geneid | 8795 |
---|---|
ensemblid | ENSG00000120889.13 |
hgncid | 11905 |
symbol | TNFRSF10B |
name | TNF receptor superfamily member 10b |
refseq_nuc | NM_003842.5 |
refseq_prot | NP_003833.4 |
ensembl_nuc | ENST00000276431.9 |
ensembl_prot | ENSP00000276431.4 |
mane_status | MANE Select |
chr | chr8 |
start | 23020133 |
end | 23069031 |
strand | - |
ver | v1.2 |
region | chr8:23020133-23069031 |
region5000 | chr8:23015133-23074031 |
regionname0 | TNFRSF10B_chr8_23020133_23069031 |
regionname5000 | TNFRSF10B_chr8_23015133_23074031 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 440 | 213 | 39 | 28 | 111 | 6 | 28 | 87 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002 | 0/0 | 440 | 56 | 16 | 16 | 13 | 7 | 4 | 10 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003 | 0/0 | 440 | 50 | 0 | 3 | 40 | 0 | 7 | 29 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0004 | 0/0 | 440 | 36 | 20 | 9 | 4 | 1 | 2 | 4 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0005 | 1/0 | 440 | 7 | 5 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0006 | 0/0 | 440 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0007 | 0/0 | 440 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0008 | 0/0 | 440 | 3 | 0 | 1 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0009 | 0/0 | 440 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0010 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0011 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0012 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0013 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0014 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0015 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0016 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0017 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1323 | 213 | 39 | 28 | 111 | 6 | 28 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0002 | 0/0 | 1323 | 56 | 16 | 16 | 13 | 7 | 4 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0003 | 0/0 | 1323 | 49 | 0 | 3 | 39 | 0 | 7 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0004 | 0/0 | 1323 | 36 | 20 | 9 | 4 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0005 | 1/0 | 1323 | 7 | 5 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0006 | 0/0 | 1323 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0007 | 0/0 | 1323 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0008 | 0/0 | 1323 | 3 | 0 | 1 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0009 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0010 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0011 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0012 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0013 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0014 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0015 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0016 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0017 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
c0018 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2676 | 161 | 38 | 22 | 73 | 3 | 24 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0002 | 0/1 | 2676 | 81 | 6 | 9 | 53 | 3 | 9 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0003 | 0/0 | 2676 | 42 | 8 | 10 | 21 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0004 | 0/0 | 2676 | 33 | 19 | 5 | 6 | 2 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0005 | 0/0 | 2676 | 19 | 1 | 7 | 7 | 3 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0006 | 0/0 | 2676 | 11 | 2 | 4 | 1 | 2 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0007 | 0/0 | 2676 | 5 | 0 | 0 | 4 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0008 | 0/0 | 2671 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0009 | 0/0 | 2676 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0010 | 0/0 | 2676 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0011 | 0/0 | 2676 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0012 | 0/0 | 2676 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0013 | 0/0 | 2676 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0014 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0015 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0016 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0017 | 0/0 | 2676 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0018 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0019 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0020 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0021 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0022 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0023 | 0/0 | 2720 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0024 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0025 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0026 | 0/0 | 2676 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0027 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0028 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0029 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0030 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0031 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
t0032 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1323 | 213 | 39 | 28 | 111 | 6 | 28 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002 | 0/0 | 1323 | 56 | 16 | 16 | 13 | 7 | 4 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0003 | 0/0 | 1323 | 49 | 0 | 3 | 39 | 0 | 7 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0016 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0004c0004 | 0/0 | 1323 | 36 | 20 | 9 | 4 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0005c0005 | 1/0 | 1323 | 7 | 5 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0006c0006 | 0/0 | 1323 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0007c0007 | 0/0 | 1323 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0008c0008 | 0/0 | 1323 | 3 | 0 | 1 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0009c0009 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0010c0010 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0011c0011 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0012c0012 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0013c0013 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0014c0015 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0015c0014 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0016c0017 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0017c0018 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3998 | 97 | 16 | 7 | 56 | 2 | 16 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0002 | 0/1 | 3998 | 57 | 5 | 9 | 33 | 3 | 6 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0003 | 0/0 | 3998 | 35 | 8 | 8 | 16 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0004 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0007 | 0/0 | 3998 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0008 | 0/0 | 3993 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0009 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0010 | 0/0 | 3998 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0011 | 0/0 | 3998 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0012 | 0/0 | 3998 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0013 | 0/0 | 3998 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0016 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0017 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0018 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0019 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0021 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0022 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0024 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0026 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0001c0001t0027 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0002 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0004 | 0/0 | 3998 | 21 | 10 | 4 | 5 | 2 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0005 | 0/0 | 3998 | 19 | 1 | 7 | 7 | 3 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0006 | 0/0 | 3998 | 10 | 1 | 4 | 1 | 2 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0015 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0028 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0029 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0031 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0002c0002t0032 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0003t0001 | 0/0 | 3998 | 16 | 0 | 1 | 10 | 0 | 5 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0003t0002 | 0/0 | 3998 | 22 | 0 | 0 | 20 | 0 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0003t0003 | 0/0 | 3998 | 7 | 0 | 2 | 5 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0003t0007 | 0/0 | 3998 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0003t0025 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0003c0016t0001 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0004c0004t0001 | 0/0 | 3998 | 33 | 17 | 9 | 4 | 1 | 2 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0004c0004t0002 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0004c0004t0009 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0004c0004t0020 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0005c0005t0001 | 1/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0005c0005t0004 | 0/0 | 3998 | 6 | 5 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0006c0006t0001 | 0/0 | 3998 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0007c0007t0004 | 0/0 | 3998 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0008c0008t0004 | 0/0 | 3998 | 2 | 0 | 1 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0008c0008t0030 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0009c0009t0001 | 0/0 | 3998 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0010c0010t0014 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0011c0011t0006 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0012c0012t0023 | 0/0 | 4042 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0013c0013t0001 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0014c0015t0001 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0015c0014t0001 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0016c0017t0001 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
a0017c0018t0001 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | copy fasta | chr8 | 23015133 | 23074031 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0011g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0011g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0012g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0013g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0013g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0016g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0017g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0019g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0021g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0022g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0024g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0026g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0001c0001t0027g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0005g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0006g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0028g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0029g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0031g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0002c0002t0032g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0003t0025g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0003c0016t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0004c0004t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0001g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0005c0005t0004g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0006c0006t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0007c0007t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0007c0007t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0007c0007t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0008c0008t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0008c0008t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0008c0008t0030g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0009c0009t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0009c0009t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0010c0010t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0011c0011t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0012c0012t0023g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0013c0013t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0014c0015t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0015c0014t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0016c0017t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
a0017c0018t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00099 | hp2 | a0002 | c0002 | t0005 | g0335 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00140 | hp1 | a0002 | c0002 | t0005 | g0313 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0306 | EUR | GBR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | FIN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00280 | hp2 | a0002 | c0002 | t0006 | g0325 | EUR | FIN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00408 | hp2 | a0002 | c0002 | t0004 | g0362 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00423 | hp2 | a0003 | c0003 | t0002 | g0091 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00438 | hp1 | a0008 | c0008 | t0004 | g0364 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0049 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00621 | hp2 | a0003 | c0003 | t0007 | g0111 | EAS | CHS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00639 | hp1 | a0004 | c0004 | t0001 | g0017 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00733 | hp2 | a0004 | c0004 | t0001 | g0206 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00735 | hp1 | a0002 | c0002 | t0004 | g0330 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00738 | hp1 | a0008 | c0008 | t0004 | g0339 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG00738 | hp2 | a0004 | c0004 | t0001 | g0138 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01069 | hp1 | a0004 | c0004 | t0001 | g0300 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01070 | hp1 | a0004 | c0004 | t0001 | g0166 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01070 | hp2 | a0002 | c0002 | t0004 | g0008 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01071 | hp2 | a0002 | c0002 | t0004 | g0008 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0095 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01099 | hp1 | a0002 | c0002 | t0006 | g0343 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01099 | hp2 | a0015 | c0014 | t0001 | g0208 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0264 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01106 | hp2 | a0002 | c0002 | t0005 | g0348 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01167 | hp1 | a0002 | c0002 | t0005 | g0368 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01167 | hp2 | a0009 | c0009 | t0001 | g0225 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01169 | hp1 | a0009 | c0009 | t0001 | g0209 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01169 | hp2 | a0002 | c0002 | t0006 | g0334 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01175 | hp1 | a0002 | c0002 | t0006 | g0338 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01175 | hp2 | a0004 | c0004 | t0001 | g0063 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01192 | hp1 | a0006 | c0006 | t0001 | g0128 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0207 | AMR | PUR | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01255 | hp1 | a0002 | c0002 | t0005 | g0329 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01255 | hp2 | a0002 | c0002 | t0005 | g0336 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01258 | hp2 | a0002 | c0002 | t0005 | g0007 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01261 | hp1 | a0016 | c0017 | t0001 | g0103 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01433 | hp1 | a0004 | c0004 | t0001 | g0062 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01433 | hp2 | a0002 | c0002 | t0004 | g0314 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0311 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01515 | hp1 | a0002 | c0002 | t0004 | g0327 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01516 | hp1 | a0002 | c0002 | t0004 | g0369 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01516 | hp2 | a0004 | c0004 | t0001 | g0065 | EUR | IBS | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01884 | hp2 | a0002 | c0002 | t0005 | g0007 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01891 | hp1 | a0011 | c0011 | t0006 | g0312 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01891 | hp2 | a0005 | c0005 | t0004 | g0321 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01934 | hp1 | a0004 | c0004 | t0001 | g0287 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01934 | hp2 | a0002 | c0002 | t0006 | g0331 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01978 | hp2 | a0001 | c0001 | t0021 | g0155 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01981 | hp1 | a0002 | c0002 | t0005 | g0324 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01981 | hp2 | a0004 | c0004 | t0001 | g0057 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01993 | hp1 | a0003 | c0003 | t0003 | g0106 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02004 | hp2 | a0001 | c0001 | t0024 | g0302 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02015 | hp1 | a0003 | c0003 | t0002 | g0083 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0197 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02040 | hp1 | a0003 | c0003 | t0007 | g0086 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02055 | hp2 | a0002 | c0002 | t0004 | g0356 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02056 | hp2 | a0002 | c0002 | t0004 | g0371 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02083 | hp2 | a0003 | c0003 | t0002 | g0045 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02135 | hp2 | a0002 | c0002 | t0004 | g0342 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0212 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02148 | hp1 | a0002 | c0002 | t0005 | g0350 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0087 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02165 | hp2 | a0003 | c0003 | t0007 | g0069 | EAS | CDX | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02257 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02258 | hp1 | a0005 | c0005 | t0004 | g0318 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02280 | hp1 | a0002 | c0002 | t0015 | g0010 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0119 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | PEL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02523 | hp1 | a0008 | c0008 | t0030 | g0365 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02572 | hp1 | a0005 | c0005 | t0004 | g0358 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0060 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02615 | hp2 | a0004 | c0004 | t0001 | g0124 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02630 | hp2 | a0002 | c0002 | t0029 | g0357 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02683 | hp2 | a0002 | c0002 | t0006 | g0363 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02717 | hp1 | a0005 | c0005 | t0004 | g0366 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02723 | hp2 | a0006 | c0006 | t0001 | g0126 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02735 | hp1 | a0004 | c0004 | t0001 | g0031 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0102 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02818 | hp1 | a0006 | c0006 | t0001 | g0222 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0123 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0140 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02886 | hp2 | a0004 | c0004 | t0001 | g0131 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0316 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02896 | hp2 | a0002 | c0002 | t0004 | g0352 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0320 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02922 | hp1 | a0004 | c0004 | t0001 | g0221 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02922 | hp2 | a0004 | c0004 | t0002 | g0021 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0204 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0118 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0375 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0243 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03098 | hp2 | a0007 | c0007 | t0004 | g0359 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03130 | hp1 | a0007 | c0007 | t0004 | g0319 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03130 | hp2 | a0004 | c0004 | t0009 | g0040 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03139 | hp1 | a0010 | c0010 | t0014 | g0009 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03139 | hp2 | a0002 | c0002 | t0032 | g0323 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03195 | hp1 | a0004 | c0004 | t0001 | g0130 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03195 | hp2 | a0002 | c0002 | t0004 | g0374 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03225 | hp1 | a0006 | c0006 | t0001 | g0127 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0088 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03453 | hp1 | a0007 | c0007 | t0004 | g0317 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03453 | hp2 | a0002 | c0002 | t0004 | g0355 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03486 | hp1 | a0002 | c0002 | t0004 | g0353 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03490 | hp1 | a0001 | c0001 | t0013 | g0246 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03516 | hp1 | a0002 | c0002 | t0028 | g0351 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03516 | hp2 | a0004 | c0004 | t0001 | g0129 | AFR | ESN | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03540 | hp1 | a0002 | c0002 | t0004 | g0361 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03540 | hp2 | a0004 | c0004 | t0001 | g0133 | AFR | GWD | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03579 | hp1 | a0005 | c0005 | t0004 | g0315 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03579 | hp2 | a0006 | c0006 | t0001 | g0029 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0078 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03704 | hp2 | a0012 | c0012 | t0023 | g0016 | SAS | PJL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03927 | hp2 | a0001 | c0001 | t0026 | g0026 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0142 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04115 | hp1 | a0005 | c0005 | t0004 | g0367 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0061 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0094 | SAS | BEB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04204 | hp2 | a0002 | c0002 | t0005 | g0333 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0100 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG04228 | hp2 | a0002 | c0002 | t0006 | g0340 | SAS | STU | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18522 | hp2 | a0004 | c0004 | t0001 | g0139 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0332 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0205 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18939 | hp2 | a0004 | c0004 | t0001 | g0270 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18942 | hp1 | a0002 | c0002 | t0005 | g0344 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18947 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18950 | hp1 | a0002 | c0002 | t0005 | g0347 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18954 | hp2 | a0001 | c0001 | t0022 | g0290 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18956 | hp2 | a0003 | c0003 | t0002 | g0110 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18959 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18961 | hp1 | a0003 | c0003 | t0025 | g0070 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18961 | hp2 | a0002 | c0002 | t0005 | g0372 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18963 | hp2 | a0003 | c0003 | t0002 | g0028 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18970 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18971 | hp1 | a0003 | c0003 | t0002 | g0099 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18974 | hp2 | a0003 | c0003 | t0002 | g0105 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18980 | hp2 | a0003 | c0003 | t0002 | g0186 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18985 | hp2 | a0003 | c0003 | t0003 | g0109 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18987 | hp1 | a0003 | c0003 | t0002 | g0116 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18987 | hp2 | a0002 | c0002 | t0005 | g0341 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0196 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18991 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18992 | hp2 | a0017 | c0018 | t0001 | g0084 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18995 | hp1 | a0002 | c0002 | t0005 | g0345 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19000 | hp1 | a0003 | c0003 | t0002 | g0187 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19002 | hp2 | a0004 | c0004 | t0001 | g0147 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19003 | hp1 | a0003 | c0016 | t0001 | g0307 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19003 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19009 | hp2 | a0003 | c0003 | t0003 | g0188 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19012 | hp2 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19030 | hp2 | a0004 | c0004 | t0001 | g0134 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19043 | hp2 | a0002 | c0002 | t0006 | g0354 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19054 | hp1 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19056 | hp1 | a0003 | c0003 | t0002 | g0112 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19057 | hp2 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19058 | hp1 | a0001 | c0001 | t0027 | g0268 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19058 | hp2 | a0004 | c0004 | t0001 | g0148 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19065 | hp1 | a0002 | c0002 | t0006 | g0349 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19065 | hp2 | a0002 | c0002 | t0005 | g0346 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19066 | hp1 | a0002 | c0002 | t0004 | g0373 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19074 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19079 | hp1 | a0004 | c0004 | t0001 | g0175 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19080 | hp2 | a0003 | c0003 | t0003 | g0121 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19081 | hp1 | a0002 | c0002 | t0004 | g0326 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19081 | hp2 | a0003 | c0003 | t0002 | g0047 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19084 | hp2 | a0002 | c0002 | t0005 | g0360 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19088 | hp2 | a0001 | c0001 | t0018 | g0169 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19090 | hp2 | a0001 | c0001 | t0019 | g0096 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19240 | hp1 | a0004 | c0004 | t0001 | g0122 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA19240 | hp2 | a0001 | c0001 | t0012 | g0228 | AFR | YRI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0132 | AFR | ASW | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ASW | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20752 | hp2 | a0002 | c0002 | t0006 | g0328 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20805 | hp2 | a0002 | c0002 | t0005 | g0337 | EUR | TSI | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20905 | hp1 | a0001 | c0001 | t0017 | g0051 | SAS | GIH | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20905 | hp2 | a0014 | c0015 | t0001 | g0079 | SAS | GIH | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG01123 | hp2 | a0002 | c0002 | t0031 | g0370 | AMR | CLM | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0322 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02109 | hp2 | a0004 | c0004 | t0020 | g0039 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03471 | hp1 | a0004 | c0004 | t0001 | g0038 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | MSL | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0223 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18955 | hp1 | a0013 | c0013 | t0001 | g0177 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA20300 | hp2 | a0006 | c0006 | t0001 | g0224 | AFR | USA | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA21309 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | LWK | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0305 | REF | REF | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
homoSapiens_grch38 | hp1 | a0005 | c0005 | t0001 | g0012 | REF | REF | TNFRSF10B_chr8_23015133_23074031 | TNFRSF10B | chr8 | 23015133 | 23074031 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23022771
|
G | A | 1 | a0015 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1223C>T | p.Thr408Met | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1360/3998 | 1223/1323 | 408/440 | chr8 | 23022771 | ||
chr8:23027732
|
C | T | 1 | a0017 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.770G>A | p.Arg257His | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/9 | 907/3998 | 770/1323 | 257/440 | chr8 | 23027732 | ||
chr8:23028412
|
C | T | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.667G>A | p.Val223Ile | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 804/3998 | 667/1323 | 223/440 | chr8 | 23028412 | ||
chr8:23028414
|
G | A | 1 | a0009 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.665C>T | p.Ala222Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 802/3998 | 665/1323 | 222/440 | chr8 | 23028414 | ||
chr8:23028417
|
G | A | 1 | a0013 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.662C>T | p.Ala221Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 799/3998 | 662/1323 | 221/440 | chr8 | 23028417 | ||
chr8:23028487
|
C | A | 1 | a0014 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.592G>T | p.Val198Leu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 729/3998 | 592/1323 | 198/440 | chr8 | 23028487 | ||
chr8:23028489
|
G | A | 2 | a0006a0007 | 9 | HG01192.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.590C>T | p.Thr197Met | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 727/3998 | 590/1323 | 197/440 | chr8 | 23028489 | ||
chr8:23028507
|
A | G | 10 | a0001a0002a0003others(7): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
missense_variant | MODERATE | c.572T>C | p.Val191Ala | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/9 | 709/3998 | 572/1323 | 191/440 | chr8 | 23028507 | ||
chr8:23029610
|
C | A | 1 | a0017 | 1 | NA18992.hp2 | missense_variant&splice_region_variant | MODERATE | c.476G>T | p.Gly159Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/9 | 613/3998 | 476/1323 | 159/440 | chr8 | 23029610 | ||
chr8:23043188
|
G | A | 4 | a0003a0008a0016others(1): Show | 55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
missense_variant | MODERATE | c.200C>T | p.Ala67Val | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/9 | 337/3998 | 200/1323 | 67/440 | chr8 | 23043188 | ||
chr8:23068800
|
G | A | 12 | a0001a0003a0004others(9): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
missense_variant | MODERATE | c.95C>T | p.Pro32Leu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 232/3998 | 95/1323 | 32/440 | chr8 | 23068800 | ||
chr8:23068833
|
C | T | 1 | a0010 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.62G>A | p.Gly21Glu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 199/3998 | 62/1323 | 21/440 | chr8 | 23068833 | ||
chr8:23068839
|
C | T | 1 | a0011 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.56G>A | p.Gly19Asp | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 193/3998 | 56/1323 | 19/440 | chr8 | 23068839 | ||
chr8:23068851
|
C | G | 1 | a0010 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.44G>C | p.Arg15Pro | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 181/3998 | 44/1323 | 15/440 | chr8 | 23068851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23022982
|
G | A | 1 | a0003c0016 | 1 | NA19003.hp1 | splice_region_variant&synonymous_variant | LOW | c.1012C>T | p.Leu338Leu | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1149/3998 | 1012/1323 | 338/440 | chr8 | 23022982 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23020184
|
A | T | 3 | a0001c0001t0009a0001c0001t0011a0004c0004t0009 | 4 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2487T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2487 | chr8 | 23020184 | |||||
chr8:23020235
|
T | A | 1 | a0004c0004t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2436A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2436 | chr8 | 23020235 | |||||
chr8:23020488
|
T | A | 3 | a0001c0001t0009a0001c0001t0011a0004c0004t0009 | 4 | HG01243.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2183A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2183 | chr8 | 23020488 | |||||
chr8:23020546
|
G | A | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2125C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2125 | chr8 | 23020546 | |||||
chr8:23020657
|
A | G | 1 | a0001c0001t0024 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2014T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 2014 | chr8 | 23020657 | |||||
chr8:23020683
|
T | C | 1 | a0002c0002t0031 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1988 | chr8 | 23020683 | |||||
chr8:23020706
|
TAAAAG | T | 2 | a0001c0001t0008a0002c0002t0032 | 4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1960_*1964delCTTT others(1): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1960 | chr8 | 23020706 | |||||
chr8:23020813
|
G | C | 1 | a0001c0001t0013 | 2 | HG01496.hp2 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1858C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1858 | chr8 | 23020813 | |||||
chr8:23021180
|
CTGAGGTC others(16): Show |
C | 1 | a0001c0001t0019 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1468_*1490delTCTA others(19): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1468 | chr8 | 23021180 | |||||
chr8:23021232
|
G | A | 1 | a0001c0001t0027 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1439C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1439 | chr8 | 23021232 | |||||
chr8:23021322
|
G | A | 1 | a0001c0001t0021 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1349 | chr8 | 23021322 | |||||
chr8:23021509
|
A | G | 1 | a0001c0001t0026 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1162T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 1162 | chr8 | 23021509 | |||||
chr8:23021856
|
A | G | 1 | a0001c0001t0018 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 815 | chr8 | 23021856 | |||||
chr8:23022056
|
C | T | 2 | a0001c0001t0010a0002c0002t0029 | 3 | HG02630.hp2 HG02976.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*615G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 615 | chr8 | 23022056 | |||||
chr8:23022167
|
G | A | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*504C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 504 | chr8 | 23022167 | |||||
chr8:23022168
|
G | A | 1 | a0003c0003t0025 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 503 | chr8 | 23022168 | |||||
chr8:23022185
|
G | C | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 486 | chr8 | 23022185 | |||||
chr8:23022221
|
T | C | 12 | a0001c0001t0002a0001c0001t0007a0001c0001t0013others(9): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 450 | chr8 | 23022221 | |||||
chr8:23022432
|
G | A | 1 | a0001c0001t0022 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 239 | chr8 | 23022432 | |||||
chr8:23022510
|
T | TACAGGAT others(37): Show |
1 | a0012c0012t0023 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*160dupGAAACT others(38): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 160 | chr8 | 23022510 | |||||
chr8:23022527
|
A | G | 2 | a0001c0001t0009a0004c0004t0009 | 2 | HG02723.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 144 | chr8 | 23022527 | |||||
chr8:23022590
|
C | G | 1 | a0001c0001t0017 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 81 | chr8 | 23022590 | |||||
chr8:23022594
|
C | T | 1 | a0002c0002t0028 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 77 | chr8 | 23022594 | |||||
chr8:23022649
|
G | C | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(14): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 22 | chr8 | 23022649 | |||||
chr8:23022660
|
G | A | 2 | a0001c0001t0008a0002c0002t0032 | 4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 9/9 | 11 | chr8 | 23022660 | |||||
chr8:23068906
|
A | T | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 12 | chr8 | 23068906 | |||||
chr8:23068908
|
G | C | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-14C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 14 | chr8 | 23068908 | |||||
chr8:23068910
|
T | G | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 16 | chr8 | 23068910 | |||||
chr8:23068911
|
C | T | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 17 | chr8 | 23068911 | |||||
chr8:23068914
|
A | C | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 20 | chr8 | 23068914 | |||||
chr8:23068985
|
G | A | 14 | a0001c0001t0004a0002c0002t0004a0002c0002t0005others(11): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | chr8 | 23068985 | ||||||
chr8:23068988
|
A | T | 1 | a0001c0001t0016 | 1 | NA19057.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 94 | chr8 | 23068988 | |||||
chr8:23068995
|
G | T | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-101C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 101 | chr8 | 23068995 | |||||
chr8:23069001
|
C | G | 2 | a0002c0002t0015a0010c0010t0014 | 2 | HG02280.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-107G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 107 | chr8 | 23069001 | |||||
chr8:23069002
|
C | T | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 108 | chr8 | 23069002 | |||||
chr8:23069004
|
G | T | 1 | a0010c0010t0014 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/9 | 110 | chr8 | 23069004 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:23022988
|
G | A | 1 | a0001c0001t0012g0140 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.1010-4C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23022988 | ||||||
chr8:23023124
|
G | A | 1 | a0004c0004t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1010-140C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023124 | ||||||
chr8:23023145
|
C | T | 1 | a0004c0004t0001g0017 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1010-161G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023145 | ||||||
chr8:23023192
|
CAA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(91): Show | 98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1010-210_1010-209d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023192 | ||||||
chr8:23023275
|
A | C | 2 | a0001c0001t0012g0140a0001c0001t0012g0228 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1010-291T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023275 | ||||||
chr8:23023310
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1010-326C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023310 | ||||||
chr8:23023460
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1010-476C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023460 | ||||||
chr8:23023478
|
GT | G | 4 | a0001c0001t0008g0036a0001c0001t0008g0118a0001c0001t0008g0123others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-495delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023478 | ||||||
chr8:23023492
|
ACT | A | 3 | a0001c0001t0010g0204a0001c0001t0010g0205a0002c0002t0029g0357 | 3 | HG02630.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1010-510_1010-509d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023492 | ||||||
chr8:23023629
|
A | G | 1 | a0004c0004t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1009+559T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023629 | ||||||
chr8:23023907
|
A | G | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(326): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1009+281T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23023907 | ||||||
chr8:23024019
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0066a0001c0001t0001g0247 | 3 | HG02145.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1009+169C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23024019 | ||||||
chr8:23024020
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0066a0001c0001t0001g0247 | 3 | HG02145.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1009+168T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23024020 | ||||||
chr8:23024126
|
C | T | 2 | a0001c0001t0002g0161a0002c0002t0031g0370 | 2 | HG00735.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1009+62G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 8/8 | chr8 | 23024126 | ||||||
chr8:23024339
|
T | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(318): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.937-79A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024339 | ||||||
chr8:23024524
|
AT | A | 45 | a0001c0001t0001g0014a0001c0001t0001g0213a0001c0001t0001g0238others(42): Show | 46 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.937-265delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024524 | ||||||
chr8:23024696
|
C | T | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(317): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.937-436G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024696 | ||||||
chr8:23024780
|
G | A | 106 | a0001c0001t0002g0015a0001c0001t0002g0050a0001c0001t0002g0053others(103): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.937-520C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024780 | ||||||
chr8:23024870
|
G | A | 2 | a0002c0002t0005g0346a0002c0002t0005g0360 | 2 | NA19065.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.937-610C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024870 | ||||||
chr8:23024977
|
AAAAATAA others(3): Show |
A | 66 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(63): Show | 67 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.937-727_937-718del others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23024977 | ||||||
chr8:23025018
|
G | A | 22 | a0001c0001t0003g0042a0001c0001t0003g0068a0001c0001t0003g0152others(19): Show | 23 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.937-758C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23025018 | ||||||
chr8:23025234
|
C | T | 4 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0218others(1): Show | 4 | HG02572.hp2 HG02922.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-974G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23025234 | ||||||
chr8:23025797
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.936+1336G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23025797 | ||||||
chr8:23026011
|
G | T | 2 | a0001c0001t0009g0215a0004c0004t0009g0040 | 2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.936+1122C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026011 | ||||||
chr8:23026087
|
T | C | 9 | a0006c0006t0001g0029a0006c0006t0001g0126a0006c0006t0001g0127others(6): Show | 9 | HG01192.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.936+1046A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026087 | ||||||
chr8:23026112
|
A | T | 1 | a0003c0003t0001g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.936+1021T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026112 | ||||||
chr8:23026221
|
A | C | 5 | a0001c0001t0002g0154a0001c0001t0002g0161a0001c0001t0002g0303others(2): Show | 5 | HG00280.hp1 HG00735.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+912T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026221 | ||||||
chr8:23026266
|
G | GT | 114 | a0001c0001t0001g0037a0001c0001t0001g0219a0001c0001t0002g0015others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.936+866dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026266 | ||||||
chr8:23026266
|
GT | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(91): Show | 98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.936+866delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026266 | ||||||
chr8:23026272
|
T | G | 2 | a0001c0001t0011g0207a0001c0001t0011g0223 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.936+861A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026272 | ||||||
chr8:23026288
|
T | G | 1 | a0001c0001t0003g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.936+845A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026288 | ||||||
chr8:23026462
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(316): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.936+671C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026462 | ||||||
chr8:23026514
|
T | C | 2 | a0001c0001t0009g0215a0004c0004t0009g0040 | 2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.936+619A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026514 | ||||||
