr4:114608708
|
A | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+9734A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608708 | ||||||
chr4:114608771
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-3+9797A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608771 | ||||||
chr4:114608867
|
G | C | 2 | a0001c0001t0009g0206a0001c0001t0009g0207 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-3+9893G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608867 | ||||||
chr4:114608935
|
A | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+9961A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608935 | ||||||
chr4:114609179
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-3+10205G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609179 | ||||||
chr4:114609194
|
C | A | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+10220C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609194 | ||||||
chr4:114609253
|
A | G | 6 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0022others(3): Show | 6 | HG00323.hp2 HG00438.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+10279A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609253 | ||||||
chr4:114609299
|
A | G | 1 | a0002c0002t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3+10325A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609299 | ||||||
chr4:114609479
|
A | G | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3+10505A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609479 | ||||||
chr4:114609801
|
C | T | 1 | a0002c0002t0002g0162 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-3+10827C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609801 | ||||||
chr4:114609876
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0108 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-3+10902A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609876 | ||||||
chr4:114610043
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0020 | 3 | NA18947.hp1 NA18961.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-3+11069G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610043 | ||||||
chr4:114610074
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+11100A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610074 | ||||||
chr4:114610144
|
A | T | 1 | a0002c0002t0002g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3+11170A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610144 | ||||||
chr4:114610189
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+11215T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610189 | ||||||
chr4:114610466
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+11492C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610466 | ||||||
chr4:114610549
|
A | G | 1 | a0001c0001t0015g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3+11575A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610549 | ||||||
chr4:114610616
|
T | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+11642T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610616 | ||||||
chr4:114610699
|
G | A | 41 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0028others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-3+11725G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610699 | ||||||
chr4:114610801
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11827C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610801 | ||||||
chr4:114610820
|
G | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(255): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-3+11846G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610820 | ||||||
chr4:114610859
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3+11885G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610859 | ||||||
chr4:114610870
|
A | T | 1 | a0002c0002t0002g0177 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-3+11896A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610870 | ||||||
chr4:114610978
|
T | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-11901T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610978 | ||||||
chr4:114611064
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-2-11815T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611064 | ||||||
chr4:114611278
|
ATT | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216 | 4 | HG02145.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-11600_-2-11599d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611278 | ||||||
chr4:114611403
|
C | CAT | 11 | a0001c0001t0002g0006a0001c0001t0002g0020a0001c0001t0002g0022others(8): Show | 12 | HG00558.hp2 HG01175.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-11434_-2-11433d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CAT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0181others(11): Show | 15 | HG00741.hp2 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-11434_-2-11433d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATAT | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0166a0001c0001t0001g0167others(11): Show | 14 | HG02040.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-11436_-2-11433d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATAT | C | 11 | a0001c0001t0003g0005a0001c0001t0003g0115a0001c0001t0003g0211others(8): Show | 13 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-11438_-2-11433d others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATATA others(1): Show |
C | 11 | a0001c0001t0003g0214a0001c0001t0003g0217a0001c0001t0003g0218others(8): Show | 13 | HG00738.hp2 HG02015.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-11440_-2-11433d others(10): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATATA others(3): Show |
C | 33 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170others(30): Show | 39 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-2-11442_-2-11433d others(12): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATATA others(5): Show |
C | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-11444_-2-11433d others(14): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATATA others(9): Show |
C | 3 | a0002c0002t0002g0137a0002c0002t0002g0138a0002c0002t0002g0163 | 3 | HG02698.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-2-11448_-2-11433d others(18): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0099a0001c0001t0004g0239 | 2 | HG01975.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-2-11454_-2-11433d others(24): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611403
|
CATATATA others(17): Show |
C | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-2-11456_-2-11433d others(26): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | |||||
chr4:114611415
|
TATATATA others(25): Show |
T | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-11462_-2-11431d others(34): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611415 | |||||
chr4:114611423
|
T | C | 1 | a0002c0002t0002g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-2-11456T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611423 | ||||||
chr4:114611427
|
TATATATA others(13): Show |
T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-11450_-2-11431d others(22): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611427 | |||||
chr4:114611431
|
T | TATACATA others(27): Show |
2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-11445_-2-11444i others(36): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611431 | |||||
chr4:114611441
|
T | TATAC | 2 | a0001c0001t0003g0016a0001c0001t0003g0215 | 3 | HG03098.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-11435_-2-11434i others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611441 | |||||
chr4:114611442
|
A | G | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-11437A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611442 | ||||||
chr4:114611443
|
T | C | 5 | a0001c0001t0003g0211a0001c0001t0003g0217a0001c0001t0008g0012others(2): Show | 6 | HG00140.hp2 HG02451.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11436T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611443 | ||||||
chr4:114611443
|
T | TAC | 3 | a0001c0001t0004g0242a0001c0001t0004g0243a0001c0001t0012g0256 | 3 | HG00639.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-2-11435_-2-11434i others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611443 | |||||
chr4:114611445
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(113): Show | 124 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-2-11434T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611445 | ||||||
chr4:114611445
|
T | TACAC | 3 | a0001c0001t0010g0223a0001c0001t0010g0224a0001c0001t0010g0225 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-2-11424_-2-11421d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611445 | |||||
chr4:114611445
|
T | TATAC | 11 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0042others(8): Show | 11 | HG01099.hp2 HG01255.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-11433_-2-11432i others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611445 | |||||
chr4:114611445
|
T | TATATAC | 3 | a0001c0001t0001g0044a0001c0003t0005g0197a0001c0003t0005g0198 | 3 | HG02074.hp2 HG02280.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-2-11433_-2-11432i others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611445 | |||||
chr4:114611457
|
C | CAG | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-11418_-2-11417d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611457 | |||||
chr4:114611457
|
C | G | 103 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0028others(100): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-2-11422C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611457 | ||||||
chr4:114611460
|
A | C | 2 | a0002c0002t0002g0014a0002c0002t0002g0179 | 3 | HG00597.hp2 HG01074.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-2-11419A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611460 | ||||||
chr4:114611516
|
G | A | 1 | a0001c0003t0005g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-2-11363G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611516 | ||||||
chr4:114611528
|
C | CAT | 15 | a0001c0001t0003g0005a0001c0001t0003g0211a0001c0001t0003g0213others(12): Show | 17 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-11333_-2-11332d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611528 | |||||
chr4:114611528
|
CAT | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-11333_-2-11332d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611528 | |||||
chr4:114611546
|
T | C | 8 | a0001c0001t0001g0111a0001c0001t0001g0180a0001c0001t0001g0201others(5): Show | 8 | HG00323.hp1 HG01109.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-11333T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611546 | ||||||
chr4:114611546
|
T | TAC | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(164): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-2-11323_-2-11322d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611546 | |||||
chr4:114611546
|
T | TATAC | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0181others(26): Show | 31 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-2-11332_-2-11331i others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611546 | |||||
chr4:114611746
|
G | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-11133G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611746 | ||||||
chr4:114611949
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216 | 4 | HG02145.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-10930T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611949 | ||||||
chr4:114611970
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-2-10909T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611970 | ||||||
chr4:114611981
|
G | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG00423.hp2 NA18983.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-10898G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611981 | ||||||
chr4:114612482
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-2-10397C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612482 | ||||||
chr4:114612619
|
G | A | 23 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(20): Show | 26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-10260G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612619 | ||||||
chr4:114612732
|
A | G | 3 | a0001c0001t0006g0158a0001c0001t0006g0159a0001c0001t0006g0160 | 3 | HG02723.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-2-10147A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612732 | ||||||
chr4:114612871
|
A | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-10008A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612871 | ||||||
chr4:114612966
|
T | A | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-9913T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612966 | ||||||
chr4:114613169
|
T | G | 1 | a0001c0001t0004g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-9710T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613169 | ||||||
chr4:114613406
|
A | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-9473A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613406 | ||||||
chr4:114613543
|
G | A | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-9336G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613543 | ||||||
chr4:114613573
|
T | C | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2-9306T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613573 | ||||||
chr4:114613660
|
T | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-9219T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613660 | ||||||
chr4:114613678
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2-9201A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613678 | ||||||
chr4:114613749
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-9130C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613749 | ||||||
chr4:114613788
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(118): Show | 126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.-2-9091A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613788 | ||||||
chr4:114614102
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(125): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-2-8777G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614102 | ||||||
chr4:114614235
|
G | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(234): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-2-8644G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614235 | ||||||
chr4:114614659
|
G | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-8220G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614659 | ||||||
chr4:114614666
