geneid | 944 |
---|---|
ensemblid | ENSG00000106952.8 |
hgncid | 11938 |
symbol | TNFSF8 |
name | TNF superfamily member 8 |
refseq_nuc | NM_001244.4 |
refseq_prot | NP_001235.1 |
ensembl_nuc | ENST00000223795.3 |
ensembl_prot | ENSP00000223795.2 |
mane_status | MANE Select |
chr | chr9 |
start | 114901145 |
end | 114930591 |
strand | - |
ver | v1.2 |
region | chr9:114901145-114930591 |
region5000 | chr9:114896145-114935591 |
regionname0 | TNFSF8_chr9_114901145_114930591 |
regionname5000 | TNFSF8_chr9_114896145_114935591 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 234 | 403 | 92 | 80 | 173 | 12 | 44 | 133 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0002 | 0/0 | 234 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 705 | 278 | 78 | 41 | 123 | 7 | 28 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
c0002 | 0/1 | 705 | 125 | 14 | 39 | 50 | 5 | 16 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
c0003 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3075 | 141 | 17 | 19 | 72 | 7 | 25 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0002 | 0/1 | 3075 | 104 | 13 | 31 | 40 | 4 | 15 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0003 | 0/0 | 3075 | 53 | 42 | 9 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0004 | 0/0 | 3075 | 34 | 0 | 8 | 26 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0005 | 0/0 | 3075 | 12 | 11 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0006 | 0/0 | 3075 | 9 | 0 | 0 | 9 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0007 | 0/0 | 3075 | 8 | 0 | 0 | 8 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0008 | 0/0 | 3073 | 5 | 0 | 1 | 3 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0009 | 0/0 | 3075 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0010 | 0/0 | 3075 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0011 | 0/0 | 3073 | 4 | 0 | 4 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0012 | 0/0 | 3073 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0013 | 0/0 | 3075 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0014 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0015 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0016 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0017 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0018 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0019 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0020 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0021 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0022 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0023 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0024 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0025 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0026 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0027 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0028 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0029 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0030 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0031 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0032 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
t0033 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 6 | 6 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0005 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0007 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0016 | 0/1 | 3 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0024 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 705 | 278 | 78 | 41 | 123 | 7 | 28 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002 | 0/1 | 705 | 125 | 14 | 39 | 50 | 5 | 16 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0002c0003 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3779 | 141 | 17 | 19 | 72 | 7 | 25 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0003 | 0/0 | 3779 | 53 | 42 | 9 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0004 | 0/0 | 3779 | 34 | 0 | 8 | 26 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0005 | 0/0 | 3779 | 12 | 11 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0006 | 0/0 | 3779 | 9 | 0 | 0 | 9 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0007 | 0/0 | 3779 | 7 | 0 | 0 | 7 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0009 | 0/0 | 3779 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0013 | 0/0 | 3779 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0015 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0018 | 0/0 | 3779 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0021 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0022 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0023 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0024 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0025 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0026 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0027 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0028 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0029 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0030 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0031 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0032 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0001t0033 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0002 | 0/1 | 3779 | 104 | 13 | 31 | 40 | 4 | 15 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0008 | 0/0 | 3777 | 5 | 0 | 1 | 3 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0010 | 0/0 | 3779 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0011 | 0/0 | 3777 | 4 | 0 | 4 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0012 | 0/0 | 3777 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0014 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0016 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0017 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0019 | 0/0 | 3779 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0001c0002t0020 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
a0002c0003t0007 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | copy fasta | chr9 | 114896145 | 114935591 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0005 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0024 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0001 | 0/0 | 12 | 0 | 6 | 6 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0007g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0009g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0009g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0013g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0018g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0021g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0022g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0023g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0024g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0025g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0026g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0027g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0028g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0029g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0030g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0031g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0032g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0007 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0016 | 0/1 | 3 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0008g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0010g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0010g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0010g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0011g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0011g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0011g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0012g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0014g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0016g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0019g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0001c0002t0020g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
a0002c0003t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0191 | EUR | GBR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0187 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00673 | hp2 | a0001 | c0001 | t0029 | g0079 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00733 | hp1 | a0001 | c0002 | t0011 | g0037 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0172 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01081 | hp2 | a0001 | c0001 | t0027 | g0064 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0224 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01167 | hp1 | a0001 | c0002 | t0014 | g0055 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01192 | hp2 | a0001 | c0001 | t0031 | g0263 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0226 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01255 | hp2 | a0001 | c0002 | t0016 | g0166 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01261 | hp2 | a0001 | c0001 | t0028 | g0112 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0161 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01358 | hp2 | a0001 | c0002 | t0008 | g0196 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01515 | hp1 | a0001 | c0002 | t0008 | g0130 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0220 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0126 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01928 | hp2 | a0001 | c0002 | t0020 | g0229 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0164 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0297 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02004 | hp2 | a0001 | c0002 | t0011 | g0201 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02027 | hp1 | a0001 | c0002 | t0008 | g0175 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0302 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02074 | hp2 | a0001 | c0001 | t0009 | g0287 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02148 | hp2 | a0001 | c0002 | t0011 | g0209 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0252 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02293 | hp1 | a0001 | c0001 | t0032 | g0290 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02293 | hp2 | a0001 | c0002 | t0011 | g0037 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0271 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02886 | hp1 | a0001 | c0001 | t0022 | g0248 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03130 | hp2 | a0001 | c0001 | t0024 | g0234 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0235 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0171 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0186 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03704 | hp1 | a0001 | c0001 | t0018 | g0217 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0185 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0250 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0170 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04184 | hp1 | a0001 | c0002 | t0019 | g0160 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18747 | hp1 | a0001 | c0001 | t0030 | g0077 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0101 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18945 | hp2 | a0001 | c0002 | t0012 | g0039 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18949 | hp2 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18950 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18957 | hp1 | a0001 | c0002 | t0010 | g0053 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18960 | hp1 | a0001 | c0001 | t0025 | g0134 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18965 | hp2 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18966 | hp1 | a0001 | c0002 | t0010 | g0053 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18966 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18969 | hp1 | a0001 | c0002 | t0010 | g0303 