chr8:23026637
|
C | A | 1 | a0004c0004t0001g0166 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.936+496G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026637 | ||||||
chr8:23026718
|
T | C | 35 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(32): Show | 35 | HG00408.hp1 HG00609.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.936+415A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026718 | ||||||
chr8:23026721
|
T | C | 1 | a0002c0002t0006g0363 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.936+412A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026721 | ||||||
chr8:23026765
|
C | T | 2 | a0001c0001t0011g0207a0001c0001t0011g0223 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.936+368G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026765 | ||||||
chr8:23026823
|
T | C | 14 | a0001c0001t0003g0041a0001c0001t0008g0036a0001c0001t0008g0118others(11): Show | 14 | HG01192.hp1 HG02615.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.936+310A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026823 | ||||||
chr8:23026995
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.936+138G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23026995 | ||||||
chr8:23027075
|
C | A | 65 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(62): Show | 66 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.936+58G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23027075 | ||||||
chr8:23027088
|
G | C | 65 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(62): Show | 66 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.936+45C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23027088 | ||||||
chr8:23027100
|
G | A | 2 | a0001c0001t0011g0207a0001c0001t0011g0223 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.936+33C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 7/8 | chr8 | 23027100 | ||||||
chr8:23027320
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.781-32C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027320 | ||||||
chr8:23027441
|
G | A | 3 | a0001c0001t0001g0027a0002c0002t0004g0332a0002c0002t0028g0351 | 3 | HG03516.hp1 HG03669.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.781-153C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027441 | ||||||
chr8:23027596
|
A | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.780+126T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027596 | ||||||
chr8:23027640
|
G | A | 111 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(108): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.780+82C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027640 | ||||||
chr8:23027641
|
G | A | 220 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(217): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.780+81C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 6/8 | chr8 | 23027641 | ||||||
chr8:23027818
|
A | T | 100 | a0001c0001t0002g0015a0001c0001t0002g0050a0001c0001t0002g0053others(97): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.749-65T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23027818 | ||||||
chr8:23027930
|
A | G | 2 | a0001c0001t0003g0167a0002c0002t0006g0343 | 2 | HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.749-177T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23027930 | ||||||
chr8:23028080
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.748+251C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028080 | ||||||
chr8:23028091
|
T | A | 1 | a0003c0003t0003g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.748+240A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028091 | ||||||
chr8:23028156
|
A | G | 3 | a0001c0001t0001g0219a0002c0002t0004g0322a0002c0002t0004g0353 | 3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.748+175T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028156 | ||||||
chr8:23028226
|
G | A | 1 | a0001c0001t0009g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.748+105C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028226 | ||||||
chr8:23028248
|
G | A | 4 | a0001c0001t0008g0036a0001c0001t0008g0118a0001c0001t0008g0123others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+83C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028248 | ||||||
chr8:23028318
|
A | T | 3 | a0001c0001t0001g0219a0002c0002t0004g0322a0002c0002t0004g0353 | 3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.748+13T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 5/8 | chr8 | 23028318 | ||||||
chr8:23028617
|
A | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(324): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.477-15T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028617 | ||||||
chr8:23028629
|
G | T | 1 | a0001c0001t0009g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477-27C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028629 | ||||||
chr8:23028717
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(93): Show | 100 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.477-115G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028717 | ||||||
chr8:23028742
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0198 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.477-140G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028742 | ||||||
chr8:23028812
|
C | A | 12 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0097others(9): Show | 13 | HG01993.hp2 NA18747.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.477-210G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028812 | ||||||
chr8:23028872
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.477-270A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028872 | ||||||
chr8:23028877
|
T | C | 1 | a0004c0004t0001g0133 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.477-275A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23028877 | ||||||
chr8:23029034
|
G | A | 3 | a0001c0001t0001g0219a0002c0002t0004g0322a0002c0002t0004g0353 | 3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.477-432C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029034 | ||||||
chr8:23029072
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.477-470T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029072 | ||||||
chr8:23029124
|
G | A | 1 | a0002c0002t0005g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.476+486C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029124 | ||||||
chr8:23029305
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(94): Show | 101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.476+305G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029305 | ||||||
chr8:23029319
|
C | T | 1 | a0002c0002t0004g0374 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.476+291G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029319 | ||||||
chr8:23029321
|
A | G | 1 | a0002c0002t0005g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.476+289T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029321 | ||||||
chr8:23029339
|
C | A | 1 | a0001c0001t0002g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.476+271G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029339 | ||||||
chr8:23029420
|
G | A | 5 | a0001c0001t0002g0192a0001c0001t0002g0293a0001c0001t0002g0310others(2): Show | 5 | HG01074.hp2 HG03017.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+190C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029420 | ||||||
chr8:23029471
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.476+139G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029471 | ||||||
chr8:23029472
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.476+138C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029472 | ||||||
chr8:23029500
|
C | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(316): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.476+110G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029500 | ||||||
chr8:23029595
|
C | T | 1 | a0001c0001t0009g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.476+15G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 4/8 | chr8 | 23029595 | ||||||
chr8:23029726
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.365-5G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029726 | ||||||
chr8:23029741
|
T | C | 14 | a0001c0001t0003g0041a0001c0001t0008g0036a0001c0001t0008g0118others(11): Show | 14 | HG01192.hp1 HG02615.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.365-20A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029741 | ||||||
chr8:23029968
|
G | A | 1 | a0003c0003t0001g0265 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.365-247C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029968 | ||||||
chr8:23029986
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.365-265C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23029986 | ||||||
chr8:23030095
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(97): Show | 104 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.365-374C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23030095 | ||||||
chr8:23030456
|
G | A | 204 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(201): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.364+303C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23030456 | ||||||
chr8:23030594
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364+165C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 3/8 | chr8 | 23030594 | ||||||
chr8:23030894
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(324): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.251-22C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23030894 | ||||||
chr8:23030948
|
C | T | 1 | a0006c0006t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.251-76G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23030948 | ||||||
chr8:23031108
|
C | T | 13 | a0001c0001t0008g0036a0001c0001t0008g0118a0001c0001t0008g0123others(10): Show | 13 | HG01192.hp1 HG02723.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-236G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031108 | ||||||
chr8:23031258
|
A | G | 1 | a0001c0001t0021g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.251-386T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031258 | ||||||
chr8:23031309
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.251-437G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031309 | ||||||
chr8:23031323
|
G | T | 3 | a0001c0001t0010g0204a0001c0001t0010g0205a0002c0002t0029g0357 | 3 | HG02630.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.251-451C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031323 | ||||||
chr8:23031372
|
G | A | 6 | a0001c0001t0001g0219a0001c0001t0002g0184a0001c0001t0002g0256others(3): Show | 6 | HG02109.hp1 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-500C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031372 | ||||||
chr8:23031375
|
C | CTATT | 147 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0037others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.251-507_251-504dup others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | ||||||
chr8:23031375
|
C | CTATTTAT others(1): Show |
61 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 63 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.251-511_251-504dup others(8): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | ||||||
chr8:23031375
|
C | CTATTTAT others(5): Show |
17 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0158others(14): Show | 17 | HG00438.hp1 HG02109.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.251-515_251-504dup others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | ||||||
chr8:23031375
|
CTATT | C | 60 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0080others(57): Show | 61 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.251-507_251-504del others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031375 | ||||||
chr8:23031504
|
C | G | 5 | a0001c0001t0001g0217a0001c0001t0004g0375a0001c0001t0010g0204others(2): Show | 5 | HG02630.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-632G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031504 | ||||||
chr8:23031544
|
C | T | 189 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.251-672G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031544 | ||||||
chr8:23031545
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(315): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.251-673T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031545 | ||||||
chr8:23031547
|
C | T | 1 | a0002c0002t0004g0361 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.251-675G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031547 | ||||||
chr8:23031561
|
G | C | 1 | a0001c0001t0009g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251-689C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031561 | ||||||
chr8:23031584
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG02717.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.251-712C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031584 | ||||||
chr8:23031873
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.251-1001C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031873 | ||||||
chr8:23031911
|
C | CAT | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(172): Show | 180 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.251-1041_251-1040d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031911 | ||||||
chr8:23031912
|
A | ATAT | 6 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0219others(3): Show | 6 | HG00597.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-1041_251-1040i others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031912 | ||||||
chr8:23031913
|
T | TA | 145 | a0001c0001t0001g0214a0001c0001t0001g0257a0001c0001t0002g0015others(142): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.251-1042_251-1041i others(3): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031913 | ||||||
chr8:23031915
|
T | A | 1 | a0001c0001t0007g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.251-1043A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23031915 | ||||||
chr8:23032068
|
G | A | 1 | a0004c0004t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.251-1196C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032068 | ||||||
chr8:23032140
|
C | T | 1 | a0004c0004t0001g0017 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.251-1268G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032140 | ||||||
chr8:23032270
|
C | T | 19 | a0001c0001t0003g0042a0001c0001t0003g0068a0001c0001t0003g0152others(16): Show | 20 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.251-1398G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032270 | ||||||
chr8:23032342
|
C | G | 1 | a0001c0001t0026g0026 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.251-1470G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032342 | ||||||
chr8:23032368
|
G | A | 1 | a0002c0002t0004g0342 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.251-1496C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032368 | ||||||
chr8:23032384
|
G | A | 1 | a0002c0002t0004g0356 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.251-1512C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032384 | ||||||
chr8:23032449
|
T | C | 13 | a0001c0001t0008g0036a0001c0001t0008g0118a0001c0001t0008g0123others(10): Show | 13 | HG01192.hp1 HG02723.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-1577A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032449 | ||||||
chr8:23032527
|
C | CGA | 73 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(70): Show | 74 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.251-1657_251-1656d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032527 | ||||||
chr8:23032584
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0216 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.251-1712C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032584 | ||||||
chr8:23032800
|
G | A | 1 | a0001c0001t0012g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.251-1928C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23032800 | ||||||
chr8:23033113
|
A | G | 1 | a0002c0002t0005g0372 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.251-2241T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033113 | ||||||
chr8:23033259
|
T | C | 4 | a0004c0004t0001g0147a0004c0004t0001g0148a0004c0004t0001g0175others(1): Show | 4 | NA18939.hp2 NA19002.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2387A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033259 | ||||||
chr8:23033306
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0213a0002c0002t0004g0332others(3): Show | 6 | HG02055.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2434G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033306 | ||||||
chr8:23033401
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(96): Show | 103 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.251-2529C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033401 | ||||||
chr8:23033412
|
G | A | 219 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.251-2540C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033412 | ||||||
chr8:23033444
|
G | A | 6 | a0004c0004t0001g0133a0004c0004t0001g0139a0004c0004t0001g0212others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2572C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033444 | ||||||
chr8:23033529
|
A | C | 1 | a0004c0004t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.251-2657T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033529 | ||||||
chr8:23033585
|
C | CA | 6 | a0004c0004t0001g0024a0004c0004t0001g0133a0004c0004t0001g0175others(3): Show | 6 | HG01099.hp2 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2714dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CA | C | 12 | a0003c0003t0007g0111a0004c0004t0001g0017a0004c0004t0001g0031others(9): Show | 12 | HG00621.hp2 HG00639.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.251-2714delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAA | C | 13 | a0001c0001t0002g0074a0001c0001t0002g0151a0001c0001t0002g0195others(10): Show | 13 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-2717_251-2714d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAA | C | 39 | a0001c0001t0002g0050a0001c0001t0002g0053a0001c0001t0002g0073others(36): Show | 40 | HG00621.hp1 HG01074.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.251-2718_251-2714d others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAA | C | 82 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0002g0015others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.251-2719_251-2714d others(8): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA | C | 6 | a0001c0001t0003g0068a0001c0001t0003g0152a0002c0002t0006g0354others(3): Show | 6 | HG01891.hp1 HG03017.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2720_251-2714d others(9): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(1): Show |
C | 22 | a0001c0001t0001g0234a0001c0001t0002g0054a0001c0001t0003g0005others(19): Show | 23 | HG00423.hp1 HG01106.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.251-2721_251-2714d others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0125others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-2722_251-2714d others(11): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(3): Show |
C | 36 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0064others(33): Show | 36 | HG00408.hp1 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.251-2723_251-2714d others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0280a0002c0002t0004g0342 | 2 | HG02135.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.251-2724_251-2714d others(13): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0011g0207a0001c0001t0011g0223a0001c0001t0012g0140others(1): Show | 4 | HG01243.hp2 HG02886.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2725_251-2714d others(14): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0168a0001c0001t0001g0174a0001c0001t0001g0229others(3): Show | 6 | HG01978.hp2 HG02258.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2726_251-2714d others(15): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(7): Show |
C | 42 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0032others(39): Show | 43 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.251-2727_251-2714d others(16): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(8): Show |
C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(44): Show | 50 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.251-2728_251-2714d others(17): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251-2729_251-2714d others(18): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(15): Show |
C | 2 | a0001c0001t0002g0157a0001c0001t0002g0165 | 2 | HG02602.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.251-2735_251-2714d others(24): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033585
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.251-2736_251-2714d others(25): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033585 | ||||||
chr8:23033620
|
A | AAAAAAAA others(3): Show |
2 | a0002c0002t0004g0322a0002c0002t0004g0353 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-2749_251-2748i others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033620 | ||||||
chr8:23033620
|
A | G | 75 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(72): Show | 76 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.251-2748T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033620 | ||||||
chr8:23033666
|
A | G | 1 | a0004c0004t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.251-2794T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033666 | ||||||
chr8:23033685
|
T | C | 2 | a0001c0001t0011g0207a0001c0001t0011g0223 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.251-2813A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033685 | ||||||
chr8:23033776
|
G | A | 7 | a0004c0004t0001g0038a0004c0004t0001g0124a0004c0004t0001g0131others(4): Show | 7 | HG01099.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-2904C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033776 | ||||||
chr8:23033807
|
G | A | 22 | a0001c0001t0003g0042a0001c0001t0003g0068a0001c0001t0003g0152others(19): Show | 23 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.251-2935C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033807 | ||||||
chr8:23033836
|
A | G | 1 | a0001c0001t0003g0232 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.251-2964T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033836 | ||||||
chr8:23033898
|
C | G | 3 | a0001c0001t0001g0219a0002c0002t0004g0322a0002c0002t0004g0353 | 3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-3026G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23033898 | ||||||
chr8:23034004
|
G | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(320): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.251-3132C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034004 | ||||||
chr8:23034160
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0213others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-3288C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034160 | ||||||
chr8:23034243
|
G | C | 1 | a0001c0001t0003g0241 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.251-3371C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034243 | ||||||
chr8:23034373
|
G | T | 5 | a0001c0001t0009g0215a0001c0001t0011g0207a0001c0001t0011g0223others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-3501C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034373 | ||||||
chr8:23034437
|
G | T | 1 | a0001c0001t0002g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-3565C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034437 | ||||||
chr8:23034572
|
A | T | 5 | a0004c0004t0001g0119a0004c0004t0001g0206a0009c0009t0001g0209others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-3700T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034572 | ||||||
chr8:23034644
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.251-3772G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034644 | ||||||
chr8:23034761
|
T | C | 136 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0191others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.251-3889A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034761 | ||||||
chr8:23034937
|
T | C | 80 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(77): Show | 81 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.251-4065A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23034937 | ||||||
chr8:23035058
|
T | TTGGCAAG others(8): Show |
1 | a0003c0003t0003g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.251-4201_251-4187d others(17): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035058 | ||||||
chr8:23035142
|
TA | T | 9 | a0006c0006t0001g0029a0006c0006t0001g0126a0006c0006t0001g0127others(6): Show | 9 | HG01192.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-4271delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035142 | ||||||
chr8:23035402
|
A | T | 4 | a0001c0001t0003g0005a0001c0001t0003g0172a0001c0001t0016g0011others(1): Show | 5 | NA18939.hp1 NA18941.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-4530T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035402 | ||||||
chr8:23035521
|
G | A | 133 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0191others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.251-4649C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035521 | ||||||
chr8:23035897
|
A | T | 1 | a0002c0002t0006g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.251-5025T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035897 | ||||||
chr8:23035924
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.251-5052C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035924 | ||||||
chr8:23035934
|
T | A | 3 | a0001c0001t0001g0219a0002c0002t0004g0322a0002c0002t0004g0353 | 3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-5062A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035934 | ||||||
chr8:23035953
|
C | T | 2 | a0001c0001t0011g0207a0001c0001t0011g0223 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.251-5081G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23035953 | ||||||
chr8:23036078
|
A | AGAT | 134 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0191others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.251-5207_251-5206i others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036078 | ||||||
chr8:23036079
|
T | A | 134 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0191others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.251-5207A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036079 | ||||||
chr8:23036080
|
C | A | 134 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0191others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.251-5208G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036080 | ||||||
chr8:23036150
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0213others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-5278T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036150 | ||||||
chr8:23036301
|
G | A | 3 | a0001c0001t0001g0219a0002c0002t0004g0322a0002c0002t0004g0353 | 3 | HG02109.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.251-5429C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036301 | ||||||
chr8:23036455
|
C | G | 66 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(63): Show | 67 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.251-5583G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036455 | ||||||
chr8:23036495
|
G | A | 5 | a0001c0001t0003g0041a0001c0001t0008g0036a0001c0001t0008g0118others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-5623C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036495 | ||||||
chr8:23036611
|
G | A | 130 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0191others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.251-5739C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036611 | ||||||
chr8:23036718
|
C | T | 3 | a0001c0001t0001g0272a0003c0003t0001g0095a0017c0018t0001g0084 | 3 | HG01081.hp1 NA18992.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.251-5846G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23036718 | ||||||
chr8:23037135
|
A | T | 2 | a0001c0001t0011g0207a0001c0001t0011g0223 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+6003T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037135 | ||||||
chr8:23037164
|
A | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.250+5974T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037164 | ||||||
chr8:23037252
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(102): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250+5886A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037252 | ||||||
chr8:23037359
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.250+5779A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037359 | ||||||
chr8:23037500
|
A | G | 1 | a0001c0001t0018g0169 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.250+5638T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037500 | ||||||
chr8:23037692
|
A | T | 2 | a0004c0004t0001g0024a0004c0004t0001g0057 | 2 | HG01981.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.250+5446T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037692 | ||||||
chr8:23037728
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(102): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250+5410A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037728 | ||||||
chr8:23037974
|
G | T | 1 | a0002c0002t0004g0369 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.250+5164C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23037974 | ||||||
chr8:23038005
|
A | G | 1 | a0016c0017t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.250+5133T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038005 | ||||||
chr8:23038186
|
T | C | 1 | a0003c0003t0002g0082 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.250+4952A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038186 | ||||||
chr8:23038267
|
T | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(321): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.250+4871A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038267 | ||||||
chr8:23038475
|
G | A | 1 | a0008c0008t0004g0339 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.250+4663C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038475 | ||||||
chr8:23038483
|
G | A | 1 | a0014c0015t0001g0079 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.250+4655C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038483 | ||||||
chr8:23038544
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(321): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.250+4594T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038544 | ||||||
chr8:23038595
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(102): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250+4543T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038595 | ||||||
chr8:23038709
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0011g0207a0001c0001t0011g0223 | 3 | HG01243.hp2 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+4429A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038709 | ||||||
chr8:23038877
|
G | A | 2 | a0004c0004t0001g0243a0015c0014t0001g0208 | 2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.250+4261C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038877 | ||||||
chr8:23038982
|
A | G | 3 | a0001c0001t0001g0037a0001c0001t0011g0207a0001c0001t0011g0223 | 3 | HG01243.hp2 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+4156T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23038982 | ||||||
chr8:23039179
|
C | T | 2 | a0002c0002t0004g0322a0002c0002t0004g0353 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.250+3959G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039179 | ||||||
chr8:23039191
|
G | A | 4 | a0001c0001t0002g0053a0001c0001t0003g0033a0002c0002t0015g0010others(1): Show | 4 | HG02280.hp1 HG02965.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+3947C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039191 | ||||||
chr8:23039269
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250+3869G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039269 | ||||||
chr8:23039305
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250+3833G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039305 | ||||||
chr8:23039382
|
ACAGGATA others(3): Show |
A | 1 | a0001c0001t0001g0202 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.250+3746_250+3755d others(12): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039382 | ||||||
chr8:23039544
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.250+3594G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039544 | ||||||
chr8:23039720
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.250+3418C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039720 | ||||||
chr8:23039845
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0002g0171 | 2 | HG02040.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.250+3293G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039845 | ||||||
chr8:23039922
|
G | A | 7 | a0004c0004t0001g0038a0004c0004t0020g0039a0005c0005t0004g0321others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+3216C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039922 | ||||||
chr8:23039998
|
C | G | 1 | a0006c0006t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250+3140G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23039998 | ||||||
chr8:23040039
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(193): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.250+3099T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040039 | ||||||
chr8:23040084
|
G | C | 1 | a0001c0001t0003g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.250+3054C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040084 | ||||||
chr8:23040106
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0217a0001c0001t0004g0375others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+3032T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040106 | ||||||
chr8:23040173
|
C | T | 140 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0035others(137): Show | 144 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.250+2965G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040173 | ||||||
chr8:23040255
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+2883A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040255 | ||||||
chr8:23040264
|
TAA | T | 8 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0244others(5): Show | 8 | HG01261.hp2 HG02148.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+2872_250+2873d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040264 | ||||||
chr8:23040266
|
A | T | 105 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(102): Show | 109 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.250+2872T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040266 | ||||||
chr8:23040267
|
A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(175): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.250+2871T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040267 | ||||||
chr8:23040274
|
TATAATAT others(45): Show |
T | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+2812_250+2863d others(54): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040274 | ||||||
chr8:23040276
|
T | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(174): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.250+2862A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040276 | ||||||
chr8:23040289
|
T | A | 97 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(94): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.250+2849A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040289 | ||||||
chr8:23040290
|
TAA | T | 42 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0080others(39): Show | 42 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.250+2846_250+2847d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040290 | ||||||
chr8:23040292
|
A | T | 1 | a0003c0003t0001g0060 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+2846T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040292 | ||||||
chr8:23040294
|
TATATATA others(15): Show |
T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2822_250+2843d others(24): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040294 | ||||||
chr8:23040294
|
TATATATA others(69): Show |
T | 6 | a0001c0001t0001g0202a0001c0001t0001g0274a0006c0006t0001g0126others(3): Show | 6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2768_250+2843d others(78): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040294 | ||||||
chr8:23040298
|
T | TAATATAT others(45): Show |
1 | a0003c0003t0001g0060 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+2839_250+2840i others(54): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040298 | ||||||
chr8:23040300
|
T | A | 1 | a0003c0003t0001g0060 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+2838A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040300 | ||||||
chr8:23040313
|
A | T | 1 | a0007c0007t0004g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+2825T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040313 | ||||||
chr8:23040313
|
ATAAATAT others(75): Show |
A | 1 | a0005c0005t0004g0367 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.250+2743_250+2824d others(84): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040313 | ||||||
chr8:23040318
|
TATATATA others(19): Show |
T | 1 | a0007c0007t0004g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+2794_250+2819d others(28): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040318 | ||||||
chr8:23040324
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+2814A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040324 | ||||||
chr8:23040326
|
C | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0216 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.250+2812G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040326 | ||||||
chr8:23040341
|
T | A | 1 | a0001c0001t0003g0018 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.250+2797A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040341 | ||||||
chr8:23040344
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2794T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040344 | ||||||
chr8:23040344
|
AATATATA others(21): Show |
A | 86 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(83): Show | 90 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.250+2766_250+2793d others(30): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040344 | ||||||
chr8:23040349
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2789T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040349 | ||||||
chr8:23040360
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2778T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040360 | ||||||
chr8:23040367
|
A | T | 22 | a0001c0001t0001g0247a0001c0001t0002g0015a0001c0001t0002g0113others(19): Show | 22 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.250+2771T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040367 | ||||||
chr8:23040367
|
AT | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2770delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040367 | ||||||
chr8:23040367
|
ATAAATAT others(21): Show |
A | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+2743_250+2770d others(30): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040367 | ||||||
chr8:23040370
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2768T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040370 | ||||||
chr8:23040375
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2763T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040375 | ||||||
chr8:23040383
|
AAT | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2753_250+2754d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040383 | ||||||
chr8:23040396
|
TAA | T | 6 | a0001c0001t0001g0202a0001c0001t0001g0274a0006c0006t0001g0126others(3): Show | 6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2740_250+2741d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040396 | ||||||
chr8:23040398
|
A | AAT | 14 | a0001c0001t0001g0217a0001c0001t0002g0113a0001c0001t0002g0114others(11): Show | 14 | HG02293.hp1 HG02572.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+2738_250+2739d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040398 | ||||||
chr8:23040398
|
A | AATATATA others(23): Show |
35 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0080others(32): Show | 35 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.250+2710_250+2739d others(32): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040398 | ||||||
chr8:23040405
|
A | G | 6 | a0001c0001t0001g0202a0001c0001t0001g0274a0006c0006t0001g0126others(3): Show | 6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2733T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040405 | ||||||
chr8:23040406
|
TACAAAAT others(53): Show |
T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.250+2672_250+2731d others(62): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040406 | ||||||
chr8:23040416
|
A | G | 6 | a0001c0001t0001g0202a0001c0001t0001g0274a0006c0006t0001g0126others(3): Show | 6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2722T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040416 | ||||||
chr8:23040419
|
TTTA | T | 6 | a0001c0001t0001g0202a0001c0001t0001g0274a0006c0006t0001g0126others(3): Show | 6 | HG01192.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+2716_250+2718d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040419 | ||||||
chr8:23040422
|
A | ATTATATA others(16): Show |
5 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0218others(2): Show | 5 | HG02293.hp1 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+2715_250+2716i others(25): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040422 | ||||||
chr8:23040423
|
T | A | 2 | a0001c0001t0003g0286a0001c0001t0003g0306 | 2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.250+2715A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040423 | ||||||
chr8:23040433
|
A | G | 11 | a0001c0001t0001g0202a0001c0001t0001g0274a0001c0001t0002g0113others(8): Show | 11 | HG01192.hp1 HG02293.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+2705T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040433 | ||||||
chr8:23040436
|
TACAAAAT others(23): Show |
T | 1 | a0002c0002t0005g0368 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.250+2672_250+2701d others(32): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040436 | ||||||
chr8:23040441
|
AAT | A | 11 | a0001c0001t0001g0202a0001c0001t0001g0274a0001c0001t0002g0113others(8): Show | 11 | HG01192.hp1 HG02293.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+2695_250+2696d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040441 | ||||||
chr8:23040464
|
TAC | T | 11 | a0001c0001t0001g0202a0001c0001t0001g0274a0001c0001t0002g0113others(8): Show | 11 | HG01192.hp1 HG02293.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+2672_250+2673d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040464 | ||||||
chr8:23040466
|
C | T | 152 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0030others(149): Show | 156 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.250+2672G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040466 | ||||||
chr8:23040499
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(177): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.250+2639A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040499 | ||||||
chr8:23040572
|
C | T | 111 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(108): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.250+2566G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040572 | ||||||
chr8:23040616
|
AAAAC | A | 8 | a0001c0001t0001g0217a0001c0001t0004g0375a0001c0001t0010g0204others(5): Show | 8 | HG02630.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+2518_250+2521d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040616 | ||||||
chr8:23040620
|
C | T | 77 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0101others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.250+2518G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040620 | ||||||
chr8:23040646
|
C | A | 32 | a0001c0001t0001g0030a0001c0001t0001g0080a0001c0001t0001g0098others(29): Show | 32 | HG00438.hp1 HG00609.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.250+2492G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040646 | ||||||
chr8:23040709
|
G | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(320): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.250+2429C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040709 | ||||||
chr8:23040732
|
C | T | 4 | a0001c0001t0003g0033a0001c0001t0008g0036a0001c0001t0008g0118others(1): Show | 4 | HG02280.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+2406G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040732 | ||||||
chr8:23040733
|
G | A | 2 | a0001c0001t0001g0234a0003c0003t0003g0109 | 2 | NA18975.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.250+2405C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040733 | ||||||
chr8:23040891
|
C | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0076others(137): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.250+2247G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040891 | ||||||
chr8:23040910
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0283a0001c0001t0022g0290 | 3 | NA18954.hp2 NA18993.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.250+2228A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040910 | ||||||
