geneid | 7133 |
---|---|
ensemblid | ENSG00000028137.19 |
hgncid | 11917 |
symbol | TNFRSF1B |
name | TNF receptor superfamily member 1B |
refseq_nuc | NM_001066.3 |
refseq_prot | NP_001057.1 |
ensembl_nuc | ENST00000376259.7 |
ensembl_prot | ENSP00000365435.3 |
mane_status | MANE Select |
chr | chr1 |
start | 12166991 |
end | 12209220 |
strand | + |
ver | v1.2 |
region | chr1:12166991-12209220 |
region5000 | chr1:12161991-12214220 |
regionname0 | TNFRSF1B_chr1_12166991_12209220 |
regionname5000 | TNFRSF1B_chr1_12161991_12214220 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 461 | 292 | 73 | 58 | 117 | 10 | 33 | 81 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002 | 0/0 | 461 | 56 | 16 | 11 | 18 | 4 | 7 | 15 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0003 | 0/0 | 461 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0004 | 0/0 | 461 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0005 | 0/1 | 461 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0006 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0007 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0008 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0009 | 0/0 | 461 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0010 | 0/0 | 461 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1386 | 277 | 67 | 58 | 109 | 10 | 32 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0002 | 0/0 | 1386 | 55 | 15 | 11 | 18 | 4 | 7 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0003 | 0/0 | 1386 | 8 | 6 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0004 | 0/0 | 1386 | 7 | 0 | 0 | 7 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0005 | 0/0 | 1386 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0006 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0007 | 0/1 | 1386 | 2 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0011 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0012 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
c0013 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2302 | 55 | 3 | 17 | 21 | 4 | 10 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0002 | 0/0 | 2302 | 53 | 6 | 9 | 31 | 1 | 6 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0003 | 1/0 | 2302 | 47 | 9 | 7 | 23 | 3 | 4 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0004 | 0/0 | 2302 | 17 | 2 | 2 | 12 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0005 | 0/0 | 2303 | 17 | 2 | 0 | 13 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0006 | 0/0 | 2303 | 12 | 10 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0007 | 0/0 | 2302 | 12 | 0 | 0 | 11 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0008 | 0/0 | 2302 | 9 | 8 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0009 | 0/0 | 2303 | 9 | 1 | 4 | 1 | 2 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0010 | 0/0 | 2302 | 8 | 6 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0011 | 0/0 | 2303 | 7 | 7 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0012 | 0/0 | 2302 | 7 | 2 | 1 | 3 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0013 | 0/0 | 2302 | 6 | 1 | 1 | 0 | 0 | 4 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0014 | 0/0 | 2302 | 6 | 0 | 4 | 0 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0015 | 0/0 | 2303 | 5 | 4 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0016 | 0/1 | 2306 | 5 | 0 | 4 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0017 | 0/0 | 2302 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0018 | 0/0 | 2303 | 4 | 3 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0019 | 0/0 | 2302 | 4 | 0 | 0 | 4 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0020 | 0/0 | 2303 | 3 | 0 | 2 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0021 | 0/0 | 2303 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0022 | 0/0 | 2302 | 3 | 0 | 1 | 1 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0023 | 0/0 | 2303 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0024 | 0/0 | 2302 | 3 | 0 | 0 | 2 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0025 | 0/0 | 2303 | 3 | 2 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0026 | 0/0 | 2303 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0027 | 0/0 | 2302 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0028 | 0/0 | 2302 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0029 | 0/0 | 2303 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0030 | 0/0 | 2302 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0031 | 0/0 | 2303 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0032 | 0/0 | 2303 | 2 | 1 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0033 | 0/0 | 2302 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0034 | 0/0 | 2303 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0035 | 0/0 | 2302 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0036 | 0/0 | 2306 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0037 | 0/0 | 2302 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0038 | 0/0 | 2311 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0039 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0040 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0041 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0042 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0043 | 0/0 | 2302 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0044 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0045 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0046 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0047 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0048 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0049 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0050 | 0/0 | 2302 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0051 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0052 | 0/0 | 2302 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0053 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0054 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0055 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0056 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0057 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0058 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0059 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0060 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0061 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0062 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0063 | 0/0 | 2302 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0064 | 0/0 | 2306 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0065 | 0/0 | 2302 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0066 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0067 | 0/0 | 2311 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0068 | 0/0 | 2311 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
t0069 | 0/0 | 2311 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0344 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1386 | 277 | 67 | 58 | 109 | 10 | 32 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003 | 0/0 | 1386 | 8 | 6 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0004 | 0/0 | 1386 | 7 | 0 | 0 | 7 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002 | 0/0 | 1386 | 55 | 15 | 11 | 18 | 4 | 7 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0003c0005 | 0/0 | 1386 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0004c0006 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0005c0007 | 0/1 | 1386 | 2 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0006c0013 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0007c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0008c0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0009c0012 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0010c0011 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3687 | 33 | 2 | 14 | 12 | 3 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0002 | 0/0 | 3687 | 45 | 4 | 7 | 28 | 0 | 6 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0003 | 1/0 | 3687 | 41 | 6 | 7 | 21 | 2 | 4 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0004 | 0/0 | 3687 | 17 | 2 | 2 | 12 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0005 | 0/0 | 3688 | 16 | 2 | 0 | 12 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0006 | 0/0 | 3688 | 12 | 10 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0007 | 0/0 | 3687 | 3 | 0 | 0 | 2 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0008 | 0/0 | 3687 | 7 | 6 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0009 | 0/0 | 3688 | 7 | 1 | 3 | 1 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0010 | 0/0 | 3687 | 8 | 6 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0011 | 0/0 | 3688 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0012 | 0/0 | 3687 | 6 | 2 | 1 | 2 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0013 | 0/0 | 3687 | 5 | 1 | 0 | 0 | 0 | 4 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0014 | 0/0 | 3687 | 4 | 0 | 2 | 0 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0015 | 0/0 | 3688 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0016 | 0/0 | 3691 | 4 | 0 | 4 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0017 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0018 | 0/0 | 3688 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0019 | 0/0 | 3687 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0020 | 0/0 | 3688 | 3 | 0 | 2 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0021 | 0/0 | 3688 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0022 | 0/0 | 3687 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0023 | 0/0 | 3688 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0024 | 0/0 | 3687 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0025 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0026 | 0/0 | 3688 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0027 | 0/0 | 3687 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0028 | 0/0 | 3687 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0029 | 0/0 | 3688 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0030 | 0/0 | 3687 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0032 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0033 | 0/0 | 3687 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0035 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0036 | 0/0 | 3691 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0037 | 0/0 | 3687 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0041 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0042 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0043 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0044 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0045 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0046 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0047 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0049 | 0/0 | 3688 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0050 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0051 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0052 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0053 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0054 | 0/0 | 3688 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0055 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0056 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0057 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0058 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0061 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0062 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0063 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0064 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0065 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0066 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0001t0068 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0001 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0002 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0003 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0034 | 0/0 | 3688 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0035 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0059 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0067 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0003t0069 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0004t0001 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0004t0007 | 0/0 | 3687 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0001c0004t0024 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0001 | 0/0 | 3687 | 16 | 0 | 3 | 6 | 1 | 6 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0002 | 0/0 | 3687 | 7 | 1 | 2 | 3 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0003 | 0/0 | 3687 | 3 | 1 | 0 | 1 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0005 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0007 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0008 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0009 | 0/0 | 3688 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0011 | 0/0 | 3688 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0012 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0013 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0014 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0015 | 0/0 | 3688 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0017 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0019 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0021 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0022 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0025 | 0/0 | 3688 | 2 | 1 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0031 | 0/0 | 3688 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0032 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0034 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0038 | 0/0 | 3696 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0039 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0002t0040 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0002c0009t0018 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0003c0005t0003 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0003c0005t0007 | 0/0 | 3687 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0003c0005t0019 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0004c0006t0001 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0004c0006t0060 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0005c0007t0014 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0005c0007t0016 | 0/1 | 3691 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0006c0013t0001 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0007c0008t0003 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0008c0010t0048 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0009c0012t0001 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
a0010c0011t0001 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | copy fasta | chr1 | 12161991 | 12214220 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0015g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0018g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0018g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0019g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0019g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0020g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0020g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0020g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0021g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0021g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0022g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0023g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0023g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0023g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0024g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0024g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0025g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0026g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0026g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0027g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0027g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0028g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0028g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0029g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0029g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0030g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0030g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0032g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0033g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0035g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0036g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0036g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0037g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0037g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0041g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0042g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0043g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0044g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0045g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0046g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0047g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0049g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0050g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0051g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0052g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0053g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0054g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0055g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0056g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0057g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0058g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0061g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0062g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0063g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0064g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0065g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0066g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0068g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0034g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0035g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0059g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0067g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0069g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0024g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0008g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0009g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0009g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0011g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0013g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0014g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0015g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0015g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0017g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0019g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0021g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0022g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0025g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0025g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0031g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0031g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0032g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0034g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0038g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0038g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0039g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0040g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0009t0018g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0019g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0004c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0004c0006t0060g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0005c0007t0014g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0005c0007t0016g0344 