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18974 | hp1 | a0001 | c0002 | t0010 | g0052 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18985 | hp2 | a0001 | c0002 | t0008 | g0218 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18987 | hp2 | a0001 | c0001 | t0007 | g0306 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18991 | hp1 | a0001 | c0002 | t0012 | g0039 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18994 | hp2 | a0001 | c0002 | t0008 | g0194 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19000 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19001 | hp1 | a0002 | c0003 | t0007 | g0307 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0305 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19003 | hp1 | a0001 | c0001 | t0033 | g0294 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19004 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19009 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0162 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19030 | hp2 | a0001 | c0001 | t0021 | g0280 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0300 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19059 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19062 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19062 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19070 | hp1 | a0001 | c0001 | t0009 | g0295 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19090 | hp1 | a0001 | c0002 | t0010 | g0052 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA19240 | hp2 | a0001 | c0001 | t0026 | g0091 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ASW | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | ASW | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0190 | EUR | TSI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0188 | SAS | GIH | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | USA | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
HG06807 | hp2 | a0001 | c0002 | t0017 | g0208 | AFR | USA | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0016 | REF | REF | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0024 | REF | REF | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114904017
|
T | G | 1 | a0002 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.619A>C | p.Asn207His | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 907/3779 | 619/705 | 207/234 | chr9 | 114904017 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114905862
|
C | T | 1 | a0001c0002 | 125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
synonymous_variant | LOW | c.276G>A | p.Arg92Arg | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/4 | 564/3779 | 276/705 | 92/234 | chr9 | 114905862 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114901270
|
T | C | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(14): Show | 227 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2661 | chr9 | 114901270 | |||||
chr9:114901328
|
T | G | 2 | a0001c0001t0013a0001c0001t0023 | 3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2603A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2603 | chr9 | 114901328 | |||||
chr9:114901349
|
T | C | 2 | a0001c0001t0013a0001c0001t0023 | 3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2582A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2582 | chr9 | 114901349 | |||||
chr9:114901384
|
G | T | 1 | a0001c0001t0027 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2547C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2547 | chr9 | 114901384 | |||||
chr9:114901414
|
G | A | 1 | a0001c0002t0017 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2517 | chr9 | 114901414 | |||||
chr9:114901520
|
G | C | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): Show | 229 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2411C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2411 | chr9 | 114901520 | |||||
chr9:114901604
|
G | T | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): Show | 229 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2327C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2327 | chr9 | 114901604 | |||||
chr9:114901700
|
T | C | 1 | a0001c0001t0022 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2231 | chr9 | 114901700 | |||||
chr9:114901877
|
T | C | 1 | a0001c0001t0028 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2054A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2054 | chr9 | 114901877 | |||||
chr9:114901892
|
T | C | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(16): Show | 230 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2039A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2039 | chr9 | 114901892 | |||||
chr9:114901931
|
T | C | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(16): Show | 230 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2000A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2000 | chr9 | 114901931 | |||||
chr9:114901961
|
G | A | 1 | a0001c0001t0029 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1970 | chr9 | 114901961 | |||||
chr9:114902100
|
C | T | 1 | a0001c0001t0009 | 5 | HG02074.hp2 NA18950.hp2 NA19000.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1831G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1831 | chr9 | 114902100 | |||||
chr9:114902164
|
G | A | 1 | a0001c0001t0006 | 9 | NA18747.hp2 NA18957.hp2 NA18965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1767C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1767 | chr9 | 114902164 | |||||
chr9:114902293
|
C | T | 2 | a0001c0001t0007a0002c0003t0007 | 8 | HG02074.hp1 NA18949.hp2 NA18967.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1638G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1638 | chr9 | 114902293 | |||||
chr9:114902336
|
T | G | 1 | a0001c0002t0019 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1595 | chr9 | 114902336 | |||||
chr9:114902377
|
T | A | 1 | a0001c0002t0011 | 4 | HG00733.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1554A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1554 | chr9 | 114902377 | |||||
chr9:114902461
|
A | G | 1 | a0001c0001t0024 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1470T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1470 | chr9 | 114902461 | |||||
chr9:114902470
|
G | A | 1 | a0001c0001t0005 | 12 | HG01496.hp1 HG01884.hp1 HG02572.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1461C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1461 | chr9 | 114902470 | |||||
chr9:114902613
|
C | G | 1 | a0001c0001t0023 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1318G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1318 | chr9 | 114902613 | |||||
chr9:114902654
|
T | A | 1 | a0001c0001t0030 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1277A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1277 | chr9 | 114902654 | |||||
chr9:114902907
|
A | G | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(17): Show | 231 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1024T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1024 | chr9 | 114902907 | |||||
chr9:114902913
|
C | T | 3 | a0001c0001t0007a0001c0001t0009a0002c0003t0007 | 13 | HG02074.hp1 HG02074.hp2 NA18949.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1018G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1018 | chr9 | 114902913 | |||||
chr9:114903050
|
G | T | 1 | a0001c0001t0026 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 881 | chr9 | 114903050 | |||||
chr9:114903077
|
C | T | 1 | a0001c0001t0009 | 5 | HG02074.hp2 NA18950.hp2 NA19000.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*854G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 854 | chr9 | 114903077 | |||||
chr9:114903081
|
C | A | 1 | a0001c0001t0032 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 850 | chr9 | 114903081 | |||||
chr9:114903099
|
A | G | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(16): Show | 230 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*832T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 832 | chr9 | 114903099 | |||||
chr9:114903155
|
A | G | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(23): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*776T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 776 | chr9 | 114903155 | |||||
chr9:114903290
|
C | G | 11 | a0001c0001t0018a0001c0002t0002a0001c0002t0008others(8): Show | 126 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 641 | chr9 | 114903290 | |||||
chr9:114903320
|
G | A | 1 | a0001c0001t0031 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*611C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 611 | chr9 | 114903320 | |||||
chr9:114903423
|
GGA | G | 3 | a0001c0002t0008a0001c0002t0011a0001c0002t0012 | 11 | HG00733.hp1 HG01358.hp2 HG01515.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*506_*507delTC | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 506 | chr9 | 114903423 | |||||
chr9:114903427
|
G | C | 3 | a0001c0002t0008a0001c0002t0011a0001c0002t0012 | 11 | HG00733.hp1 HG01358.hp2 HG01515.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*504C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 504 | chr9 | 114903427 | |||||
chr9:114903429
|
T | C | 3 | a0001c0002t0008a0001c0002t0011a0001c0002t0012 | 11 | HG00733.hp1 HG01358.hp2 HG01515.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*502A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 502 | chr9 | 114903429 | |||||
chr9:114903454
|
G | A | 1 | a0001c0002t0020 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 477 | chr9 | 114903454 | |||||
chr9:114903472
|
T | C | 11 | a0001c0001t0018a0001c0002t0002a0001c0002t0008others(8): Show | 126 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 459 | chr9 | 114903472 | |||||
chr9:114903568
|
C | T | 1 | a0001c0001t0021 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 363 | chr9 | 114903568 | |||||
chr9:114903586
|
G | A | 11 | a0001c0001t0018a0001c0002t0002a0001c0002t0008others(8): Show | 126 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*345C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 345 | chr9 | 114903586 | |||||
chr9:114903605
|
G | A | 4 | a0001c0001t0004a0001c0001t0009a0001c0001t0032others(1): Show | 41 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*326C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 326 | chr9 | 114903605 | |||||
chr9:114903651
|
A | T | 11 | a0001c0001t0018a0001c0002t0002a0001c0002t0008others(8): Show | 126 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*280T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 280 | chr9 | 114903651 | |||||
chr9:114903917
|
C | T | 1 | a0001c0001t0015 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 14 | chr9 | 114903917 | |||||
chr9:114930390
|
C | T | 1 | a0001c0002t0014 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/4 | 87 | chr9 | 114930390 | |||||
chr9:114930508
|
T | G | 3 | a0001c0001t0007a0001c0002t0010a0002c0003t0007 | 13 | HG02074.hp1 NA18949.hp2 NA18957.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-205A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/4 | 205 | chr9 | 114930508 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114904342
|
A | G | 1 | a0001c0002t0002g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.311-17T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904342 | ||||||
chr9:114904375
|
G | A | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.311-50C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904375 | ||||||
chr9:114904398
|
G | A | 181 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(178): Show | 244 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.311-73C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904398 | ||||||
chr9:114904496
|
G | A | 95 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(92): Show | 125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.311-171C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904496 | ||||||
chr9:114904644
|
A | T | 184 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(181): Show | 247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.311-319T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904644 | ||||||