chr8:23040922
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(89): Show | 95 | HG00597.hp1 HG00597.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.250+2216G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23040922 | ||||||
chr8:23041058
|
TTTG | T | 40 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0213others(37): Show | 41 | HG01123.hp1 HG01243.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.250+2077_250+2079d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041058 | ||||||
chr8:23041060
|
TG | T | 21 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0216others(18): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.250+2077delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041060 | ||||||
chr8:23041061
|
G | T | 19 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0066others(16): Show | 19 | HG02004.hp2 HG02027.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.250+2077C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041061 | ||||||
chr8:23041062
|
TTG | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.250+2074_250+2075d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041062 | ||||||
chr8:23041063
|
TG | T | 3 | a0001c0001t0001g0296a0002c0002t0004g0374a0004c0004t0001g0024 | 3 | HG02257.hp1 HG03195.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.250+2074delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041063 | ||||||
chr8:23041085
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.250+2053C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041085 | ||||||
chr8:23041097
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0164a0001c0001t0026g0026 | 3 | HG03654.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.250+2041G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041097 | ||||||
chr8:23041119
|
C | T | 2 | a0001c0001t0001g0238a0003c0016t0001g0307 | 2 | NA18953.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.250+2019G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041119 | ||||||
chr8:23041191
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.250+1947A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041191 | ||||||
chr8:23041223
|
A | C | 32 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0164others(29): Show | 33 | HG00639.hp1 HG01891.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.250+1915T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041223 | ||||||
chr8:23041253
|
C | T | 1 | a0004c0004t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.250+1885G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041253 | ||||||
chr8:23041255
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.250+1883G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041255 | ||||||
chr8:23041265
|
C | A | 4 | a0001c0001t0001g0149a0004c0004t0001g0147a0004c0004t0001g0148others(1): Show | 4 | NA19002.hp2 NA19058.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+1873G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041265 | ||||||
chr8:23041317
|
G | A | 2 | a0001c0001t0003g0220a0001c0001t0003g0259 | 2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.250+1821C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041317 | ||||||
chr8:23041346
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0043others(156): Show | 164 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+1792A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041346 | ||||||
chr8:23041352
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.250+1786G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041352 | ||||||
chr8:23041382
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | NA18983.hp2 NA18998.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+1756A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041382 | ||||||
chr8:23041393
|
G | A | 1 | a0003c0003t0002g0187 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.250+1745C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041393 | ||||||
chr8:23041447
|
G | A | 28 | a0001c0001t0001g0115a0001c0001t0001g0178a0001c0001t0001g0180others(25): Show | 28 | HG01123.hp1 HG02523.hp2 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.250+1691C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041447 | ||||||
chr8:23041537
|
G | GTCAA | 6 | a0001c0001t0001g0030a0001c0001t0001g0164a0001c0001t0026g0026others(3): Show | 6 | HG00639.hp1 HG02257.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+1597_250+1600d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041537 | ||||||
chr8:23041568
|
C | G | 2 | a0004c0004t0001g0017a0004c0004t0001g0024 | 2 | HG00639.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.250+1570G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041568 | ||||||
chr8:23041603
|
T | TA | 23 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0025others(20): Show | 23 | HG00738.hp2 HG01081.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.250+1534dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041603 | ||||||
chr8:23041603
|
TA | T | 60 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0098others(57): Show | 60 | HG00639.hp1 HG00738.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.250+1534delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041603 | ||||||
chr8:23041603
|
TAA | T | 37 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0071others(34): Show | 38 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.250+1533_250+1534d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041603 | ||||||
chr8:23041638
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.250+1500T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041638 | ||||||
chr8:23041663
|
C | A | 9 | a0001c0001t0001g0216a0001c0001t0001g0230a0002c0002t0004g0316others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+1475G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041663 | ||||||
chr8:23041792
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.250+1346T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041792 | ||||||
chr8:23041845
|
T | C | 9 | a0001c0001t0001g0214a0001c0001t0003g0261a0001c0001t0009g0215others(6): Show | 9 | HG00639.hp2 HG01123.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+1293A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041845 | ||||||
chr8:23041871
|
G | A | 26 | a0001c0001t0001g0115a0001c0001t0001g0178a0001c0001t0001g0180others(23): Show | 26 | HG01123.hp1 HG01433.hp2 HG02523.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+1267C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041871 | ||||||
chr8:23041912
|
C | G | 2 | a0001c0001t0001g0219a0006c0006t0001g0029 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.250+1226G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23041912 | ||||||
chr8:23042086
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0011g0223a0007c0007t0004g0317 | 3 | HG02258.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.250+1052G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042086 | ||||||
chr8:23042110
|
T | C | 1 | a0006c0006t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250+1028A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042110 | ||||||
chr8:23042119
|
T | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0216a0001c0001t0001g0217others(9): Show | 12 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+1019A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042119 | ||||||
chr8:23042120
|
C | G | 47 | a0001c0001t0001g0043a0001c0001t0001g0115a0001c0001t0001g0178others(44): Show | 48 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.250+1018G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042120 | ||||||
chr8:23042125
|
C | T | 9 | a0001c0001t0001g0037a0001c0001t0003g0232a0001c0001t0003g0261others(6): Show | 9 | HG00639.hp2 HG02257.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+1013G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042125 | ||||||
chr8:23042161
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.250+977G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042161 | ||||||
chr8:23042249
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(135): Show | 142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.250+889A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042249 | ||||||
chr8:23042250
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.250+888C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042250 | ||||||
chr8:23042252
|
G | A | 1 | a0004c0004t0001g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.250+886C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042252 | ||||||
chr8:23042265
|
T | C | 9 | a0001c0001t0001g0213a0002c0002t0004g0332a0002c0002t0004g0355others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+873A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042265 | ||||||
chr8:23042444
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.250+694G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042444 | ||||||
chr8:23042597
|
C | G | 3 | a0006c0006t0001g0126a0006c0006t0001g0127a0006c0006t0001g0128 | 3 | HG01192.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.250+541G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042597 | ||||||
chr8:23042611
|
G | T | 1 | a0004c0004t0001g0300 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.250+527C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042611 | ||||||
chr8:23042729
|
C | G | 1 | a0001c0001t0001g0274 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.250+409G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042729 | ||||||
chr8:23042974
|
G | A | 11 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0248others(8): Show | 12 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+164C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042974 | ||||||
chr8:23042984
|
T | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0098a0001c0001t0002g0097others(2): Show | 5 | HG00609.hp2 NA19004.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+154A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23042984 | ||||||
chr8:23043060
|
A | G | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.250+78T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23043060 | ||||||
chr8:23043091
|
A | C | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.250+47T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 2/8 | chr8 | 23043091 | ||||||
chr8:23043381
|
T | A | 1 | a0002c0002t0006g0340 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.145-138A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043381 | ||||||
chr8:23043436
|
C | T | 158 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.145-193G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043436 | ||||||
chr8:23043483
|
A | G | 1 | a0001c0001t0012g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145-240T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043483 | ||||||
chr8:23043533
|
T | C | 1 | a0001c0001t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.145-290A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043533 | ||||||
chr8:23043660
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0026g0026others(1): Show | 4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-417C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043660 | ||||||
chr8:23043689
|
T | C | 163 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(160): Show | 164 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.145-446A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043689 | ||||||
chr8:23043724
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.145-481G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043724 | ||||||
chr8:23043738
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.145-495C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043738 | ||||||
chr8:23043821
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.145-578T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043821 | ||||||
chr8:23043858
|
A | G | 162 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.145-615T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043858 | ||||||
chr8:23043959
|
C | T | 1 | a0005c0005t0004g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-716G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23043959 | ||||||
chr8:23044042
|
T | C | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-799A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044042 | ||||||
chr8:23044055
|
A | C | 270 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(267): Show | 274 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.145-812T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044055 | ||||||
chr8:23044096
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-853G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044096 | ||||||
chr8:23044139
|
G | A | 1 | a0003c0003t0003g0121 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.145-896C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044139 | ||||||
chr8:23044209
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-966G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044209 | ||||||
chr8:23044234
|
A | T | 1 | a0002c0002t0004g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.145-991T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044234 | ||||||
chr8:23044358
|
A | G | 162 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.145-1115T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044358 | ||||||
chr8:23044430
|
T | C | 71 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0229others(68): Show | 72 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.145-1187A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044430 | ||||||
chr8:23044436
|
T | C | 1 | a0011c0011t0006g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.145-1193A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044436 | ||||||
chr8:23044477
|
A | C | 71 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0229others(68): Show | 72 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.145-1234T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044477 | ||||||
chr8:23044693
|
A | C | 65 | a0001c0001t0001g0022a0001c0001t0001g0101a0001c0001t0001g0115others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.145-1450T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044693 | ||||||
chr8:23044698
|
A | G | 2 | a0003c0003t0007g0069a0003c0003t0025g0070 | 2 | HG02165.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.145-1455T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044698 | ||||||
chr8:23044860
|
A | C | 1 | a0001c0001t0012g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145-1617T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044860 | ||||||
chr8:23044950
|
T | A | 11 | a0001c0001t0004g0375a0001c0001t0008g0123a0001c0001t0010g0204others(8): Show | 11 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-1707A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23044950 | ||||||
chr8:23045008
|
G | A | 1 | a0011c0011t0006g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.145-1765C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045008 | ||||||
chr8:23045013
|
G | A | 69 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0229others(66): Show | 70 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.145-1770C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045013 | ||||||
chr8:23045060
|
C | CA | 123 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0043others(120): Show | 126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.145-1818dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | ||||||
chr8:23045060
|
C | CAA | 9 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0026g0026others(6): Show | 9 | HG01891.hp1 HG02135.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.145-1819_145-1818d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | ||||||
chr8:23045060
|
CA | C | 110 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.145-1818delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | ||||||
chr8:23045060
|
CAA | C | 28 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.145-1819_145-1818d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045060 | ||||||
chr8:23045100
|
T | C | 70 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0229others(67): Show | 71 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.145-1857A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045100 | ||||||
chr8:23045103
|
A | G | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.145-1860T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045103 | ||||||
chr8:23045131
|
G | A | 1 | a0001c0001t0018g0169 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.145-1888C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045131 | ||||||
chr8:23045145
|
A | G | 279 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(276): Show | 283 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.145-1902T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045145 | ||||||
chr8:23045159
|
G | T | 1 | a0002c0002t0005g0344 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.145-1916C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045159 | ||||||
chr8:23045184
|
T | C | 91 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-1941A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045184 | ||||||
chr8:23045213
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-1970C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045213 | ||||||
chr8:23045276
|
G | A | 1 | a0003c0003t0002g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.145-2033C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045276 | ||||||
chr8:23045332
|
C | T | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-2089G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045332 | ||||||
chr8:23045355
|
G | A | 2 | a0003c0003t0001g0095a0003c0003t0003g0106 | 2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.145-2112C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045355 | ||||||
chr8:23045377
|
T | C | 70 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0229others(67): Show | 71 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.145-2134A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045377 | ||||||
chr8:23045401
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-2158G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045401 | ||||||
chr8:23045560
|
G | C | 1 | a0001c0001t0002g0279 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.145-2317C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045560 | ||||||
chr8:23045575
|
A | C | 1 | a0004c0004t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-2332T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045575 | ||||||
chr8:23045696
|
C | T | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.145-2453G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045696 | ||||||
chr8:23045941
|
C | CA | 89 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.145-2699dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23045941 | ||||||
chr8:23046072
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.145-2829C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046072 | ||||||
chr8:23046119
|
G | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-2876C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046119 | ||||||
chr8:23046161
|
C | T | 66 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0229others(63): Show | 67 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.145-2918G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046161 | ||||||
chr8:23046164
|
T | C | 3 | a0001c0001t0001g0056a0001c0001t0002g0058a0004c0004t0001g0057 | 3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.145-2921A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046164 | ||||||
chr8:23046264
|
A | T | 1 | a0001c0001t0002g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.145-3021T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046264 | ||||||
chr8:23046265
|
T | C | 1 | a0001c0001t0003g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.145-3022A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046265 | ||||||
chr8:23046387
|
C | T | 79 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.145-3144G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046387 | ||||||
chr8:23046442
|
C | T | 1 | a0002c0002t0004g0361 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.145-3199G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046442 | ||||||
chr8:23046495
|
T | A | 1 | a0005c0005t0004g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-3252A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046495 | ||||||
chr8:23046548
|
C | T | 12 | a0001c0001t0001g0143a0001c0001t0001g0248a0001c0001t0001g0249others(9): Show | 13 | HG01123.hp1 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-3305G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046548 | ||||||
chr8:23046614
|
A | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-3371T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046614 | ||||||
chr8:23046615
|
TA | T | 14 | a0001c0001t0001g0115a0001c0001t0001g0269a0001c0001t0001g0274others(11): Show | 14 | HG00099.hp2 HG01515.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-3373delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046615 | ||||||
chr8:23046615
|
TAAA | T | 224 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0025others(221): Show | 228 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.145-3375_145-3373d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046615 | ||||||
chr8:23046615
|
TAAAA | T | 41 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0034others(38): Show | 41 | HG00423.hp1 HG00733.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-3376_145-3373d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046615 | ||||||
chr8:23046631
|
A | C | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3388T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046631 | ||||||
chr8:23046633
|
A | C | 188 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(185): Show | 192 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.145-3390T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046633 | ||||||
chr8:23046747
|
T | C | 2 | a0001c0001t0002g0240a0001c0001t0003g0239 | 2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.145-3504A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046747 | ||||||
chr8:23046951
|
A | C | 1 | a0003c0003t0001g0044 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.145-3708T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046951 | ||||||
chr8:23046955
|
C | T | 2 | a0001c0001t0001g0025a0004c0004t0001g0024 | 2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.145-3712G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23046955 | ||||||
chr8:23047013
|
C | T | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3770G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047013 | ||||||