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0006c0013t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0007c0008t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0008c0010t0048g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0009c0012t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0010c0011t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0063 | g0088 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0162 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00140 | hp1 | a0002 | c0002 | t0003 | g0334 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0320 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | FIN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00323 | hp2 | a0001 | c0001 | t0022 | g0056 | EUR | FIN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00408 | hp2 | a0001 | c0004 | t0007 | g0137 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00423 | hp2 | a0002 | c0002 | t0034 | g0178 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00438 | hp1 | a0001 | c0004 | t0007 | g0159 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00438 | hp2 | a0001 | c0001 | t0044 | g0236 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00544 | hp1 | a0001 | c0001 | t0030 | g0174 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00544 | hp2 | a0001 | c0001 | t0030 | g0254 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00597 | hp1 | a0003 | c0005 | t0003 | g0195 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00639 | hp1 | a0001 | c0001 | t0014 | g0212 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00673 | hp1 | a0001 | c0001 | t0019 | g0067 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0133 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00738 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00738 | hp2 | a0001 | c0001 | t0020 | g0263 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01069 | hp1 | a0001 | c0001 | t0022 | g0177 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01070 | hp1 | a0001 | c0001 | t0028 | g0305 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0233 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01071 | hp2 | a0001 | c0001 | t0028 | g0306 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01081 | hp2 | a0001 | c0001 | t0065 | g0313 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01099 | hp1 | a0001 | c0001 | t0016 | g0058 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01099 | hp2 | a0001 | c0001 | t0020 | g0052 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01106 | hp2 | a0002 | c0002 | t0013 | g0031 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01109 | hp2 | a0001 | c0001 | t0052 | g0308 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01167 | hp1 | a0001 | c0001 | t0027 | g0315 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01169 | hp1 | a0001 | c0001 | t0027 | g0048 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01192 | hp1 | a0001 | c0001 | t0018 | g0311 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01192 | hp2 | a0001 | c0001 | t0049 | g0025 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01243 | hp2 | a0002 | c0002 | t0015 | g0032 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0323 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01255 | hp2 | a0001 | c0001 | t0016 | g0060 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0339 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01261 | hp1 | a0002 | c0002 | t0031 | g0335 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01358 | hp1 | a0001 | c0001 | t0026 | g0317 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01358 | hp2 | a0005 | c0007 | t0014 | g0346 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01433 | hp1 | a0002 | c0002 | t0009 | g0276 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0059 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01515 | hp1 | a0001 | c0001 | t0009 | g0041 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01515 | hp2 | a0002 | c0002 | t0009 | g0185 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0083 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01516 | hp2 | a0001 | c0001 | t0014 | g0247 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01884 | hp1 | a0001 | c0001 | t0021 | g0238 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0015 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0203 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01934 | hp1 | a0002 | c0002 | t0031 | g0150 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01934 | hp2 | a0001 | c0001 | t0036 | g0227 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0086 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01981 | hp2 | a0001 | c0001 | t0036 | g0094 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02027 | hp1 | a0001 | c0001 | t0058 | g0332 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02040 | hp1 | a0008 | c0010 | t0048 | g0298 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02055 | hp1 | a0001 | c0001 | t0055 | g0295 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02055 | hp2 | a0002 | c0002 | t0008 | g0351 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02056 | hp1 | a0002 | c0002 | t0022 | g0157 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02056 | hp2 | a0001 | c0001 | t0019 | g0065 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02135 | hp1 | a0003 | c0005 | t0007 | g0158 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0299 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02145 | hp2 | a0001 | c0001 | t0025 | g0268 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02155 | hp1 | a0001 | c0001 | t0010 | g0241 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02165 | hp1 | a0002 | c0002 | t0007 | g0152 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02257 | hp1 | a0002 | c0002 | t0038 | g0357 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0043 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0046 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0132 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02280 | hp1 | a0004 | c0006 | t0001 | g0093 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02293 | hp2 | a0002 | c0002 | t0014 | g0319 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0318 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0229 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02523 | hp2 | a0001 | c0001 | t0041 | g0329 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02572 | hp1 | a0002 | c0002 | t0011 | g0027 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02572 | hp2 | a0001 | c0003 | t0067 | g0355 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02615 | hp1 | a0001 | c0003 | t0069 | g0354 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0294 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0353 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0259 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0341 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0124 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02647 | hp2 | a0002 | c0002 | t0015 | g0267 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02683 | hp1 | a0002 | c0002 | t0025 | g0156 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02683 | hp2 | a0001 | c0001 | t0014 | g0200 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0302 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02698 | hp2 | a0001 | c0001 | t0064 | g0265 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02717 | hp1 | a0001 | c0001 | t0047 | g0035 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02717 | hp2 | a0002 | c0002 | t0032 | g0024 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0340 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0310 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02809 | hp1 | a0004 | c0006 | t0060 | g0064 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02886 | hp1 | a0002 | c0002 | t0008 | g0023 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02886 | hp2 | a0001 | c0001 | t0023 | g0019 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02895 | hp2 | a0001 | c0001 | t0023 | g0026 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02897 | hp1 | a0001 | c0001 | t0035 | g0214 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02965 | hp1 | a0001 | c0001 | t0023 | g0242 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02970 | hp2 | a0002 | c0002 | t0017 | g0033 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03017 | hp1 | a0001 | c0001 | t0013 | g0271 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03017 | hp2 | a0001 | c0001 | t0033 | g0003 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0017 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0202 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03130 | hp2 | a0001 | c0001 | t0068 | g0356 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03195 | hp1 | a0007 | c0008 | t0003 | g0314 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03195 | hp2 | a0001 | c0001 | t0021 | g0164 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0292 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0047 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03239 | hp2 | a0001 | c0001 | t0020 | g0252 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03486 | hp1 | a0001 | c0003 | t0059 | g0044 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03486 | hp2 | a0002 | c0009 | t0018 | g0045 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03491 | hp1 | a0001 | c0001 | t0037 | g0130 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03491 | hp2 | a0001 | c0001 | t0033 | g0003 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03492 | hp1 | a0001 | c0001 | t0024 | g0337 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03492 | hp2 | a0001 | c0001 | t0037 | g0129 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03540 | hp1 | a0001 | c0001 | t0051 | g0237 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03579 | hp2 | a0001 | c0001 | t0042 | g0128 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0321 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0261 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03704 | hp1 | a0001 | c0001 | t0013 | g0037 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03704 | hp2 | a0001 | c0001 | t0029 | g0228 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03710 | hp2 | a0001 | c0001 | t0043 | g0274 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03831 | hp1 | a0010 | c0011 | t0001 | g0140 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03831 | hp2 | a0001 | c0001 | t0013 | g0169 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0309 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03927 | hp1 | a0009 | c0012 | t0001 | g0125 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03942 | hp1 | a0001 | c0001 | t0054 | g0239 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0301 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0040 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04199 | hp1 | a0001 | c0003 | t0034 | g0144 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0325 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0277 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0018 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | CHB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18906 | hp2 | a0002 | c0002 | t0017 | g0034 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18941 | hp2 | a0001 | c0001 | t0029 | g0117 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18942 | hp2 | a0001 | c0001 | t0057 | g0330 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18943 | hp1 | a0001 | c0001 | t0024 | g0225 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18944 | hp1 | a0002 | c0002 | t0019 | g0191 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18965 | hp2 | a0003 | c0005 | t0019 | g0155 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18966 | hp1 | a0006 | c0013 | t0001 | g0182 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18978 | hp1 | a0002 | c0002 | t0039 | g0136 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18978 | hp2 | a0001 | c0001 | t0032 | g0121 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0072 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0287 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0006 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18995 | hp2 | a0001 | c0001 | t0012 | g0204 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19000 | hp2 | a0001 | c0004 | t0007 | g0216 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19002 | hp2 | a0001 | c0001 | t0056 | g0270 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19005 | hp2 | a0001 | c0001 | t0053 | g0110 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19007 | hp2 | a0002 | c0002 | t0040 | g0211 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19009 | hp1 | a0001 | c0003 | t0001 | g0345 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19011 | hp1 | a0003 | c0005 | t0007 | g0135 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19012 | hp2 | a0002 | c0002 | t0012 | g0209 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19030 | hp1 | a0001 | c0001 | t0045 | g0226 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19030 | hp2 | a0002 | c0002 | t0021 | g0179 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0288 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0256 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19055 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19056 | hp2 | a0001 | c0004 | t0007 | g0220 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19063 | hp1 | a0001 | c0004 | t0007 | g0139 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19063 | hp2 | a0001 | c0001 | t0061 | g0245 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19065 | hp2 | a0001 | c0001 | t0010 | g0081 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19066 | hp2 | a0001 | c0004 | t0024 | g0138 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19074 | hp1 | a0002 | c0002 | t0005 | g0141 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0322 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19084 | hp1 | a0001 | c0001 | t0066 | g0250 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19088 | hp2 | a0003 | c0005 | t0007 | g0184 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19089 | hp1 | a0001 | c0001 | t0046 | g0101 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19089 | hp2 | a0001 | c0001 | t0062 | g0106 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19240 | hp1 | a0002 | c0002 | t0038 | g0358 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | ASW | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20129 | hp2 | a0002 | c0002 | t0015 | g0013 | AFR | ASW | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0165 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0312 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0051 | SAS | GIH | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0131 | SAS | GIH | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01123 | hp2 | a0001 | c0001 | t0050 | g0109 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02109 | hp1 | a0001 | c0003 | t0002 | g0342 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0153 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02559 | hp1 | a0002 | c0002 | t0025 | g0194 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0266 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03471 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0291 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG06807 | hp1 | a0001 | c0003 | t0035 | g0029 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG06807 | hp2 | a0002 | c0002 | t0011 | g0324 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18955 | hp2 | a0001 | c0004 | t0001 | g0338 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20300 | hp1 | a0001 | c0001 | t0026 | g0262 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0316 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0092 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA21309 | hp2 | a0002 | c0002 | t0003 | g0028 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
homoSapiens_chm13v2 | hp1 | a0005 | c0007 | t0016 | g0344 | REF | REF | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0123 | REF | REF | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12188806
|
C | T | 1 | a0006 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.89C>T | p.Thr30Ile | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/10 | 190/3687 | 89/1386 | 30/461 | chr1 | 12188806 | ||
chr1:12192870
|
G | A | 1 | a0007 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.559G>A | p.Val187Met | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 660/3687 | 559/1386 | 187/461 | chr1 | 12192870 | ||
chr1:12192898
|
T | G | 4 | a0002a0005a0009others(1): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
missense_variant | MODERATE | c.587T>G | p.Met196Arg | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 688/3687 | 587/1386 | 196/461 | chr1 | 12192898 | ||
chr1:12192919
|
C | T | 1 | a0009 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.608C>T | p.Thr203Met | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 709/3687 | 608/1386 | 203/461 | chr1 | 12192919 | ||
chr1:12193005
|
G | A | 2 | a0003a0005 | 7 | HG00597.hp1 HG01358.hp2 HG02135.hp1 others(4): Show |
missense_variant | MODERATE | c.694G>A | p.Glu232Lys | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 795/3687 | 694/1386 | 232/461 | chr1 | 12193005 | ||
chr1:12193958
|
T | C | 1 | a0004 | 2 | HG02280.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.791T>C | p.Leu264Pro | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/10 | 892/3687 | 791/1386 | 264/461 | chr1 | 12193958 | ||
chr1:12201985
|
A | G | 1 | a0008 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.919A>G | p.Lys307Glu | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/10 | 1020/3687 | 919/1386 | 307/461 | chr1 | 12201985 | ||
chr1:12206881
|
C | T | 1 | a0010 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1247C>T | p.Pro416Leu | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1348/3687 | 1247/1386 | 416/461 | chr1 | 12206881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12188885
|
A | G | 5 | a0001c0003a0002c0002a0005c0007others(2): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