chr9:114904746
|
T | C | 1 | a0001c0001t0001g0025 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.311-421A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904746 | ||||||
chr9:114904849
|
C | G | 1 | a0001c0001t0027g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311-524G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904849 | ||||||
chr9:114904881
|
A | G | 95 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(92): Show | 125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.311-556T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904881 | ||||||
chr9:114904962
|
C | T | 95 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(92): Show | 125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.311-637G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904962 | ||||||
chr9:114905163
|
T | C | 88 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(85): Show | 121 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(118): Show |
intron_variant | MODIFIER | c.310+665A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905163 | ||||||
chr9:114905169
|
C | T | 3 | a0001c0002t0011g0037a0001c0002t0011g0201a0001c0002t0011g0209 | 4 | HG00733.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+659G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905169 | ||||||
chr9:114905172
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310+656C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905172 | ||||||
chr9:114905183
|
A | C | 17 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0049others(14): Show | 36 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.310+645T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905183 | ||||||
chr9:114905491
|
T | C | 185 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(182): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.310+337A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905491 | ||||||
chr9:114905569
|
G | A | 1 | a0001c0001t0021g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.310+259C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905569 | ||||||
chr9:114905608
|
G | T | 11 | a0001c0002t0002g0013a0001c0002t0002g0129a0001c0002t0002g0131others(8): Show | 13 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.310+220C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905608 | ||||||
chr9:114905657
|
G | A | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.310+171C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905657 | ||||||
chr9:114905657
|
G | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0049others(17): Show | 41 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.310+171C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905657 | ||||||
chr9:114905713
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0149 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.310+115T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905713 | ||||||
chr9:114905774
|
A | G | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.310+54T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905774 | ||||||
chr9:114905939
|
G | A | 1 | a0001c0001t0003g0272 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239-40C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114905939 | ||||||
chr9:114906081
|
A | T | 91 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(88): Show | 125 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-182T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906081 | ||||||
chr9:114906239
|
GAGGGGTA others(28): Show |
G | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.239-375_239-341del others(35): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906239 | ||||||
chr9:114906273
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0251 | 4 | HG01243.hp2 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-374T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906273 | ||||||
chr9:114906827
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0289 | 3 | NA18971.hp1 NA18972.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.239-928T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906827 | ||||||
chr9:114906990
|
C | T | 29 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0049others(26): Show | 52 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.239-1091G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906990 | ||||||
chr9:114907019
|
A | G | 184 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(181): Show | 247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.239-1120T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907019 | ||||||
chr9:114907035
|
G | A | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239-1136C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907035 | ||||||
chr9:114907037
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239-1138G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907037 | ||||||
chr9:114907129
|
G | A | 1 | a0001c0002t0002g0226 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.239-1230C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907129 | ||||||
chr9:114907305
|
C | T | 277 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(274): Show | 364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.239-1406G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907305 | ||||||
chr9:114907352
|
G | A | 1 | a0001c0001t0004g0296 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.239-1453C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907352 | ||||||
chr9:114907419
|
A | T | 91 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(88): Show | 125 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-1520T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907419 | ||||||
chr9:114907462
|
C | T | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.239-1563G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907462 | ||||||
chr9:114907534
|
C | G | 92 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.239-1635G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907534 | ||||||
chr9:114907585
|
C | T | 2 | a0001c0001t0013g0271a0001c0001t0013g0300 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239-1686G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907585 | ||||||
chr9:114907660
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-1761G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907660 | ||||||
chr9:114907673
|
T | C | 1 | a0001c0001t0003g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.239-1774A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907673 | ||||||
chr9:114907685
|
C | T | 1 | a0001c0001t0004g0051 | 2 | NA18953.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.239-1786G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907685 | ||||||
chr9:114907978
|
G | C | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.239-2079C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907978 | ||||||
chr9:114907994
|
C | T | 5 | a0001c0001t0007g0054a0001c0001t0007g0304a0001c0001t0007g0306others(2): Show | 6 | NA18949.hp2 NA18967.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-2095G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907994 | ||||||
chr9:114908107
|
C | T | 2 | a0001c0001t0013g0271a0001c0001t0013g0300 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239-2208G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908107 | ||||||
chr9:114908384
|
A | T | 184 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(181): Show | 247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.239-2485T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908384 | ||||||
chr9:114908469
|
T | A | 1 | a0001c0002t0002g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.239-2570A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908469 | ||||||
chr9:114908645
|
G | GA | 93 | a0001c0001t0001g0137a0001c0001t0003g0018a0001c0001t0003g0019others(90): Show | 127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.239-2747dupT | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908645 | ||||||
chr9:114908964
|
A | C | 1 | a0001c0001t0025g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.239-3065T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908964 | ||||||
chr9:114909156
|
C | T | 1 | a0001c0002t0002g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.239-3257G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909156 | ||||||
chr9:114909245
|
G | T | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 402 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.239-3346C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909245 | ||||||
chr9:114909335
|
G | A | 1 | a0001c0002t0002g0205 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.239-3436C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909335 | ||||||
chr9:114909413
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.239-3514T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909413 | ||||||
chr9:114909419
|
G | A | 17 | a0001c0001t0003g0046a0001c0001t0003g0268a0001c0001t0003g0278others(14): Show | 20 | HG01496.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-3520C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909419 | ||||||
chr9:114909515
|
G | A | 2 | a0001c0001t0013g0271a0001c0001t0013g0300 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239-3616C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909515 | ||||||
chr9:114909697
|
C | T | 1 | a0001c0002t0002g0225 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.239-3798G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909697 | ||||||
chr9:114909964
|
T | C | 61 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(58): Show | 72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.239-4065A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909964 | ||||||
chr9:114909973
|
C | G | 2 | a0001c0002t0002g0163a0001c0002t0002g0189 | 2 | HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.239-4074G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909973 | ||||||
chr9:114909992
|
A | C | 2 | a0001c0001t0003g0261a0001c0001t0003g0265 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.239-4093T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909992 | ||||||
chr9:114910033
|
A | G | 1 | a0001c0001t0004g0293 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.239-4134T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910033 | ||||||
chr9:114910386
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-4487C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910386 | ||||||
chr9:114910452
|
C | G | 1 | a0001c0001t0003g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239-4553G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910452 | ||||||
chr9:114910480
|
T | C | 185 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(182): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.239-4581A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910480 | ||||||
chr9:114910651
|
A | T | 1 | a0001c0001t0003g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-4752T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910651 | ||||||
chr9:114910854
|
C | T | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.239-4955G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910854 | ||||||
chr9:114910866
|
A | C | 92 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(89): Show | 127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.239-4967T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910866 | ||||||
chr9:114911189
|
C | T | 1 | a0001c0001t0003g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-5290G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911189 | ||||||
chr9:114911190
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-5291C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911190 | ||||||
chr9:114911293
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.239-5394G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911293 | ||||||
chr9:114911307
|
A | G | 2 | a0001c0001t0003g0046a0001c0001t0003g0268 | 3 | HG02109.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.239-5408T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911307 | ||||||
chr9:114911330
|