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(199): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-2-8213C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614666 | ||||||
chr4:114614675
|
CT | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(199): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-2-8203delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614675 | ||||||
chr4:114614794
|
C | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-8085C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614794 | ||||||
chr4:114614838
|
GA | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8040delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614838 | ||||||
chr4:114614839
|
A | C | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-8040A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614839 | ||||||
chr4:114614840
|
C | CT | 8 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0003g0005others(5): Show | 10 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-8019dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114614840 | |||||
chr4:114614840
|
CT | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(176): Show | 194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.-2-8019delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114614840 | |||||
chr4:114614841
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8038T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614841 | ||||||
chr4:114614852
|
T | C | 1 | a0001c0003t0005g0194 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-2-8027T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614852 | ||||||
chr4:114614872
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0020 | 3 | NA18947.hp1 NA18961.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-2-8007A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614872 | ||||||
chr4:114614891
|
T | A | 3 | a0001c0003t0005g0183a0001c0003t0005g0184a0001c0003t0005g0185 | 3 | HG00423.hp1 HG01981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-2-7988T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614891 | ||||||
chr4:114615411
|
T | C | 1 | a0001c0014t0018g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2-7468T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615411 | ||||||
chr4:114615452
|
T | A | 1 | a0002c0002t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2-7427T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615452 | ||||||
chr4:114615466
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-2-7413C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615466 | ||||||
chr4:114615659
|
G | A | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-7220G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615659 | ||||||
chr4:114615862
|
T | TAGTGGGC others(6747): Show |
1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6754): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | |||||
chr4:114615862
|
T | TAGTGGGC others(6727): Show |
2 | a0001c0001t0011g0203a0001c0001t0012g0202 | 2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6734): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | |||||
chr4:114615862
|
T | TAGTGGGC others(6727): Show |
2 | a0001c0001t0011g0204a0001c0001t0011g0205 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6734): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | |||||
chr4:114615862
|
T | TAGTGGGC others(6726): Show |
2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6733): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | |||||
chr4:114615890
|
AG | A | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6987delG | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615890 | |||||
chr4:114615891
|
GGCAGCAG others(7): Show |
G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-6987_-2-6974del others(14): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615891 | ||||||
chr4:114615987
|
A | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6892A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615987 | ||||||
chr4:114616051
|
A | T | 1 | a0001c0001t0004g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-6828A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616051 | ||||||
chr4:114616095
|
C | T | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6784C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616095 | ||||||
chr4:114616144
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6735T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616144 | ||||||
chr4:114616254
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-6625C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616254 | ||||||
chr4:114616267
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-6612C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616267 | ||||||
chr4:114616292
|
G | A | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6587G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616292 | ||||||
chr4:114616312
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-6567C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616312 | ||||||
chr4:114616404
|
G | A | 1 | a0001c0001t0008g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-2-6475G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616404 | ||||||
chr4:114616567
|
C | T | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2-6312C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616567 | ||||||
chr4:114616575
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-6304C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616575 | ||||||
chr4:114616586
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2-6293C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616586 | ||||||
chr4:114616677
|
G | A | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-2-6202G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616677 | ||||||
chr4:114616747
|
T | C | 4 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216others(1): Show | 5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-6132T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616747 | ||||||
chr4:114616846
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6033T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616846 | ||||||
chr4:114616890
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-2-5989C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616890 | ||||||
chr4:114616986
|
C | T | 29 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(26): Show | 33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.-2-5893C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616986 | ||||||
chr4:114616989
|
A | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-5890A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616989 | ||||||
chr4:114617024
|
A | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-5855A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617024 | ||||||
chr4:114617123
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(253): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-2-5756A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617123 | ||||||
chr4:114617140
|
G | A | 1 | a0002c0002t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2-5739G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617140 | ||||||
chr4:114617264
|
A | G | 1 | a0002c0002t0002g0151 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-2-5615A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617264 | ||||||
chr4:114617270
|
C | A | 1 | a0001c0001t0002g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-2-5609C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617270 | ||||||
chr4:114617314
|
C | T | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-5565C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617314 | ||||||
chr4:114617357
|
A | G | 114 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0002g0006others(111): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-2-5522A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617357 | ||||||
chr4:114617415
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-2-5464A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617415 | ||||||
chr4:114617501
|
G | A | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-5378G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617501 | ||||||
chr4:114617504
|
G | A | 1 | a0001c0001t0006g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-5375G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617504 | ||||||
chr4:114617728
|
G | A | 1 | a0001c0001t0004g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-2-5151G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617728 | ||||||
chr4:114617883
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-4996G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617883 | ||||||
chr4:114618077
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2-4802A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618077 | ||||||
chr4:114618077
|
ATCT | A | 16 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0003g0233others(13): Show | 16 | HG01255.hp1 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-4797_-2-4795del others(3): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114618077 | |||||
chr4:114618148
|
A | G | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-2-4731A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618148 | ||||||
chr4:114618241
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0099 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-2-4638A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618241 | ||||||
chr4:114618354
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-2-4525C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618354 | ||||||
chr4:114618672
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-2-4207A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618672 | ||||||
chr4:114618710
|
T | C | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2-4169T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618710 | ||||||
chr4:114618772
|
G | A | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-4107G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618772 | ||||||
chr4:114619264
|
T | A | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-3615T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619264 | ||||||
chr4:114619275
|
A | T | 2 | a0001c0006t0003g0234a0001c0006t0003g0240 | 2 | HG00738.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-3604A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619275 | ||||||
chr4:114619375
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-2-3504A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619375 | ||||||
chr4:114619420
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-3459C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619420 | ||||||
chr4:114619438
|
C | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-3441C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619438 | ||||||
chr4:114619496
|
C | T | 4 | a0001c0001t0003g0005a0001c0001t0003g0219a0001c0001t0003g0220others(1): Show | 6 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-3383C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619496 | ||||||
chr4:114619599
|
A | G | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-3280A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619599 | ||||||
chr4:114619641
|
C | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3238C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619641 | ||||||
chr4:114619696
|
G | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-3183G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619696 | ||||||
chr4:114620100
|
TA | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-2774delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114620100 | |||||
chr4:114620195
|
C | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-2684C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620195 | ||||||
chr4:114620229
|
A | G | 1 | a0005c0009t0004g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-2650A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620229 | ||||||
chr4:114620444
|
C | T | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-2435C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620444 | ||||||
chr4:114620589
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-2290G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620589 | ||||||
chr4:114620633
|
G | A | 22 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(19): Show | 25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-2246G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620633 | ||||||
chr4:114620675
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0005g0110 | 2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-2-2204T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620675 | ||||||
chr4:114620748
|
A | G | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-2131A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620748 | ||||||
chr4:114620805
|
T | C | 29 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(26): Show | 32 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2-2074T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620805 | ||||||
chr4:114620905
|
G | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1974G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620905 | ||||||
chr4:114620912
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2-1967A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620912 | ||||||
chr4:114621056
|
G | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-1823G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621056 | ||||||
chr4:114621060
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2-1819G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621060 | ||||||
chr4:114621085
|
TC | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1790delC | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114621085 | |||||
chr4:114621243
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-2-1636T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621243 | ||||||
chr4:114621831
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-2-1048T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621831 | ||||||
chr4:114621913
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-966A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621913 | ||||||
chr4:114621954
|
CT | C | 22 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(19): Show | 25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-916delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114621954 | |||||
chr4:114622049
|
G | A | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-830G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622049 | ||||||
chr4:114622088
|
A | G | 22 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(19): Show | 25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-791A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622088 | ||||||
