geneid | 8600 |
---|---|
ensemblid | ENSG00000120659.16 |
hgncid | 11926 |
symbol | TNFSF11 |
name | TNF superfamily member 11 |
refseq_nuc | NM_003701.4 |
refseq_prot | NP_003692.1 |
ensembl_nuc | ENST00000398795.7 |
ensembl_prot | ENSP00000381775.3 |
mane_status | MANE Select |
chr | chr13 |
start | 42574152 |
end | 42608013 |
strand | + |
ver | v1.2 |
region | chr13:42574152-42608013 |
region5000 | chr13:42569152-42613013 |
regionname0 | TNFSF11_chr13_42574152_42608013 |
regionname5000 | TNFSF11_chr13_42569152_42613013 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 317 | 406 | 84 | 73 | 204 | 11 | 32 | 162 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0002 | 0/0 | 317 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0003 | 0/0 | 317 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0004 | 0/0 | 317 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 954 | 221 | 36 | 39 | 121 | 4 | 19 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0002 | 0/0 | 954 | 158 | 38 | 33 | 69 | 7 | 11 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0003 | 0/0 | 954 | 16 | 1 | 0 | 14 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0004 | 0/0 | 954 | 7 | 6 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0005 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0006 | 0/0 | 954 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0007 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0008 | 0/0 | 954 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0009 | 0/0 | 954 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
c0010 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1248 | 233 | 49 | 40 | 121 | 4 | 18 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0002 | 0/0 | 1248 | 125 | 13 | 30 | 62 | 8 | 12 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0003 | 0/0 | 1248 | 21 | 6 | 1 | 12 | 0 | 2 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0004 | 0/0 | 1248 | 8 | 7 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0005 | 0/0 | 1248 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0006 | 1/0 | 1248 | 4 | 3 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0007 | 0/0 | 1248 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0008 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0009 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0010 | 0/0 | 1248 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0011 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0012 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0013 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
t0014 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0002 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0004 | 0/1 | 5 | 0 | 1 | 1 | 0 | 2 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0007 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0008 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0011 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 954 | 221 | 36 | 39 | 121 | 4 | 19 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002 | 0/0 | 954 | 158 | 38 | 33 | 69 | 7 | 11 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0003 | 0/0 | 954 | 16 | 1 | 0 | 14 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0004 | 0/0 | 954 | 7 | 6 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0005 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0007 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0008 | 0/0 | 954 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0002c0006 | 0/0 | 954 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0003c0010 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0004c0009 | 0/0 | 954 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2201 | 209 | 30 | 37 | 119 | 4 | 18 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0001t0002 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0001t0006 | 1/0 | 2201 | 4 | 3 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0001t0007 | 0/0 | 2201 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0001t0010 | 0/0 | 2201 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0001t0012 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0001t0014 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0001 | 0/0 | 2201 | 19 | 15 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0002 | 0/0 | 2201 | 123 | 13 | 30 | 62 | 7 | 11 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0004 | 0/0 | 2201 | 8 | 7 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0005 | 0/0 | 2201 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0007 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0011 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0002t0013 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0003t0003 | 0/0 | 2201 | 14 | 1 | 0 | 12 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0003t0008 | 0/0 | 2201 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0004t0001 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0004t0003 | 0/0 | 2201 | 5 | 4 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0005t0009 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0007t0003 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0001c0008t0003 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0002c0006t0001 | 0/0 | 2201 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0003c0010t0001 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
a0004c0009t0002 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | copy fasta | chr13 | 42569152 | 42613013 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0004 | 0/1 | 5 | 0 | 1 | 1 | 0 | 2 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0006g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0010g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0001t0014g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0002 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0007 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0005g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0002t0013g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0008g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0003t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0004t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0004t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0004t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0005t0009g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0005t0009g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0007t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0001c0008t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0002c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0002c0006t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0003c0010t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
a0004c0009t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0124 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0132 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0131 | EUR | FIN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00280 | hp2 | a0004 | c0009 | t0002 | g0083 | EUR | FIN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00438 | hp2 | a0001 | c0002 | t0005 | g0016 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00621 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00639 | hp1 | a0002 | c0006 | t0001 | g0317 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00673 | hp1 | a0001 | c0003 | t0003 | g0310 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0155 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01069 | hp1 | a0001 | c0001 | t0010 | g0043 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01071 | hp2 | a0001 | c0001 | t0010 | g0043 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0095 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0313 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0312 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01256 | hp1 | a0001 | c0008 | t0003 | g0295 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01496 | hp2 | a0001 | c0002 | t0004 | g0224 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0101 | EUR | IBS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0060 | EUR | IBS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01884 | hp2 | a0001 | c0002 | t0013 | g0229 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0311 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0121 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02055 | hp1 | a0001 | c0004 | t0003 | g0266 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | CDX | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0022 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0220 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0143 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02622 | hp1 | a0001 | c0002 | t0007 | g0233 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0186 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0084 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02717 | hp1 | a0001 | c0007 | t0003 | g0290 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02723 | hp1 | a0001 | c0002 | t0004 | g0221 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0110 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0219 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02818 | hp1 | a0001 | c0002 | t0011 | g0230 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02895 | hp2 | a0001 | c0004 | t0003 | g0267 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02922 | hp1 | a0001 | c0005 | t0009 | g0316 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02922 | hp2 | a0003 | c0010 | t0001 | g0056 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02965 | hp2 | a0001 | c0002 | t0004 | g0226 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0136 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0223 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0222 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03453 | hp1 | a0001 | c0004 | t0003 | g0268 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03453 | hp2 | a0001 | c0003 | t0003 | g0227 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0096 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03540 | hp2 | a0001 | c0005 | t0009 | g0315 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0097 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03654 | hp1 | a0001 | c0003 | t0003 | g0307 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0115 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0294 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04199 | hp1 | a0001 | c0004 | t0003 | g0078 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0149 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18939 | hp1 | a0001 | c0003 | t0003 | g0308 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18944 | hp1 | a0001 | c0003 | t0003 | g0306 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18962 | hp1 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18964 | hp2 | a0001 | c0001 | t0014 | g0280 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18965 | hp1 | a0001 | c0003 | t0008 | g0304 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18971 | hp1 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18979 | hp1 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18980 | hp1 | a0001 | c0003 | t0003 | g0301 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18981 | hp1 | a0001 | c0003 | t0003 | g0300 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18985 | hp2 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18995 | hp1 | a0001 | c0003 | t0003 | g0297 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19043 | hp1 | a0001 | c0002 | t0004 | g0225 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19064 | hp1 | a0001 | c0003 | t0008 | g0303 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19066 | hp1 | a0001 | c0003 | t0003 | g0305 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19075 | hp2 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19080 | hp2 | a0001 | c0003 | t0003 | g0298 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0309 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0302 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0022 | AFR | ASW | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ASW | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0100 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0199 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0022 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20300 | hp1 | a0002 | c0006 | t0001 | g0269 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0065 | REF | REF | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42574410