synonymous_variant | LOW | c.168A>G | p.Lys56Lys | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/10 | 269/3687 | 168/1386 | 56/461 | chr1 | 12188885 | ||
chr1:12192516
|
C | T | 1 | a0001c0004 | 7 | HG00408.hp2 HG00438.hp1 NA18955.hp2 others(4): Show |
synonymous_variant | LOW | c.543C>T | p.Pro181Pro | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 5/10 | 644/3687 | 543/1386 | 181/461 | chr1 | 12192516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12167002
|
A | C | 4 | a0001c0001t0068a0001c0003t0067a0001c0003t0069others(1): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-90A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 90 | chr1 | 12167002 | |||||
chr1:12167008
|
C | A | 1 | a0002c0002t0039 | 1 | NA18978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 84 | chr1 | 12167008 | |||||
chr1:12167017
|
G | A | 1 | a0002c0002t0040 | 1 | NA19007.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 75 | chr1 | 12167017 | |||||
chr1:12167017
|
G | T | 1 | a0001c0001t0066 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-75G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 75 | chr1 | 12167017 | |||||
chr1:12167039
|
T | TGCGAGGG others(1): Show |
4 | a0001c0001t0068a0001c0003t0067a0001c0003t0069others(1): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-29dupGCGAGGGC | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 28 | INFO_REALIGN_3_PRIME | chr1 | 12167039 | ||||
chr1:12207208
|
A | G | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(51): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*188A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 188 | chr1 | 12207208 | |||||
chr1:12207213
|
T | G | 4 | a0001c0001t0020a0001c0001t0026a0001c0001t0027others(1): Show | 9 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*193T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 193 | chr1 | 12207213 | |||||
chr1:12207235
|
C | T | 44 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(41): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*215C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 215 | chr1 | 12207235 | |||||
chr1:12207407
|
C | A | 21 | a0001c0001t0004a0001c0001t0012a0001c0001t0013others(18): Show | 58 | HG00621.hp1 HG00733.hp2 HG01099.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*387C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 387 | chr1 | 12207407 | |||||
chr1:12207473
|
A | G | 2 | a0001c0001t0021a0002c0002t0021 | 3 | HG01884.hp1 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 453 | chr1 | 12207473 | |||||
chr1:12207490
|
C | A | 1 | a0001c0001t0042 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 470 | chr1 | 12207490 | |||||
chr1:12207492
|
T | C | 3 | a0001c0001t0033a0001c0001t0037a0001c0001t0043 | 5 | HG03017.hp2 HG03491.hp1 HG03491.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*472T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 472 | chr1 | 12207492 | |||||
chr1:12207498
|
C | G | 7 | a0001c0001t0008a0001c0001t0035a0001c0001t0049others(4): Show | 14 | HG01167.hp2 HG01192.hp2 HG01891.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*478C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 478 | chr1 | 12207498 | |||||
chr1:12207649
|
C | T | 1 | a0001c0001t0042 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*629C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 629 | chr1 | 12207649 | |||||
chr1:12207778
|
C | T | 1 | a0008c0010t0048 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 758 | chr1 | 12207778 | |||||
chr1:12207842
|
G | A | 1 | a0001c0001t0044 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 822 | chr1 | 12207842 | |||||
chr1:12207858
|
C | G | 12 | a0001c0001t0007a0001c0001t0019a0001c0001t0024others(9): Show | 22 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*838C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 838 | chr1 | 12207858 | |||||
chr1:12207914
|
G | GA | 35 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(32): Show | 88 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*904dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 905 | INFO_REALIGN_3_PRIME | chr1 | 12207914 | ||||
chr1:12207942
|
C | T | 44 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(41): Show | 120 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 922 | chr1 | 12207942 | |||||
chr1:12207966
|
G | GTGAA | 5 | a0001c0001t0016a0001c0001t0036a0001c0001t0053others(2): Show | 9 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*950dupTGAA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 951 | INFO_REALIGN_3_PRIME | chr1 | 12207966 | ||||
chr1:12208168
|
C | T | 2 | a0001c0001t0017a0002c0002t0017 | 4 | HG02970.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1148C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1148 | chr1 | 12208168 | |||||
chr1:12208268
|
C | T | 1 | a0001c0001t0043 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1248C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1248 | chr1 | 12208268 | |||||
chr1:12208329
|
T | C | 2 | a0001c0001t0029a0001c0001t0054 | 3 | HG03704.hp2 HG03942.hp1 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1309T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1309 | chr1 | 12208329 | |||||
chr1:12208330
|
C | T | 2 | a0001c0001t0052a0001c0001t0063 | 2 | HG00099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1310 | chr1 | 12208330 | |||||
chr1:12208331
|
C | A | 2 | a0001c0001t0052a0001c0001t0063 | 2 | HG00099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1311C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1311 | chr1 | 12208331 | |||||
chr1:12208375
|
G | A | 1 | a0001c0001t0056 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1355G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1355 | chr1 | 12208375 | |||||
chr1:12208438
|
T | C | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1418 | chr1 | 12208438 | |||||
chr1:12208442
|
G | A | 12 | a0001c0001t0005a0001c0001t0009a0001c0001t0018others(9): Show | 38 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1422G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1422 | chr1 | 12208442 | |||||
chr1:12208514
|
A | G | 11 | a0001c0001t0016a0001c0001t0017a0001c0001t0036others(8): Show | 17 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1494A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1494 | chr1 | 12208514 | |||||
chr1:12208521
|
T | G | 2 | a0001c0001t0023a0002c0002t0038 | 5 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1501T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1501 | chr1 | 12208521 | |||||
chr1:12208567
|
G | A | 1 | a0001c0001t0057 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1547 | chr1 | 12208567 | |||||
chr1:12208580
|
C | T | 4 | a0001c0001t0014a0001c0001t0028a0002c0002t0014others(1): Show | 8 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1560C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1560 | chr1 | 12208580 | |||||
chr1:12208664
|
G | A | 8 | a0001c0001t0016a0001c0001t0017a0001c0001t0036others(5): Show | 14 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1644G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1644 | chr1 | 12208664 | |||||
chr1:12209005
|
A | C | 1 | a0001c0001t0058 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1985A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1985 | chr1 | 12209005 | |||||
chr1:12209024
|
C | G | 1 | a0001c0001t0051 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2004C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 2004 | chr1 | 12209024 | |||||
chr1:12209097
|
C | T | 3 | a0001c0003t0067a0001c0003t0069a0004c0006t0060 | 3 | HG02572.hp2 HG02615.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2077C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 2077 | chr1 | 12209097 | |||||
chr1:12209163
|
A | C | 1 | a0001c0001t0045 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 2143 | chr1 | 12209163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12167245
|
C | G | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+76C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167245 | ||||||
chr1:12167319
|
A | C | 1 | a0001c0001t0006g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+150A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167319 | ||||||
chr1:12167471
|
T | C | 1 | a0001c0001t0005g0005 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.78+302T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167471 | ||||||
chr1:12167674
|
G | C | 1 | a0001c0001t0012g0006 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.78+505G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167674 | ||||||
chr1:12167784
|
G | C | 14 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+615G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167784 | ||||||
chr1:12167808
|
A | G | 14 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+639A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167808 | ||||||
chr1:12167814
|
C | G | 14 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+645C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167814 | ||||||
chr1:12167838
|
A | C | 1 | a0001c0001t0002g0352 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.78+669A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167838 | ||||||
chr1:12168115
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78+946G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168115 | ||||||
chr1:12168176
|
G | A | 3 | a0002c0002t0002g0022a0002c0002t0008g0023a0002c0002t0032g0024 | 3 | HG02717.hp2 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.78+1007G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168176 | ||||||
chr1:12168208
|
C | T | 2 | a0002c0002t0038g0357a0002c0002t0038g0358 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.78+1039C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168208 | ||||||
chr1:12168445
|
G | A | 1 | a0001c0001t0049g0025 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78+1276G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168445 | ||||||
chr1:12168534
|
C | T | 1 | a0002c0002t0008g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78+1365C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168534 | ||||||
chr1:12168712
|
C | A | 1 | a0001c0001t0023g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.78+1543C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168712 | ||||||
chr1:12168712
|
C | T | 1 | a0001c0001t0001g0350 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.78+1543C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168712 | ||||||
chr1:12168753
|
G | C | 33 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(30): Show | 33 | HG01106.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.78+1584G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168753 | ||||||
chr1:12168791
|
C | G | 1 | a0001c0001t0002g0349 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.78+1622C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168791 | ||||||
chr1:12168804
|
C | G | 2 | a0001c0001t0002g0347a0001c0001t0003g0348 | 2 | NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.78+1635C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168804 | ||||||
chr1:12168921
|
C | A | 1 | a0001c0001t0003g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.78+1752C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168921 | ||||||
chr1:12168953
|
C | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.78+1784C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168953 | ||||||
chr1:12168960
|
C | T | 3 | a0002c0002t0002g0022a0002c0002t0008g0023a0002c0002t0032g0024 | 3 | HG02717.hp2 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.78+1791C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168960 | ||||||
chr1:12168974
|
TC | T | 14 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+1810delC | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12168974 | |||||
chr1:12169649
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.78+2480C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169649 | ||||||
chr1:12169650
|
G | A | 1 | a0001c0001t0013g0037 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.78+2481G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169650 | ||||||
chr1:12169954
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.78+2785G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169954 | ||||||
chr1:12169990
|
G | C | 1 | a0001c0001t0005g0038 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.78+2821G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169990 | ||||||
chr1:12170024
|
G | A | 7 | a0001c0003t0035g0029a0002c0002t0002g0030a0002c0002t0003g0028others(4): Show | 7 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+2855G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170024 | ||||||
chr1:12170070
|
C | T | 1 | a0001c0003t0002g0342 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.78+2901C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170070 | ||||||
chr1:12170175
|
CCATT | C | 33 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(30): Show | 33 | HG01106.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.78+3024_78+3027del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12170175 | |||||
chr1:12170248
|
G | C | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+3079G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170248 | ||||||
chr1:12170388
|
G | T | 14 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+3219G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170388 | ||||||
chr1:12170472
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.78+3303G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170472 | ||||||
chr1:12170492
|
C | T | 1 | a0001c0001t0068g0356 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78+3323C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170492 | ||||||
chr1:12170574
|
G | C | 19 | a0001c0001t0002g0011a0001c0001t0003g0016a0001c0001t0006g0014others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.78+3405G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170574 | ||||||
chr1:12170833
|
A | AT | 8 | a0001c0001t0004g0339a0001c0001t0004g0341a0001c0001t0008g0340others(5): Show | 8 | HG01257.hp2 HG01358.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+3678dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12170833 | |||||
chr1:12170866
|
G | A | 1 | a0001c0001t0004g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.78+3697G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170866 | ||||||
chr1:12170936
|
A | C | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.78+3767A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170936 | ||||||
chr1:12171176
|
C | CT | 13 | a0001c0001t0005g0336a0001c0001t0023g0026a0001c0003t0001g0345others(10): Show | 13 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.78+4024dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12171176 | |||||
chr1:12171176
|
CT | C | 13 | a0001c0001t0002g0049a0001c0001t0003g0036a0001c0001t0003g0050others(10): Show | 13 | HG01074.hp1 HG01169.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+4024delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12171176 | |||||
chr1:12171197
|
A | G | 1 | a0002c0002t0031g0335 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.78+4028A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171197 | ||||||
chr1:12171294
|
G | A | 1 | a0001c0001t0020g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.78+4125G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171294 | ||||||
chr1:12171447
|
G | T | 1 | a0002c0002t0003g0334 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.78+4278G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171447 | ||||||
chr1:12171597
|
C | T | 7 | a0001c0001t0003g0016a0001c0001t0006g0014a0001c0001t0011g0015others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+4428C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171597 | ||||||
chr1:12172231
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.78+5062C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172231 | ||||||
chr1:12172297
|
C | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | NA19055.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.78+5128C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172297 | ||||||
chr1:12172459
|
T | A | 3 | a0001c0001t0023g0026a0001c0001t0047g0035a0002c0002t0017g0034 | 3 | HG02717.hp1 HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.78+5290T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172459 | ||||||
chr1:12172597
|
A | G | 8 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0328others(5): Show | 8 | HG00558.hp2 HG02027.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+5428A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172597 | ||||||
chr1:12172747
|
A | G | 1 | a0001c0001t0005g0325 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.78+5578A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172747 | ||||||
chr1:12172749
|
T | C | 94 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.78+5580T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172749 | ||||||
chr1:12172948
|
A | G | 3 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033 | 3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.78+5779A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172948 | ||||||
chr1:12172951
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+5782C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172951 | ||||||
chr1:12173004
|
A | G | 342 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(339): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.78+5835A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173004 | ||||||
chr1:12173205
|
C | T | 3 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033 | 3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.78+6036C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173205 | ||||||
chr1:12173697
|
T | C | 271 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.78+6528T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173697 | ||||||
chr1:12173776
|
T | C | 1 | a0003c0005t0007g0135 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.78+6607T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173776 | ||||||
chr1:12174122
|
T | TTTC | 10 | a0001c0001t0003g0302a0001c0001t0003g0312a0001c0001t0004g0284others(7): Show | 10 | HG00639.hp1 HG02027.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+6994_78+6996dup others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTC | 7 | a0001c0001t0006g0288a0001c0001t0009g0051a0001c0001t0013g0271others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+6991_78+6996dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(2): Show |
6 | a0001c0001t0003g0251a0001c0001t0003g0273a0001c0001t0007g0322others(3): Show | 6 | HG00741.hp2 HG01192.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+6988_78+6996dup others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(5): Show |
8 | a0001c0001t0001g0297a0001c0001t0005g0325a0001c0001t0006g0353others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+6985_78+6996dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(8): Show |
4 | a0001c0001t0004g0272a0001c0001t0004g0300a0001c0003t0002g0342others(1): Show | 4 | HG02040.hp2 HG02109.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6982_78+6996dup others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(11): Show |
2 | a0001c0001t0004g0316a0001c0001t0056g0270 | 2 | NA19002.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.78+6979_78+6996dup others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(14): Show |