chr4:114622105
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2-774T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622105 | ||||||
chr4:114622111
|
C | G | 1 | a0001c0001t0003g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2-768C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622111 | ||||||
chr4:114622200
|
C | T | 22 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(19): Show | 25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-679C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622200 | ||||||
chr4:114622201
|
G | A | 15 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(12): Show | 15 | HG00280.hp1 HG00642.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-678G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622201 | ||||||
chr4:114622369
|
G | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-2-510G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622369 | ||||||
chr4:114622403
|
C | T | 41 | a0001c0001t0003g0217a0001c0001t0006g0135a0001c0001t0006g0140others(38): Show | 48 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-2-476C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622403 | ||||||
chr4:114622615
|
T | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-264T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622615 | ||||||
chr4:114622674
|
T | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0089a0001c0011t0001g0047others(3): Show | 7 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-205T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622674 | ||||||
chr4:114622752
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-127G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622752 | ||||||
chr4:114622759
|
A | AT | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(218): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-2-110dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114622759 | |||||
chr4:114622759
|
A | ATT | 12 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0218others(9): Show | 14 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2-111_-2-110dupTT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114622759 | |||||
chr4:114623769
|
G | T | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+67G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114623769 | ||||||
chr4:114623836
|
C | T | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+134C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114623836 | ||||||
chr4:114624205
|
T | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.822+503T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624205 | ||||||
chr4:114624206
|
T | C | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+504T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624206 | ||||||
chr4:114624315
|
A | G | 42 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0006g0135others(39): Show | 49 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.822+613A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624315 | ||||||
chr4:114624730
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+1028C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624730 | ||||||
chr4:114624787
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.822+1085G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624787 | ||||||
chr4:114624891
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.822+1189G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624891 | ||||||
chr4:114624907
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.822+1205A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624907 | ||||||
chr4:114625069
|
C | CACACCTT others(7): Show |
5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1367_822+1368i others(16): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625069 | ||||||
chr4:114625142
|
C | G | 4 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216others(1): Show | 5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+1440C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625142 | ||||||
chr4:114625204
|
T | C | 1 | a0004c0005t0003g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.822+1502T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625204 | ||||||
chr4:114625338
|
C | T | 22 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(19): Show | 25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+1636C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625338 | ||||||
chr4:114625368
|
G | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1666G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625368 | ||||||
chr4:114625449
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0011g0203a0001c0001t0011g0204others(2): Show | 5 | HG01074.hp2 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1747C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625449 | ||||||
chr4:114625466
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.822+1764A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625466 | ||||||
chr4:114625483
|
C | CCTAGGTG others(11): Show |
7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+1783_822+1800d others(20): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625483 | |||||
chr4:114625509
|
T | TA | 62 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(59): Show | 63 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.822+1832dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | |||||
chr4:114625509
|
T | TAA | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(65): Show | 72 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.822+1831_822+1832d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | |||||
chr4:114625509
|
T | TAAA | 9 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0050others(6): Show | 10 | HG00438.hp1 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+1830_822+1832d others(5): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | |||||
chr4:114625509
|
TA | T | 29 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(26): Show | 33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.822+1832delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | |||||
chr4:114625509
|
TAA | T | 21 | a0001c0001t0002g0178a0001c0001t0003g0005a0001c0001t0003g0016others(18): Show | 24 | HG00738.hp1 HG01106.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.822+1831_822+1832d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | |||||
chr4:114625849
|
C | A | 8 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0218others(5): Show | 8 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+2147C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625849 | ||||||
chr4:114626003
|
A | C | 1 | a0001c0001t0023g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.822+2301A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626003 | ||||||
chr4:114626033
|
A | C | 1 | a0001c0001t0006g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.822+2331A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626033 | ||||||
chr4:114626296
|
T | C | 1 | a0001c0001t0003g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.822+2594T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626296 | ||||||
chr4:114626394
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168others(1): Show | 4 | HG01109.hp2 HG02615.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2692G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626394 | ||||||
chr4:114626414
|
A | G | 4 | a0001c0001t0010g0222a0001c0001t0010g0223a0001c0001t0010g0224others(1): Show | 4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2712A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626414 | ||||||
chr4:114626452
|
G | A | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+2750G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626452 | ||||||
chr4:114626515
|
G | C | 42 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0006g0135others(39): Show | 49 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.822+2813G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626515 | ||||||
chr4:114626880
|
T | A | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+3178T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626880 | ||||||
chr4:114627255
|
C | CT | 6 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0001g0105others(3): Show | 6 | HG01168.hp2 HG01175.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+3572dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114627255 | |||||
chr4:114627255
|
CT | C | 47 | a0001c0001t0001g0097a0001c0001t0001g0114a0001c0001t0002g0011others(44): Show | 51 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(48): Show |
intron_variant | MODIFIER | c.822+3572delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114627255 | |||||
chr4:114627255
|
CTT | C | 6 | a0001c0001t0002g0171a0001c0001t0011g0203a0001c0001t0011g0204others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+3571_822+3572d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114627255 | |||||
chr4:114627451
|
A | G | 7 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+3749A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627451 | ||||||
chr4:114627509
|
C | T | 1 | a0001c0001t0015g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.822+3807C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627509 | ||||||
chr4:114627582
|
G | A | 1 | a0001c0001t0020g0121 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.822+3880G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627582 | ||||||
chr4:114627667
|
T | G | 4 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0001t0008g0175others(1): Show | 6 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+3965T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627667 | ||||||
chr4:114627881
|
A | G | 2 | a0001c0001t0009g0015a0001c0001t0009g0209 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+4179A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627881 | ||||||
chr4:114628208
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+4506T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628208 | ||||||
chr4:114628218
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+4516T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628218 | ||||||
chr4:114628382
|
C | A | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+4680C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628382 | ||||||
chr4:114628383
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(231): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.822+4681A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628383 | ||||||
chr4:114628406
|
C | T | 1 | a0001c0001t0006g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+4704C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628406 | ||||||
chr4:114628574
|
G | A | 29 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(26): Show | 32 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.822+4872G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628574 | ||||||
chr4:114628661
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(202): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.822+4959A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628661 | ||||||
chr4:114628767
|
T | TAAGAAAG others(316): Show |
3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628767
|
T | TAAGAAAG others(313): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01074.hp2 HG01496.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(322): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628767
|
T | TAAGAAAG others(314): Show |
100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(97): Show | 105 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(323): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628767
|
T | TAAGAAAG others(315): Show |
17 | a0001c0001t0001g0024a0001c0001t0001g0052a0001c0001t0001g0053others(14): Show | 17 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(324): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628767
|
T | TAAGAAAG others(316): Show |
1 | a0001c0014t0018g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628767
|
T | TAAGAAAG others(319): Show |
1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(328): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628767
|
T | TAAGAAAG others(314): Show |
1 | a0003c0004t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(323): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | |||||
chr4:114628769
|
A | AGAAAGTG others(317): Show |
12 | a0001c0001t0006g0135a0001c0001t0006g0158a0002c0002t0002g0136others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(326): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | |||||
chr4:114628769
|
A | AGAAAGTG others(316): Show |
26 | a0001c0001t0003g0217a0001c0001t0006g0140a0001c0001t0006g0141others(23): Show | 33 | HG00140.hp1 HG00558.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | |||||
chr4:114628769
|
A | AGAAAGTG others(315): Show |
1 | a0001c0001t0006g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(324): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | |||||
chr4:114628769
|
A | AGAAAGTG others(316): Show |
1 | a0001c0001t0006g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | |||||
chr4:114628769
|
A | AGAAAGTG others(317): Show |
1 | a0002c0002t0002g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.822+5072_822+5073i others(326): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | |||||
chr4:114628778
|
A | G | 1 | a0001c0003t0005g0191 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.822+5076A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628778 | ||||||
chr4:114628873
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0085 | 3 | NA18947.hp2 NA18955.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.822+5171T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628873 | ||||||
chr4:114628956
|
A | G | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(229): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.822+5254A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628956 | ||||||
chr4:114629112
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+5410C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629112 | ||||||
chr4:114629240
|
G | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+5538G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629240 | ||||||
chr4:114629264
|
A | G | 2 | a0001c0001t0015g0231a0001c0001t0016g0227 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.822+5562A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629264 | ||||||
chr4:114629320
|
T | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+5618T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629320 | ||||||
chr4:114629358
|
C | G | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+5656C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629358 | ||||||
chr4:114629442