|
C | G | 1 | a0002 | 2 | HG00639.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.107C>G | p.Pro36Arg | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 259/2201 | 107/954 | 36/317 | chr13 | 42574410 | ||
chr13:42581145
|
C | T | 1 | a0003 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.239C>T | p.Ser80Leu | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/5 | 391/2201 | 239/954 | 80/317 | chr13 | 42581145 | ||
chr13:42600784
|
C | G | 1 | a0004 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.420C>G | p.Ile140Met | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 3/5 | 572/2201 | 420/954 | 140/317 | chr13 | 42600784 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42574348
|
G | A | 1 | a0001c0007 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.45G>A | p.Ser15Ser | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 197/2201 | 45/954 | 15/317 | chr13 | 42574348 | ||
chr13:42574429
|
T | C | 6 | a0001c0002a0001c0003a0001c0007others(3): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
synonymous_variant | LOW | c.126T>C | p.Pro42Pro | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 278/2201 | 126/954 | 42/317 | chr13 | 42574429 | ||
chr13:42574450
|
C | T | 1 | a0001c0005 | 2 | HG02922.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.147C>T | p.Phe49Phe | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 299/2201 | 147/954 | 49/317 | chr13 | 42574450 | ||
chr13:42581230
|
T | C | 1 | a0001c0008 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.324T>C | p.Asp108Asp | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/5 | 476/2201 | 324/954 | 108/317 | chr13 | 42581230 | ||
chr13:42600760
|
A | G | 1 | a0003c0010 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.396A>G | p.Gln132Gln | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 3/5 | 548/2201 | 396/954 | 132/317 | chr13 | 42600760 | ||
chr13:42606888
|
T | C | 4 | a0001c0003a0001c0004a0001c0007others(1): Show | 25 | HG00673.hp1 HG01256.hp1 HG02055.hp1 others(22): Show |
synonymous_variant | LOW | c.924T>C | p.Phe308Phe | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 1076/2201 | 924/954 | 308/317 | chr13 | 42606888 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42574163
|
C | T | 1 | a0001c0002t0005 | 5 | HG00438.hp2 HG02129.hp1 NA18971.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-141C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | chr13 | 42574163 | ||||||
chr13:42574177
|
C | G | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(20): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
5_prime_UTR_variant | MODIFIER | c.-127C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 127 | chr13 | 42574177 | |||||
chr13:42574300
|
C | T | 1 | a0001c0001t0014 | 1 | NA18964.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 4 | chr13 | 42574300 | |||||
chr13:42606966
|
T | C | 1 | a0001c0002t0004 | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 48 | chr13 | 42606966 | |||||
chr13:42606992
|
A | G | 1 | a0001c0002t0013 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 74 | chr13 | 42606992 | |||||
chr13:42607074
|
C | T | 1 | a0001c0001t0010 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*156C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 156 | chr13 | 42607074 | |||||
chr13:42607077
|
G | A | 1 | a0001c0003t0008 | 2 | NA18965.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*159G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 159 | chr13 | 42607077 | |||||
chr13:42607182
|
G | T | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(19): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 264 | chr13 | 42607182 | |||||
chr13:42607301
|
C | T | 5 | a0001c0003t0003a0001c0003t0008a0001c0004t0003others(2): Show | 23 | HG00673.hp1 HG01256.hp1 HG02055.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*383C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 383 | chr13 | 42607301 | |||||
chr13:42607458
|
A | G | 1 | a0001c0001t0012 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 540 | chr13 | 42607458 | |||||
chr13:42607622
|
G | A | 1 | a0001c0005t0009 | 2 | HG02922.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*704G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 704 | chr13 | 42607622 | |||||
chr13:42607660
|
G | A | 2 | a0001c0001t0007a0001c0002t0007 | 4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*742G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 742 | chr13 | 42607660 | |||||
chr13:42607866
|
G | T | 4 | a0001c0001t0002a0001c0002t0002a0001c0002t0005others(1): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*948G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 948 | chr13 | 42607866 | |||||
chr13:42607917
|
T | C | 1 | a0001c0002t0011 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 999 | chr13 | 42607917 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42574538
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.219+16C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574538 | ||||||
chr13:42574596
|
T | A | 9 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(6): Show | 9 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+74T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574596 | ||||||
chr13:42574708
|
G | A | 1 | a0001c0002t0002g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.219+186G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574708 | ||||||
chr13:42574757
|
G | A | 2 | a0001c0002t0002g0058a0001c0002t0002g0059 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.219+235G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574757 | ||||||
chr13:42574926
|
G | A | 9 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(6): Show | 9 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+404G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574926 | ||||||
chr13:42575100
|
C | T | 1 | a0002c0006t0001g0317 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.219+578C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575100 | ||||||
chr13:42575661
|
A | T | 2 | a0001c0005t0009g0315a0001c0005t0009g0316 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.219+1139A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575661 | ||||||
chr13:42575753
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.219+1231A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575753 | ||||||
chr13:42575822
|
A | T | 2 | a0001c0002t0002g0312a0001c0002t0002g0313 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.219+1300A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575822 | ||||||
chr13:42575881
|
A | G | 1 | a0001c0002t0002g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219+1359A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575881 | ||||||
chr13:42575974
|
C | G | 16 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(13): Show | 16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.219+1452C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575974 | ||||||
chr13:42576033
|
A | G | 1 | a0001c0002t0002g0294 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.219+1511A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576033 | ||||||
chr13:42576149
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.219+1627A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576149 | ||||||
chr13:42576225
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219+1703G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576225 | ||||||
chr13:42576264
|
G | A | 2 | a0001c0002t0002g0060a0001c0002t0002g0061 | 2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.219+1742G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576264 | ||||||
chr13:42576360
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+1838C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576360 | ||||||
chr13:42576499
|
A | T | 318 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.219+1977A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576499 | ||||||
chr13:42576552
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+2030C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576552 | ||||||
chr13:42576866
|
T | C | 1 | a0001c0008t0003g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.219+2344T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576866 | ||||||
chr13:42576939
|
C | T | 1 | a0001c0007t0003g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.219+2417C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576939 | ||||||
chr13:42576962
|
A | G | 1 | a0001c0002t0001g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+2440A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576962 | ||||||
chr13:42577050
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0012others(19): Show | 34 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.219+2528T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577050 | ||||||
chr13:42577061
|
T | C | 1 | a0001c0003t0003g0296 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.219+2539T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577061 | ||||||
chr13:42577364
|
G | A | 105 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(102): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.219+2842G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577364 | ||||||
chr13:42577424
|
C | T | 1 | a0001c0007t0003g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.219+2902C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577424 | ||||||
chr13:42577500
|
GA | G | 10 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(7): Show | 10 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+2986delA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42577500 | |||||
chr13:42577693
|
G | A | 2 | a0001c0005t0009g0315a0001c0005t0009g0316 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.219+3171G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577693 | ||||||
chr13:42577864
|
C | T | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.220-3262C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577864 | ||||||
chr13:42577968
|
G | C | 2 | a0001c0003t0003g0296a0001c0003t0003g0297 | 2 | NA18995.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.220-3158G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577968 | ||||||
chr13:42578043
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220-3083A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578043 | ||||||
chr13:42578196
|
G | T | 1 | a0001c0002t0002g0161 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-2930G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578196 | ||||||