chr8:23047080
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.145-3837T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047080 | ||||||
chr8:23047097
|
T | C | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3854A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047097 | ||||||
chr8:23047107
|
G | A | 1 | a0002c0002t0005g0348 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.145-3864C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047107 | ||||||
chr8:23047135
|
G | A | 2 | a0001c0001t0001g0025a0004c0004t0001g0024 | 2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.145-3892C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047135 | ||||||
chr8:23047191
|
C | G | 29 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.145-3948G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047191 | ||||||
chr8:23047232
|
C | T | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-3989G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047232 | ||||||
chr8:23047234
|
G | A | 86 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.145-3991C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047234 | ||||||
chr8:23047234
|
G | ATAATCCC others(1072): Show |
1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-3991_145-3990i others(1081): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047234 | ||||||
chr8:23047272
|
A | G | 202 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(199): Show | 205 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.145-4029T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047272 | ||||||
chr8:23047294
|
T | C | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-4051A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047294 | ||||||
chr8:23047309
|
A | G | 114 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(111): Show | 117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.145-4066T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047309 | ||||||
chr8:23047357
|
C | CA | 74 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.145-4115dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | ||||||
chr8:23047357
|
C | CAAAAAAA others(1074): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02257.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-4115_145-4114i others(1083): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | ||||||
chr8:23047357
|
C | CAAAAAAA others(1075): Show |
1 | a0001c0001t0008g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.145-4115_145-4114i others(1084): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | ||||||
chr8:23047357
|
CA | C | 156 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(153): Show | 159 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.145-4115delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | ||||||
chr8:23047357
|
CAA | C | 6 | a0001c0001t0003g0052a0001c0001t0003g0210a0001c0001t0003g0211others(3): Show | 6 | HG02602.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-4116_145-4115d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047357 | ||||||
chr8:23047404
|
T | C | 4 | a0001c0001t0001g0125a0006c0006t0001g0126a0006c0006t0001g0127others(1): Show | 4 | HG01192.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-4161A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047404 | ||||||
chr8:23047423
|
C | T | 4 | a0001c0001t0008g0118a0004c0004t0001g0119a0005c0005t0004g0367others(1): Show | 4 | HG02280.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-4180G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047423 | ||||||
chr8:23047699
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0003g0220a0004c0004t0001g0221 | 3 | HG02922.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.145-4456G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23047699 | ||||||
chr8:23048162
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02257.hp2 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-4919C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048162 | ||||||
chr8:23048162
|
G | GGTGGCTC others(1073): Show |
1 | a0004c0004t0020g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.145-4920_145-4919i others(1082): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048162 | ||||||
chr8:23048209
|
G | T | 1 | a0003c0003t0002g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.145-4966C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048209 | ||||||
chr8:23048264
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.145-5021A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048264 | ||||||
chr8:23048337
|
A | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-5094T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048337 | ||||||
chr8:23048343
|
G | A | 8 | a0001c0001t0010g0204a0001c0001t0010g0205a0001c0001t0011g0207others(5): Show | 8 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.145-5100C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048343 | ||||||
chr8:23048358
|
C | G | 2 | a0001c0001t0004g0375a0002c0002t0004g0374 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.145-5115G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048358 | ||||||
chr8:23048435
|
G | C | 91 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-5192C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048435 | ||||||
chr8:23048437
|
C | CA | 46 | a0001c0001t0001g0194a0001c0001t0001g0247a0001c0001t0001g0248others(43): Show | 47 | HG01123.hp1 HG01175.hp2 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.145-5195dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048437 | ||||||
chr8:23048437
|
CA | C | 16 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(13): Show | 16 | HG01884.hp1 HG02004.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.145-5195delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048437 | ||||||
chr8:23048437
|
CAA | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.145-5196_145-5195d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048437 | ||||||
chr8:23048457
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.145-5214G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048457 | ||||||
chr8:23048667
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(55): Show | 60 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.145-5424A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048667 | ||||||
chr8:23048793
|
T | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-5550A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048793 | ||||||
chr8:23048851
|
C | T | 1 | a0003c0003t0003g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.145-5608G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048851 | ||||||
chr8:23048856
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.145-5613G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048856 | ||||||
chr8:23048870
|
G | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02809.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-5627C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048870 | ||||||
chr8:23048937
|
A | T | 34 | a0001c0001t0001g0125a0001c0001t0001g0229a0001c0001t0001g0230others(31): Show | 34 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.145-5694T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048937 | ||||||
chr8:23048982
|
A | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02809.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-5739T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23048982 | ||||||
chr8:23049031
|
G | A | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0006c0006t0001g0029 | 3 | HG02572.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.145-5788C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049031 | ||||||
chr8:23049128
|
A | G | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-5885T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049128 | ||||||
chr8:23049295
|
G | C | 1 | a0004c0004t0001g0133 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-6052C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049295 | ||||||
chr8:23049509
|
A | C | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-6266T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049509 | ||||||
chr8:23049554
|
C | A | 4 | a0001c0001t0001g0125a0006c0006t0001g0126a0006c0006t0001g0127others(1): Show | 4 | HG01192.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-6311G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049554 | ||||||
chr8:23049577
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0002g0097 | 2 | NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.145-6334A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049577 | ||||||
chr8:23049614
|
T | C | 1 | a0003c0003t0002g0099 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.145-6371A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049614 | ||||||
chr8:23049677
|
G | T | 2 | a0001c0001t0003g0286a0004c0004t0001g0287 | 2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.145-6434C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049677 | ||||||
chr8:23049728
|
T | G | 79 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.145-6485A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049728 | ||||||
chr8:23049772
|
T | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-6529A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049772 | ||||||
chr8:23049783
|
C | T | 3 | a0001c0001t0002g0141a0004c0004t0001g0122a0004c0004t0001g0142 | 3 | HG01123.hp1 HG03942.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.145-6540G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049783 | ||||||
chr8:23049795
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.145-6552G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049795 | ||||||
chr8:23049817
|
C | A | 80 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.145-6574G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049817 | ||||||
chr8:23049817
|
C | CTTATTGG others(24): Show |
1 | a0003c0003t0002g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.145-6605_145-6575d others(33): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049817 | ||||||
chr8:23049873
|
T | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-6630A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049873 | ||||||
chr8:23049909
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.145-6666T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049909 | ||||||
chr8:23049944
|
G | C | 19 | a0001c0001t0001g0149a0001c0001t0001g0170a0001c0001t0001g0174others(16): Show | 19 | HG02040.hp2 NA18939.hp1 NA18955.hp1 others(16): Show |
intron_variant | MODIFIER | c.145-6701C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049944 | ||||||
chr8:23049949
|
G | A | 5 | a0001c0001t0001g0254a0001c0001t0001g0257a0001c0001t0002g0255others(2): Show | 5 | HG02015.hp2 NA18941.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-6706C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23049949 | ||||||
chr8:23050012
|
G | T | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-6769C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050012 | ||||||
chr8:23050208
|
G | C | 10 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0210others(7): Show | 11 | HG02717.hp2 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-6965C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050208 | ||||||
chr8:23050243
|
G | T | 1 | a0001c0001t0009g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.145-7000C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050243 | ||||||
chr8:23050293
|
G | GT | 97 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(94): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.145-7051dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050293 | ||||||
chr8:23050301
|
G | A | 1 | a0004c0004t0001g0133 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-7058C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050301 | ||||||
chr8:23050412
|
G | A | 91 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-7169C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050412 | ||||||
chr8:23050463
|
T | C | 10 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0210others(7): Show | 11 | HG02717.hp2 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-7220A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050463 | ||||||
chr8:23050472
|
G | A | 1 | a0015c0014t0001g0208 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.145-7229C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050472 | ||||||
chr8:23050805
|
G | A | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7562C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050805 | ||||||
chr8:23050823
|
C | T | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7580G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050823 | ||||||
chr8:23050840
|
G | A | 1 | a0004c0004t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.145-7597C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050840 | ||||||
chr8:23050863
|
C | A | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-7620G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050863 | ||||||
chr8:23050868
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.145-7625C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050868 | ||||||
chr8:23050950
|
T | C | 28 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.145-7707A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050950 | ||||||
chr8:23050953
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.145-7710T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050953 | ||||||
chr8:23050968
|
G | A | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7725C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050968 | ||||||
chr8:23050994
|
T | A | 93 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.145-7751A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23050994 | ||||||
chr8:23051000
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.145-7757C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051000 | ||||||
chr8:23051025
|
G | C | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7782C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051025 | ||||||
chr8:23051060
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.145-7817C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051060 | ||||||
chr8:23051083
|
C | T | 84 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.145-7840G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051083 | ||||||
chr8:23051100
|
C | T | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7857G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051100 | ||||||
chr8:23051105
|
A | G | 79 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.145-7862T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051105 | ||||||
chr8:23051170
|
CAA | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0026g0026others(1): Show | 4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-7929_145-7928d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051170 | ||||||
chr8:23051200
|
A | AAAAT | 92 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.145-7958_145-7957i others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051200 | ||||||
chr8:23051545
|
CT | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-8303delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051545 | ||||||
chr8:23051546
|
T | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.145-8303A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051546 | ||||||
chr8:23051547
|
CT | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0056others(155): Show | 163 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.145-8305delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051547 | ||||||
chr8:23051548
|
T | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.145-8305A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051548 | ||||||
chr8:23051550
|
T | C | 1 | a0004c0004t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.145-8307A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051550 | ||||||
chr8:23051584
|
G | A | 96 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(93): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.145-8341C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051584 | ||||||
chr8:23051607
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0026g0026others(1): Show | 4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-8364G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051607 | ||||||
chr8:23051621
|
T | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-8378A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051621 | ||||||
chr8:23051638
|
G | A | 1 | a0004c0004t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-8395C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051638 | ||||||
chr8:23051694
|
G | A | 84 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.145-8451C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051694 | ||||||
chr8:23051698
|
C | G | 1 | a0001c0001t0012g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145-8455G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051698 | ||||||
chr8:23051701
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.145-8458G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051701 | ||||||
chr8:23051765
|
C | G | 1 | a0003c0003t0003g0003 | 2 | NA18970.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.145-8522G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051765 | ||||||
chr8:23051785
|
C | T | 1 | a0002c0002t0006g0334 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.145-8542G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051785 | ||||||
chr8:23051878
|
A | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-8635T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23051878 | ||||||
chr8:23052033
|
G | A | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-8790C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052033 | ||||||
chr8:23052150
|
C | T | 1 | a0005c0005t0004g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-8907G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052150 | ||||||
chr8:23052163
|
G | C | 78 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.145-8920C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052163 | ||||||
chr8:23052239
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(49): Show | 54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.145-8996C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052239 | ||||||
chr8:23052285
|
C | CT | 113 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0043others(110): Show | 116 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.145-9043dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | ||||||
chr8:23052285
|
C | CTTTT | 75 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.145-9046_145-9043d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | ||||||
chr8:23052285
|
C | CTTTTT | 12 | a0001c0001t0001g0149a0001c0001t0001g0159a0001c0001t0001g0160others(9): Show | 12 | HG00597.hp1 HG00733.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-9047_145-9043d others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | ||||||
chr8:23052285
|
CT | C | 6 | a0001c0001t0001g0288a0001c0001t0002g0308a0001c0001t0003g0286others(3): Show | 6 | HG01934.hp1 HG02293.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-9043delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052285 | ||||||
chr8:23052398
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.145-9155C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052398 | ||||||
chr8:23052436
|
C | A | 11 | a0001c0001t0008g0123a0001c0001t0010g0204a0001c0001t0010g0205others(8): Show | 11 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-9193G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052436 | ||||||
chr8:23052488
|
G | A | 1 | a0006c0006t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.145-9245C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052488 | ||||||
chr8:23052529
|
G | A | 2 | a0001c0001t0004g0375a0002c0002t0004g0374 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.145-9286C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052529 | ||||||
chr8:23052577
|
C | A | 1 | a0001c0001t0002g0195 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.145-9334G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052577 | ||||||
chr8:23052602
|
T | G | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.145-9359A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052602 | ||||||
chr8:23052675
|
C | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(248): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.145-9432G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052675 | ||||||
chr8:23052745
|
G | A | 1 | a0001c0001t0008g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.145-9502C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052745 | ||||||
chr8:23052865
|
A | C | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0216others(3): Show | 6 | HG01884.hp1 HG02004.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-9622T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052865 | ||||||
chr8:23052958
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.145-9715G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23052958 | ||||||
chr8:23053236
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0007g0203 | 2 | NA18991.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.145-9993C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053236 | ||||||
chr8:23053314
|
C | T | 27 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(24): Show | 27 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.145-10071G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053314 | ||||||
chr8:23053349
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0002g0050 | 2 | HG03491.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.145-10106A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053349 | ||||||
chr8:23053368
|
G | T | 35 | a0001c0001t0001g0125a0001c0001t0001g0229a0001c0001t0001g0230others(32): Show | 35 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.145-10125C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053368 | ||||||
chr8:23053404
|
A | G | 2 | a0001c0001t0008g0123a0004c0004t0001g0124 | 2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-10161T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053404 | ||||||
chr8:23053426
|
A | G | 1 | a0002c0002t0005g0333 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.145-10183T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053426 | ||||||
chr8:23053444
|
A | C | 1 | a0002c0002t0004g0369 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.145-10201T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053444 | ||||||
chr8:23053457
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.145-10214C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053457 | ||||||
chr8:23053481
|