|
T | C | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+5740T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629442 | ||||||
chr4:114629688
|
C | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+5986C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629688 | ||||||
chr4:114629888
|
A | G | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+6186A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629888 | ||||||
chr4:114630017
|
G | A | 3 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252 | 3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.822+6315G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630017 | ||||||
chr4:114630144
|
CT | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(75): Show | 83 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.822+6444delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114630144 | |||||
chr4:114630286
|
C | T | 1 | a0001c0001t0023g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.822+6584C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630286 | ||||||
chr4:114630310
|
C | T | 6 | a0001c0001t0003g0217a0001c0001t0011g0203a0001c0001t0011g0204others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+6608C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630310 | ||||||
chr4:114630311
|
G | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+6609G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630311 | ||||||
chr4:114630360
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+6658C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630360 | ||||||
chr4:114630395
|
G | A | 11 | a0001c0003t0001g0192a0001c0003t0005g0041a0001c0003t0005g0183others(8): Show | 11 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.822+6693G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630395 | ||||||
chr4:114630431
|
A | G | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+6729A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630431 | ||||||
chr4:114630639
|
A | ATT | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+6948_822+6949d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114630639 | |||||
chr4:114630639
|
AT | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG01934.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+6949delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114630639 | |||||
chr4:114630739
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.822+7037A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630739 | ||||||
chr4:114630867
|
A | C | 4 | a0001c0001t0004g0241a0001c0001t0004g0244a0001c0001t0004g0253others(1): Show | 4 | HG02717.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+7165A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630867 | ||||||
chr4:114630894
|
G | A | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+7192G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630894 | ||||||
chr4:114630937
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.822+7235T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630937 | ||||||
chr4:114631210
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+7508A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631210 | ||||||
chr4:114631741
|
T | A | 4 | a0001c0001t0003g0005a0001c0001t0003g0219a0001c0001t0003g0220others(1): Show | 6 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+8039T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631741 | ||||||
chr4:114631796
|
G | A | 2 | a0002c0002t0002g0137a0002c0002t0002g0138 | 2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.822+8094G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631796 | ||||||
chr4:114631939
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+8237C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631939 | ||||||
chr4:114632027
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.822+8325G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632027 | ||||||
chr4:114632109
|
C | T | 1 | a0001c0001t0008g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.822+8407C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632109 | ||||||
chr4:114632200
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.822+8498G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632200 | ||||||
chr4:114632419
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.822+8717G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632419 | ||||||
chr4:114632439
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+8737C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632439 | ||||||
chr4:114632518
|
C | A | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+8816C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632518 | ||||||
chr4:114632758
|
C | A | 2 | a0001c0001t0005g0057a0001c0001t0007g0058 | 2 | NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.822+9056C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632758 | ||||||
chr4:114632825
|
C | T | 41 | a0001c0001t0003g0217a0001c0001t0006g0135a0001c0001t0006g0140others(38): Show | 48 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.822+9123C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632825 | ||||||
chr4:114632831
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.822+9129C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632831 | ||||||
chr4:114632833
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+9131G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632833 | ||||||
chr4:114632920
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.822+9218A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632920 | ||||||
chr4:114632934
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+9232A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632934 | ||||||
chr4:114632969
|
G | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+9267G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632969 | ||||||
chr4:114633051
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.822+9349G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633051 | ||||||
chr4:114633122
|
A | T | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+9420A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633122 | ||||||
chr4:114633181
|
T | G | 2 | a0001c0006t0003g0234a0001c0006t0003g0240 | 2 | HG00738.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.822+9479T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633181 | ||||||
chr4:114633283
|
A | G | 29 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(26): Show | 33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.822+9581A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633283 | ||||||
chr4:114633292
|
A | C | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+9590A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633292 | ||||||
chr4:114633409
|
A | AG | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0106 | 3 | NA18983.hp1 NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.822+9709dupG | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114633409 | |||||
chr4:114633520
|
T | C | 1 | a0002c0002t0002g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+9818T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633520 | ||||||
chr4:114633799
|
C | A | 1 | a0001c0001t0001g0040 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.822+10097C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633799 | ||||||
chr4:114633805
|
G | A | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+10103G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633805 | ||||||
chr4:114634223
|
T | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+10521T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634223 | ||||||
chr4:114634226
|
A | G | 4 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216others(1): Show | 5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+10524A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634226 | ||||||
chr4:114634257
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0188 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.822+10555T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634257 | ||||||
chr4:114634303
|
T | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.822+10601T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634303 | ||||||
chr4:114634422
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.822+10720C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634422 | ||||||
chr4:114634426
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+10724T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634426 | ||||||
chr4:114634463
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0201 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.822+10761G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634463 | ||||||
chr4:114634539
|
G | A | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+10837G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634539 | ||||||
chr4:114634577
|
AT | A | 22 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0180others(19): Show | 22 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.822+10876delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634577 | ||||||
chr4:114634767
|
C | CT | 5 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+11072dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114634767 | |||||
chr4:114635028
|
C | CT | 19 | a0001c0001t0001g0082a0001c0001t0001g0180a0001c0001t0001g0181others(16): Show | 19 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.822+11339dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114635028 | |||||
chr4:114635028
|
C | CTGTT | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+11327_822+1132 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114635028 | |||||
chr4:114635328
|
G | T | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+11626G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635328 | ||||||
chr4:114635417
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0186 | 2 | HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.822+11715C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635417 | ||||||
chr4:114635497
|
G | A | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+11795G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635497 | ||||||
chr4:114635682
|
C | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+11980C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635682 | ||||||
chr4:114635719
|
T | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.822+12017T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635719 | ||||||
chr4:114635841
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+12139A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635841 | ||||||
chr4:114635869
|
A | G | 22 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0115others(19): Show | 25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+12167A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635869 | ||||||
chr4:114636002
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 7 | HG00597.hp1 HG01169.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+12300T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636002 | ||||||
chr4:114636089
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.822+12387G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636089 | ||||||
chr4:114636184
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.822+12482C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636184 | ||||||
chr4:114636264
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.822+12562G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636264 | ||||||
chr4:114636384
|
T | A | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+12682T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636384 | ||||||
chr4:114636525
|
T | TGTAAAGC others(1): Show |
5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+12824_822+1282 others(12): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114636525 | |||||
chr4:114636536
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+12834A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636536 | ||||||
chr4:114636549
|
A | C | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+12847A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636549 | ||||||
chr4:114636954
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+13252T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636954 | ||||||
chr4:114636987
|
T | C | 1 | a0001c0003t0005g0197 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.822+13285T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636987 | ||||||
chr4:114637033
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+13331A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637033 | ||||||
chr4:114637085
|
T | C | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+13383T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637085 | ||||||
chr4:114637290
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.822+13588T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637290 | ||||||
chr4:114637341
|
G | A | 6 | a0001c0001t0003g0005a0001c0001t0003g0115a0001c0001t0003g0214others(3): Show | 8 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+13639G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637341 | ||||||
chr4:114637388
|
T | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+13686T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637388 | ||||||
chr4:114637487
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+13785A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637487 | ||||||
chr4:114637758
|
T | G | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+14056T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637758 | ||||||
chr4:114637932
|
C | T | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+14230C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637932 | ||||||
chr4:114637981
|
T | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+14279T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637981 | ||||||
chr4:114638290
|
A | G | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+14588A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638290 | ||||||
chr4:114638567
|
T | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+14865T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638567 | ||||||
chr4:114638668
|
C | T | 16 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0142others(13): Show | 21 | HG00621.hp2 HG02015.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+14966C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638668 | ||||||
chr4:114638987
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+15285C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638987 | ||||||
chr4:114639152
|
T | C | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168others(1): Show | 4 | HG01109.hp2 HG02615.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+15450T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114639152 | ||||||