chr13:42578433
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.220-2693T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578433 | ||||||
chr13:42578514
|
C | T | 16 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(13): Show | 16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-2612C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578514 | ||||||
chr13:42578585
|
A | C | 1 | a0001c0001t0014g0280 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.220-2541A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578585 | ||||||
chr13:42578627
|
C | T | 105 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(102): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.220-2499C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578627 | ||||||
chr13:42578751
|
G | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(82): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.220-2375G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578751 | ||||||
chr13:42579006
|
T | C | 1 | a0001c0002t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-2120T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579006 | ||||||
chr13:42579022
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(234): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.220-2104A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579022 | ||||||
chr13:42579119
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-2007G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579119 | ||||||
chr13:42579415
|
C | CA | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.220-1695dupA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579415 | |||||
chr13:42579415
|
CA | C | 13 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0273others(10): Show | 15 | HG01361.hp2 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.220-1695delA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579415 | |||||
chr13:42579704
|
C | CTTTTT | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0282others(5): Show | 8 | HG00099.hp1 HG01884.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-1402_220-1398d others(7): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
C | CTTTTTT | 41 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0031others(38): Show | 53 | HG00642.hp1 HG01192.hp1 HG01433.hp2 others(50): Show |
intron_variant | MODIFIER | c.220-1403_220-1398d others(8): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
C | CTTTTTTT | 24 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 41 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.220-1404_220-1398d others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0037a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 7 | HG00408.hp1 HG00423.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-1405_220-1398d others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0207 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.220-1408_220-1398d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220-1411_220-1398d others(16): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
CT | C | 37 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(34): Show | 43 | HG00597.hp1 HG00673.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.220-1398delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
CTT | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(181): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.220-1399_220-1398d others(4): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
CTTT | C | 11 | a0001c0001t0001g0046a0001c0001t0001g0273a0001c0001t0001g0274others(8): Show | 12 | HG01361.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.220-1400_220-1398d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579704
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.220-1408_220-1398d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | |||||
chr13:42579733
|
A | T | 2 | a0002c0006t0001g0269a0002c0006t0001g0317 | 2 | HG00639.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.220-1393A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579733 | ||||||
chr13:42579824
|
A | G | 1 | a0001c0002t0002g0141 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.220-1302A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579824 | ||||||
chr13:42579975
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.220-1151C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579975 | ||||||
chr13:42580224
|
C | T | 4 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0267others(1): Show | 5 | HG02572.hp1 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-902C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580224 | ||||||
chr13:42580349
|
G | A | 14 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(11): Show | 14 | HG01256.hp1 HG03654.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-777G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580349 | ||||||
chr13:42580368
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220-758A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580368 | ||||||
chr13:42580409
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220-717G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580409 | ||||||
chr13:42580460
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220-666A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580460 | ||||||
chr13:42580670
|
G | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(76): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.220-456G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580670 | ||||||
chr13:42580823
|
T | A | 2 | a0001c0002t0002g0082a0001c0002t0002g0142 | 2 | NA18980.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.220-303T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580823 | ||||||
chr13:42580823
|
T | G | 103 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(100): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.220-303T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580823 | ||||||
chr13:42581032
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.220-94G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42581032 | ||||||
chr13:42581051
|
T | G | 3 | a0001c0002t0002g0084a0001c0002t0002g0143a0004c0009t0002g0083 | 3 | HG00280.hp2 HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.220-75T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42581051 | ||||||
chr13:42581101
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-25C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42581101 | ||||||
chr13:42581307
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+14G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581307 | ||||||
chr13:42581395
|
T | G | 1 | a0001c0002t0007g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387+102T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581395 | ||||||
chr13:42581585
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+292G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581585 | ||||||
chr13:42581695
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.387+402C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581695 | ||||||
chr13:42581696
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+403A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581696 | ||||||
chr13:42582016
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.387+723G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582016 | ||||||
chr13:42582140
|
G | C | 2 | a0001c0005t0009g0315a0001c0005t0009g0316 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.387+847G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582140 | ||||||
chr13:42582164
|
C | T | 2 | a0001c0002t0001g0228a0001c0002t0013g0229 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.387+871C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582164 | ||||||
chr13:42582222
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+929A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582222 | ||||||
chr13:42582289
|
A | T | 1 | a0001c0002t0002g0140 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.387+996A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582289 | ||||||
chr13:42582377
|
G | A | 2 | a0001c0002t0002g0085a0001c0002t0002g0086 | 2 | NA18987.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.387+1084G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582377 | ||||||
chr13:42582422
|
C | CGA | 3 | a0001c0001t0001g0031a0001c0001t0001g0166a0001c0001t0001g0189 | 4 | NA18944.hp2 NA18953.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1129_387+1130i others(4): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582422 | ||||||
chr13:42582458
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.387+1165T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582458 | ||||||
chr13:42582560
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+1267G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582560 | ||||||
chr13:42582602
|
G | A | 7 | a0001c0002t0002g0013a0001c0002t0002g0087a0001c0002t0002g0088others(4): Show | 9 | NA18948.hp1 NA18990.hp2 NA19005.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+1309G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582602 | ||||||
chr13:42582629
|
T | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18969.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.387+1336T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582629 | ||||||
chr13:42582698
|
A | G | 1 | a0001c0007t0003g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.387+1405A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582698 | ||||||
chr13:42582961
|
A | C | 1 | a0001c0002t0002g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.387+1668A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582961 | ||||||
chr13:42583008
|
G | A | 1 | a0001c0002t0002g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.387+1715G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583008 | ||||||
chr13:42583067
|
T | A | 5 | a0001c0002t0001g0217a0001c0002t0001g0218a0001c0002t0001g0231others(2): Show | 5 | HG02451.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1774T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583067 | ||||||
chr13:42583122
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.387+1829C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583122 | ||||||
chr13:42583131
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+1838G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583131 | ||||||
chr13:42583176
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+1883C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583176 | ||||||
chr13:42583304
|
C | G | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+2011C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583304 | ||||||
chr13:42583358
|
G | A | 5 | a0001c0002t0001g0217a0001c0002t0001g0218a0001c0002t0001g0231others(2): Show | 5 | HG02451.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2065G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583358 | ||||||
chr13:42583359
|
C | T | 5 | a0001c0002t0001g0217a0001c0002t0001g0218a0001c0002t0001g0231others(2): Show | 5 | HG02451.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2066C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583359 | ||||||
chr13:42583417
|
T | TA | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(59): Show | 91 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.387+2145dupA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA | 7 | a0001c0002t0002g0086a0001c0002t0002g0136a0001c0002t0002g0137others(4): Show | 7 | HG00733.hp2 HG01168.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+2139_387+2145d others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(1): Show |