2 | a0001c0003t0003g0047a0002c0002t0002g0030 | 2 | HG02004.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.78+6976_78+6996dup others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(17): Show |
1 | a0001c0001t0001g0275 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.78+6973_78+6996dup others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(20): Show |
1 | a0001c0001t0006g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+6970_78+6996dup others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(23): Show |
2 | a0001c0001t0001g0134a0001c0001t0012g0133 | 2 | HG00733.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.78+6967_78+6996dup others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
T | TTTCTTCT others(26): Show |
1 | a0001c0001t0058g0332 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.78+6964_78+6996dup others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
TTTC | T | 10 | a0001c0001t0002g0171a0001c0001t0003g0002a0001c0001t0003g0091others(7): Show | 10 | HG00735.hp2 HG01934.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+6994_78+6996del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174122
|
TTTCTTC | T | 3 | a0001c0004t0007g0137a0001c0004t0007g0139a0001c0004t0024g0138 | 3 | HG00408.hp2 NA19063.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78+6991_78+6996del others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | |||||
chr1:12174139
|
TCTTCTTC others(50): Show |
T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+6976_78+7032del others(57): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174139 | |||||
chr1:12174148
|
T | TCTCCTTC others(20): Show |
1 | a0001c0001t0001g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.78+6981_78+6982ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
T | TCTCCTTC others(26): Show |
2 | a0001c0001t0001g0055a0001c0001t0022g0056 | 2 | HG00323.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.78+6981_78+6982ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
T | TCTTCTCC others(11): Show |
1 | a0001c0001t0016g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.78+6984_78+6985ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
T | TCTTCTCC others(29): Show |
2 | a0001c0001t0016g0058a0002c0002t0039g0136 | 2 | HG01099.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.78+6984_78+6985ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
TCTTCTTC others(11): Show |
T | 2 | a0001c0001t0008g0007a0001c0004t0001g0338 | 2 | HG01891.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.78+6985_78+7002del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
TCTTCTTC others(23): Show |
T | 3 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010 | 3 | HG01167.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.78+6985_78+7014del others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
TCTTCTTC others(29): Show |
T | 2 | a0001c0001t0002g0011a0001c0001t0017g0012 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.78+6985_78+7020del others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174148
|
TCTTCTTC others(41): Show |
T | 1 | a0002c0002t0015g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.78+6985_78+7032del others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | |||||
chr1:12174151
|
TCTTCTTC others(26): Show |
T | 2 | a0001c0001t0006g0014a0001c0001t0011g0015 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.78+6988_78+7020del others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174151 | |||||
chr1:12174151
|
TCTTCTTC others(32): Show |
T | 2 | a0001c0001t0003g0016a0002c0002t0008g0351 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78+6988_78+7026del others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174151 | |||||
chr1:12174154
|
T | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0016g0058others(4): Show | 7 | HG00323.hp2 HG01099.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6985T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174154 | ||||||
chr1:12174154
|
T | TCTC | 5 | a0001c0001t0002g0148a0001c0001t0005g0063a0002c0002t0001g0146others(2): Show | 5 | HG00423.hp1 HG01952.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+6987_78+6988ins others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTCCTTC others(8): Show |
4 | a0001c0001t0001g0145a0001c0001t0005g0062a0001c0003t0034g0144others(1): Show | 4 | HG04199.hp1 NA18954.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6987_78+6988ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTCCTTC others(14): Show |
1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.78+6987_78+6988ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTCCTTC others(20): Show |
2 | a0001c0001t0001g0061a0002c0002t0005g0141 | 2 | HG01123.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.78+6987_78+6988ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(5): Show |
2 | a0001c0001t0003g0278a0003c0005t0019g0155 | 2 | HG02273.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(11): Show |
3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0006g0154 | 3 | HG01175.hp2 HG01496.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(17): Show |
2 | a0001c0001t0009g0068a0001c0001t0015g0153 | 2 | HG00639.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(23): Show |
1 | a0001c0001t0019g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.78+6990_78+6991ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(29): Show |
3 | a0001c0001t0001g0066a0002c0002t0001g0151a0002c0002t0007g0152 | 3 | HG02165.hp1 HG02818.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(35): Show |
2 | a0001c0001t0002g0333a0001c0001t0019g0065 | 2 | HG00408.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
T | TCTTCTCC others(41): Show |
1 | a0004c0006t0060g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+6990_78+6991ins others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
TCTTCTTC others(11): Show |
T | 1 | a0002c0002t0013g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.78+6991_78+7008del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174154
|
TCTTCTTC others(17): Show |
T | 1 | a0002c0002t0015g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.78+6991_78+7014del others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | |||||
chr1:12174157
|
TCTTCTTC others(2): Show |
T | 5 | a0001c0001t0009g0092a0001c0001t0030g0174a0001c0001t0032g0121others(2): Show | 5 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+6994_78+7002del others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174157 | |||||
chr1:12174157
|
TCTTCTTC others(8): Show |
T | 1 | a0002c0002t0017g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.78+6994_78+7008del others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174157 | |||||
chr1:12174160
|
T | C | 45 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(42): Show | 45 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.78+6991T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174160 | ||||||
chr1:12174160
|
T | TCTC | 3 | a0001c0001t0002g0090a0001c0001t0016g0086a0002c0002t0031g0335 | 3 | HG01261.hp1 HG01978.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(2): Show |
8 | a0001c0001t0001g0166a0001c0001t0002g0054a0001c0001t0002g0087others(5): Show | 8 | HG00099.hp1 HG01074.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(8): Show |
7 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0002g0039others(4): Show | 7 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(14): Show |
6 | a0001c0001t0001g0078a0001c0001t0002g0053a0001c0001t0003g0082others(3): Show | 6 | HG00673.hp2 HG01496.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(20): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0079 | 3 | HG01243.hp1 HG01257.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(26): Show |
2 | a0001c0001t0001g0074a0001c0001t0005g0038 | 2 | HG01258.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(32): Show |
2 | a0001c0001t0003g0161a0001c0001t0005g0075 | 2 | NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTCCTTC others(38): Show |
2 | a0001c0001t0002g0160a0001c0001t0005g0073 | 2 | NA19009.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTC | 4 | a0001c0001t0002g0183a0001c0001t0003g0103a0001c0001t0003g0181others(1): Show | 4 | HG01261.hp2 HG02523.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+7087_78+7092dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTCC others(5): Show |
1 | a0001c0001t0002g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.78+7081_78+7092dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTCC others(11): Show |
6 | a0001c0001t0002g0100a0001c0001t0002g0180a0001c0001t0022g0177others(3): Show | 6 | HG00423.hp2 HG01069.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+7075_78+7092dup others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTCC others(17): Show |
4 | a0001c0001t0001g0098a0001c0001t0002g0099a0001c0001t0004g0280others(1): Show | 4 | HG00621.hp2 HG01981.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+7069_78+7092dup others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTCC others(23): Show |
5 | a0001c0001t0001g0095a0001c0001t0001g0343a0001c0001t0002g0097others(2): Show | 5 | HG00735.hp1 HG04115.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+7063_78+7092dup others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTCC others(29): Show |
3 | a0001c0001t0002g0175a0001c0001t0004g0176a0001c0001t0024g0337 | 3 | HG00621.hp1 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.78+7057_78+7092dup others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTCC others(35): Show |
1 | a0004c0006t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.78+7051_78+7092dup others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(2): Show |
4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0004g0108others(1): Show | 4 | HG01175.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(8): Show |
9 | a0001c0001t0001g0201a0001c0001t0002g0349a0001c0001t0003g0199others(6): Show | 9 | HG01891.hp2 HG02683.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(14): Show |
9 | a0001c0001t0001g0107a0001c0001t0003g0192a0001c0001t0003g0197others(6): Show | 9 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(20): Show |
3 | a0001c0001t0009g0001a0001c0001t0062g0106a0002c0002t0002g0042 | 4 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(32): Show |
2 | a0001c0001t0002g0190a0001c0001t0005g0005 | 2 | NA18948.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(38): Show |
1 | a0001c0001t0001g0189 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(44): Show |
2 | a0001c0001t0003g0187a0001c0001t0003g0188 | 2 | NA18966.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(51): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(50): Show |
1 | a0001c0001t0003g0186 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(57): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(5): Show |
6 | a0001c0001t0001g0350a0001c0001t0004g0235a0001c0001t0021g0238others(3): Show | 6 | HG00438.hp2 HG01884.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(11): Show |
7 | a0001c0001t0001g0230a0001c0001t0003g0231a0001c0001t0005g0113others(4): Show | 7 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(17): Show |
7 | a0001c0001t0002g0224a0001c0001t0002g0347a0001c0001t0007g0287others(4): Show | 7 | HG01934.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(23): Show |
7 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0002g0222others(4): Show | 7 | HG01981.hp1 HG02293.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(29): Show |
5 | a0001c0001t0002g0219a0001c0001t0003g0217a0001c0001t0003g0218others(2): Show | 5 | HG03209.hp1 NA18945.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(41): Show |
1 | a0001c0001t0035g0214 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(8): Show |
2 | a0001c0001t0005g0249a0001c0001t0013g0037 | 2 | HG03704.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(14): Show |
7 | a0001c0001t0006g0248a0001c0001t0011g0291a0001c0001t0012g0006others(4): Show | 7 | HG01516.hp2 HG02976.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(20): Show |
2 | a0001c0001t0061g0245a0005c0007t0014g0346 | 2 | HG01358.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(26): Show |
4 | a0001c0001t0001g0244a0001c0001t0002g0116a0001c0001t0003g0348others(1): Show | 4 | HG01256.hp1 HG02273.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(32): Show |
3 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0033g0003 | 4 | HG03017.hp2 HG03491.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(38): Show |
1 | a0001c0001t0002g0352 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(44): Show |
1 | a0001c0001t0002g0243 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(51): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(11): Show |
4 | a0001c0001t0004g0258a0001c0001t0004g0260a0001c0001t0006g0259others(1): Show | 4 | HG02622.hp2 HG03579.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(17): Show |
4 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0257others(1): Show | 4 | HG01109.hp1 HG02083.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(23): Show |
1 | a0001c0001t0004g0339 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(29): Show |
3 | a0001c0001t0002g0327a0001c0001t0003g0118a0001c0001t0008g0256 | 3 | HG00558.hp2 HG02129.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(35): Show |
3 | a0001c0001t0002g0326a0001c0001t0003g0255a0001c0001t0030g0254 | 3 | HG00544.hp2 NA18747.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(47): Show |
1 | a0001c0001t0002g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(54): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(14): Show |
3 | a0001c0001t0015g0299a0001c0001t0025g0268a0002c0002t0015g0267 | 3 | HG02145.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(20): Show |
1 | a0008c0010t0048g0298 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(26): Show |
1 | a0001c0001t0041g0329 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(32): Show |
2 | a0001c0001t0002g0328a0001c0001t0011g0266 | 2 | HG02080.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(38): Show |
1 | a0001c0001t0064g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(56): Show |
1 | a0001c0001t0002g0264 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(63): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(23): Show |
4 | a0001c0001t0003g0131a0001c0001t0012g0046a0001c0001t0037g0129others(1): Show | 4 | HG02258.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(29): Show |
1 | a0002c0009t0018g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(47): Show |
1 | a0001c0001t0002g0304 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(54): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(20): Show |
1 | a0001c0001t0004g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(38): Show |
2 | a0001c0001t0003g0309a0001c0001t0007g0310 | 2 | HG02735.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(23): Show |
2 | a0001c0001t0027g0048a0001c0001t0027g0315 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(29): Show |
1 | a0001c0001t0043g0274 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(35): Show |
1 | a0001c0001t0057g0330 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(26): Show |
1 | a0001c0001t0003g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(32): Show |
1 | a0001c0001t0002g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(35): Show |
1 | a0001c0001t0004g0331 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
T | TCTTCTTC others(32): Show |
1 | a0001c0001t0003g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
TCTTCTC | T | 8 | a0001c0001t0003g0021a0001c0001t0008g0340a0001c0001t0020g0052others(5): Show | 8 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+7087_78+7092del others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
TCTTCTCC others(5): Show |
T | 2 | a0001c0001t0004g0341a0002c0002t0001g0321 | 2 | HG02630.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.78+7081_78+7092del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
TCTTCTCC others(11): Show |
T | 3 | a0001c0001t0002g0289a0001c0001t0006g0290a0001c0003t0059g0044 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.78+7075_78+7092del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
TCTTCTCC others(23): Show |
T | 3 | a0001c0001t0023g0026a0002c0002t0002g0022a0002c0002t0017g0034 | 3 | HG02895.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.78+7063_78+7092del others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174160
|
TCTTCTCC others(35): Show |
T | 1 | a0001c0001t0047g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.78+7051_78+7092del others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | |||||
chr1:12174163
|
TCTC | T | 12 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0003g0213others(9): Show | 13 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.78+6997_78+6999del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | |||||
chr1:12174163
|
TCTCCTTC others(2): Show |
T | 4 | a0001c0001t0002g0293a0001c0001t0002g0303a0001c0001t0011g0020others(1): Show | 4 | HG02280.hp2 HG03195.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6997_78+7005del others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | |||||
chr1:12174163
|
TCTCCTTC others(8): Show |
T | 4 | a0001c0001t0006g0296a0001c0001t0008g0294a0001c0001t0020g0252others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6997_78+7011del others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | |||||
chr1:12174163
|
TCTCCTTC others(14): Show |
T | 2 | a0002c0002t0008g0023a0002c0002t0032g0024 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.78+6997_78+7017del others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | |||||
chr1:12174166
|
C | T | 31 | a0001c0001t0001g0134a0001c0001t0001g0240a0001c0001t0001g0307others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.78+6997C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174166 | ||||||
chr1:12174172
|
C | T | 34 | a0001c0001t0001g0307a0001c0001t0003g0021a0001c0001t0003g0269others(31): Show | 35 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.78+7003C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174172 | ||||||
chr1:12174178
|
C | T | 28 | a0001c0001t0001g0307a0001c0001t0002g0293a0001c0001t0002g0303others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.78+7009C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174178 | ||||||
chr1:12174184
|
C | T | 20 | a0001c0001t0002g0289a0001c0001t0002g0303a0001c0001t0003g0021others(17): Show | 20 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.78+7015C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174184 | ||||||
chr1:12174190
|
C | CCTTCTCC others(22): Show |
1 | a0001c0001t0005g0063 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.78+7023_78+7051dup others(29): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174190 | |||||
chr1:12174190
|
C | T | 5 | a0001c0003t0059g0044a0002c0002t0001g0321a0002c0002t0008g0023others(2): Show | 5 | HG02717.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7021C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174190 | ||||||
chr1:12174196
|
C | T | 2 | a0002c0002t0001g0321a0002c0002t0032g0024 | 2 | HG02717.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.78+7027C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174196 | ||||||
chr1:12174246
|