chr4:114639255
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+15553A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114639255 | ||||||
chr4:114639584
|
A | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.822+15882A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114639584 | ||||||
chr4:114640033
|
G | GT | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(160): Show | 176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.822+16346dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640033 | |||||
chr4:114640033
|
G | GTT | 5 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0199others(2): Show | 5 | HG00597.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+16345_822+1634 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640033 | |||||
chr4:114640033
|
GT | G | 5 | a0001c0001t0002g0132a0001c0001t0010g0222a0001c0001t0010g0223others(2): Show | 5 | HG00323.hp2 HG01243.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+16346delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640033 | |||||
chr4:114640069
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+16367C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640069 | ||||||
chr4:114640199
|
T | A | 1 | a0001c0001t0006g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.822+16497T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640199 | ||||||
chr4:114640240
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+16538C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640240 | ||||||
chr4:114640282
|
G | A | 1 | a0008c0008t0001g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.822+16580G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640282 | ||||||
chr4:114640312
|
G | A | 1 | a0001c0001t0001g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.822+16610G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640312 | ||||||
chr4:114640438
|
C | A | 1 | a0001c0006t0003g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.822+16736C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640438 | ||||||
chr4:114640455
|
A | AT | 24 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(21): Show | 26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.822+16760dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640455 | |||||
chr4:114640717
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.822+17015A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640717 | ||||||
chr4:114640765
|
T | A | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+17063T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640765 | ||||||
chr4:114640914
|
C | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+17212C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640914 | ||||||
chr4:114641011
|
G | A | 6 | a0001c0001t0004g0242a0001c0001t0004g0243a0001c0001t0008g0012others(3): Show | 8 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+17309G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114641011 | ||||||
chr4:114641285
|
C | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+17583C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114641285 | ||||||
chr4:114641536
|
G | A | 1 | a0001c0001t0007g0063 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.822+17834G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114641536 | ||||||
chr4:114642053
|
G | C | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+18351G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642053 | ||||||
chr4:114642195
|
G | A | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+18493G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642195 | ||||||
chr4:114642214
|
C | CT | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+18523dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114642214 | |||||
chr4:114642234
|
A | G | 1 | a0001c0001t0005g0077 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.822+18532A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642234 | ||||||
chr4:114642290
|
G | A | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+18588G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642290 | ||||||
chr4:114642383
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.822+18681A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642383 | ||||||
chr4:114642457
|
A | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+18755A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642457 | ||||||
chr4:114642666
|
T | G | 4 | a0001c0001t0010g0222a0001c0001t0010g0223a0001c0001t0010g0224others(1): Show | 4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+18964T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642666 | ||||||
chr4:114642903
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.822+19201T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642903 | ||||||
chr4:114642937
|
G | T | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+19235G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642937 | ||||||
chr4:114642998
|
T | A | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+19296T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642998 | ||||||
chr4:114643113
|
G | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+19411G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643113 | ||||||
chr4:114643204
|
GT | G | 4 | a0001c0001t0010g0222a0001c0001t0010g0223a0001c0001t0010g0224others(1): Show | 4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+19503delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643204 | ||||||
chr4:114643256
|
A | G | 1 | a0008c0008t0001g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.822+19554A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643256 | ||||||
chr4:114643274
|
T | G | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+19572T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643274 | ||||||
chr4:114643513
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(254): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.822+19811A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643513 | ||||||
chr4:114643741
|
G | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+20039G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643741 | ||||||
chr4:114643924
|
C | T | 1 | a0001c0001t0005g0110 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.823-20071C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643924 | ||||||
chr4:114644083
|
A | G | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823-19912A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644083 | ||||||
chr4:114644111
|
C | T | 1 | a0001c0001t0003g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.823-19884C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644111 | ||||||
chr4:114644266
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-19729C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644266 | ||||||
chr4:114644306
|
A | T | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-19689A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644306 | ||||||
chr4:114644503
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.823-19492A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644503 | ||||||
chr4:114644657
|
A | G | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-19338A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644657 | ||||||
chr4:114644723
|
T | C | 2 | a0001c0001t0011g0204a0001c0001t0011g0205 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.823-19272T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644723 | ||||||
chr4:114644733
|
A | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-19262A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644733 | ||||||
chr4:114644740
|
T | G | 2 | a0001c0003t0001g0192a0001c0003t0005g0194 | 2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.823-19255T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644740 | ||||||
chr4:114644934
|
A | G | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-19061A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644934 | ||||||
chr4:114644955
|
A | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-19040A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644955 | ||||||
chr4:114645039
|
C | CACAG | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.823-18949_823-1894 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114645039 | |||||
chr4:114645057
|
C | A | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-18938C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645057 | ||||||
chr4:114645246
|
C | A | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-18749C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645246 | ||||||
chr4:114645573
|
G | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-18422G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645573 | ||||||
chr4:114645598
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.823-18397T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645598 | ||||||
chr4:114645687
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.823-18308G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645687 | ||||||
chr4:114645805
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-18190G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645805 | ||||||
chr4:114645835
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.823-18160A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645835 | ||||||
chr4:114645869
|
C | T | 6 | a0001c0001t0005g0057a0001c0001t0007g0058a0001c0001t0007g0063others(3): Show | 6 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-18126C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645869 | ||||||
chr4:114646049
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.823-17946T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646049 | ||||||
chr4:114646127
|
A | G | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-17868A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646127 | ||||||
chr4:114646277
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.823-17718A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646277 | ||||||
chr4:114646391
|
A | C | 1 | a0001c0001t0003g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.823-17604A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646391 | ||||||
chr4:114646474
|
T | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0014t0018g0168 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-17521T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646474 | ||||||
chr4:114646856
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-17139A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646856 | ||||||
chr4:114647356
|
T | TTG | 51 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0064others(48): Show | 59 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.823-16603_823-1660 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | |||||
chr4:114647356
|
T | TTGTG | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(108): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-16605_823-1660 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | |||||
chr4:114647356
|
T | TTGTGTG | 31 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0060others(28): Show | 33 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-16607_823-1660 others(10): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | |||||
chr4:114647356
|
T | TTGTGTGT others(1): Show |
5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0106others(2): Show | 5 | HG00738.hp1 HG01109.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-16609_823-1660 others(12): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | |||||
chr4:114647356
|
TTG | T | 3 | a0001c0001t0003g0233a0001c0001t0009g0206a0001c0001t0009g0207 | 3 | HG02572.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.823-16603_823-1660 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | |||||
chr4:114647356
|
TTGTG | T | 6 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(3): Show | 6 | HG01257.hp2 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-16605_823-1660 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | |||||
chr4:114647516
|
A | G | 1 | a0001c0001t0009g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.823-16479A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647516 | ||||||
chr4:114647657
|
G | A | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.823-16338G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647657 | ||||||
chr4:114647690
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823-16305G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647690 | ||||||
chr4:114647874
|
T | G | 40 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(37): Show | 45 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.823-16121T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647874 | ||||||
chr4:114647914
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.823-16081G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647914 | ||||||
chr4:114648371
|
GT | G | 10 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0106others(7): Show | 11 | HG00621.hp1 HG00741.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-15603delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114648371 | |||||
chr4:114648371
|
GTT | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(193): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.823-15604_823-1560 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114648371 | |||||
chr4:114648433
|
G | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-15562G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648433 | ||||||
chr4:114648451
|
T | TG | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-15541dupG | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114648451 | |||||
chr4:114648505
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.823-15490A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648505 | ||||||
chr4:114648506
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.823-15489G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648506 | ||||||
chr4:114648658
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-15337A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648658 | ||||||
chr4:114649082
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.823-14913C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649082 | ||||||
chr4:114649114
|
G | T | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.823-14881G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649114 | ||||||
chr4:114649537
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0040others(1): Show | 4 | HG01081.hp2 HG01975.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-14458A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649537 | ||||||
chr4:114649552
|