63 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0001g0228others(60): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.387+2138_387+2145d others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(2): Show |
36 | a0001c0002t0002g0007a0001c0002t0002g0014a0001c0002t0002g0026others(33): Show | 41 | HG00597.hp1 HG00738.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.387+2137_387+2145d others(11): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(3): Show |
10 | a0001c0002t0001g0215a0001c0002t0002g0087a0001c0002t0002g0095others(7): Show | 10 | HG01106.hp1 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+2136_387+2145d others(12): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(4): Show |
9 | a0001c0002t0001g0048a0001c0002t0001g0053a0001c0002t0002g0025others(6): Show | 10 | HG01169.hp2 HG02622.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+2135_387+2145d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(5): Show |
8 | a0001c0002t0001g0052a0001c0002t0001g0231a0001c0002t0001g0232others(5): Show | 8 | HG00673.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.387+2134_387+2145d others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(6): Show |
4 | a0001c0002t0004g0222a0001c0002t0004g0223a0001c0002t0004g0224others(1): Show | 4 | HG01496.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+2133_387+2145d others(15): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(7): Show |
3 | a0001c0002t0004g0220a0001c0002t0004g0221a0001c0002t0011g0230 | 3 | HG02572.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.387+2132_387+2145d others(16): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(8): Show |
1 | a0001c0002t0001g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.387+2131_387+2145d others(17): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(9): Show |
6 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0002t0001g0051others(3): Show | 6 | HG02145.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+2130_387+2145d others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(10): Show |
1 | a0001c0002t0004g0219 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.387+2129_387+2145d others(19): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583417
|
T | TAAAAAAA others(11): Show |
1 | a0001c0002t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+2128_387+2145d others(20): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | |||||
chr13:42583433
|
A | AAAAAAAA others(1): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 6 | HG02647.hp1 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+2145_387+2146i others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583433 | |||||
chr13:42583433
|
A | AAAAAAAG | 36 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0012others(33): Show | 49 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.387+2145_387+2146i others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583433 | |||||
chr13:42583434
|
A | AAAAAAG | 39 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0023others(36): Show | 56 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.387+2145_387+2146i others(8): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583434 | |||||
chr13:42583439
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(230): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.387+2146G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583439 | ||||||
chr13:42583443
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(127): Show | 162 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.387+2150G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583443 | ||||||
chr13:42583444
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(232): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.387+2151G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583444 | ||||||
chr13:42583447
|
G | A | 1 | a0001c0001t0001g0047 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+2154G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583447 | ||||||
chr13:42583448
|
A | G | 105 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(102): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.387+2155A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583448 | ||||||
chr13:42583763
|
G | A | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+2470G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583763 | ||||||
chr13:42583779
|
G | A | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+2486G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583779 | ||||||
chr13:42583797
|
G | A | 1 | a0001c0002t0007g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387+2504G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583797 | ||||||
chr13:42583903
|
G | T | 1 | a0001c0007t0003g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.387+2610G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583903 | ||||||
chr13:42583966
|
A | G | 1 | a0001c0002t0002g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.387+2673A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583966 | ||||||
chr13:42583996
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.387+2703C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583996 | ||||||
chr13:42584083
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.387+2790A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584083 | ||||||
chr13:42584252
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.387+2959G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584252 | ||||||
chr13:42584365
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+3072T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584365 | ||||||
chr13:42584451
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(234): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.387+3158A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584451 | ||||||
chr13:42584460
|
C | A | 1 | a0001c0002t0002g0087 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.387+3167C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584460 | ||||||
chr13:42584491
|
C | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0198a0001c0001t0001g0201 | 3 | NA18987.hp2 NA18997.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.387+3198C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584491 | ||||||
chr13:42584598
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(234): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.387+3305C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584598 | ||||||
chr13:42584599
|
T | A | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+3306T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584599 | ||||||
chr13:42584617
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.387+3324G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584617 | ||||||
chr13:42584660
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.387+3367C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584660 | ||||||
chr13:42584736
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(235): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.387+3443C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584736 | ||||||
chr13:42584955
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+3662G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584955 | ||||||
chr13:42584999
|
G | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(75): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.387+3706G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584999 | ||||||
chr13:42585031
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.387+3738G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585031 | ||||||
chr13:42585041
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00642.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.387+3748C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585041 | ||||||
chr13:42585111
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.387+3818A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585111 | ||||||
chr13:42585138
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387+3845G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585138 | ||||||
chr13:42585215
|
G | A | 2 | a0001c0002t0001g0048a0001c0002t0001g0053 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.387+3922G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585215 | ||||||
chr13:42585225
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.387+3932G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585225 | ||||||
chr13:42585265
|
G | A | 105 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(102): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.387+3972G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585265 | ||||||
chr13:42585380
|
T | C | 106 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(103): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.387+4087T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585380 | ||||||
chr13:42585413
|
T | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0279 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.387+4120T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585413 | ||||||
chr13:42585525
|
C | G | 1 | a0001c0002t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.387+4232C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585525 | ||||||
chr13:42585668
|
G | A | 138 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(135): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.387+4375G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585668 | ||||||
chr13:42585789
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(234): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.387+4496G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585789 | ||||||
chr13:42586247
|
G | A | 4 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0267others(1): Show | 5 | HG02572.hp1 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+4954G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586247 | ||||||
chr13:42586441
|
A | T | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+5148A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586441 | ||||||
chr13:42586544
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.387+5251A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586544 | ||||||
chr13:42586583
|
G | A | 4 | a0001c0002t0002g0027a0001c0002t0002g0097a0001c0002t0002g0112others(1): Show | 5 | HG02647.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+5290G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586583 | ||||||
chr13:42586584
|
A | T | 9 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(6): Show | 9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.387+5291A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586584 | ||||||
chr13:42586794
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(225): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.387+5501A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586794 | ||||||
chr13:42586828
|
T | G | 1 | a0001c0002t0002g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.387+5535T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586828 | ||||||
chr13:42586993
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.387+5700T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586993 | ||||||
chr13:42587082
|
G | A | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+5789G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587082 | ||||||
chr13:42587230
|
T | C | 5 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0267others(2): Show | 6 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+5937T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587230 | ||||||