T | C | 1 | a0010c0011t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.78+7077T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174246 | ||||||
chr1:12174250
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7081C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174250 | ||||||
chr1:12174256
|
C | T | 6 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(3): Show | 6 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+7087C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174256 | ||||||
chr1:12174262
|
T | C | 13 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0076others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+7093T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174262 | ||||||
chr1:12174263
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7094C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174263 | ||||||
chr1:12174266
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7097C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174266 | ||||||
chr1:12174267
|
T | A | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7098T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174267 | ||||||
chr1:12174267
|
T | TCCTTCTC others(23): Show |
1 | a0001c0003t0001g0345 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.78+7098_78+7099ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174267 | ||||||
chr1:12174267
|
T | TTCTTCTT others(11): Show |
1 | a0005c0007t0016g0344 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.78+7098_78+7099ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174267 | ||||||
chr1:12174461
|
T | A | 2 | a0001c0001t0023g0026a0002c0002t0017g0034 | 2 | HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.78+7292T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174461 | ||||||
chr1:12174468
|
G | C | 2 | a0001c0001t0008g0007a0001c0001t0008g0008 | 2 | HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.78+7299G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174468 | ||||||
chr1:12174540
|
G | A | 1 | a0003c0005t0019g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.78+7371G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174540 | ||||||
chr1:12174550
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.78+7381C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174550 | ||||||
chr1:12174565
|
A | G | 8 | a0001c0001t0068g0356a0001c0003t0001g0345a0001c0003t0067g0355others(5): Show | 8 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+7396A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174565 | ||||||
chr1:12174685
|
G | A | 2 | a0001c0001t0005g0119a0001c0001t0032g0121 | 2 | NA18978.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.78+7516G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174685 | ||||||
chr1:12174710
|
C | A | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.78+7541C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174710 | ||||||
chr1:12174720
|
G | A | 3 | a0001c0001t0004g0339a0001c0001t0004g0341a0001c0001t0008g0340 | 3 | HG01257.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.78+7551G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174720 | ||||||
chr1:12174736
|
A | G | 1 | a0001c0001t0023g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.78+7567A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174736 | ||||||
chr1:12174769
|
G | C | 1 | a0001c0001t0061g0245 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.78+7600G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174769 | ||||||
chr1:12174828
|
T | C | 8 | a0001c0001t0068g0356a0001c0003t0001g0345a0001c0003t0067g0355others(5): Show | 8 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+7659T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174828 | ||||||
chr1:12174926
|
G | A | 4 | a0001c0001t0003g0016a0001c0001t0006g0014a0001c0001t0007g0322others(1): Show | 4 | HG01884.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+7757G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174926 | ||||||
chr1:12174983
|
C | T | 1 | a0001c0001t0017g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.78+7814C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174983 | ||||||
chr1:12175075
|
G | A | 2 | a0001c0001t0002g0224a0001c0001t0006g0215 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78+7906G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175075 | ||||||
chr1:12175114
|
G | A | 3 | a0001c0001t0009g0092a0001c0001t0022g0177a0002c0002t0001g0151 | 3 | HG01069.hp1 HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.78+7945G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175114 | ||||||
chr1:12175223
|
C | T | 3 | a0001c0001t0002g0148a0001c0001t0002g0171a0001c0001t0003g0170 | 3 | HG00423.hp1 HG02129.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.78+8054C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175223 | ||||||
chr1:12175242
|
C | T | 1 | a0001c0001t0043g0274 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78+8073C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175242 | ||||||
chr1:12175374
|
A | G | 3 | a0001c0001t0003g0231a0001c0001t0006g0232a0001c0001t0006g0233 | 3 | HG01069.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.78+8205A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175374 | ||||||
chr1:12175391
|
C | T | 3 | a0001c0001t0003g0197a0001c0001t0006g0154a0001c0001t0015g0153 | 3 | HG02109.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.78+8222C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175391 | ||||||
chr1:12175399
|
C | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.78+8230C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175399 | ||||||
chr1:12175667
|
C | G | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.78+8498C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175667 | ||||||
chr1:12175820
|
C | T | 1 | a0002c0002t0008g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78+8651C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175820 | ||||||
chr1:12176053
|
G | GA | 53 | a0001c0001t0001g0145a0001c0001t0002g0053a0001c0001t0002g0054others(50): Show | 53 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.78+8900dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176053 | |||||
chr1:12176053
|
GA | G | 11 | a0001c0001t0002g0049a0001c0001t0003g0050a0001c0001t0003g0111others(8): Show | 11 | HG01358.hp2 HG02109.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.78+8900delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176053 | |||||
chr1:12176060
|
A | G | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+8891A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176060 | ||||||
chr1:12176103
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+8934C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176103 | ||||||
chr1:12176161
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.78+8992G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176161 | ||||||
chr1:12176173
|
C | T | 1 | a0001c0001t0003g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.78+9004C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176173 | ||||||
chr1:12176175
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.78+9006C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176175 | ||||||
chr1:12176269
|
AG | A | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+9102delG | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176269 | |||||
chr1:12176971
|
TCCTGAGC | T | 8 | a0001c0001t0068g0356a0001c0003t0001g0345a0001c0003t0067g0355others(5): Show | 8 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+9819_78+9825del others(7): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176971 | |||||
chr1:12177148
|
G | A | 26 | a0001c0001t0001g0297a0001c0001t0002g0326a0001c0001t0002g0327others(23): Show | 27 | HG00558.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+9979G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177148 | ||||||
chr1:12177282
|
C | T | 1 | a0002c0002t0009g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.78+10113C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177282 | ||||||
chr1:12177313
|
G | A | 1 | a0001c0001t0006g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+10144G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177313 | ||||||
chr1:12177364
|
G | A | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+10195G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177364 | ||||||
chr1:12177394
|
G | A | 2 | a0001c0004t0007g0216a0001c0004t0007g0220 | 2 | NA19000.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.78+10225G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177394 | ||||||
chr1:12177520
|
C | T | 4 | a0001c0001t0023g0026a0001c0001t0047g0035a0002c0002t0008g0351others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+10351C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177520 | ||||||
chr1:12177717
|
C | T | 4 | a0001c0003t0067g0355a0001c0003t0069g0354a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+10548C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177717 | ||||||
chr1:12177751
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.78+10582G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177751 | ||||||
chr1:12177760
|
C | G | 1 | a0001c0001t0002g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.78+10591C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177760 | ||||||
chr1:12177764
|
A | G | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.78+10595A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177764 | ||||||
chr1:12177794
|
C | CA | 37 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0297others(34): Show | 38 | HG00558.hp1 HG00558.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+10641dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12177794 | |||||
chr1:12177794
|
CA | C | 17 | a0001c0001t0001g0230a0001c0001t0002g0304a0001c0001t0006g0248others(14): Show | 17 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.78+10641delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12177794 | |||||
chr1:12177821
|
C | T | 1 | a0001c0001t0016g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.78+10652C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177821 | ||||||
chr1:12177921
|
C | T | 8 | a0001c0001t0068g0356a0001c0003t0001g0345a0001c0003t0067g0355others(5): Show | 8 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+10752C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177921 | ||||||
chr1:12178139
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-10657C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178139 | ||||||
chr1:12178303
|
G | A | 1 | a0001c0001t0065g0313 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79-10493G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178303 | ||||||
chr1:12178333
|
CG | C | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-10460delG | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12178333 | |||||
chr1:12178582
|
G | C | 1 | a0001c0001t0024g0225 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79-10214G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178582 | ||||||
chr1:12178689
|
G | A | 3 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033 | 3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.79-10107G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178689 | ||||||
chr1:12178772
|
C | G | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-10024C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178772 | ||||||
chr1:12178830
|
C | T | 5 | a0001c0001t0068g0356a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-9966C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178830 | ||||||
chr1:12178913
|
C | T | 11 | a0001c0001t0002g0224a0001c0001t0003g0251a0001c0001t0006g0154others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-9883C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178913 | ||||||
chr1:12178970
|
G | T | 3 | a0001c0001t0023g0026a0001c0001t0047g0035a0002c0002t0017g0034 | 3 | HG02717.hp1 HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.79-9826G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178970 | ||||||
chr1:12178972
|
G | A | 3 | a0001c0001t0011g0291a0001c0001t0018g0318a0002c0002t0011g0324 | 3 | HG02451.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.79-9824G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178972 | ||||||
chr1:12179032
|
G | A | 17 | a0001c0001t0023g0026a0001c0001t0047g0035a0001c0003t0001g0345others(14): Show | 17 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-9764G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179032 | ||||||
chr1:12179094
|
C | T | 4 | a0001c0003t0001g0345a0002c0002t0015g0013a0005c0007t0014g0346others(1): Show | 4 | HG01358.hp2 NA19009.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-9702C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179094 | ||||||
chr1:12179299
|
C | T | 2 | a0001c0001t0002g0180a0003c0005t0007g0184 | 2 | NA18975.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.79-9497C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179299 | ||||||
chr1:12179308
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.79-9488G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179308 | ||||||
chr1:12179463
|
C | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-9333C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179463 | ||||||
chr1:12179473
|
G | A | 14 | a0001c0001t0023g0026a0001c0001t0047g0035a0001c0003t0035g0029others(11): Show | 14 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-9323G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179473 | ||||||
chr1:12179756
|
G | A | 1 | a0001c0001t0001g0350 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.79-9040G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179756 | ||||||
chr1:12180031
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.79-8765G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180031 | ||||||
chr1:12180040
|
G | A | 4 | a0001c0003t0067g0355a0001c0003t0069g0354a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-8756G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180040 | ||||||
chr1:12180089
|
A | T | 2 | a0001c0001t0022g0177a0002c0002t0001g0151 | 2 | HG01069.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.79-8707A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180089 | ||||||
chr1:12180152
|
G | A | 1 | a0001c0001t0002g0304 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.79-8644G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180152 | ||||||
chr1:12180358
|
C | G | 1 | a0001c0001t0022g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.79-8438C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180358 | ||||||
chr1:12180539
|
A | T | 4 | a0001c0003t0067g0355a0001c0003t0069g0354a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-8257A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180539 | ||||||
chr1:12180619
|
G | A | 47 | a0001c0001t0001g0145a0001c0001t0002g0053a0001c0001t0002g0054others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.79-8177G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180619 | ||||||
chr1:12180635
|
C | T | 3 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033 | 3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.79-8161C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180635 | ||||||
chr1:12180665
|
T | G | 14 | a0001c0001t0023g0026a0001c0001t0047g0035a0001c0003t0035g0029others(11): Show | 14 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-8131T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180665 | ||||||
chr1:12180751
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.79-8045C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180751 | ||||||
chr1:12180767
|
T | G | 71 | a0001c0001t0001g0145a0001c0001t0002g0053a0001c0001t0002g0054others(68): Show | 71 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.79-8029T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180767 | ||||||
chr1:12180833
|
A | G | 2 | a0001c0001t0002g0347a0001c0001t0003g0348 | 2 | NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.79-7963A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180833 | ||||||
chr1:12180993
|
T | C | 14 | a0001c0001t0002g0289a0001c0001t0018g0043a0001c0001t0023g0026others(11): Show | 14 | HG01192.hp2 HG01358.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-7803T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180993 | ||||||
chr1:12181017
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-7779G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181017 | ||||||
chr1:12181086
|
G | A | 1 | a0001c0001t0008g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.79-7710G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181086 | ||||||
chr1:12181126
|
A | G | 2 | a0001c0001t0018g0043a0001c0001t0049g0025 | 2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.79-7670A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181126 | ||||||
chr1:12181205
|
T | C | 4 | a0001c0003t0067g0355a0001c0003t0069g0354a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-7591T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181205 | ||||||
chr1:12181267
|
T | C | 1 | a0001c0001t0056g0270 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.79-7529T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181267 | ||||||
chr1:12181412
|
A | G | 12 | a0001c0001t0001g0107a0001c0001t0018g0043a0001c0001t0021g0164others(9): Show | 12 | HG00597.hp2 HG01192.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.79-7384A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181412 | ||||||
chr1:12181546
|
C | T | 1 | a0002c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79-7250C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181546 | ||||||
chr1:12181554
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79-7242G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181554 | ||||||
chr1:12181615
|
G | A | 3 | a0001c0001t0004g0316a0001c0001t0028g0305a0001c0001t0028g0306 | 3 | HG01070.hp1 HG01071.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.79-7181G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181615 | ||||||
chr1:12181780
|
G | A | 1 | a0002c0002t0014g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.79-7016G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181780 | ||||||
chr1:12181798
|
T | G | 24 | a0001c0001t0002g0289a0001c0001t0003g0197a0001c0001t0009g0051others(21): Show | 24 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.79-6998T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181798 | ||||||
chr1:12181934
|
G | A | 58 | a0001c0001t0001g0297a0001c0001t0002g0289a0001c0001t0002g0328others(55): Show | 59 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.79-6862G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181934 | ||||||
chr1:12182022
|
C | T | 4 | a0001c0003t0067g0355a0001c0003t0069g0354a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-6774C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182022 | ||||||
chr1:12182039
|
C | T | 5 | a0001c0001t0021g0164a0001c0003t0001g0345a0002c0002t0008g0351others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-6757C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182039 | ||||||
chr1:12182140
|
G | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-6656G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182140 | ||||||
chr1:12182148
|
G | A | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-6648G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182148 | ||||||
chr1:12182401
|