A | G | 6 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0218others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-14443A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649552 | ||||||
chr4:114649718
|
C | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-14277C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649718 | ||||||
chr4:114649811
|
T | TA | 38 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(35): Show | 45 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.823-14175dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114649811 | |||||
chr4:114649812
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.823-14183A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649812 | ||||||
chr4:114649863
|
CT | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-14128delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114649863 | |||||
chr4:114650125
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13870T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650125 | ||||||
chr4:114650189
|
C | G | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-13806C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650189 | ||||||
chr4:114650219
|
G | C | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-13776G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650219 | ||||||
chr4:114650269
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13726C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650269 | ||||||
chr4:114650270
|
C | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13725C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650270 | ||||||
chr4:114650390
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13605C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650390 | ||||||
chr4:114650424
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.823-13571A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650424 | ||||||
chr4:114650495
|
A | C | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823-13500A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650495 | ||||||
chr4:114650549
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.823-13446T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650549 | ||||||
chr4:114650667
|
A | G | 39 | a0001c0001t0003g0217a0001c0001t0006g0135a0001c0001t0006g0140others(36): Show | 46 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.823-13328A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650667 | ||||||
chr4:114650870
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.823-13125A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650870 | ||||||
chr4:114650928
|
G | A | 1 | a0001c0001t0008g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823-13067G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650928 | ||||||
chr4:114650975
|
T | C | 1 | a0006c0010t0002g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.823-13020T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650975 | ||||||
chr4:114651169
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.823-12826C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651169 | ||||||
chr4:114651169
|
C | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(204): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.823-12826C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651169 | ||||||
chr4:114651235
|
A | G | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(229): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.823-12760A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651235 | ||||||
chr4:114651492
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.823-12503C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651492 | ||||||
chr4:114651574
|
A | G | 1 | a0002c0002t0002g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.823-12421A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651574 | ||||||
chr4:114651766
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.823-12229T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651766 | ||||||
chr4:114652219
|
G | T | 1 | a0001c0003t0005g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.823-11776G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652219 | ||||||
chr4:114652396
|
A | AT | 5 | a0001c0001t0002g0125a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG01934.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-11585dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114652396 | |||||
chr4:114652396
|
AT | A | 7 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(4): Show | 8 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-11585delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114652396 | |||||
chr4:114652412
|
A | G | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-11583A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652412 | ||||||
chr4:114652469
|
C | A | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.823-11526C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652469 | ||||||
chr4:114652513
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0170 | 3 | HG01257.hp1 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.823-11482T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652513 | ||||||
chr4:114652516
|
G | A | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-11479G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652516 | ||||||
chr4:114652811
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823-11184A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652811 | ||||||
chr4:114652815
|
T | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-11180T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652815 | ||||||
chr4:114652827
|
C | G | 39 | a0001c0001t0003g0217a0001c0001t0006g0135a0001c0001t0006g0140others(36): Show | 46 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.823-11168C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652827 | ||||||
chr4:114652891
|
A | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(234): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.823-11104A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652891 | ||||||
chr4:114653017
|
C | T | 1 | a0001c0001t0007g0074 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.823-10978C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114653017 | ||||||
chr4:114653291
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-10704A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114653291 | ||||||
chr4:114653334
|
C | T | 1 | a0003c0004t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.823-10661C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114653334 | ||||||
chr4:114654071
|
G | A | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-9924G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654071 | ||||||
chr4:114654112
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.823-9883C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654112 | ||||||
chr4:114654255
|
T | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.823-9740T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654255 | ||||||
chr4:114654273
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0036 | 2 | HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.823-9722C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654273 | ||||||
chr4:114654322
|
C | A | 1 | a0002c0002t0002g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.823-9673C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654322 | ||||||
chr4:114654379
|
T | A | 1 | a0001c0001t0003g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.823-9616T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654379 | ||||||
chr4:114654706
|
A | AAG | 3 | a0002c0002t0002g0010a0002c0002t0002g0136a0002c0002t0002g0177 | 4 | HG00558.hp1 NA18986.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-9279_823-9278d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114654706 | |||||
chr4:114654823
|
C | T | 1 | a0002c0002t0002g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.823-9172C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654823 | ||||||
chr4:114655066
|
G | GT | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-8918dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114655066 | |||||
chr4:114655139
|
AT | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-8853delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114655139 | |||||
chr4:114655155
|
C | T | 1 | a0001c0001t0011g0205 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.823-8840C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655155 | ||||||
chr4:114655186
|
T | C | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.823-8809T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655186 | ||||||
chr4:114655202
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.823-8793A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655202 | ||||||
chr4:114655205
|
A | G | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-8790A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655205 | ||||||
chr4:114655281
|
G | T | 1 | a0007c0012t0006g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.823-8714G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655281 | ||||||
chr4:114655828
|
A | G | 3 | a0001c0001t0005g0110a0001c0003t0005g0195a0001c0003t0005g0197 | 3 | HG02074.hp2 NA18948.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.823-8167A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655828 | ||||||
chr4:114656041
|
G | A | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-7954G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656041 | ||||||
chr4:114656225
|
C | T | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-7770C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656225 | ||||||
chr4:114656668
|
G | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-7327G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656668 | ||||||
chr4:114656697
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-7298T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656697 | ||||||
chr4:114656748
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.823-7247C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656748 | ||||||
chr4:114656841
|
C | G | 29 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(26): Show | 33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-7154C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656841 | ||||||
chr4:114656953
|
G | C | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-7042G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656953 | ||||||
chr4:114657125
|
C | A | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-6870C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657125 | ||||||
chr4:114657364
|
G | C | 1 | a0001c0003t0005g0197 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.823-6631G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657364 | ||||||
chr4:114657607
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.823-6388A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657607 | ||||||
chr4:114657609
|
T | C | 4 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216others(1): Show | 5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-6386T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657609 | ||||||
chr4:114657617
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-6378A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657617 | ||||||
chr4:114657632
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-6363G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657632 | ||||||
chr4:114657873
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0215a0001c0001t0003g0216 | 4 | HG02145.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-6122G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657873 | ||||||
chr4:114657878
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823-6117C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657878 | ||||||
chr4:114658072
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-5923G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658072 | ||||||
chr4:114658247
|
G | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-5748G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658247 | ||||||
chr4:114658285
|
C | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(162): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.823-5710C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658285 | ||||||
chr4:114658499
|
C | T | 2 | a0001c0014t0018g0168a0001c0015t0021g0165 | 2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-5496C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658499 | ||||||
chr4:114658605
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-5390T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658605 | ||||||
chr4:114658706
|
T | TA | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.823-5280dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114658706 | |||||
chr4:114658983
|
TA | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-5011delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658983 | ||||||
chr4:114659132
|
A | C | 1 | a0002c0002t0002g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.823-4863A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659132 | ||||||
chr4:114659160
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.823-4835C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659160 | ||||||
chr4:114659174
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.823-4821A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659174 | ||||||
chr4:114659290
|
A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0111 | 2 | HG00323.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.823-4705A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659290 | ||||||
chr4:114659367
|
T | C | 1 | a0001c0001t0004g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.823-4628T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659367 | ||||||
chr4:114659402
|
A | G | 1 | a0002c0002t0002g0149 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.823-4593A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659402 | ||||||
chr4:114659524
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(209): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.823-4471A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659524 | ||||||
chr4:114659545
|
T | C | 2 | a0001c0014t0018g0168a0001c0015t0021g0165 | 2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-4450T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659545 | ||||||
chr4:114659650
|
C | T | 1 | a0001c0001t0002g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.823-4345C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659650 | ||||||
chr4:114659777
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823-4218A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659777 | ||||||
chr4:114659801
|