chr13:42587245
|
T | G | 1 | a0001c0001t0006g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.387+5952T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587245 | ||||||
chr13:42587455
|
A | G | 1 | a0001c0002t0001g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387+6162A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587455 | ||||||
chr13:42587543
|
T | C | 1 | a0001c0008t0003g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.387+6250T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587543 | ||||||
chr13:42587597
|
G | C | 1 | a0001c0002t0002g0089 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.387+6304G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587597 | ||||||
chr13:42587603
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.387+6310A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587603 | ||||||
chr13:42587767
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.387+6474A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587767 | ||||||
chr13:42587894
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.387+6601A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587894 | ||||||
chr13:42587927
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(81): Show | 115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.387+6634G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587927 | ||||||
chr13:42588058
|
T | C | 1 | a0001c0001t0006g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.387+6765T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588058 | ||||||
chr13:42588062
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+6769C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588062 | ||||||
chr13:42588549
|
G | A | 5 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0267others(2): Show | 6 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+7256G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588549 | ||||||
chr13:42588998
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+7705C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588998 | ||||||
chr13:42589145
|
G | A | 1 | a0001c0003t0003g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.387+7852G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589145 | ||||||
chr13:42589159
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(224): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.387+7866C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589159 | ||||||
chr13:42589234
|
G | T | 9 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(6): Show | 9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.387+7941G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589234 | ||||||
chr13:42589390
|
C | A | 8 | a0001c0002t0004g0219a0001c0002t0004g0220a0001c0002t0004g0221others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.387+8097C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589390 | ||||||
chr13:42589401
|
C | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.387+8108C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589401 | ||||||
chr13:42589443
|
C | A | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+8150C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589443 | ||||||
chr13:42589461
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.387+8168C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589461 | ||||||
chr13:42589466
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.387+8173C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589466 | ||||||
chr13:42589501
|
T | C | 1 | a0001c0002t0002g0113 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.387+8208T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589501 | ||||||
chr13:42589505
|
T | G | 15 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(12): Show | 15 | HG01496.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.387+8212T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589505 | ||||||
chr13:42589645
|
C | T | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+8352C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589645 | ||||||
chr13:42589663
|
G | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(228): Show | 289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.387+8370G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589663 | ||||||
chr13:42589720
|
A | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.387+8427A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589720 | ||||||
chr13:42589743
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.387+8450G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589743 | ||||||
chr13:42589814
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.387+8521G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589814 | ||||||
chr13:42590011
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+8718C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590011 | ||||||
chr13:42590035
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+8742T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590035 | ||||||
chr13:42590405
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(233): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+9112G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590405 | ||||||
chr13:42590450
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.387+9157T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590450 | ||||||
chr13:42590488
|
C | T | 16 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(13): Show | 16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.387+9195C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590488 | ||||||
chr13:42590559
|
A | G | 16 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(13): Show | 16 | HG01496.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+9266A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590559 | ||||||
chr13:42590574
|
C | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(87): Show | 121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.387+9281C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590574 | ||||||
chr13:42590592
|
A | G | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+9299A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590592 | ||||||
chr13:42590730
|
G | A | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+9437G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590730 | ||||||
chr13:42590816
|
T | G | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+9523T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590816 | ||||||
chr13:42590914
|
A | G | 1 | a0001c0003t0003g0307 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.387+9621A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590914 | ||||||
chr13:42591006
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.387+9713T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591006 | ||||||
chr13:42591022
|
G | T | 3 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0011g0230 | 3 | HG02818.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.387+9729G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591022 | ||||||
chr13:42591246
|
G | T | 105 | a0001c0002t0001g0126a0001c0002t0001g0157a0001c0002t0002g0002others(102): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.388-9506G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591246 | ||||||
chr13:42591332
|
A | G | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(67): Show | 100 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.388-9420A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591332 | ||||||
chr13:42591369
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(87): Show | 121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.388-9383C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591369 | ||||||
chr13:42591372
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0066others(1): Show | 12 | NA18939.hp2 NA18941.hp1 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-9380C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591372 | ||||||
chr13:42591399
|
T | A | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-9353T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591399 | ||||||
chr13:42591567
|
C | T | 16 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(13): Show | 16 | HG01496.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.388-9185C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591567 | ||||||
chr13:42591602
|
A | G | 1 | a0001c0003t0003g0307 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.388-9150A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591602 | ||||||
chr13:42591824
|
G | C | 3 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0011g0230 | 3 | HG02818.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.388-8928G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591824 | ||||||
chr13:42592027
|
G | T | 1 | a0001c0001t0001g0185 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.388-8725G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592027 | ||||||
chr13:42592110
|
C | T | 1 | a0001c0002t0002g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.388-8642C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592110 | ||||||
chr13:42592148
|
G | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.388-8604G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592148 | ||||||
chr13:42592159
|
A | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.388-8593A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592159 | ||||||
chr13:42592222
|
G | C | 2 | a0001c0002t0002g0099a0001c0002t0002g0114 | 2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.388-8530G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592222 | ||||||
chr13:42592233
|
C | G | 16 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(13): Show | 16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-8519C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592233 | ||||||
chr13:42592488
|
C | G | 1 | a0001c0003t0003g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.388-8264C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592488 | ||||||
chr13:42592645
|
G | A | 16 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(13): Show | 16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-8107G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592645 | ||||||
chr13:42592797
|
C | T | 4 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-7955C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592797 | ||||||
chr13:42592810
|
A | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.388-7942A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592810 | ||||||
chr13:42593078
|
G | A | 2 | a0001c0005t0009g0315a0001c0005t0009g0316 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.388-7674G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593078 | ||||||
chr13:42593078
|
G | C | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-7674G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593078 | ||||||
chr13:42593197
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(227): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.388-7555T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593197 | ||||||
chr13:42593262
|
T | C | 8 | a0001c0002t0004g0219a0001c0002t0004g0220a0001c0002t0004g0221others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-7490T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593262 | ||||||
chr13:42593338
|
A | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.388-7414A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593338 | ||||||
chr13:42593377