T | C | 69 | a0001c0001t0004g0284a0001c0001t0008g0009a0001c0001t0008g0010others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.79-6395T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182401 | ||||||
chr1:12182520
|
T | C | 1 | a0001c0001t0017g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79-6276T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182520 | ||||||
chr1:12182562
|
T | C | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.79-6234T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182562 | ||||||
chr1:12182562
|
T | TTGAA | 60 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.79-6216_79-6213dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12182562 | |||||
chr1:12182647
|
G | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.79-6149G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182647 | ||||||
chr1:12182702
|
T | A | 7 | a0002c0002t0001g0321a0002c0002t0002g0030a0002c0002t0003g0028others(4): Show | 7 | HG00140.hp1 HG02004.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-6094T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182702 | ||||||
chr1:12182736
|
T | G | 64 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.79-6060T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182736 | ||||||
chr1:12182813
|
G | A | 38 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0034g0144others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-5983G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182813 | ||||||
chr1:12182857
|
G | A | 2 | a0001c0001t0027g0048a0001c0001t0027g0315 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.79-5939G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182857 | ||||||
chr1:12182892
|
A | G | 61 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.79-5904A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182892 | ||||||
chr1:12183084
|
C | T | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5712C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183084 | ||||||
chr1:12183133
|
C | T | 4 | a0001c0001t0002g0190a0001c0001t0002g0219a0001c0001t0002g0253others(1): Show | 4 | HG02132.hp2 NA18984.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5663C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183133 | ||||||
chr1:12183217
|
C | T | 64 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.79-5579C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183217 | ||||||
chr1:12183320
|
G | C | 67 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-5476G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183320 | ||||||
chr1:12183446
|
T | TTC | 10 | a0001c0001t0005g0325a0001c0003t0002g0342a0001c0003t0003g0047others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-5324_79-5323dup others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183446 | |||||
chr1:12183446
|
TTC | T | 320 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.79-5324_79-5323del others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183446 | |||||
chr1:12183492
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.79-5304A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183492 | ||||||
chr1:12183545
|
A | T | 1 | a0001c0001t0005g0089 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.79-5251A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183545 | ||||||
chr1:12183587
|
T | A | 1 | a0002c0002t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.79-5209T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183587 | ||||||
chr1:12183597
|
TTATC | T | 5 | a0001c0003t0001g0345a0001c0003t0035g0029a0002c0002t0011g0027others(2): Show | 5 | HG01358.hp2 HG02572.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-5185_79-5182del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183597 | |||||
chr1:12183605
|
CTATCTAT others(5): Show |
C | 3 | a0002c0002t0001g0172a0002c0002t0001g0173a0002c0002t0031g0150 | 3 | HG01168.hp2 HG01169.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.79-5189_79-5178del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183605 | |||||
chr1:12183609
|
CTATCTGT others(1): Show |
C | 35 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0034g0144others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-5185_79-5178del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183609 | |||||
chr1:12183617
|
T | C | 26 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(23): Show | 26 | HG00140.hp1 HG01106.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.79-5179T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183617 | ||||||
chr1:12183654
|
TTTTATCT others(3): Show |
T | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-5140_79-5131del others(10): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183654 | |||||
chr1:12183656
|
T | TTATC | 57 | a0001c0001t0001g0069a0001c0001t0001g0095a0001c0001t0001g0145others(54): Show | 59 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-5088_79-5085dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183656
|
T | TTATCTAT others(1): Show |
18 | a0001c0001t0001g0066a0001c0001t0002g0148a0001c0001t0002g0333others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5092_79-5085dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183656
|
T | TTATCTAT others(5): Show |
2 | a0001c0001t0002g0102a0001c0001t0007g0310 | 2 | HG02083.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.79-5096_79-5085dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183656
|
TTATC | T | 82 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0077others(79): Show | 83 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.79-5088_79-5085del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183656
|
TTATCTAT others(1): Show |
T | 31 | a0001c0001t0001g0055a0001c0001t0001g0134a0001c0001t0001g0230others(28): Show | 31 | HG00558.hp1 HG00738.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.79-5092_79-5085del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183656
|
TTATCTAT others(5): Show |
T | 19 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0001g0350others(16): Show | 19 | HG00438.hp2 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.79-5096_79-5085del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183656
|
TTATCTAT others(9): Show |
T | 5 | a0001c0001t0002g0116a0001c0001t0003g0126a0001c0001t0003g0127others(2): Show | 5 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-5100_79-5085del others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | |||||
chr1:12183675
|
T | G | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5121T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183675 | ||||||
chr1:12183679
|
TCTA | T | 3 | a0002c0002t0002g0162a0002c0002t0002g0163a0009c0012t0001g0125 | 3 | HG00099.hp2 HG03927.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.79-5116_79-5114del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183679 | ||||||
chr1:12183683
|
TCTA | T | 20 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0147others(17): Show | 20 | HG00423.hp2 HG01074.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-5112_79-5110del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183683 | ||||||
chr1:12183687
|
TCTA | T | 11 | a0002c0002t0001g0146a0002c0002t0001g0149a0002c0002t0001g0167others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-5108_79-5106del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183687 | ||||||
chr1:12183695
|
T | A | 2 | a0002c0002t0011g0027a0002c0002t0015g0267 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.79-5101T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183695 | ||||||
chr1:12183699
|
T | G | 7 | a0001c0003t0003g0047a0002c0002t0013g0031a0002c0002t0015g0032others(4): Show | 7 | HG01106.hp2 HG01243.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-5097T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183699 | ||||||
chr1:12183699
|
T | TCTATCTA others(9): Show |
1 | a0001c0003t0002g0342 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79-5090_79-5089ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183699 | |||||
chr1:12183699
|
T | TCTATCTA others(13): Show |
1 | a0001c0003t0059g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79-5086_79-5085ins others(20): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183699 | |||||
chr1:12183702
|
A | ATCTAGCT others(14): Show |
1 | a0002c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79-5090_79-5089ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183702 | |||||
chr1:12183703
|
T | A | 2 | a0002c0002t0002g0030a0002c0002t0003g0334 | 2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.79-5093T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183703 | ||||||
chr1:12183703
|
T | G | 2 | a0002c0002t0008g0351a0002c0002t0011g0324 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.79-5093T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183703 | ||||||
chr1:12183703
|
TCTATCTA others(5): Show |
T | 1 | a0002c0002t0003g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-5092_79-5081del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183703 | ||||||
chr1:12183706
|
A | AGCTAGCT others(10): Show |
1 | a0001c0003t0069g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.79-5090_79-5089ins others(17): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183706 | ||||||
chr1:12183707
|
T | A | 2 | a0002c0002t0001g0321a0002c0002t0014g0319 | 2 | HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.79-5089T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183707 | ||||||
chr1:12183707
|
T | G | 4 | a0001c0003t0035g0029a0002c0002t0008g0023a0002c0002t0011g0324others(1): Show | 4 | HG02717.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5089T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183707 | ||||||
chr1:12183710
|
A | AGCTAGCT others(17): Show |
1 | a0001c0003t0067g0355 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.79-5086_79-5085ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183710 | ||||||
chr1:12183710
|
A | AGCTATCT others(9): Show |
1 | a0001c0003t0035g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.79-5086_79-5085ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183710 | ||||||
chr1:12183710
|
AT | A | 38 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0146others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.79-5084delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183710 | |||||
chr1:12183711
|
T | A | 3 | a0001c0003t0035g0029a0001c0003t0067g0355a0002c0002t0011g0324 | 3 | HG02572.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.79-5085T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183711 | ||||||
chr1:12183711
|
T | TCTAGCTA others(9): Show |
1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79-5085_79-5084ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183711 | ||||||
chr1:12183711
|
T | TTCTA | 70 | a0001c0001t0001g0142a0001c0001t0001g0166a0001c0001t0001g0189others(67): Show | 70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.79-5080_79-5077dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | |||||
chr1:12183711
|
T | TTCTATCT others(5): Show |
1 | a0002c0002t0032g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79-5077_79-5076ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | |||||
chr1:12183711
|
T | TTCTATCT others(9): Show |
1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.79-5077_79-5076ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | |||||
chr1:12183711
|
T | TTCTATCT others(17): Show |
2 | a0001c0001t0002g0219a0001c0001t0024g0225 | 2 | NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.79-5077_79-5076ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | |||||
chr1:12183711
|
TTCTATCT others(42): Show |
T | 6 | a0001c0001t0037g0129a0001c0001t0037g0130a0002c0002t0002g0193others(3): Show | 6 | HG02572.hp1 HG02647.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-5084_79-5036del others(49): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183711 | ||||||
chr1:12183716
|
T | G | 1 | a0002c0002t0011g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-5080T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183716 | ||||||
chr1:12183720
|
C | A | 1 | a0002c0002t0003g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-5076C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183720 | ||||||
chr1:12183720
|
C | CCTAT | 27 | a0001c0001t0002g0102a0001c0001t0002g0115a0001c0001t0002g0293others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.79-5048_79-5045dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | |||||
chr1:12183720
|
C | CCTATCTA others(1): Show |
4 | a0001c0001t0011g0291a0001c0001t0055g0295a0002c0009t0018g0045others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5052_79-5045dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | |||||
chr1:12183720
|
C | CCTATCTA others(5): Show |
3 | a0001c0001t0003g0127a0001c0001t0006g0290a0001c0001t0010g0124 | 3 | HG01109.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-5056_79-5045dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | |||||
chr1:12183720
|
C | CCTATCTA others(9): Show |
1 | a0001c0001t0006g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-5060_79-5045dup others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | |||||
chr1:12183720
|
C | T | 66 | a0001c0001t0002g0160a0001c0001t0002g0175a0001c0001t0002g0219others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-5076C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183720 | ||||||
chr1:12183720
|
CCTAT | C | 18 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0002g0071others(15): Show | 18 | HG01081.hp2 HG01168.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5048_79-5045del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | |||||
chr1:12183724
|
T | C | 2 | a0001c0001t0001g0307a0001c0001t0005g0336 | 2 | HG03098.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.79-5072T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183724 | ||||||
chr1:12183728
|
T | C | 1 | a0001c0001t0066g0250 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.79-5068T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183728 | ||||||
chr1:12183728
|
TCTATCTA others(33): Show |
T | 4 | a0002c0002t0001g0146a0002c0002t0002g0030a0002c0002t0002g0163others(1): Show | 4 | HG00140.hp1 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5059_79-5020del others(40): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183728 | |||||
chr1:12183732
|
TCTATCTA others(29): Show |
T | 13 | a0002c0002t0001g0165a0002c0002t0001g0167a0002c0002t0001g0168others(10): Show | 13 | HG00099.hp2 HG01433.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-5055_79-5020del others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183732 | |||||
chr1:12183736
|
TCTATCTA others(25): Show |
T | 10 | a0002c0002t0001g0147a0002c0002t0001g0149a0002c0002t0001g0151others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-5051_79-5020del others(32): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183736 | |||||
chr1:12183740
|
TCTATCTA others(21): Show |
T | 9 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0207others(6): Show | 9 | HG00423.hp2 HG01074.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-5047_79-5020del others(28): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183740 | |||||
chr1:12183744
|
T | G | 2 | a0001c0001t0007g0287a0001c0001t0016g0059 | 2 | HG01433.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-5052T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183744 | ||||||
chr1:12183744
|
T | TCTAG | 3 | a0001c0001t0002g0011a0001c0001t0017g0012a0001c0001t0018g0318 | 3 | HG02451.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.79-5049_79-5048ins others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183744 | |||||
chr1:12183744
|
TCTATCTA others(17): Show |
T | 3 | a0002c0002t0003g0028a0002c0002t0009g0185a0002c0002t0031g0150 | 3 | HG01515.hp2 HG01934.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79-5044_79-5021del others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183744 | |||||
chr1:12183748
|
T | G | 83 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(80): Show | 84 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.79-5048T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183748 | ||||||
chr1:12183748
|
T | TCTAG | 14 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(11): Show | 14 | HG00639.hp2 HG00673.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-5028_79-5025dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
T | TCTAGCTA others(1): Show |
13 | a0001c0001t0001g0189a0001c0001t0002g0183a0001c0001t0002g0205others(10): Show | 13 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-5032_79-5025dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
T | TCTATCTA others(1): Show |
34 | a0001c0001t0001g0142a0001c0001t0001g0166a0001c0001t0001g0275others(31): Show | 34 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.79-5045_79-5044ins others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
T | TCTATCTA others(5): Show |
1 | a0001c0001t0014g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.79-5045_79-5044ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
T | TCTATCTA others(5): Show |
11 | a0001c0001t0001g0240a0001c0001t0002g0253a0001c0001t0002g0326others(8): Show | 11 | HG02040.hp2 HG02132.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-5045_79-5044ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
T | TCTATCTA others(33): Show |
1 | a0001c0001t0001g0343 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79-5045_79-5044ins others(40): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
T | TCTATCTA others(9): Show |
8 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0244others(5): Show | 8 | HG01069.hp1 HG01934.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-5045_79-5044ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183748
|
TCTAGCTA others(1): Show |
T | 4 | a0001c0001t0001g0134a0001c0001t0003g0131a0001c0001t0012g0132others(1): Show | 4 | HG00733.hp2 HG02258.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5032_79-5025del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | |||||
chr1:12183752
|
G | T | 16 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0003t0002g0342others(13): Show | 16 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.79-5044G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183752 | ||||||
chr1:12183755
|
A | ATCTATCT others(2): Show |
8 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(5): Show | 8 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-5041_79-5040ins others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183755 | ||||||
chr1:12183755
|
AGCTAGCT others(8): Show |
A | 1 | a0001c0003t0003g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-5040_79-5026del others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183755 | ||||||
chr1:12183756
|
G | T | 18 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0035g0029others(15): Show | 18 | HG01106.hp2 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5040G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183756 | ||||||
chr1:12183759
|
AGCTAGCT others(4): Show |
A | 1 | a0001c0003t0002g0342 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79-5036_79-5026del others(11): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183759 | ||||||
chr1:12183760
|
G | T | 18 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0059g0044others(15): Show | 18 | HG01243.hp2 HG01358.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.79-5036G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183760 | ||||||