A | C | 1 | a0001c0001t0002g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.823-4194A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659801 | ||||||
chr4:114660209
|
A | G | 8 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0218others(5): Show | 8 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-3786A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660209 | ||||||
chr4:114660224
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(236): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.823-3771T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660224 | ||||||
chr4:114660242
|
AT | A | 3 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252 | 3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823-3752delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660242 | ||||||
chr4:114660313
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823-3682C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660313 | ||||||
chr4:114660316
|
CAG | C | 3 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252 | 3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823-3676_823-3675d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660316 | |||||
chr4:114660546
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.823-3449G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660546 | ||||||
chr4:114660692
|
A | G | 2 | a0001c0006t0003g0234a0001c0006t0003g0240 | 2 | HG00738.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823-3303A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660692 | ||||||
chr4:114660710
|
G | A | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-3285G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660710 | ||||||
chr4:114660753
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.823-3242G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660753 | ||||||
chr4:114660890
|
C | CA | 20 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0003g0016others(17): Show | 21 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-3085dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660890 | |||||
chr4:114660890
|
C | CAA | 10 | a0001c0001t0004g0239a0001c0001t0004g0241a0001c0001t0004g0242others(7): Show | 10 | HG01109.hp2 HG01975.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-3086_823-3085d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660890 | |||||
chr4:114660890
|
CA | C | 11 | a0001c0001t0001g0188a0001c0001t0002g0011a0001c0001t0002g0169others(8): Show | 13 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-3085delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660890 | |||||
chr4:114660906
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(118): Show | 126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.823-3089A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660906 | ||||||
chr4:114660958
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.823-3037A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660958 | ||||||
chr4:114661002
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.823-2993T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661002 | ||||||
chr4:114661138
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-2857A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661138 | ||||||
chr4:114661153
|
A | G | 29 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(26): Show | 33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-2842A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661153 | ||||||
chr4:114661360
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823-2635T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661360 | ||||||
chr4:114661484
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-2511C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661484 | ||||||
chr4:114661718
|
C | T | 2 | a0001c0001t0003g0228a0001c0001t0003g0229 | 2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.823-2277C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661718 | ||||||
chr4:114661850
|
C | G | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823-2145C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661850 | ||||||
chr4:114662002
|
C | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-1993C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662002 | ||||||
chr4:114662005
|
C | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-1990C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662005 | ||||||
chr4:114662008
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823-1987A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662008 | ||||||
chr4:114662048
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.823-1947A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662048 | ||||||
chr4:114662334
|
G | A | 1 | a0008c0008t0001g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.823-1661G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662334 | ||||||
chr4:114662414
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.823-1581G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662414 | ||||||
chr4:114662448
|
A | G | 1 | a0002c0002t0002g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823-1547A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662448 | ||||||
chr4:114662567
|
C | T | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(207): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.823-1428C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662567 | ||||||
chr4:114662779
|
CTTAA | C | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-1211_823-1208d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662779 | |||||
chr4:114662816
|
CTT | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 44 | HG00597.hp2 HG01168.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.823-1153_823-1152d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662816 | |||||
chr4:114662816
|
CTTT | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(184): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.823-1154_823-1152d others(5): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662816 | |||||
chr4:114662816
|
CTTTT | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0002g0011others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-1155_823-1152d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662816 | |||||
chr4:114662865
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.823-1130G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662865 | ||||||
chr4:114662889
|
A | G | 16 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0003g0233others(13): Show | 16 | HG01255.hp1 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-1106A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662889 | ||||||
chr4:114662899
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-1096C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662899 | ||||||
chr4:114662990
|
T | C | 40 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(37): Show | 47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.823-1005T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662990 | ||||||
chr4:114663066
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(207): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.823-929A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663066 | ||||||
chr4:114663122
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.823-873C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663122 | ||||||
chr4:114663214
|
G | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-781G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663214 | ||||||
chr4:114663401
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-594C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663401 | ||||||
chr4:114663407
|
G | A | 1 | a0001c0001t0010g0222 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-588G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663407 | ||||||
chr4:114663465
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.823-530T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663465 | ||||||
chr4:114663650
|
C | A | 3 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252 | 3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823-345C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663650 | ||||||
chr4:114663707
|
A | G | 7 | a0001c0001t0007g0058a0001c0001t0007g0063a0001c0001t0007g0068others(4): Show | 7 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-288A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663707 | ||||||
chr4:114663873
|
C | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(165): Show | 181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.823-122C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663873 | ||||||
chr4:114663886
|
T | C | 4 | a0002c0002t0002g0139a0002c0002t0002g0145a0002c0002t0002g0146others(1): Show | 4 | HG00140.hp1 HG00733.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-109T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663886 | ||||||
chr4:114664251
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.965+114G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664251 | ||||||
chr4:114664359
|
A | G | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.965+222A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664359 | ||||||
chr4:114664680
|
C | T | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.965+543C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664680 | ||||||
chr4:114664755
|
C | T | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+618C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664755 | ||||||
chr4:114664791
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.965+654G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664791 | ||||||
chr4:114664943
|
C | T | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.966-737C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664943 | ||||||
chr4:114665137
|
T | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.966-543T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665137 | ||||||
chr4:114665320
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(207): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.966-360T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665320 | ||||||
chr4:114665419
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.966-261A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665419 | ||||||
chr4:114665540
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(202): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.966-140A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665540 | ||||||
chr4:114665548
|
A | G | 1 | a0001c0001t0009g0015 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.966-132A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665548 | ||||||
chr4:114665586
|
A | C | 1 | a0001c0001t0023g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.966-94A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665586 | ||||||
chr4:114665623
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.966-57C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665623 | ||||||
chr4:114665640
|
T | C | 6 | a0001c0001t0003g0005a0001c0001t0003g0115a0001c0001t0003g0214others(3): Show | 8 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.966-40T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665640 | ||||||
chr4:114665786
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1042+30G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114665786 | ||||||
chr4:114665816
|
C | CT | 12 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0178others(9): Show | 12 | HG00639.hp1 HG00738.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042+75dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 114665816 | |||||
chr4:114666275
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1042+519C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666275 | ||||||
chr4:114666658
|
G | A | 4 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042+902G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666658 | ||||||
chr4:114666914
|
G | C | 1 | a0001c0001t0003g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1042+1158G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666914 | ||||||
chr4:114666993
|
A | G | 1 | a0003c0004t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1043-1092A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666993 | ||||||
chr4:114667067
|
T | A | 3 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252 | 3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1043-1018T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667067 | ||||||
chr4:114667081
|
C | A | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1043-1004C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667081 | ||||||
chr4:114667118
|
A | C | 1 | a0003c0004t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1043-967A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667118 | ||||||
chr4:114667120
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1043-965G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667120 | ||||||
chr4:114667131
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1043-954G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667131 | ||||||
chr4:114667219
|
C | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1043-866C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667219 | ||||||
chr4:114667355
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1043-730A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667355 | ||||||
chr4:114667471
|
T | A | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043-614T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667471 | ||||||
chr4:114667531
|
A | G | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1043-554A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667531 | ||||||
chr4:114667805
|
T | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(164): Show | 179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1043-280T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667805 | ||||||
chr4:114668003
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(209): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1043-82C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114668003 | ||||||
chr4:114668584
|
T | C | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1262+280T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114668584 | ||||||
chr4:114668587
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1262+283T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114668587 | ||||||
chr4:114668819
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1262+515C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114668819 | ||||||
chr4:114669067
|
C | G | 16 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0003g0233others(13): Show | 16 | HG01255.hp1 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.1262+763C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669067 | ||||||