G | A | 2 | a0001c0002t0002g0211a0001c0002t0002g0212 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.239-5431C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911330 | ||||||
chr9:114911692
|
G | A | 1 | a0001c0002t0017g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.239-5793C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911692 | ||||||
chr9:114911731
|
C | T | 1 | a0001c0001t0007g0308 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.239-5832G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911731 | ||||||
chr9:114911873
|
T | C | 2 | a0001c0001t0003g0238a0001c0001t0003g0246 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.239-5974A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911873 | ||||||
chr9:114911895
|
A | G | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.239-5996T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911895 | ||||||
chr9:114911912
|
C | T | 1 | a0001c0001t0003g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-6013G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911912 | ||||||
chr9:114911930
|
G | T | 2 | a0001c0001t0003g0281a0001c0001t0003g0282 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.239-6031C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911930 | ||||||
chr9:114911970
|
A | G | 61 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(58): Show | 72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.239-6071T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911970 | ||||||
chr9:114912040
|
C | T | 48 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0017others(45): Show | 66 | HG00558.hp1 HG00597.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.238+6056G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912040 | ||||||
chr9:114912096
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0108others(1): Show | 7 | HG02698.hp2 HG03017.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+6000C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912096 | ||||||
chr9:114912253
|
A | C | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+5843T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912253 | ||||||
chr9:114912333
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.238+5763T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912333 | ||||||
chr9:114912452
|
C | T | 1 | a0001c0001t0004g0049 | 2 | NA18956.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.238+5644G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912452 | ||||||
chr9:114912493
|
G | T | 5 | a0001c0001t0001g0122a0001c0001t0001g0149a0001c0001t0001g0178others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+5603C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912493 | ||||||
chr9:114912499
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.238+5597G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912499 | ||||||
chr9:114912503
|
C | T | 1 | a0001c0001t0003g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.238+5593G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912503 | ||||||
chr9:114912522
|
T | G | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+5574A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912522 | ||||||
chr9:114912534
|
C | T | 92 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.238+5562G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912534 | ||||||
chr9:114912546
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.238+5550A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912546 | ||||||
chr9:114912556
|
A | C | 1 | a0001c0001t0003g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.238+5540T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912556 | ||||||
chr9:114912564
|
A | AT | 34 | a0001c0001t0003g0236a0001c0001t0004g0001a0001c0001t0004g0003others(31): Show | 58 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.238+5531dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912564 | ||||||
chr9:114912568
|
T | C | 1 | a0001c0002t0002g0224 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.238+5528A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912568 | ||||||
chr9:114912673
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.238+5423G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912673 | ||||||
chr9:114912691
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0178 | 3 | HG03516.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.238+5405C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912691 | ||||||
chr9:114912698
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.238+5398G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912698 | ||||||
chr9:114912721
|
T | A | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+5375A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912721 | ||||||
chr9:114913160
|
C | T | 1 | a0001c0001t0003g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238+4936G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913160 | ||||||
chr9:114913165
|
A | G | 14 | a0001c0001t0003g0048a0001c0001t0003g0236a0001c0001t0003g0240others(11): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+4931T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913165 | ||||||
chr9:114913170
|
G | A | 1 | a0001c0001t0004g0296 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.238+4926C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913170 | ||||||
chr9:114913174
|
A | G | 93 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(90): Show | 121 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.238+4922T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913174 | ||||||
chr9:114913190
|
C | T | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+4906G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913190 | ||||||
chr9:114913221
|
T | G | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.238+4875A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913221 | ||||||
chr9:114913533
|
G | A | 92 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.238+4563C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913533 | ||||||
chr9:114913622
|
T | A | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+4474A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913622 | ||||||
chr9:114913727
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.238+4369C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913727 | ||||||
chr9:114913869
|
A | G | 1 | a0001c0001t0023g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.238+4227T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913869 | ||||||
chr9:114913870
|
C | T | 1 | a0001c0001t0007g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.238+4226G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913870 | ||||||
chr9:114913999
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.238+4097C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913999 | ||||||
chr9:114914006
|
G | T | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+4090C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914006 | ||||||
chr9:114914034
|
T | C | 183 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(180): Show | 246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.238+4062A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914034 | ||||||
chr9:114914238
|
T | C | 183 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(180): Show | 246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.238+3858A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914238 | ||||||
chr9:114914247
|
A | G | 1 | a0001c0001t0003g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.238+3849T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914247 | ||||||
chr9:114914261
|
A | G | 91 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(88): Show | 119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.238+3835T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914261 | ||||||
chr9:114914495
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0153 | 3 | NA18945.hp1 NA19000.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.238+3601C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914495 | ||||||
chr9:114914550
|
G | A | 182 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(179): Show | 245 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.238+3546C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914550 | ||||||
chr9:114914553
|
A | C | 183 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(180): Show | 246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.238+3543T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914553 | ||||||
chr9:114914651
|
G | C | 93 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(90): Show | 121 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.238+3445C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914651 | ||||||
chr9:114914937
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.238+3159G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914937 | ||||||
chr9:114914983
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.238+3113G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914983 | ||||||
chr9:114915025
|
A | C | 182 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(179): Show | 245 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.238+3071T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915025 | ||||||
chr9:114915036
|
C | T | 1 | a0001c0002t0002g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+3060G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915036 | ||||||
chr9:114915078
|
A | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0230 | 3 | NA18939.hp1 NA18984.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.238+3018T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915078 | ||||||
chr9:114915080
|
C | T | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+3016G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915080 | ||||||
chr9:114915126
|
G | A | 31 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(28): Show | 55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+2970C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915126 | ||||||
chr9:114915149
|
T | A | 1 | a0001c0001t0028g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+2947A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915149 | ||||||
chr9:114915286
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0028others(25): Show | 36 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.238+2810T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915286 | ||||||
chr9:114915337
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.238+2759C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915337 | ||||||
chr9:114915339
|
C | T | 1 | a0001c0002t0002g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+2757G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915339 | ||||||
chr9:114915450
|
G | T | 1 | a0001c0002t0010g0052 | 2 | NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.238+2646C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915450 | ||||||
chr9:114915545
|
G | A | 59 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(56): Show | 70 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.238+2551C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915545 | ||||||
chr9:114915773
|
A | AG | 185 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(182): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.238+2322_238+2323i others(3): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915773 | ||||||
chr9:114915847
|
T | C | 1 | a0001c0002t0002g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238+2249A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915847 | ||||||
chr9:114915859
|
C | T | 1 | a0001c0002t0002g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238+2237G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915859 | ||||||
chr9:114915860
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+2236C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915860 | ||||||
chr9:114915924
|
T | A | 1 | a0001c0002t0002g0206 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.238+2172A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915924 | ||||||
chr9:114915956
|