chr1:12183764
|
G | C | 8 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(5): Show | 8 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-5032G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183764 | ||||||
chr1:12183764
|
G | T | 21 | a0001c0001t0002g0049a0001c0001t0003g0050a0001c0001t0003g0197others(18): Show | 21 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-5032G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183764 | ||||||
chr1:12183767
|
AGCT | A | 4 | a0002c0002t0015g0032a0002c0002t0017g0033a0002c0002t0038g0357others(1): Show | 4 | HG01243.hp2 HG02257.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5028_79-5026del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183767 | ||||||
chr1:12183768
|
G | C | 10 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(7): Show | 10 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-5028G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183768 | ||||||
chr1:12183768
|
G | T | 10 | a0001c0001t0037g0129a0001c0001t0037g0130a0002c0002t0002g0193others(7): Show | 10 | HG01106.hp2 HG01358.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-5028G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183768 | ||||||
chr1:12183771
|
A | T | 8 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-5025A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183771 | ||||||
chr1:12183772
|
T | C | 2 | a0002c0002t0021g0179a0002c0002t0025g0194 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-5024T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183772 | ||||||
chr1:12183775
|
AT | A | 14 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(11): Show | 14 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-5019delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183775 | |||||
chr1:12183776
|
T | TCTA | 6 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-5020_79-5019ins others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183776 | ||||||
chr1:12183781
|
T | C | 10 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(7): Show | 10 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-5015T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183781 | ||||||
chr1:12183785
|
C | G | 6 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-5011C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183785 | ||||||
chr1:12183785
|
C | T | 4 | a0002c0002t0002g0022a0002c0002t0021g0179a0002c0002t0025g0194others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5011C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183785 | ||||||
chr1:12183789
|
C | CCTAT | 47 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0034g0144others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.79-4995_79-4992dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183789 | |||||
chr1:12183789
|
C | G | 2 | a0002c0002t0002g0022a0002c0002t0032g0024 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79-5007C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183789 | ||||||
chr1:12183789
|
C | T | 18 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(15): Show | 18 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5007C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183789 | ||||||
chr1:12183793
|
T | G | 2 | a0002c0002t0021g0179a0002c0002t0025g0194 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-5003T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183793 | ||||||
chr1:12183796
|
A | AT | 6 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-4999dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183796 | |||||
chr1:12183805
|
G | C | 5 | a0001c0003t0035g0029a0001c0003t0067g0355a0001c0003t0069g0354others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-4991G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183805 | ||||||
chr1:12183805
|
G | T | 5 | a0001c0001t0029g0228a0001c0001t0054g0239a0001c0003t0001g0345others(2): Show | 5 | HG02717.hp2 HG03579.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-4991G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183805 | ||||||
chr1:12183808
|
A | T | 2 | a0002c0002t0021g0179a0002c0002t0025g0194 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-4988A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183808 | ||||||
chr1:12183809
|
T | C | 2 | a0002c0002t0002g0022a0002c0002t0032g0024 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79-4987T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183809 | ||||||
chr1:12183816
|
AT | A | 10 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(7): Show | 10 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-4978delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183816 | |||||
chr1:12183817
|
T | TTCTATCT others(1): Show |
3 | a0002c0002t0002g0030a0002c0002t0038g0357a0002c0002t0038g0358 | 3 | HG02004.hp2 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.79-4978_79-4971dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183817 | |||||
chr1:12183817
|
T | TTCTATCT others(5): Show |
6 | a0002c0002t0001g0321a0002c0002t0003g0028a0002c0002t0003g0334others(3): Show | 6 | HG00140.hp1 HG02056.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-4971_79-4970ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183817 | |||||
chr1:12183817
|
T | TTCTATCT others(9): Show |
1 | a0002c0002t0011g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.79-4971_79-4970ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183817 | |||||
chr1:12183826
|
C | CCTAT | 20 | a0001c0001t0001g0085a0001c0001t0001g0142a0001c0001t0001g0221others(17): Show | 20 | HG01069.hp1 HG01167.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-4946_79-4943dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183826 | |||||
chr1:12183826
|
C | CCTATCTA others(5): Show |
1 | a0002c0002t0011g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-4954_79-4943dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183826 | |||||
chr1:12183826
|
C | T | 59 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-4970C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183826 | ||||||
chr1:12183842
|
T | C | 1 | a0001c0003t0001g0345 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.79-4954T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183842 | ||||||
chr1:12183846
|
T | C | 1 | a0001c0003t0001g0345 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.79-4950T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183846 | ||||||
chr1:12183850
|
T | C | 4 | a0001c0001t0010g0241a0001c0003t0001g0345a0001c0003t0035g0029others(1): Show | 4 | HG02155.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-4946T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183850 | ||||||
chr1:12183850
|
T | TCTATCTA others(5): Show |
1 | a0005c0007t0016g0344 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.79-4943_79-4942ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | |||||
chr1:12183850
|
T | TCTATCTA others(5): Show |
18 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0151others(15): Show | 18 | HG00099.hp2 HG00423.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-4943_79-4942ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | |||||
chr1:12183850
|
T | TCTATCTA others(9): Show |
1 | a0005c0007t0014g0346 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79-4943_79-4942ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | |||||
chr1:12183850
|
T | TCTATCTA others(9): Show |
9 | a0002c0002t0001g0146a0002c0002t0001g0165a0002c0002t0001g0172others(6): Show | 9 | HG01074.hp1 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-4943_79-4942ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | |||||
chr1:12183850
|
T | TCTATCTA others(13): Show |
10 | a0001c0001t0037g0129a0001c0001t0037g0130a0002c0002t0001g0149others(7): Show | 10 | HG01106.hp2 HG01243.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-4943_79-4942ins others(20): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | |||||
chr1:12183850
|
T | TCTATCTA others(17): Show |
1 | a0002c0002t0025g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.79-4943_79-4942ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | |||||
chr1:12184111
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0085a0004c0006t0001g0093others(1): Show | 4 | HG02280.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-4685A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184111 | ||||||
chr1:12184180
|
GA | G | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-4615delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184180 | ||||||
chr1:12184201
|
A | G | 67 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-4595A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184201 | ||||||
chr1:12184261
|
T | C | 68 | a0001c0001t0004g0280a0001c0001t0037g0129a0001c0001t0037g0130others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.79-4535T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184261 | ||||||
chr1:12184345
|
AT | A | 7 | a0001c0001t0001g0107a0001c0001t0004g0339a0001c0001t0051g0237others(4): Show | 7 | HG00597.hp2 HG01106.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-4436delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12184345 | |||||
chr1:12184443
|
A | G | 4 | a0002c0002t0021g0179a0002c0002t0025g0194a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02559.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-4353A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184443 | ||||||
chr1:12184482
|
G | C | 1 | a0001c0001t0011g0291 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79-4314G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184482 | ||||||
chr1:12184570
|
G | A | 1 | a0002c0002t0011g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-4226G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184570 | ||||||
chr1:12184594
|
C | T | 1 | a0001c0001t0024g0225 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79-4202C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184594 | ||||||
chr1:12184647
|
C | T | 4 | a0001c0001t0006g0259a0001c0001t0011g0266a0001c0001t0025g0268others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-4149C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184647 | ||||||
chr1:12184657
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0009g0068 | 2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.79-4139G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184657 | ||||||
chr1:12184855
|
C | T | 1 | a0001c0001t0014g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.79-3941C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184855 | ||||||
chr1:12184949
|
C | T | 1 | a0002c0002t0008g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-3847C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184949 | ||||||
chr1:12184972
|
T | C | 67 | a0001c0001t0023g0026a0001c0001t0037g0129a0001c0001t0037g0130others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-3824T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184972 | ||||||
chr1:12185095
|
G | A | 2 | a0001c0001t0002g0180a0003c0005t0003g0195 | 2 | HG00597.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.79-3701G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185095 | ||||||
chr1:12185095
|
GCAGTTAG others(23): Show |
G | 1 | a0002c0002t0008g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-3700_79-3671del others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185095 | ||||||
chr1:12185179
|
G | A | 1 | a0001c0001t0009g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.79-3617G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185179 | ||||||
chr1:12185298
|
G | A | 1 | a0001c0001t0009g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79-3498G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185298 | ||||||
chr1:12185303
|
CCTTTTT | C | 64 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.79-3482_79-3477del others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12185303 | |||||
chr1:12185344
|
C | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-3452C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185344 | ||||||
chr1:12185437
|
T | TC | 38 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0034g0144others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-3353dupC | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12185437 | |||||
chr1:12185443
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.79-3353C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185443 | ||||||
chr1:12185559
|
G | T | 1 | a0001c0001t0003g0312 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79-3237G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185559 | ||||||
chr1:12185651
|
T | G | 67 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0001g0345others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-3145T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185651 | ||||||
chr1:12185675
|
T | A | 38 | a0001c0001t0037g0129a0001c0001t0037g0130a0001c0003t0034g0144others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-3121T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185675 | ||||||
chr1:12186118
|
C | T | 79 | a0001c0001t0001g0142a0001c0001t0001g0166a0001c0001t0001g0189others(76): Show | 79 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-2678C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186118 | ||||||
chr1:12186126
|
C | A | 7 | a0001c0003t0035g0029a0001c0003t0067g0355a0001c0003t0069g0354others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-2670C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186126 | ||||||
chr1:12186143
|
G | A | 1 | a0001c0001t0026g0317 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.79-2653G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186143 | ||||||
chr1:12186212
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.79-2584G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186212 | ||||||
chr1:12186275
|
C | T | 1 | a0001c0001t0029g0117 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.79-2521C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186275 | ||||||
chr1:12186419
|
G | A | 1 | a0001c0001t0003g0192 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.79-2377G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186419 | ||||||
chr1:12186526
|
ATATGTTA others(41): Show |
A | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-2269_79-2222del others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186526 | ||||||
chr1:12186723
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.79-2073G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186723 | ||||||
chr1:12186951
|
C | G | 36 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0146others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.79-1845C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186951 | ||||||
chr1:12187071
|
C | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79-1725C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187071 | ||||||
chr1:12187253
|
A | G | 42 | a0001c0001t0001g0297a0001c0001t0002g0053a0001c0001t0002g0054others(39): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.79-1543A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187253 | ||||||
chr1:12187309
|
A | G | 4 | a0002c0002t0021g0179a0002c0002t0025g0194a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02559.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-1487A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187309 | ||||||
chr1:12187438
|
C | T | 3 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044 | 3 | HG02109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-1358C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187438 | ||||||
chr1:12187453
|
C | T | 1 | a0002c0002t0008g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-1343C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187453 | ||||||
chr1:12187470
|
C | T | 3 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044 | 3 | HG02109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-1326C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187470 | ||||||
chr1:12187681
|
A | AAGTCTTG others(3): Show |
1 | a0001c0001t0032g0121 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.79-1112_79-1103dup others(10): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12187681 | |||||
chr1:12187883
|
C | T | 10 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(7): Show | 10 | HG01358.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-913C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187883 | ||||||
chr1:12187886
|
G | T | 8 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(5): Show | 8 | HG01106.hp2 HG01243.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-910G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187886 | ||||||
chr1:12187953
|
G | A | 1 | a0002c0002t0040g0211 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.79-843G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187953 | ||||||
chr1:12188183
|
ATG | A | 36 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0146others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.79-612_79-611delTG | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188183 | ||||||
chr1:12188234
|
G | C | 67 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-562G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188234 | ||||||
chr1:12188290
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-506C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188290 | ||||||
chr1:12188293
|
G | A | 2 | a0001c0001t0002g0099a0001c0001t0002g0100 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.79-503G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188293 | ||||||
chr1:12188368
|
T | A | 67 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-428T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188368 | ||||||
chr1:12188446
|
G | A | 36 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0146others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.79-350G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188446 | ||||||
chr1:12188470
|
C | T | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-326C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188470 | ||||||
chr1:12188501
|
G | A | 4 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-295G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188501 | ||||||
chr1:12188542
|
A | T | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-254A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188542 | ||||||
chr1:12188596
|
G | GGGGGAGG others(74): Show |
1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-199_79-198insGG others(79): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12188596 | |||||
chr1:12188598
|
T | A | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-198T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188598 | ||||||
chr1:12188628
|
G | A | 4 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-168G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188628 | ||||||
chr1:12188639
|
C | T | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-157C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188639 | ||||||
chr1:12188655
|
G | A | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-141G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188655 | ||||||
chr1:12188682
|
A | T | 6 | a0001c0001t0002g0049a0001c0001t0003g0050a0001c0001t0003g0197others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-114A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188682 | ||||||
chr1:12188683
|