|
A | G | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(67): Show | 100 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.388-7375A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593377 | ||||||
chr13:42593925
|
T | A | 3 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199 | 3 | HG02630.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.388-6827T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593925 | ||||||
chr13:42593937
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.388-6815C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593937 | ||||||
chr13:42593938
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.388-6814A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593938 | ||||||
chr13:42594172
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-6580C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594172 | ||||||
chr13:42594365
|
G | C | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-6387G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594365 | ||||||
chr13:42594402
|
G | A | 138 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(135): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.388-6350G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594402 | ||||||
chr13:42594524
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 124 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-6228G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594524 | ||||||
chr13:42594723
|
G | C | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.388-6029G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594723 | ||||||
chr13:42594752
|
C | T | 1 | a0001c0002t0004g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388-6000C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594752 | ||||||
chr13:42594892
|
C | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.388-5860C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594892 | ||||||
chr13:42594905
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.388-5847G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594905 | ||||||
chr13:42594945
|
AT | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(76): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.388-5804delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42594945 | |||||
chr13:42594948
|
T | TA | 8 | a0001c0002t0002g0084a0001c0002t0002g0101a0001c0002t0002g0115others(5): Show | 8 | HG00280.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-5793dupA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42594948 | |||||
chr13:42595059
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.388-5693A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595059 | ||||||
chr13:42595255
|
T | A | 1 | a0001c0002t0002g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.388-5497T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595255 | ||||||
chr13:42595305
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-5447T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595305 | ||||||
chr13:42595435
|
A | T | 1 | a0001c0002t0002g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.388-5317A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595435 | ||||||
chr13:42595611
|
T | G | 10 | a0001c0001t0001g0318a0001c0002t0001g0048a0001c0002t0001g0049others(7): Show | 10 | HG01109.hp2 HG01192.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-5141T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595611 | ||||||
chr13:42595956
|
C | G | 2 | a0001c0002t0002g0116a0001c0002t0002g0161 | 2 | HG01099.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.388-4796C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595956 | ||||||
chr13:42596079
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.388-4673G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596079 | ||||||
chr13:42596081
|
G | A | 6 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0266others(3): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-4671G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596081 | ||||||
chr13:42596303
|
C | T | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-4449C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596303 | ||||||
chr13:42596443
|
T | C | 1 | a0001c0002t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.388-4309T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596443 | ||||||
chr13:42596637
|
C | G | 1 | a0001c0001t0010g0043 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.388-4115C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596637 | ||||||
chr13:42596720
|
G | A | 8 | a0001c0002t0002g0084a0001c0002t0002g0101a0001c0002t0002g0115others(5): Show | 8 | HG00280.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-4032G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596720 | ||||||
chr13:42596751
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.388-4001G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596751 | ||||||
chr13:42596942
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0191 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.388-3810T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596942 | ||||||
chr13:42596962
|
G | A | 8 | a0001c0002t0004g0219a0001c0002t0004g0220a0001c0002t0004g0221others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-3790G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596962 | ||||||
chr13:42597050
|
G | A | 6 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0266others(3): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-3702G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597050 | ||||||
chr13:42597175
|
T | TACATGTC | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.388-3577_388-3576i others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597175 | ||||||
chr13:42597246
|
C | A | 20 | a0001c0001t0001g0038a0001c0001t0001g0184a0001c0001t0001g0209others(17): Show | 21 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.388-3506C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597246 | ||||||
chr13:42597311
|
A | G | 1 | a0001c0002t0005g0029 | 2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.388-3441A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597311 | ||||||
chr13:42597340
|
C | CT | 40 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0167others(37): Show | 41 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.388-3391dupT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | |||||
chr13:42597340
|
C | CTT | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.388-3392_388-3391d others(4): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | |||||
chr13:42597340
|
C | CTTT | 21 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0170others(18): Show | 23 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-3393_388-3391d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | |||||
chr13:42597340
|
CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0038a0001c0001t0001g0184a0001c0001t0001g0209others(17): Show | 21 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.388-3400_388-3391d others(12): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | |||||
chr13:42597432
|
G | A | 16 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(13): Show | 16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-3320G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597432 | ||||||
chr13:42597514
|
TC | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-3235delC | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597514 | |||||
chr13:42597530
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(56): Show | 88 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.388-3222C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597530 | ||||||
chr13:42597801
|
G | A | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-2951G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597801 | ||||||
chr13:42597823
|
G | A | 9 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(6): Show | 9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.388-2929G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597823 | ||||||
chr13:42597855
|
C | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(286): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.388-2897C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597855 | ||||||
chr13:42597873
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.388-2879G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597873 | ||||||
chr13:42597949
|
A | T | 8 | a0001c0002t0004g0219a0001c0002t0004g0220a0001c0002t0004g0221others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-2803A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597949 | ||||||
chr13:42598006
|
T | G | 1 | a0001c0003t0003g0299 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.388-2746T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598006 | ||||||
chr13:42598421
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.388-2331T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598421 | ||||||
chr13:42598476
|
G | A | 4 | a0001c0001t0001g0235a0001c0001t0001g0244a0001c0001t0001g0248others(1): Show | 4 | NA18947.hp2 NA18951.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-2276G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598476 | ||||||
chr13:42598659
|
A | T | 1 | a0001c0008t0003g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.388-2093A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598659 | ||||||
chr13:42598741
|
G | A | 9 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(6): Show | 9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.388-2011G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598741 | ||||||
chr13:42598742
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.388-2010C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598742 | ||||||
chr13:42598921
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.388-1831G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598921 | ||||||
chr13:42599062
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 227 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.388-1690T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599062 | ||||||
chr13:42599077
|
G | C | 1 | a0003c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-1675G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599077 | ||||||
chr13:42599174
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.388-1578A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599174 | ||||||
chr13:42599303
|
CTCTA | C | 4 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0007g0186others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1406_388-1403d others(6): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599303 | |||||
chr13:42599321
|
C | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0270a0001c0001t0001g0272 | 5 | NA18953.hp1 NA18960.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-1431C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599321 | ||||||
chr13:42599329
|
CTATCTAT others(2): Show |
C | 2 | a0001c0001t0001g0039a0001c0001t0001g0246 | 3 | HG01070.hp2 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.388-1422_388-1414d others(11): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599329 | ||||||
chr13:42599330
|
T | TATCTATC others(4): Show |
1 | a0001c0002t0002g0137 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.388-1421_388-1411d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599330 | |||||
chr13:42599330
|
T | TATCTATC others(8): Show |
1 | a0001c0005t0009g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388-1421_388-1407d others(17): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599330 | |||||