T | C | 185 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(182): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.238+2140A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915956 | ||||||
chr9:114916025
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.238+2071G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916025 | ||||||
chr9:114916073
|
G | T | 1 | a0001c0001t0003g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.238+2023C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916073 | ||||||
chr9:114916527
|
C | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1569G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916527 | ||||||
chr9:114916529
|
G | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1567C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916529 | ||||||
chr9:114916530
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1566C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916530 | ||||||
chr9:114916531
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1565C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916531 | ||||||
chr9:114916532
|
T | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1564A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916532 | ||||||
chr9:114916533
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1563C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916533 | ||||||
chr9:114916551
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1545C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916551 | ||||||
chr9:114916552
|
T | A | 2 | a0001c0002t0002g0207a0001c0002t0002g0210 | 2 | NA18975.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.238+1544A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916552 | ||||||
chr9:114916553
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1543C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916553 | ||||||
chr9:114916556
|
A | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1540T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916556 | ||||||
chr9:114916557
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1539C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916557 | ||||||
chr9:114916559
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1537C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916559 | ||||||
chr9:114916560
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1536C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916560 | ||||||
chr9:114916562
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1534C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916562 | ||||||
chr9:114916564
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1532C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916564 | ||||||
chr9:114916565
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1531C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916565 | ||||||
chr9:114916568
|
C | A | 1 | a0001c0001t0004g0286 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.238+1528G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916568 | ||||||
chr9:114916575
|
T | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1521A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916575 | ||||||
chr9:114916577
|
T | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1519A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916577 | ||||||
chr9:114916589
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.238+1507G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916589 | ||||||
chr9:114916598
|
T | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1498A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916598 | ||||||
chr9:114916599
|
T | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1497A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916599 | ||||||
chr9:114916600
|
T | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1496A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916600 | ||||||
chr9:114916602
|
C | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1494G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916602 | ||||||
chr9:114916603
|
A | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1493T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916603 | ||||||
chr9:114916605
|
A | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1491T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916605 | ||||||
chr9:114916607
|
C | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1489G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916607 | ||||||
chr9:114916609
|
C | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1487G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916609 | ||||||
chr9:114916611
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1485C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916611 | ||||||
chr9:114916612
|
T | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1484A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916612 | ||||||
chr9:114916613
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1483C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916613 | ||||||
chr9:114916615
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1481C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916615 | ||||||
chr9:114916619
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1477C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916619 | ||||||
chr9:114916622
|
C | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1474G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916622 | ||||||
chr9:114916624
|
T | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1472A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916624 | ||||||
chr9:114916626
|
A | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1470T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916626 | ||||||
chr9:114916629
|
T | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1467A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916629 | ||||||
chr9:114916633
|
T | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1463A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916633 | ||||||
chr9:114916639
|
A | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1457T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916639 | ||||||
chr9:114916642
|
C | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1454G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916642 | ||||||
chr9:114916644
|
T | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1452A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916644 | ||||||
chr9:114916652
|
C | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1444G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916652 | ||||||
chr9:114916657
|
C | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1439G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916657 | ||||||
chr9:114916660
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1436C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916660 | ||||||
chr9:114916661
|
C | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1435G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916661 | ||||||
chr9:114916666
|
A | AATATAAC others(3): Show |
1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1429_238+1430i others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916666 | ||||||
chr9:114916668
|
T | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1428A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916668 | ||||||
chr9:114916674
|
A | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1422T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916674 | ||||||
chr9:114916676
|
T | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1420A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916676 | ||||||
chr9:114916679
|
A | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1417T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916679 | ||||||
chr9:114916680
|
T | C | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1416A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916680 | ||||||
chr9:114916686
|
A | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1410T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916686 | ||||||
chr9:114916687
|
A | G | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1409T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916687 | ||||||
chr9:114916688
|
A | T | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1408T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916688 | ||||||
chr9:114916726
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1370C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916726 | ||||||
chr9:114916998
|
G | A | 1 | a0001c0002t0002g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+1098C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916998 | ||||||
chr9:114917067
|
G | T | 1 | a0001c0002t0002g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+1029C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917067 | ||||||
chr9:114917090
|
G | C | 185 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(182): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.238+1006C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917090 | ||||||
chr9:114917194
|
C | T | 39 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(36): Show | 49 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.238+902G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917194 | ||||||
chr9:114917205
|
C | T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.238+891G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917205 | ||||||
chr9:114917450
|
G | C | 21 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(18): Show | 42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.238+646C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917450 | ||||||
chr9:114917491
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0003g0279a0001c0001t0003g0299others(1): Show | 4 | HG01891.hp2 HG02132.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+605C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917491 | ||||||
chr9:114917522
|
G | A | 90 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(87): Show | 125 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(122): Show |
intron_variant | MODIFIER | c.238+574C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917522 | ||||||
chr9:114917870
|
T | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0251 | 4 | HG01243.hp2 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+226A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917870 | ||||||
chr9:114917956
|
A | G | 1 | a0001c0002t0002g0220 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.238+140T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917956 | ||||||
chr9:114918067
|
C | T | 1 | a0001c0002t0002g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.238+29G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114918067 | ||||||
chr9:114918452
|
A | G | 56 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(53): Show | 67 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.196-314T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918452 | ||||||
chr9:114918453
|
CT | C | 91 | a0001c0001t0001g0133a0001c0001t0004g0291a0001c0002t0002g0002others(88): Show | 118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.196-316delA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918453 | ||||||
chr9:114918471
|
A | G | 1 | a0001c0001t0004g0292 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.196-333T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918471 | ||||||
chr9:114918552
|
C | T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-414G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918552 | ||||||
chr9:114918688
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.196-550C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918688 | ||||||
chr9:114918791
|
G | A | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-653C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918791 | ||||||
chr9:114918848
|
C | T | 1 | a0001c0001t0023g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-710G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918848 | ||||||