TAAAATA | T | 83 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.145-10244_145-1023 others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053481 | ||||||
chr8:23053526
|
A | C | 29 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.145-10283T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053526 | ||||||
chr8:23053534
|
T | A | 1 | a0004c0004t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-10291A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053534 | ||||||
chr8:23053536
|
CTG | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-10295_145-1029 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053536 | ||||||
chr8:23053544
|
A | G | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-10301T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053544 | ||||||
chr8:23053560
|
A | G | 83 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.145-10317T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053560 | ||||||
chr8:23053667
|
TA | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0002c0002t0002g0013 | 3 | HG03704.hp1 NA18980.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.145-10425delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053667 | ||||||
chr8:23053670
|
G | T | 1 | a0003c0003t0003g0121 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.145-10427C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053670 | ||||||
chr8:23053785
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.145-10542T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053785 | ||||||
chr8:23053815
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.145-10572C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23053815 | ||||||
chr8:23054001
|
C | T | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-10758G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054001 | ||||||
chr8:23054012
|
T | C | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0004c0004t0001g0006others(5): Show | 9 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-10769A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054012 | ||||||
chr8:23054114
|
G | A | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.145-10871C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054114 | ||||||
chr8:23054189
|
A | G | 2 | a0001c0001t0012g0140a0004c0004t0001g0138 | 2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.145-10946T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054189 | ||||||
chr8:23054386
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.145-11143T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054386 | ||||||
chr8:23054453
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0026g0026others(1): Show | 4 | HG02735.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-11210C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054453 | ||||||
chr8:23054723
|
G | C | 89 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.145-11480C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054723 | ||||||
chr8:23054774
|
G | A | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-11531C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054774 | ||||||
chr8:23054800
|
G | A | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(2): Show | 5 | HG02698.hp1 HG02738.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-11557C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054800 | ||||||
chr8:23054915
|
G | C | 3 | a0002c0002t0004g0371a0002c0002t0004g0373a0002c0002t0005g0372 | 3 | HG02056.hp2 NA18961.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.145-11672C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054915 | ||||||
chr8:23054929
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.145-11686T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054929 | ||||||
chr8:23054935
|
A | T | 94 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.145-11692T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23054935 | ||||||
chr8:23055026
|
T | C | 2 | a0001c0001t0002g0181a0002c0002t0005g0368 | 2 | HG00099.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.145-11783A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055026 | ||||||
chr8:23055037
|
G | A | 1 | a0005c0005t0004g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-11794C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055037 | ||||||
chr8:23055154
|
C | G | 1 | a0002c0002t0005g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.145-11911G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055154 | ||||||
chr8:23055228
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.145-11985C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055228 | ||||||
chr8:23055445
|
C | A | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-12202G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055445 | ||||||
chr8:23055519
|
C | CT | 77 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.145-12277dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055519 | ||||||
chr8:23055521
|
T | TAA | 8 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-12280_145-1227 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TAAA | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0026g0026others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-12281_145-1227 others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TAAAAAAA others(2): Show |
34 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(31): Show | 36 | HG00280.hp1 HG01069.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.145-12287_145-1227 others(13): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TAAAAAAA others(3): Show |
13 | a0001c0001t0001g0247a0001c0001t0001g0291a0001c0001t0001g0296others(10): Show | 13 | HG00140.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-12288_145-1227 others(14): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TAAAAAAA others(4): Show |
3 | a0001c0001t0001g0299a0001c0001t0002g0310a0001c0001t0003g0271 | 3 | HG01074.hp2 HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.145-12289_145-1227 others(15): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0004g0375 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.145-12292_145-1227 others(18): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TAAAAAAA others(11): Show |
1 | a0004c0004t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145-12296_145-1227 others(22): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TTAAAAAA others(3): Show |
1 | a0004c0004t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.145-12279_145-1227 others(14): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TTAAAAAA others(4): Show |
2 | a0001c0001t0012g0140a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.145-12279_145-1227 others(15): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
T | TTAAAAAA others(5): Show |
1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145-12279_145-1227 others(16): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
TA | T | 84 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0076others(81): Show | 87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.145-12279delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055521
|
TAA | T | 39 | a0001c0001t0001g0043a0001c0001t0001g0059a0001c0001t0001g0064others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.145-12280_145-1227 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055521 | ||||||
chr8:23055522
|
A | T | 13 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0216others(10): Show | 13 | HG01167.hp1 HG01884.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.145-12279T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055522 | ||||||
chr8:23055596
|
T | C | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-12353A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055596 | ||||||
chr8:23055615
|
A | C | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145-12372T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055615 | ||||||
chr8:23055647
|
C | A | 3 | a0002c0002t0004g0326a0002c0002t0004g0342a0002c0002t0005g0341 | 3 | HG02135.hp2 NA18987.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.145-12404G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055647 | ||||||
chr8:23055818
|
C | T | 1 | a0001c0001t0027g0268 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.145-12575G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055818 | ||||||
chr8:23055853
|
T | C | 89 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.145-12610A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055853 | ||||||
chr8:23055878
|
T | C | 1 | a0016c0017t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.145-12635A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055878 | ||||||
chr8:23055915
|
A | T | 2 | a0004c0004t0001g0062a0004c0004t0001g0063 | 2 | HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.145-12672T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055915 | ||||||
chr8:23055962
|
G | C | 88 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(85): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.145-12719C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055962 | ||||||
chr8:23055968
|
C | T | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-12725G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23055968 | ||||||
chr8:23056067
|
G | C | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+12684C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056067 | ||||||
chr8:23056140
|
C | G | 1 | a0004c0004t0001g0300 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.144+12611G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056140 | ||||||
chr8:23056216
|
C | CATAT | 94 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12534_144+1253 others(8): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056216 | ||||||
chr8:23056259
|
G | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(4): Show | 7 | HG02257.hp1 HG02717.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+12492C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056259 | ||||||
chr8:23056300
|
A | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+12451T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056300 | ||||||
chr8:23056347
|
T | G | 1 | a0004c0004t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.144+12404A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056347 | ||||||
chr8:23056422
|
C | T | 1 | a0001c0001t0002g0273 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.144+12329G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056422 | ||||||
chr8:23056540
|
A | G | 89 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.144+12211T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056540 | ||||||
chr8:23056541
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0002g0058a0004c0004t0001g0057 | 3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.144+12210G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056541 | ||||||
chr8:23056544
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12207T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056544 | ||||||
chr8:23056600
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12151T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056600 | ||||||
chr8:23056650
|
C | CA | 107 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0025others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.144+12100dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056650 | ||||||
chr8:23056735
|
T | A | 94 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+12016A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056735 | ||||||
chr8:23056822
|
T | C | 2 | a0001c0001t0012g0140a0004c0004t0001g0138 | 2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+11929A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23056822 | ||||||
chr8:23057003
|
C | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+11748G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057003 | ||||||
chr8:23057036
|
C | CT | 22 | a0001c0001t0017g0051a0002c0002t0004g0316a0002c0002t0004g0320others(19): Show | 22 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.144+11714dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | ||||||
chr8:23057036
|
CT | C | 152 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(149): Show | 157 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.144+11714delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | ||||||
chr8:23057036
|
CTT | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(63): Show | 68 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.144+11713_144+1171 others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | ||||||
chr8:23057036
|
CTTT | C | 93 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.144+11712_144+1171 others(7): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057036 | ||||||
chr8:23057058
|
CGGAGTCT others(390): Show |
C | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+11296_144+1169 others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057058 | ||||||
chr8:23057072
|
G | A | 1 | a0002c0002t0006g0343 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.144+11679C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057072 | ||||||
chr8:23057122
|
C | T | 2 | a0001c0001t0012g0140a0004c0004t0001g0138 | 2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+11629G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057122 | ||||||
chr8:23057292
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0012g0140a0004c0004t0001g0024others(1): Show | 4 | HG00738.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+11459C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057292 | ||||||
chr8:23057297
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(253): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.144+11454T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057297 | ||||||
chr8:23057337
|
G | A | 1 | a0001c0001t0003g0005 | 2 | NA18941.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.144+11414C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057337 | ||||||
chr8:23057378
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(289): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.144+11373T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057378 | ||||||
chr8:23057429
|
A | AT | 19 | a0001c0001t0001g0185a0001c0001t0001g0248a0001c0001t0002g0156others(16): Show | 19 | HG00733.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.144+11321dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057429 | ||||||
chr8:23057429
|
AT | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0115others(65): Show | 70 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.144+11321delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057429 | ||||||
chr8:23057502
|
G | A | 94 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+11249C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057502 | ||||||
chr8:23057519
|
G | A | 1 | a0001c0001t0003g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+11232C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057519 | ||||||
chr8:23057589
|
C | T | 2 | a0003c0003t0001g0060a0003c0003t0001g0061 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.144+11162G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057589 | ||||||
chr8:23057622
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.144+11129T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057622 | ||||||
chr8:23057741
|
G | A | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0004c0004t0001g0006others(5): Show | 9 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+11010C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057741 | ||||||
chr8:23057885
|
G | A | 1 | a0004c0004t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.144+10866C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057885 | ||||||
chr8:23057975
|
A | C | 1 | a0001c0001t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+10776T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23057975 | ||||||
chr8:23058371
|
C | G | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.144+10380G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058371 | ||||||
chr8:23058483
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.144+10268A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058483 | ||||||
chr8:23058491
|
C | CT | 164 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(161): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.144+10259dupA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058491 | ||||||
chr8:23058542
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.144+10209T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058542 | ||||||
chr8:23058555
|
G | T | 2 | a0001c0001t0001g0025a0004c0004t0001g0024 | 2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.144+10196C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058555 | ||||||
chr8:23058568
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+10183G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058568 | ||||||
chr8:23058636
|
T | C | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+10115A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058636 | ||||||
chr8:23058685
|
G | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+10066C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058685 | ||||||
chr8:23058775
|
G | A | 36 | a0001c0001t0001g0125a0001c0001t0001g0229a0001c0001t0001g0230others(33): Show | 36 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.144+9976C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058775 | ||||||
chr8:23058846
|
A | T | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9905T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058846 | ||||||
chr8:23058937
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.144+9814C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058937 | ||||||
chr8:23058964
|
C | T | 2 | a0002c0002t0005g0350a0002c0002t0006g0349 | 2 | HG02148.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.144+9787G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23058964 | ||||||
chr8:23059027
|
C | T | 91 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.144+9724G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059027 | ||||||
chr8:23059392
|
C | T | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9359G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059392 | ||||||
chr8:23059483
|
T | C | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9268A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059483 | ||||||
chr8:23059509
|
G | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(173): Show | 182 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.144+9242C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059509 | ||||||
chr8:23059514
|
T | TTTCG | 9 | a0001c0001t0001g0136a0001c0001t0002g0301a0001c0001t0002g0303others(6): Show | 9 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+9236_144+9237i others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059514 | ||||||
chr8:23059514
|
T | TTTTG | 166 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(163): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.144+9233_144+9236d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059514 | ||||||
chr8:23059530
|
A | C | 1 | a0001c0001t0012g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.144+9221T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059530 | ||||||
chr8:23059530
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(169): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.144+9221T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059530 | ||||||
chr8:23059539
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(173): Show | 182 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.144+9212A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059539 | ||||||
chr8:23059592
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0002g0058a0004c0004t0001g0057 | 3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.144+9159G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059592 | ||||||
chr8:23059651
|
C | T | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0004c0004t0001g0006others(5): Show | 9 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+9100G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059651 | ||||||
chr8:23059652
|
G | A | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+9099C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059652 | ||||||
chr8:23059655
|
T | C | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+9096A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059655 | ||||||
chr8:23059663
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.144+9088G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059663 | ||||||
chr8:23059680
|
TG | T | 110 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(107): Show | 114 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.144+9070delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059680 | ||||||
chr8:23059683
|
AT | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(207): Show | 216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.144+9067delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059683 | ||||||
chr8:23059684
|
T | A | 1 | a0001c0001t0004g0375 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.144+9067A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059684 | ||||||
chr8:23059702
|
C | T | 2 | a0001c0001t0003g0041a0001c0001t0003g0232 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.144+9049G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059702 | ||||||
chr8:23059754
|
C | T | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+8997G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059754 | ||||||
chr8:23059792
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(299): Show | 308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.144+8959T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059792 | ||||||
chr8:23059802
|
G | A | 2 | a0001c0001t0012g0140a0004c0004t0001g0138 | 2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+8949C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059802 | ||||||
chr8:23059833
|
T | A | 2 | a0002c0002t0015g0010a0011c0011t0006g0312 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.144+8918A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059833 | ||||||
chr8:23059921
|
A | T | 1 | a0001c0001t0001g0231 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.144+8830T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23059921 | ||||||
chr8:23060026
|
T | G | 1 | a0002c0002t0005g0348 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.144+8725A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060026 | ||||||
chr8:23060110
|
G | T | 3 | a0002c0002t0004g0371a0002c0002t0004g0373a0002c0002t0005g0372 | 3 | HG02056.hp2 NA18961.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.144+8641C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060110 | ||||||
chr8:23060118
|
T | A | 1 | a0004c0004t0001g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.144+8633A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060118 | ||||||