chr13:42599333
|
CT | C | 3 | a0001c0001t0001g0235a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | NA18947.hp2 NA18951.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.388-1418delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599333 | ||||||
chr13:42599333
|
CTATCT | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0314 | 3 | HG00423.hp2 HG02132.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.388-1418_388-1414d others(7): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599333 | ||||||
chr13:42599334
|
T | TATCTATC others(4): Show |
5 | a0001c0001t0001g0170a0001c0001t0001g0197a0001c0002t0001g0049others(2): Show | 5 | HG03041.hp2 HG03540.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-1417_388-1407d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599334 | |||||
chr13:42599337
|
CT | C | 6 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0250others(3): Show | 6 | HG02004.hp1 HG02165.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-1414delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599337 | ||||||
chr13:42599338
|
T | TATC | 26 | a0001c0001t0001g0176a0001c0001t0001g0188a0001c0001t0001g0194others(23): Show | 31 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.388-1413_388-1411d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | |||||
chr13:42599338
|
T | TATCATCT others(31): Show |
1 | a0001c0001t0001g0264 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.388-1411_388-1410i others(40): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | |||||
chr13:42599338
|
T | TATCTATC | 24 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0032others(21): Show | 31 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.388-1413_388-1407d others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | |||||
chr13:42599338
|
T | TATCTATC others(4): Show |
2 | a0001c0003t0003g0296a0001c0003t0003g0297 | 2 | NA18995.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.388-1407_388-1406i others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | |||||
chr13:42599341
|
CT | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0044others(54): Show | 84 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.388-1410delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599341 | ||||||
chr13:42599342
|
T | TATC | 38 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0041others(35): Show | 48 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.388-1409_388-1407d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599342 | |||||
chr13:42599345
|
CT | C | 12 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0260others(9): Show | 13 | HG01081.hp2 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.388-1406delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599345 | ||||||
chr13:42599346
|
TATC | T | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0067others(22): Show | 27 | HG00423.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.388-1402_388-1400d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599346 | |||||
chr13:42599349
|
C | CATCCATC others(5): Show |
3 | a0001c0003t0003g0298a0001c0003t0003g0300a0001c0003t0003g0302 | 3 | NA18981.hp1 NA19080.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.388-1400_388-1399i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCCATC others(9): Show |
2 | a0001c0003t0003g0301a0001c0003t0003g0308 | 2 | NA18939.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.388-1400_388-1399i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCCATC others(17): Show |
1 | a0001c0004t0003g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.388-1400_388-1399i others(26): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCT | 10 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0196others(7): Show | 12 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-1370_388-1367d others(6): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCTATC others(1): Show |
33 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(30): Show | 51 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.388-1374_388-1367d others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCTATC others(5): Show |
21 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0033others(18): Show | 27 | HG00140.hp2 HG00408.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.388-1378_388-1367d others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCTATC others(9): Show |
1 | a0001c0001t0001g0201 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.388-1382_388-1367d others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CATCTATC others(13): Show |
1 | a0001c0001t0001g0203 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.388-1386_388-1367d others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | |||||
chr13:42599349
|
C | CT | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(159): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(3): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(12): Show |
1 | a0001c0003t0003g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.388-1403_388-1402i others(21): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(9): Show |
2 | a0001c0003t0003g0309a0001c0008t0003g0295 | 2 | HG01256.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(13): Show |
2 | a0001c0003t0003g0299a0001c0003t0003g0306 | 2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(17): Show |
1 | a0001c0003t0008g0303 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(26): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(21): Show |
1 | a0001c0003t0003g0305 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(30): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(1): Show |
4 | a0001c0001t0001g0071a0001c0002t0001g0048a0001c0002t0001g0051others(1): Show | 4 | HG00140.hp1 HG02129.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(5): Show |
17 | a0001c0001t0001g0021a0001c0001t0001g0066a0001c0001t0001g0068others(14): Show | 20 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(9): Show |
7 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0173others(4): Show | 10 | HG00597.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCATC others(13): Show |
3 | a0001c0001t0001g0212a0001c0001t0001g0243a0001c0002t0001g0055 | 3 | HG01975.hp1 HG02257.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCTAT others(21): Show |
1 | a0001c0003t0008g0304 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(30): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCTAT others(9): Show |
2 | a0001c0001t0001g0262a0001c0002t0004g0224 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCTAT others(9): Show |
1 | a0001c0001t0001g0270 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599349
|
C | CTATCTAT others(13): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0272 | 4 | NA18953.hp1 NA18960.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | ||||||
chr13:42599372
|
C | CTATCTAT others(9): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0210a0001c0001t0001g0263others(1): Show | 5 | HG00735.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-1367_388-1366i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599372 | |||||
chr13:42599372
|
C | CTATCTAT others(5): Show |
4 | a0001c0001t0001g0184a0001c0001t0001g0211a0001c0001t0001g0213others(1): Show | 4 | HG01361.hp1 HG04204.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1369_388-1368i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599372 | |||||
chr13:42599372
|
C | T | 2 | a0001c0001t0001g0209a0001c0005t0009g0315 | 2 | HG03540.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.388-1380C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599372 | ||||||
chr13:42599380
|
C | T | 1 | a0001c0002t0002g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.388-1372C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599380 | ||||||
chr13:42599382
|
A | ATCTATCT others(5): Show |
3 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0007t0003g0290 | 4 | HG02572.hp1 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1367_388-1366i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599382 | |||||
chr13:42599382
|
A | G | 4 | a0001c0003t0003g0227a0001c0004t0003g0266a0001c0004t0003g0267others(1): Show | 4 | HG02055.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1370A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599382 | ||||||
chr13:42599454
|
C | T | 4 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1298C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599454 | ||||||
chr13:42599505
|
G | C | 4 | a0001c0002t0004g0219a0001c0002t0004g0220a0001c0002t0004g0221others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1247G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599505 | ||||||
chr13:42599519
|
G | A | 11 | a0001c0001t0001g0318a0001c0002t0001g0048a0001c0002t0001g0049others(8): Show | 11 | HG01109.hp2 HG01192.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-1233G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599519 | ||||||
chr13:42599521
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-1231G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599521 | ||||||
chr13:42599677
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-1075C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599677 | ||||||
chr13:42599678
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0212 | 2 | NA18981.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.388-1074G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599678 | ||||||
chr13:42599754
|
G | A | 14 | a0001c0003t0003g0296a0001c0003t0003g0297a0001c0003t0003g0298others(11): Show | 14 | HG01256.hp1 HG03654.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-998G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599754 | ||||||
chr13:42599842
|
T | C | 2 | a0001c0002t0002g0312a0001c0002t0002g0313 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.388-910T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599842 | ||||||
chr13:42599880
|
T | A | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-872T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599880 | ||||||
chr13:42599901
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.388-851T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599901 | ||||||
chr13:42599964
|
A | G | 144 | a0001c0001t0001g0038a0001c0001t0001g0184a0001c0001t0001g0209others(141): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.388-788A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599964 | ||||||
chr13:42600353
|
C | A | 10 | a0001c0001t0001g0038a0001c0001t0001g0184a0001c0001t0001g0209others(7): Show | 11 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-399C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600353 | ||||||
chr13:42600361
|
G | A | 23 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(20): Show | 24 | HG01496.hp2 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.388-391G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600361 | ||||||
chr13:42600473
|
G | C | 1 | a0001c0002t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388-279G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600473 | ||||||
chr13:42600544
|
T | C | 1 | a0001c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.388-208T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600544 | ||||||
chr13:42600719
|
T | C | 1 | a0001c0002t0001g0228 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.388-33T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600719 | ||||||
chr13:42601085
|
C | T | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.532+104C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601085 | ||||||