chr9:114918969
|
T | C | 1 | a0001c0002t0002g0195 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.196-831A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918969 | ||||||
chr9:114918976
|
C | A | 1 | a0001c0002t0002g0041 | 2 | NA18939.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.196-838G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918976 | ||||||
chr9:114919020
|
G | GT | 75 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0062others(72): Show | 89 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.196-883dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919020 | ||||||
chr9:114919072
|
C | T | 93 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(90): Show | 128 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(125): Show |
intron_variant | MODIFIER | c.196-934G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919072 | ||||||
chr9:114919097
|
C | T | 31 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(28): Show | 55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-959G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919097 | ||||||
chr9:114919243
|
C | T | 93 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(90): Show | 128 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(125): Show |
intron_variant | MODIFIER | c.196-1105G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919243 | ||||||
chr9:114919282
|
A | G | 31 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(28): Show | 55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-1144T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919282 | ||||||
chr9:114919299
|
A | G | 2 | a0001c0001t0006g0073a0001c0001t0006g0074 | 2 | NA18982.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.196-1161T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919299 | ||||||
chr9:114919590
|
G | T | 91 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(88): Show | 118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.196-1452C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919590 | ||||||
chr9:114919652
|
T | C | 1 | a0001c0001t0003g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196-1514A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919652 | ||||||
chr9:114919757
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0137 | 2 | HG00597.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.196-1619G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919757 | ||||||
chr9:114919797
|
G | C | 154 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(151): Show | 193 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.196-1659C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919797 | ||||||
chr9:114920212
|
C | T | 92 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.196-2074G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920212 | ||||||
chr9:114920228
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.196-2090T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920228 | ||||||
chr9:114920265
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.196-2127T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920265 | ||||||
chr9:114920768
|
G | T | 1 | a0001c0001t0007g0306 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.196-2630C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920768 | ||||||
chr9:114920934
|
G | T | 1 | a0001c0001t0003g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.196-2796C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920934 | ||||||
chr9:114921186
|
AC | A | 10 | a0001c0001t0007g0054a0001c0001t0007g0302a0001c0001t0007g0304others(7): Show | 13 | HG02074.hp1 NA18949.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-3049delG | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921186 | ||||||
chr9:114921259
|
C | G | 1 | a0001c0001t0023g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-3121G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921259 | ||||||
chr9:114921355
|
A | C | 1 | a0001c0001t0025g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.196-3217T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921355 | ||||||
chr9:114921484
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.196-3346T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921484 | ||||||
chr9:114921675
|
G | T | 2 | a0001c0001t0004g0288a0001c0001t0004g0301 | 2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.196-3537C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921675 | ||||||
chr9:114921722
|
A | C | 1 | a0001c0002t0016g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.196-3584T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921722 | ||||||
chr9:114921808
|
C | T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-3670G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921808 | ||||||
chr9:114921934
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0120 | 3 | HG00280.hp1 HG00642.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.196-3796T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921934 | ||||||
chr9:114922072
|
CT | C | 40 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(37): Show | 50 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.196-3935delA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922072 | ||||||
chr9:114922267
|
C | T | 92 | a0001c0001t0024g0234a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.196-4129G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922267 | ||||||
chr9:114922430
|
G | A | 2 | a0001c0001t0003g0279a0001c0001t0021g0280 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196-4292C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922430 | ||||||
chr9:114922651
|
G | C | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-4513C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922651 | ||||||
chr9:114922669
|
C | T | 2 | a0001c0002t0010g0052a0001c0002t0010g0303 | 3 | NA18969.hp1 NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.196-4531G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922669 | ||||||
chr9:114922675
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.196-4537T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922675 | ||||||
chr9:114922796
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196-4658C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922796 | ||||||
chr9:114923006
|
G | C | 1 | a0001c0002t0002g0226 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-4868C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923006 | ||||||
chr9:114923069
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196-4931T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923069 | ||||||
chr9:114923118
|
A | G | 184 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(181): Show | 247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.196-4980T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923118 | ||||||
chr9:114923137
|
T | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0149 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.196-4999A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923137 | ||||||
chr9:114923223
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.196-5085G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923223 | ||||||
chr9:114923268
|
G | A | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196-5130C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923268 | ||||||
chr9:114923397
|
A | C | 1 | a0001c0001t0003g0239 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.196-5259T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923397 | ||||||
chr9:114923472
|
C | T | 1 | a0001c0002t0002g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196-5334G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923472 | ||||||
chr9:114923473
|
T | C | 1 | a0001c0002t0002g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196-5335A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923473 | ||||||
chr9:114923478
|
T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.196-5341_196-5340i others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
T | TTCTTTTT others(5): Show |
1 | a0001c0001t0001g0102 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.196-5341_196-5340i others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
T | TTTTC | 17 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0059others(14): Show | 19 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-5344_196-5341d others(6): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
T | TTTTCTTT others(1): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(19): Show | 33 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.196-5348_196-5341d others(10): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
T | TTTTCTTT others(5): Show |
14 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(11): Show | 20 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-5352_196-5341d others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
T | TTTTCTTT others(9): Show |
12 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01069.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-5356_196-5341d others(18): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
T | TTTTCTTT others(13): Show |
4 | a0001c0001t0001g0067a0001c0001t0001g0092a0001c0001t0001g0143others(1): Show | 4 | HG00438.hp1 HG02615.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-5360_196-5341d others(22): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
TTTTC | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(7): Show | 11 | HG01261.hp2 HG01891.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-5344_196-5341d others(6): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
TTTTCTTT others(1): Show |
T | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0021others(7): Show | 17 | HG00558.hp2 HG02015.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.196-5348_196-5341d others(10): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
TTTTCTTT others(5): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.196-5352_196-5341d others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923478
|
TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-5356_196-5341d others(18): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | ||||||
chr9:114923507
|
TTTCTTTC others(8): Show |
T | 8 | a0001c0001t0007g0302a0001c0001t0007g0304a0001c0001t0007g0305others(5): Show | 10 | HG02074.hp1 NA18949.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5384_196-5370d others(17): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923507 | ||||||
chr9:114923508
|
TTCTTTCT others(3): Show |
T | 1 | a0001c0002t0002g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196-5380_196-5371d others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923508 | ||||||
chr9:114923508
|
TTCTTTCT others(7): Show |
T | 15 | a0001c0002t0002g0002a0001c0002t0002g0017a0001c0002t0002g0038others(12): Show | 26 | HG00558.hp1 HG00597.hp1 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-5384_196-5371d others(16): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923508 | ||||||
chr9:114923509
|
TCTTTCTT others(6): Show |
T | 1 | a0001c0002t0002g0193 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.196-5384_196-5372d others(15): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923509 | ||||||
chr9:114923511
|
TTTCTTTC others(4): Show |
T | 5 | a0001c0001t0003g0272a0001c0001t0007g0054a0001c0001t0007g0306others(2): Show | 6 | HG01192.hp1 HG02074.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-5384_196-5374d others(13): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923511 | ||||||
chr9:114923514
|
CTTTCTTT others(5): Show |
C | 2 | a0001c0001t0001g0121a0001c0001t0001g0124 | 2 | HG02056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.196-5388_196-5377d others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923514 | ||||||
chr9:114923515
|
TTTCTTTC | T | 11 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0049others(8): Show | 26 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-5384_196-5378d others(9): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923515 | ||||||
chr9:114923519
|