chr4:114669381
|
C | CAT | 9 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0214others(6): Show | 9 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+1102_1262+110 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669381
|
CAT | C | 12 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0250others(9): Show | 12 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1262+1102_1262+110 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669381
|
CATAT | C | 28 | a0001c0001t0002g0006a0001c0001t0002g0020a0001c0001t0002g0133others(25): Show | 32 | HG00438.hp2 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1262+1100_1262+110 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669381
|
CATATAT | C | 71 | a0001c0001t0002g0009a0001c0001t0002g0019a0001c0001t0002g0021others(68): Show | 82 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1262+1098_1262+110 others(10): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669381
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1262+1094_1262+110 others(14): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669381
|
CATATATA others(5): Show |
C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(118): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1262+1092_1262+110 others(16): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669381
|
CATATATA others(7): Show |
C | 1 | a0003c0004t0001g0007 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1262+1090_1262+110 others(18): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | |||||
chr4:114669387
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0020 | 3 | NA18947.hp1 NA18961.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1262+1083T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669387 | ||||||
chr4:114669467
|
T | G | 1 | a0002c0002t0002g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1262+1163T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669467 | ||||||
chr4:114669633
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1262+1329C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669633 | ||||||
chr4:114669653
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0188 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1262+1349A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669653 | ||||||
chr4:114669665
|
A | G | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1262+1361A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669665 | ||||||
chr4:114669693
|
T | C | 1 | a0002c0002t0002g0230 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1262+1389T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669693 | ||||||
chr4:114670073
|
G | T | 1 | a0001c0001t0004g0244 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1262+1769G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670073 | ||||||
chr4:114670088
|
T | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+1784T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670088 | ||||||
chr4:114670115
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1262+1811A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670115 | ||||||
chr4:114670348
|
G | A | 6 | a0001c0001t0009g0015a0001c0001t0009g0206a0001c0001t0009g0207others(3): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1262+2044G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670348 | ||||||
chr4:114670430
|
C | CA | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(149): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1262+2151dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114670430 | |||||
chr4:114670430
|
C | CAA | 38 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0056others(35): Show | 40 | HG01081.hp1 HG01081.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1262+2150_1262+215 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114670430 | |||||
chr4:114670430
|
CA | C | 6 | a0001c0001t0003g0217a0001c0001t0003g0258a0001c0001t0004g0253others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+2151delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114670430 | |||||
chr4:114670479
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1262+2175G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670479 | ||||||
chr4:114670587
|
C | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(123): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1262+2283C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670587 | ||||||
chr4:114670801
|
C | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+2497C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670801 | ||||||
chr4:114671101
|
C | G | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1262+2797C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671101 | ||||||
chr4:114671127
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1262+2823G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671127 | ||||||
chr4:114671186
|
C | G | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1262+2882C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671186 | ||||||
chr4:114671363
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1262+3059A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671363 | ||||||
chr4:114671570
|
T | C | 1 | a0001c0001t0006g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1262+3266T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671570 | ||||||
chr4:114671591
|
A | G | 24 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(21): Show | 26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1262+3287A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671591 | ||||||
chr4:114671715
|
T | TA | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+3416dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114671715 | |||||
chr4:114671856
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1262+3552G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671856 | ||||||
chr4:114672054
|
C | A | 1 | a0001c0001t0008g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1262+3750C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672054 | ||||||
chr4:114672384
|
A | G | 7 | a0001c0001t0007g0058a0001c0001t0007g0063a0001c0001t0007g0068others(4): Show | 7 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263-3541A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672384 | ||||||
chr4:114672386
|
A | C | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-3539A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672386 | ||||||
chr4:114672508
|
G | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(253): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1263-3417G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672508 | ||||||
chr4:114672548
|
C | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0117a0001c0001t0002g0118others(3): Show | 7 | HG00741.hp2 HG01099.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263-3377C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672548 | ||||||
chr4:114672622
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(162): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1263-3303G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672622 | ||||||
chr4:114672666
|
G | T | 4 | a0001c0001t0006g0135a0001c0001t0006g0140a0001c0001t0006g0141others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-3259G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672666 | ||||||
chr4:114672701
|
G | A | 35 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0019others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1263-3224G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672701 | ||||||
chr4:114672737
|
T | G | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1263-3188T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672737 | ||||||
chr4:114672781
|
T | C | 1 | a0001c0014t0018g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1263-3144T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672781 | ||||||
chr4:114672838
|
T | A | 1 | a0001c0014t0018g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1263-3087T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672838 | ||||||
chr4:114672909
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1263-3016C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672909 | ||||||
chr4:114673035
|
A | G | 2 | a0001c0014t0018g0168a0001c0015t0021g0165 | 2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1263-2890A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673035 | ||||||
chr4:114673168
|
AT | A | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(233): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1263-2752delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114673168 | |||||
chr4:114673217
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0169a0001c0001t0002g0170 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-2708A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673217 | ||||||
chr4:114673260
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1263-2665C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673260 | ||||||
chr4:114673296
|
T | TAAAAAAA others(26): Show |
1 | a0001c0001t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1263-2628_1263-262 others(37): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114673296 | |||||
chr4:114673298
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1263-2627C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673298 | ||||||
chr4:114673300
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1263-2625T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673300 | ||||||
chr4:114673332
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1263-2593A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673332 | ||||||
chr4:114673424
|
A | T | 1 | a0001c0015t0021g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1263-2501A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673424 | ||||||
chr4:114673444
|
G | T | 1 | a0001c0001t0015g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1263-2481G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673444 | ||||||
chr4:114674020
|
C | T | 2 | a0001c0007t0014g0255a0001c0007t0019g0254 | 2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1263-1905C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674020 | ||||||
chr4:114674073
|
G | T | 1 | a0002c0002t0002g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1263-1852G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674073 | ||||||
chr4:114674113
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-1812A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674113 | ||||||
chr4:114674201
|
G | T | 1 | a0001c0001t0012g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1263-1724G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674201 | ||||||
chr4:114674241
|
TAATCATT others(9): Show |
T | 4 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0080others(1): Show | 4 | HG01256.hp2 HG01516.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-1682_1263-166 others(20): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114674241 | |||||
chr4:114674243
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1263-1682A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674243 | ||||||
chr4:114674378
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1263-1547T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674378 | ||||||
chr4:114674491
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(207): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1263-1434T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674491 | ||||||
chr4:114674545
|
A | G | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-1380A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674545 | ||||||
chr4:114674589
|
A | C | 5 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0252others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263-1336A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674589 | ||||||
chr4:114674866
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1263-1059T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674866 | ||||||
chr4:114674879
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1263-1046G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674879 | ||||||
chr4:114674892
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(255): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1263-1033A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674892 | ||||||
chr4:114674936
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1263-989G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674936 | ||||||
chr4:114675190
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(207): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1263-735A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675190 | ||||||
chr4:114675469
|
G | A | 1 | a0001c0001t0016g0227 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1263-456G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675469 | ||||||
chr4:114675490
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-435C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675490 | ||||||
chr4:114675515
|
C | T | 5 | a0001c0001t0011g0203a0001c0001t0011g0204a0001c0001t0011g0205others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-410C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675515 | ||||||
chr4:114675536
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(209): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1263-389T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675536 | ||||||
chr4:114675556
|
C | T | 1 | a0002c0002t0017g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1263-369C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675556 | ||||||
chr4:114675568
|
G | A | 3 | a0001c0001t0004g0241a0001c0001t0004g0253a0005c0009t0004g0235 | 3 | HG03209.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1263-357G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675568 | ||||||
chr4:114675735
|
G | T | 1 | a0001c0013t0003g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1263-190G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675735 | ||||||
chr4:114675739
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(115): Show | 127 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1263-159dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114675739 | |||||
chr4:114675739
|
C | CAA | 43 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(40): Show | 46 | HG00323.hp2 HG00558.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1263-160_1263-159d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114675739 | |||||
chr4:114675739
|
C | CAAA | 9 | a0001c0001t0002g0020a0001c0001t0002g0116a0001c0001t0002g0117others(6): Show | 9 | HG00438.hp2 HG01099.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1263-161_1263-159d others(5): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114675739 |