chr13:42601208
|
A | G | 3 | a0001c0003t0003g0309a0001c0003t0003g0310a0001c0004t0003g0078 | 3 | HG00673.hp1 HG04199.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.532+227A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601208 | ||||||
chr13:42601326
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.532+345A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601326 | ||||||
chr13:42601464
|
G | C | 1 | a0001c0002t0002g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.532+483G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601464 | ||||||
chr13:42601591
|
C | A | 1 | a0001c0002t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.532+610C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601591 | ||||||
chr13:42601782
|
A | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+801A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601782 | ||||||
chr13:42601934
|
A | G | 1 | a0001c0002t0002g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.532+953A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601934 | ||||||
chr13:42601975
|
C | T | 62 | a0001c0001t0002g0240a0001c0002t0002g0007a0001c0002t0002g0008others(59): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.532+994C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601975 | ||||||
chr13:42602016
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.532+1035A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602016 | ||||||
chr13:42602308
|
C | G | 1 | a0001c0002t0001g0228 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.532+1327C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602308 | ||||||
chr13:42602328
|
T | G | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.532+1347T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602328 | ||||||
chr13:42602337
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+1356T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602337 | ||||||
chr13:42602462
|
G | A | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.532+1481G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602462 | ||||||
chr13:42602466
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.532+1485C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602466 | ||||||
chr13:42602579
|
A | G | 25 | a0001c0001t0001g0038a0001c0001t0001g0209a0001c0001t0001g0210others(22): Show | 26 | HG00673.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.532+1598A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602579 | ||||||
chr13:42602683
|
T | C | 1 | a0001c0002t0002g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.532+1702T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602683 | ||||||
chr13:42602691
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.532+1710G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602691 | ||||||
chr13:42602794
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+1813C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602794 | ||||||
chr13:42602977
|
G | A | 2 | a0001c0005t0009g0315a0001c0005t0009g0316 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.532+1996G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602977 | ||||||
chr13:42603027
|
T | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0209a0001c0001t0001g0210others(16): Show | 20 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.532+2046T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603027 | ||||||
chr13:42603033
|
T | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0023others(46): Show | 66 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.532+2052T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603033 | ||||||
chr13:42603116
|
C | T | 15 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(12): Show | 15 | HG01496.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.532+2135C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603116 | ||||||
chr13:42603128
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.532+2147A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603128 | ||||||
chr13:42603487
|
G | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 5 | HG01361.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+2506G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603487 | ||||||
chr13:42603852
|
A | C | 1 | a0001c0001t0001g0046 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.533-2645A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603852 | ||||||
chr13:42603853
|
G | C | 6 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0266others(3): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-2644G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603853 | ||||||
chr13:42603858
|
C | A | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-2639C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603858 | ||||||
chr13:42604002
|
G | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0241 | 2 | HG00140.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.533-2495G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604002 | ||||||
chr13:42604324
|
G | A | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-2173G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604324 | ||||||
chr13:42604447
|
C | T | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(60): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.533-2050C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604447 | ||||||
chr13:42604469
|
T | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0191 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.533-2028T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604469 | ||||||
chr13:42604503
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.533-1994G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604503 | ||||||
chr13:42604516
|
C | A | 1 | a0001c0002t0002g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.533-1981C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604516 | ||||||
chr13:42604535
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 217 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.533-1962G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604535 | ||||||
chr13:42604546
|
G | A | 3 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199 | 3 | HG02630.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.533-1951G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604546 | ||||||
chr13:42604605
|
T | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0172a0001c0001t0001g0178others(2): Show | 6 | NA18943.hp1 NA18992.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-1892T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604605 | ||||||
chr13:42604728
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.533-1769C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604728 | ||||||
chr13:42604832
|
G | A | 105 | a0001c0001t0002g0240a0001c0002t0001g0157a0001c0002t0002g0002others(102): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.533-1665G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604832 | ||||||
chr13:42604865
|
C | A | 4 | a0001c0001t0007g0186a0001c0001t0007g0187a0001c0001t0007g0199others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-1632C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604865 | ||||||
chr13:42604925
|
G | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 10 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-1572G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604925 | ||||||
chr13:42604939
|
G | A | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-1558G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604939 | ||||||
chr13:42605005
|
G | A | 8 | a0001c0002t0004g0219a0001c0002t0004g0220a0001c0002t0004g0221others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.533-1492G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605005 | ||||||
chr13:42605019
|
A | G | 6 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0266others(3): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-1478A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605019 | ||||||
chr13:42605127
|
T | C | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-1370T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605127 | ||||||
chr13:42605149
|
G | A | 7 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(4): Show | 7 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.533-1348G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605149 | ||||||
chr13:42605250
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.533-1247A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605250 | ||||||
chr13:42605303
|
C | G | 6 | a0001c0004t0001g0022a0001c0004t0003g0022a0001c0004t0003g0266others(3): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-1194C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605303 | ||||||
chr13:42605499
|
G | C | 3 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0011g0230 | 3 | HG02818.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.533-998G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605499 | ||||||
chr13:42605579
|
GAAGGTTC others(6): Show |
G | 7 | a0001c0001t0001g0038a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 8 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.533-915_533-903del others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 42605579 | |||||
chr13:42605945
|
T | G | 1 | a0001c0001t0001g0047 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.533-552T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605945 | ||||||
chr13:42605948
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.533-549A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605948 | ||||||
chr13:42605958
|
CAT | C | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-538_533-537del others(2): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605958 | ||||||
chr13:42606081
|
C | T | 24 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(21): Show | 25 | HG00673.hp1 HG01256.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.533-416C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606081 | ||||||
chr13:42606174
|
A | G | 3 | a0001c0002t0001g0163a0001c0002t0001g0216a0001c0002t0001g0228 | 3 | HG02280.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.533-323A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606174 | ||||||
chr13:42606185
|
T | C | 1 | a0001c0002t0004g0219 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.533-312T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606185 | ||||||
chr13:42606203
|
A | G | 1 | a0001c0002t0002g0150 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.533-294A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606203 | ||||||
chr13:42606296
|
G | A | 2 | a0001c0002t0001g0231a0001c0002t0001g0232 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.533-201G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606296 | ||||||
chr13:42606367
|
G | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 10 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-130G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606367 | ||||||
chr13:42606404
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.533-93A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606404 | ||||||
chr13:42606440
|
A | C | 18 | a0001c0003t0003g0227a0001c0003t0003g0296a0001c0003t0003g0297others(15): Show | 18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-57A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606440 | ||||||
chr13:42606463
|
T | A | 10 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(7): Show | 10 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.533-34T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606463 |