chr8:23060128
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144+8623C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060128 | ||||||
chr8:23060130
|
G | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+8621C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060130 | ||||||
chr8:23060151
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144+8600G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060151 | ||||||
chr8:23060161
|
AT | A | 36 | a0001c0001t0001g0125a0001c0001t0001g0229a0001c0001t0001g0230others(33): Show | 36 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.144+8589delA | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060161 | ||||||
chr8:23060180
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(173): Show | 182 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.144+8571T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060180 | ||||||
chr8:23060197
|
T | G | 1 | a0003c0016t0001g0307 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.144+8554A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060197 | ||||||
chr8:23060279
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.144+8472G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060279 | ||||||
chr8:23060286
|
A | C | 2 | a0004c0004t0001g0212a0006c0006t0001g0222 | 2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.144+8465T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060286 | ||||||
chr8:23060290
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144+8461A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060290 | ||||||
chr8:23060334
|
G | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.144+8417C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060334 | ||||||
chr8:23060378
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.144+8373G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060378 | ||||||
chr8:23060394
|
C | T | 5 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(2): Show | 5 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+8357G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060394 | ||||||
chr8:23060403
|
C | T | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+8348G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060403 | ||||||
chr8:23060573
|
G | A | 1 | a0005c0005t0004g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.144+8178C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060573 | ||||||
chr8:23060614
|
G | A | 2 | a0001c0001t0002g0120a0001c0001t0002g0182 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.144+8137C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060614 | ||||||
chr8:23060711
|
T | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0248a0001c0001t0001g0249others(9): Show | 13 | HG01123.hp1 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.144+8040A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060711 | ||||||
chr8:23060734
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.144+8017A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060734 | ||||||
chr8:23060751
|
A | T | 1 | a0002c0002t0015g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.144+8000T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060751 | ||||||
chr8:23060835
|
T | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+7916A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060835 | ||||||
chr8:23060910
|
T | C | 1 | a0001c0001t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+7841A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060910 | ||||||
chr8:23060952
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0002g0058a0004c0004t0001g0057 | 3 | HG01192.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.144+7799T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060952 | ||||||
chr8:23060980
|
C | T | 1 | a0004c0004t0001g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.144+7771G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23060980 | ||||||
chr8:23061138
|
T | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+7613A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061138 | ||||||
chr8:23061517
|
C | T | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+7234G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061517 | ||||||
chr8:23061718
|
A | G | 1 | a0004c0004t0002g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.144+7033T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061718 | ||||||
chr8:23061809
|
C | T | 101 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(98): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.144+6942G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061809 | ||||||
chr8:23061844
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(258): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.144+6907C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061844 | ||||||
chr8:23061970
|
G | A | 2 | a0001c0001t0012g0140a0004c0004t0001g0138 | 2 | HG00738.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.144+6781C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23061970 | ||||||
chr8:23062097
|
A | T | 2 | a0001c0001t0004g0375a0002c0002t0004g0374 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.144+6654T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062097 | ||||||
chr8:23062110
|
G | A | 1 | a0005c0005t0004g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.144+6641C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062110 | ||||||
chr8:23062128
|
G | C | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0004c0004t0001g0142 | 3 | HG01123.hp1 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.144+6623C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062128 | ||||||
chr8:23062312
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144+6439G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062312 | ||||||
chr8:23062402
|
G | A | 1 | a0011c0011t0006g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.144+6349C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062402 | ||||||
chr8:23062498
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG00738.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.144+6253C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062498 | ||||||
chr8:23062636
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(73): Show | 78 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.144+6115G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062636 | ||||||
chr8:23062672
|
C | A | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144+6079G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062672 | ||||||
chr8:23062743
|
A | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+6008T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062743 | ||||||
chr8:23062885
|
A | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+5866T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062885 | ||||||
chr8:23062925
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144+5826T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23062925 | ||||||
chr8:23063035
|
A | G | 1 | a0001c0001t0017g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.144+5716T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063035 | ||||||
chr8:23063120
|
G | A | 1 | a0002c0002t0005g0313 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.144+5631C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063120 | ||||||
chr8:23063137
|
C | CAGG | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5613_144+5614i others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063137 | ||||||
chr8:23063179
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.144+5572G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063179 | ||||||
chr8:23063191
|
T | C | 1 | a0006c0006t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.144+5560A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063191 | ||||||
chr8:23063225
|
G | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5526C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063225 | ||||||
chr8:23063297
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(49): Show | 54 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.144+5454C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063297 | ||||||
chr8:23063304
|
C | T | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+5447G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063304 | ||||||
chr8:23063323
|
G | A | 2 | a0002c0002t0005g0350a0002c0002t0006g0349 | 2 | HG02148.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.144+5428C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063323 | ||||||
chr8:23063346
|
C | CA | 151 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0056others(148): Show | 156 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.144+5404dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | ||||||
chr8:23063346
|
C | CAA | 12 | a0001c0001t0001g0043a0001c0001t0001g0107a0001c0001t0001g0108others(9): Show | 12 | HG00621.hp2 HG02572.hp2 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.144+5403_144+5404d others(4): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | ||||||
chr8:23063346
|
C | CAAAAAAA others(3544): Show |
1 | a0003c0003t0003g0106 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.144+5404_144+5405i others(3553): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | ||||||
chr8:23063346
|
CA | C | 36 | a0001c0001t0001g0125a0001c0001t0001g0229a0001c0001t0001g0231others(33): Show | 36 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.144+5404delT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063346 | ||||||
chr8:23063411
|
G | A | 1 | a0002c0002t0006g0363 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.144+5340C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063411 | ||||||
chr8:23063425
|
GCAGGTCT others(7): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.144+5312_144+5325d others(16): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063425 | ||||||
chr8:23063492
|
G | A | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020 | 3 | HG01496.hp1 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.144+5259C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063492 | ||||||
chr8:23063513
|
TTTC | T | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5235_144+5237d others(5): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063513 | ||||||
chr8:23063699
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0012g0228 | 3 | HG02258.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.144+5052G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063699 | ||||||
chr8:23063739
|
G | T | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+5012C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063739 | ||||||
chr8:23063809
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+4942G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063809 | ||||||
chr8:23063848
|
T | C | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+4903A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063848 | ||||||
chr8:23063916
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.144+4835A>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063916 | ||||||
chr8:23063921
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(207): Show | 215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.144+4830G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063921 | ||||||
chr8:23063938
|
G | A | 1 | a0002c0002t0004g0361 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.144+4813C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063938 | ||||||
chr8:23063941
|
C | T | 1 | a0002c0002t0005g0324 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.144+4810G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063941 | ||||||
chr8:23063957
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(15): Show | 18 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.144+4794G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063957 | ||||||
chr8:23063959
|
T | A | 1 | a0001c0001t0002g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.144+4792A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063959 | ||||||
chr8:23063990
|
T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(4): Show | 7 | HG02257.hp1 HG02717.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+4761A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23063990 | ||||||
chr8:23064075
|
G | A | 1 | a0002c0002t0005g0360 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.144+4676C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064075 | ||||||
chr8:23064266
|
A | T | 1 | a0001c0001t0003g0227 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.144+4485T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064266 | ||||||
chr8:23064418
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(286): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.144+4333G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064418 | ||||||
chr8:23064437
|
G | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+4314C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064437 | ||||||
chr8:23064871
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.144+3880G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064871 | ||||||
chr8:23064905
|
T | C | 1 | a0002c0002t0004g0361 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.144+3846A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064905 | ||||||
chr8:23064923
|
T | C | 1 | a0004c0004t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.144+3828A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064923 | ||||||
chr8:23064965
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.144+3786C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23064965 | ||||||
chr8:23065172
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.144+3579C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065172 | ||||||
chr8:23065234
|
C | T | 3 | a0001c0001t0001g0149a0004c0004t0001g0147a0004c0004t0001g0148 | 3 | NA19002.hp2 NA19058.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.144+3517G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065234 | ||||||
chr8:23065235
|
G | A | 1 | a0001c0001t0003g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+3516C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065235 | ||||||
chr8:23065504
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.144+3247T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065504 | ||||||
chr8:23065648
|
C | T | 9 | a0002c0002t0004g0316a0002c0002t0004g0320a0002c0002t0004g0322others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.144+3103G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065648 | ||||||
chr8:23065664
|
T | C | 10 | a0001c0001t0008g0123a0001c0001t0010g0204a0001c0001t0010g0205others(7): Show | 10 | HG00733.hp2 HG01099.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.144+3087A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065664 | ||||||
chr8:23065697
|
A | G | 1 | a0001c0001t0003g0226 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.144+3054T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065697 | ||||||
chr8:23065705
|
G | C | 1 | a0001c0001t0002g0310 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.144+3046C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065705 | ||||||
chr8:23065759
|
G | A | 4 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(1): Show | 4 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+2992C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065759 | ||||||
chr8:23065761
|
G | A | 1 | a0001c0001t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+2990C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065761 | ||||||
chr8:23065799
|
A | C | 5 | a0001c0001t0004g0375a0001c0001t0012g0140a0002c0002t0015g0010others(2): Show | 5 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+2952T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23065799 | ||||||
chr8:23066011
|
G | A | 1 | a0006c0006t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144+2740C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066011 | ||||||
chr8:23066058
|
G | C | 1 | a0001c0001t0013g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.144+2693C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066058 | ||||||
chr8:23066070
|
C | T | 1 | a0002c0002t0004g0314 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.144+2681G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066070 | ||||||
chr8:23066383
|
T | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.144+2368A>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066383 | ||||||
chr8:23066518
|
T | C | 102 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(99): Show | 105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.144+2233A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066518 | ||||||
chr8:23066678
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+2073G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066678 | ||||||
chr8:23066814
|
G | A | 1 | a0004c0004t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.144+1937C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066814 | ||||||
chr8:23066845
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(296): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.144+1906A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066845 | ||||||
chr8:23066855
|
C | A | 3 | a0001c0001t0012g0140a0002c0002t0015g0010a0011c0011t0006g0312 | 3 | HG01891.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.144+1896G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066855 | ||||||
chr8:23066898
|
AAAAC | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(53): Show | 58 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.144+1849_144+1852d others(6): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066898 | ||||||
chr8:23066898
|
AAAACAAA others(1): Show |
A | 5 | a0001c0001t0012g0140a0002c0002t0015g0010a0004c0004t0001g0138others(2): Show | 5 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+1845_144+1852d others(10): Show |
TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066898 | ||||||
chr8:23066929
|
A | T | 1 | a0006c0006t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.144+1822T>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23066929 | ||||||
chr8:23067015
|
G | T | 1 | a0006c0006t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+1736C>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067015 | ||||||
chr8:23067112
|
G | A | 1 | a0001c0001t0011g0223 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.144+1639C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067112 | ||||||
chr8:23067205
|
T | C | 1 | a0003c0003t0002g0116 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144+1546A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067205 | ||||||
chr8:23067230
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0004c0004t0001g0142 | 3 | HG01123.hp1 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.144+1521C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067230 | ||||||
chr8:23067397
|
A | G | 79 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0158others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.144+1354T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067397 | ||||||
chr8:23067445
|
T | TA | 102 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.144+1305dupT | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067445 | ||||||
chr8:23067455
|
A | C | 1 | a0002c0002t0004g0374 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.144+1296T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067455 | ||||||
chr8:23067456
|
C | A | 28 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.144+1295G>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067456 | ||||||
chr8:23067480
|
A | C | 108 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(105): Show | 111 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.144+1271T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067480 | ||||||
chr8:23067532
|
A | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0026g0026others(1): Show | 4 | HG02257.hp1 HG03654.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1219T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067532 | ||||||
chr8:23067641
|
A | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(308): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.144+1110T>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067641 | ||||||
chr8:23067694
|
G | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.144+1057C>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067694 | ||||||
chr8:23067804
|
C | G | 1 | a0001c0001t0001g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.144+947G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067804 | ||||||
chr8:23067839
|
AG | A | 9 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 9 | HG02015.hp2 HG03704.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.144+911delC | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067839 | ||||||
chr8:23067851
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.144+900C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067851 | ||||||
chr8:23067915
|
T | C | 1 | a0001c0001t0003g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+836A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067915 | ||||||
chr8:23067943
|
G | A | 1 | a0003c0003t0001g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.144+808C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067943 | ||||||
chr8:23067945
|
T | C | 1 | a0002c0002t0004g0374 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.144+806A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067945 | ||||||
chr8:23067964
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.144+787G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23067964 | ||||||
chr8:23068002
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(309): Show | 318 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.144+749C>T | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068002 | ||||||
chr8:23068051
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.144+700T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068051 | ||||||
chr8:23068239
|
C | G | 1 | a0012c0012t0023g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.144+512G>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068239 | ||||||
chr8:23068247
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.144+504G>A | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068247 | ||||||
chr8:23068373
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144+378T>C | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068373 | ||||||
chr8:23068498
|
T | C | 51 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0001g0269others(48): Show | 51 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.144+253A>G | TNFRSF10B | ENSG00000120889.13 | transcript | ENST00000276431.9 | protein_coding | 1/8 | chr8 | 23068498 |