TTTC | T | 12 | a0001c0001t0001g0106a0001c0001t0003g0240a0001c0001t0003g0253others(9): Show | 19 | HG01496.hp1 HG02280.hp1 HG02965.hp2 others(16): Show |
intron_variant | MODIFIER | c.196-5384_196-5382d others(5): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923519 | ||||||
chr9:114923520
|
TTC | T | 7 | a0001c0002t0002g0040a0001c0002t0002g0165a0001c0002t0002g0223others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-5384_196-5383d others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923520 | ||||||
chr9:114923522
|
C | CT | 9 | a0001c0001t0003g0046a0001c0001t0003g0241a0001c0001t0003g0254others(6): Show | 10 | HG01109.hp1 HG01109.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-5385dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTT | 7 | a0001c0002t0002g0015a0001c0002t0002g0185a0001c0002t0002g0215others(4): Show | 10 | HG01175.hp2 HG01255.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-5386_196-5385d others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCT | 11 | a0001c0001t0001g0107a0001c0001t0003g0043a0001c0001t0003g0044others(8): Show | 13 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(7): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTT | 14 | a0001c0002t0002g0007a0001c0002t0002g0016a0001c0002t0002g0041others(11): Show | 20 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(8): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT | 8 | a0001c0002t0002g0163a0001c0002t0002g0164a0001c0002t0002g0170others(5): Show | 8 | HG01433.hp2 HG01516.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(9): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(2): Show |
17 | a0001c0001t0003g0018a0001c0001t0003g0048a0001c0001t0003g0237others(14): Show | 21 | HG00733.hp2 HG01891.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(11): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(3): Show |
10 | a0001c0002t0002g0014a0001c0002t0002g0035a0001c0002t0002g0129others(7): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(4): Show |
5 | a0001c0002t0002g0171a0001c0002t0002g0184a0001c0002t0002g0187others(2): Show | 5 | HG00323.hp1 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(13): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(6): Show |
14 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0003g0019others(11): Show | 17 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(15): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(7): Show |
8 | a0001c0001t0003g0249a0001c0002t0002g0013a0001c0002t0002g0036others(5): Show | 11 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(16): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(8): Show |
1 | a0001c0002t0002g0214 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.196-5385_196-5384i others(17): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(10): Show |
5 | a0001c0001t0003g0251a0001c0001t0003g0265a0001c0001t0003g0275others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(19): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(11): Show |
5 | a0001c0002t0002g0131a0001c0002t0002g0161a0001c0002t0002g0168others(2): Show | 5 | HG00099.hp1 HG01070.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(20): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(12): Show |
2 | a0001c0002t0002g0159a0001c0002t0002g0188 | 2 | HG02886.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.196-5385_196-5384i others(21): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(15): Show |
1 | a0001c0002t0002g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196-5385_196-5384i others(24): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923522
|
C | CTTTCTTT others(5): Show |
1 | a0001c0002t0002g0186 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.196-5385_196-5384i others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | ||||||
chr9:114923523
|
T | TTTCTTTC others(4): Show |
1 | a0001c0001t0005g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-5386_196-5385i others(13): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923523 | ||||||
chr9:114923523
|
T | TTTCTTTC others(8): Show |
1 | a0001c0002t0002g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196-5386_196-5385i others(17): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923523 | ||||||
chr9:114923523
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.196-5386_196-5385i others(21): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923523 | ||||||
chr9:114923524
|
T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196-5387_196-5386i others(16): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923524 | ||||||
chr9:114923524
|
T | TTCTTTCT others(11): Show |
2 | a0001c0001t0006g0095a0001c0001t0021g0280 | 2 | NA18965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196-5387_196-5386i others(20): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923524 | ||||||
chr9:114923525
|
T | TCTTTCTT others(14): Show |
1 | a0001c0001t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196-5388_196-5387i others(23): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923525 | ||||||
chr9:114923526
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.196-5388A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923526 | ||||||
chr9:114923528
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0158 | 2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.196-5390A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923528 | ||||||
chr9:114923532
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196-5394A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923532 | ||||||
chr9:114923931
|
T | C | 1 | a0001c0002t0002g0231 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.196-5793A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923931 | ||||||
chr9:114924029
|
G | C | 10 | a0001c0002t0002g0013a0001c0002t0002g0129a0001c0002t0002g0131others(7): Show | 12 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.196-5891C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924029 | ||||||
chr9:114924138
|
C | T | 1 | a0001c0001t0004g0286 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.195+5971G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924138 | ||||||
chr9:114924177
|
A | G | 153 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(150): Show | 192 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.195+5932T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924177 | ||||||
chr9:114924201
|
G | T | 1 | a0001c0001t0013g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+5908C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924201 | ||||||
chr9:114924215
|
T | G | 1 | a0001c0002t0002g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.195+5894A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924215 | ||||||
chr9:114924234
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.195+5875A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924234 | ||||||
chr9:114924321
|
T | C | 21 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(18): Show | 42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+5788A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924321 | ||||||
chr9:114924425
|
T | TATTGAAT others(20): Show |
1 | a0001c0001t0001g0062 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.195+5657_195+5683d others(29): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924425 | ||||||
chr9:114924452
|
A | T | 92 | a0001c0001t0024g0234a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.195+5657T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924452 | ||||||
chr9:114924567
|
C | A | 91 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(88): Show | 119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.195+5542G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924567 | ||||||
chr9:114924578
|
C | G | 21 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(18): Show | 42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+5531G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924578 | ||||||
chr9:114924756
|
C | A | 91 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0013others(88): Show | 119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.195+5353G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924756 | ||||||
chr9:114924835
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.195+5274T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924835 | ||||||
chr9:114924871
|
G | T | 92 | a0001c0001t0024g0234a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.195+5238C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924871 | ||||||
chr9:114925128
|
C | G | 1 | a0001c0002t0002g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.195+4981G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925128 | ||||||
chr9:114925130
|
G | A | 1 | a0001c0002t0002g0214 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.195+4979C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925130 | ||||||
chr9:114925131
|
G | T | 1 | a0001c0001t0003g0239 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.195+4978C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925131 | ||||||
chr9:114925717
|
T | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG00323.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.195+4392A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925717 | ||||||
chr9:114925838
|
A | G | 1 | a0001c0001t0003g0043 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.195+4271T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925838 | ||||||
chr9:114925982
|
TAAGAG | T | 21 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(18): Show | 42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+4122_195+4126d others(7): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925982 | ||||||
chr9:114926299
|
G | A | 1 | a0001c0001t0013g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+3810C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926299 | ||||||
chr9:114926658
|
G | A | 2 | a0001c0001t0013g0271a0001c0001t0013g0300 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.195+3451C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926658 | ||||||
chr9:114926719
|
A | C | 1 | a0001c0001t0003g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195+3390T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926719 | ||||||
chr9:114926845
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.195+3264T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926845 | ||||||
chr9:114926904
|
A | G | 92 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.195+3205T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926904 | ||||||
chr9:114926953
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.195+3156T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926953 | ||||||
chr9:114926982
|
A | AATATTTA others(22): Show |
3 | a0001c0001t0003g0236a0001c0001t0003g0268a0001c0001t0003g0272 | 3 | HG01192.hp1 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.195+3098_195+3126d others(31): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926982 | ||||||
chr9:114926982
|
A | AATATTTA others(25): Show |
39 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(36): Show | 49 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.195+3095_195+3126d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926982 | ||||||
chr9:114926982
|
A | AATATTTA others(57): Show |
4 | a0001c0002t0002g0161a0001c0002t0002g0162a0001c0002t0002g0181others(1): Show | 4 | HG01346.hp1 HG03579.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+3126_195+3127i others(66): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926982 | ||||||
chr9:114926993
|
T | TATAAAAT others(25): Show |
1 | a0001c0001t0001g0034 | 2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.195+3084_195+3115d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926993 | ||||||
chr9:114926993
|
TATAAAAT others(25): Show |
T | 1 | a0001c0002t0002g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.195+3084_195+3115d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926993 | ||||||
chr9:114927009
|
TATA | T | 51 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(48): Show | 60 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.195+3097_195+3099d others(5): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927009 | ||||||
chr9:114927009
|
TATAATAT others(28): Show |
T | 8 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0237others(5): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+3065_195+3099d others(37): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927009 | ||||||
chr9:114927025
|
C | T | 145 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(142): Show | 182 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.195+3084G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927025 | ||||||
chr9:114927025
|
CATAAAAT others(25): Show |
C | 8 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0001g0122others(5): Show | 9 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+3052_195+3083d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927025 | ||||||
chr9:114927092
|
A | G | 1 | a0001c0001t0023g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+3017T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927092 | ||||||
chr9:114927211
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.195+2898A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927211 | ||||||
chr9:114927268
|
T | C | 61 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(58): Show | 72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.195+2841A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927268 | ||||||
chr9:114927352
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195+2757G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927352 | ||||||
chr9:114927482
|
T | G | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+2627A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927482 | ||||||
chr9:114927512
|
G | A | 1 | a0001c0002t0008g0218 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.195+2597C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927512 | ||||||
chr9:114927558
|
A | G | 61 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(58): Show | 72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.195+2551T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927558 | ||||||
chr9:114927598
|
C | G | 21 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(18): Show | 42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+2511G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927598 | ||||||
chr9:114928027
|
A | G | 5 | a0001c0002t0002g0013a0001c0002t0002g0131a0001c0002t0002g0161others(2): Show | 7 | HG01070.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+2082T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928027 | ||||||
chr9:114928043
|
T | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(5): Show | 13 | HG00673.hp1 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+2066A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928043 | ||||||
chr9:114928410
|
G | T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1699C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928410 | ||||||
chr9:114928452
|
A | C | 6 | a0001c0002t0002g0014a0001c0002t0002g0036a0001c0002t0002g0159others(3): Show | 9 | HG02280.hp2 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+1657T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928452 | ||||||
chr9:114928478
|
T | C | 185 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(182): Show | 248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.195+1631A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928478 | ||||||
chr9:114928573
|
T | G | 2 | a0001c0002t0002g0013a0001c0002t0002g0131 | 4 | HG01070.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+1536A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928573 | ||||||
chr9:114928584
|
C | T | 31 | a0001c0001t0001g0289a0001c0001t0004g0001a0001c0001t0004g0003others(28): Show | 55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.195+1525G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928584 | ||||||
chr9:114928921
|
C | T | 93 | a0001c0001t0018g0217a0001c0001t0024g0234a0001c0002t0002g0002others(90): Show | 121 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.195+1188G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928921 | ||||||
chr9:114928937
|
T | G | 1 | a0001c0002t0002g0233 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.195+1172A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928937 | ||||||
chr9:114928939
|
A | G | 1 | a0001c0001t0015g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.195+1170T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928939 | ||||||
chr9:114928990
|
A | G | 154 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(151): Show | 193 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.195+1119T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928990 | ||||||
chr9:114928995
|
G | T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1114C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928995 | ||||||
chr9:114928996
|
A | T | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1113T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928996 | ||||||
chr9:114929033
|
T | C | 92 | a0001c0001t0018g0217a0001c0002t0002g0002a0001c0002t0002g0007others(89): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.195+1076A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929033 | ||||||
chr9:114929084
|
T | A | 92 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(89): Show | 127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.195+1025A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929084 | ||||||
chr9:114929095
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.195+1014T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929095 | ||||||
chr9:114929278
|
C | T | 93 | a0001c0001t0001g0069a0001c0001t0001g0289a0001c0001t0003g0018others(90): Show | 128 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(125): Show |
intron_variant | MODIFIER | c.195+831G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929278 | ||||||
chr9:114929288
|
G | A | 1 | a0001c0001t0005g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.195+821C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929288 | ||||||
chr9:114929357
|
C | CT | 20 | a0001c0001t0001g0068a0001c0001t0001g0105a0001c0001t0003g0236others(17): Show | 22 | HG01192.hp1 HG01928.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.195+751dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929357 | ||||||
chr9:114929357
|
CT | C | 7 | a0001c0001t0001g0103a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG01070.hp2 HG02451.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+751delA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929357 | ||||||
chr9:114929378
|
C | T | 61 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0042others(58): Show | 72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.195+731G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929378 | ||||||
chr9:114929396
|
G | A | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+713C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929396 | ||||||
chr9:114929544
|
A | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0001g0148 | 4 | HG02056.hp1 HG02602.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+565T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929544 | ||||||
chr9:114929874
|
CAT | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0012others(83): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.195+233_195+234del others(2): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929874 | ||||||
chr9:114929874
|
CATAT | C | 137 | a0001c0001t0001g0289a0001c0001t0003g0042a0001c0001t0003g0043others(134): Show | 186 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(183): Show |
intron_variant | MODIFIER | c.195+231_195+234del others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929874 | ||||||
chr9:114929875
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.195+234T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929875 | ||||||
chr9:114929892
|
T | C | 2 | a0001c0002t0008g0218a0001c0002t0012g0039 | 3 | NA18945.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.195+217A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929892 | ||||||
chr9:114929962
|
G | GTA | 3 | a0001c0001t0001g0125a0001c0001t0005g0270a0001c0001t0007g0302 | 3 | HG02074.hp1 NA18522.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.195+145_195+146dup others(2): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929962 | ||||||
chr9:114929962
|
G | GTATA | 7 | a0001c0002t0002g0126a0001c0002t0002g0127a0001c0002t0002g0128others(4): Show | 7 | HG00597.hp1 HG01070.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+143_195+146dup others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929962 | ||||||
chr9:114929962
|
GTA | G | 2 | a0001c0002t0010g0052a0001c0002t0010g0303 | 3 | NA18969.hp1 NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.195+145_195+146del others(2): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929962 | ||||||
chr9:114929967
|
T | A | 1 | a0001c0001t0004g0298 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.195+142A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929967 | ||||||
chr9:114929971
|
T | TAGAG | 19 | a0001c0002t0002g0007a0001c0002t0002g0040a0001c0002t0002g0041others(16): Show | 24 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.195+137_195+138ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929971 | ||||||
chr9:114929973
|
T | G | 22 | a0001c0001t0003g0299a0001c0001t0004g0301a0001c0001t0013g0300others(19): Show | 27 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.195+136A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929973 | ||||||
chr9:114929973
|
T | TAGAG | 6 | a0001c0001t0018g0217a0001c0002t0002g0038a0001c0002t0002g0213others(3): Show | 7 | HG01257.hp1 HG02896.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+135_195+136ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929973 | ||||||
chr9:114929975
|
T | G | 55 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(52): Show | 80 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.195+134A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929975 | ||||||
chr9:114929975
|
T | TAGAG | 18 | a0001c0002t0002g0017a0001c0002t0002g0197a0001c0002t0002g0198others(15): Show | 21 | HG00558.hp1 HG00733.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.195+133_195+134ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929975 | ||||||
chr9:114929975
|
T | TAGAGAG | 2 | a0001c0002t0008g0218a0001c0002t0012g0039 | 3 | NA18945.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.195+133_195+134ins others(6): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929975 | ||||||
chr9:114929977
|
T | G | 124 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 167 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.195+132A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929977 | ||||||
chr9:114929977
|
T | TAGAG | 21 | a0001c0002t0002g0002a0001c0002t0002g0014a0001c0002t0002g0015others(18): Show | 36 | HG00099.hp1 HG00323.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.195+128_195+131dup others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929977 | ||||||
chr9:114929977
|
T | TATAG | 19 | a0001c0002t0002g0013a0001c0002t0002g0035a0001c0002t0002g0159others(16): Show | 22 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+131_195+132ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929977 | ||||||
chr9:114929979
|
G | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0056others(27): Show | 33 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.195+130C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929979 | ||||||
chr9:114929981
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG00741.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.195+128C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929981 | ||||||
chr9:114930062
|
C | A | 1 | a0001c0001t0024g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+47G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114930062 | ||||||
chr9:114930064
|
G | A | 92 | a0001c0001t0001g0289a0001c0001t0003g0018a0001c0001t0003g0019others(89): Show | 127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.195+45C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114930064 |