G | C | 2 | a0001c0001t0018g0043a0001c0001t0049g0025 | 2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.79-113G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188683 | ||||||
chr1:12188710
|
C | A | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-86C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188710 | ||||||
chr1:12188722
|
G | A | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-74G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188722 | ||||||
chr1:12188739
|
G | A | 1 | a0002c0002t0040g0211 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.79-57G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188739 | ||||||
chr1:12188744
|
G | C | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-52G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188744 | ||||||
chr1:12188748
|
A | G | 1 | a0001c0001t0005g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-48A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188748 | ||||||
chr1:12188908
|
A | G | 67 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.178+13A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12188908 | ||||||
chr1:12188963
|
C | T | 63 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.178+68C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12188963 | ||||||
chr1:12188974
|
A | G | 212 | a0001c0001t0001g0142a0001c0001t0001g0166a0001c0001t0001g0189others(209): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.178+79A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12188974 | ||||||
chr1:12189027
|
C | G | 6 | a0001c0003t0035g0029a0001c0003t0067g0355a0001c0003t0069g0354others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+132C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189027 | ||||||
chr1:12189069
|
C | T | 2 | a0002c0002t0021g0179a0002c0002t0025g0194 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.178+174C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189069 | ||||||
chr1:12189157
|
C | A | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+262C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189157 | ||||||
chr1:12189175
|
T | A | 50 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0034g0144others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.178+280T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189175 | ||||||
chr1:12189175
|
T | C | 13 | a0001c0003t0001g0345a0001c0003t0035g0029a0001c0003t0067g0355others(10): Show | 13 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+280T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189175 | ||||||
chr1:12189248
|
C | T | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.178+353C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189248 | ||||||
chr1:12189265
|
G | T | 2 | a0001c0001t0018g0043a0001c0001t0049g0025 | 2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.178+370G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189265 | ||||||
chr1:12189287
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.178+392T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189287 | ||||||
chr1:12189369
|
C | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.178+474C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189369 | ||||||
chr1:12189417
|
C | T | 1 | a0002c0002t0001g0321 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.178+522C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189417 | ||||||
chr1:12189466
|
G | T | 3 | a0002c0002t0002g0022a0002c0002t0011g0324a0002c0002t0032g0024 | 3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.178+571G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189466 | ||||||
chr1:12189511
|
A | C | 19 | a0001c0003t0001g0345a0002c0002t0001g0321a0002c0002t0002g0022others(16): Show | 19 | HG00140.hp1 HG01106.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+616A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189511 | ||||||
chr1:12189515
|
G | C | 1 | a0002c0002t0003g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178+620G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189515 | ||||||
chr1:12189558
|
A | G | 1 | a0001c0001t0002g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.178+663A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189558 | ||||||
chr1:12189586
|
A | T | 64 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.178+691A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189586 | ||||||
chr1:12189713
|
G | A | 60 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.178+818G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189713 | ||||||
chr1:12189720
|
C | T | 3 | a0001c0001t0012g0006a0001c0001t0012g0204a0001c0001t0061g0245 | 3 | NA18993.hp2 NA18995.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.178+825C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189720 | ||||||
chr1:12189759
|
C | T | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+864C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189759 | ||||||
chr1:12189772
|
A | G | 60 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.178+877A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189772 | ||||||
chr1:12189808
|
G | C | 60 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.178+913G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189808 | ||||||
chr1:12189826
|
A | G | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+931A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189826 | ||||||
chr1:12189881
|
G | A | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+986G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189881 | ||||||
chr1:12189931
|
G | A | 60 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.179-1026G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189931 | ||||||
chr1:12189947
|
T | C | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.179-1010T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189947 | ||||||
chr1:12190037
|
T | C | 5 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-920T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190037 | ||||||
chr1:12190131
|
C | A | 3 | a0001c0003t0001g0345a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 NA19009.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.179-826C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190131 | ||||||
chr1:12190380
|
G | A | 64 | a0001c0003t0001g0345a0001c0003t0002g0342a0001c0003t0003g0047others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.179-577G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190380 | ||||||
chr1:12190458
|
C | CA | 42 | a0001c0001t0001g0275a0001c0001t0002g0104a0001c0001t0002g0183others(39): Show | 42 | HG00323.hp1 HG00639.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-477dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | |||||
chr1:12190458
|
C | CAAA | 6 | a0001c0003t0002g0342a0001c0003t0059g0044a0002c0002t0008g0023others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-479_179-477dup others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | |||||
chr1:12190458
|
C | CAAAAA | 35 | a0001c0003t0034g0144a0002c0002t0001g0143a0002c0002t0001g0146others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.179-481_179-477dup others(5): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | |||||
chr1:12190458
|
C | CAAAAAA | 10 | a0002c0002t0001g0147a0002c0002t0001g0167a0002c0002t0001g0207others(7): Show | 10 | HG02683.hp1 HG03654.hp2 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.179-482_179-477dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | |||||
chr1:12190458
|
CA | C | 8 | a0001c0001t0001g0189a0001c0001t0001g0230a0001c0001t0002g0114others(5): Show | 8 | HG03041.hp1 NA18942.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-477delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | |||||
chr1:12190831
|
T | C | 11 | a0001c0001t0001g0134a0001c0001t0003g0131a0001c0001t0009g0051others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-126T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190831 | ||||||
chr1:12190837
|
T | G | 6 | a0001c0001t0002g0049a0001c0001t0003g0050a0001c0001t0003g0197others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-120T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190837 | ||||||
chr1:12190922
|
C | T | 9 | a0002c0002t0001g0321a0002c0002t0002g0030a0002c0002t0003g0028others(6): Show | 9 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-35C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190922 | ||||||
chr1:12191134
|
T | A | 42 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0147others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.307+49T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191134 | ||||||
chr1:12191195
|
T | C | 3 | a0002c0002t0002g0022a0002c0002t0011g0324a0002c0002t0032g0024 | 3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.307+110T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191195 | ||||||
chr1:12191221
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0006g0014a0001c0001t0011g0015 | 3 | HG01884.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.307+136T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191221 | ||||||
chr1:12191224
|
C | A | 2 | a0001c0001t0002g0219a0001c0001t0002g0264 | 2 | NA18984.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.307+139C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191224 | ||||||
chr1:12191261
|
G | A | 46 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0147others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.307+176G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191261 | ||||||
chr1:12191284
|
A | C | 13 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(10): Show | 13 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.307+199A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191284 | ||||||
chr1:12191353
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.307+268G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191353 | ||||||
chr1:12191443
|
C | T | 3 | a0001c0001t0003g0231a0001c0001t0006g0232a0001c0001t0006g0233 | 3 | HG01069.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.308-331C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191443 | ||||||
chr1:12191465
|
A | G | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.308-309A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191465 | ||||||
chr1:12191489
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0002g0349a0001c0001t0002g0352 | 3 | HG01256.hp1 NA19074.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.308-285G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191489 | ||||||
chr1:12191549
|
AGGACTGC others(11): Show |
A | 4 | a0002c0002t0013g0031a0002c0002t0015g0032a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-189_308-172del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 12191549 | |||||
chr1:12191685
|
C | T | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.308-89C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191685 | ||||||
chr1:12191690
|
T | G | 1 | a0001c0001t0019g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.308-84T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191690 | ||||||
chr1:12191699
|
G | C | 1 | a0002c0002t0034g0178 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.308-75G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191699 | ||||||
chr1:12191708
|
T | G | 63 | a0001c0001t0064g0265a0001c0003t0002g0342a0001c0003t0003g0047others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.308-66T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191708 | ||||||
chr1:12191751
|
T | G | 109 | a0001c0001t0001g0297a0001c0001t0002g0053a0001c0001t0002g0054others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.308-23T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191751 | ||||||
chr1:12192276
|
C | CTG | 85 | a0001c0001t0001g0055a0001c0001t0001g0066a0001c0001t0001g0069others(82): Show | 87 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.458-125_458-124dup others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | |||||
chr1:12192276
|
C | CTGTG | 21 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0077others(18): Show | 21 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.458-127_458-124dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | |||||
chr1:12192276
|
C | CTGTGTG | 10 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-129_458-124dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | |||||
chr1:12192276
|
CTG | C | 11 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0102others(8): Show | 11 | HG00738.hp2 HG01358.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-125_458-124del others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | |||||
chr1:12192276
|
CTGTG | C | 25 | a0001c0001t0013g0037a0001c0001t0032g0121a0002c0002t0001g0147others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.458-127_458-124del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | |||||
chr1:12192276
|
CTGTGTGT others(1): Show |
C | 19 | a0002c0002t0001g0143a0002c0002t0001g0151a0002c0002t0001g0198others(16): Show | 19 | HG00423.hp2 HG01074.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-131_458-124del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | |||||
chr1:12192393
|
T | G | 1 | a0003c0005t0019g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.458-38T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | chr1 | 12192393 | ||||||
chr1:12192595
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.551+71C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 5/9 | chr1 | 12192595 | ||||||
chr1:12192835
|
C | T | 59 | a0001c0003t0002g0342a0001c0003t0003g0047a0001c0003t0059g0044others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.552-28C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 5/9 | chr1 | 12192835 | ||||||
chr1:12193294
|
T | C | 53 | a0001c0001t0002g0304a0002c0002t0001g0143a0002c0002t0001g0147others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.787+196T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193294 | ||||||
chr1:12193406
|
T | A | 1 | a0005c0007t0014g0346 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.787+308T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193406 | ||||||
chr1:12193735
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0009g0068 | 2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.788-220G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193735 | ||||||
chr1:12193842
|
C | T | 4 | a0002c0002t0021g0179a0002c0002t0025g0194a0002c0002t0038g0357others(1): Show | 4 | HG02257.hp1 HG02559.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-113C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193842 | ||||||
chr1:12194144
|
G | A | 45 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0147others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.865+112G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194144 | ||||||
chr1:12194356
|
C | T | 1 | a0001c0004t0007g0137 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.866-228C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194356 | ||||||
chr1:12194381
|
G | T | 1 | a0001c0001t0047g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.866-203G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194381 | ||||||
chr1:12194573
|
C | G | 1 | a0006c0013t0001g0182 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.866-11C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194573 | ||||||
chr1:12194986
|
A | T | 1 | a0001c0001t0056g0270 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.900+368A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12194986 | ||||||
chr1:12195178
|
T | A | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.900+560T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195178 | ||||||
chr1:12195275
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0004g0235 | 2 | NA18942.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.900+657A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195275 | ||||||
chr1:12195303
|
A | C | 45 | a0001c0001t0003g0021a0001c0001t0006g0353a0001c0001t0008g0009others(42): Show | 45 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.900+685A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195303 | ||||||
chr1:12195501
|
C | G | 5 | a0002c0002t0002g0022a0002c0002t0008g0023a0002c0002t0008g0351others(2): Show | 5 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+883C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195501 | ||||||
chr1:12195691
|
G | C | 26 | a0001c0001t0001g0107a0001c0001t0001g0201a0001c0001t0001g0230others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.900+1073G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195691 | ||||||
chr1:12195747
|
C | G | 1 | a0001c0001t0006g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.900+1129C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195747 | ||||||
chr1:12195844
|
G | A | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.900+1226G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195844 | ||||||
chr1:12196007
|
A | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.900+1389A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196007 | ||||||
chr1:12196114
|
A | G | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.900+1496A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196114 | ||||||
chr1:12196685
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.900+2067C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196685 | ||||||
chr1:12196782
|
C | T | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.900+2164C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196782 | ||||||
chr1:12196800
|
G | A | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.900+2182G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196800 | ||||||
chr1:12196804
|
G | A | 1 | a0002c0002t0031g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.900+2186G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196804 | ||||||
chr1:12196813
|
G | T | 3 | a0001c0001t0003g0016a0001c0001t0006g0296a0001c0001t0055g0295 | 3 | HG02055.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.900+2195G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196813 | ||||||
chr1:12196852
|
C | T | 1 | a0001c0001t0017g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.900+2234C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196852 | ||||||
chr1:12196884
|
C | G | 9 | a0002c0002t0001g0151a0002c0002t0001g0321a0002c0002t0002g0030others(6): Show | 9 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.900+2266C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196884 | ||||||
chr1:12196940
|
A | AT | 53 | a0001c0001t0003g0021a0001c0001t0006g0353a0002c0002t0001g0143others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.900+2332dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12196940 | |||||
chr1:12196948
|
T | C | 1 | a0001c0001t0009g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.900+2330T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196948 | ||||||
chr1:12196963
|
T | C | 2 | a0001c0001t0005g0249a0001c0001t0005g0336 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.900+2345T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196963 | ||||||
chr1:12196987
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.900+2369G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196987 | ||||||
chr1:12197310
|
T | C | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.900+2692T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197310 | ||||||
chr1:12197333
|
A | G | 12 | a0001c0001t0006g0353a0001c0001t0008g0009a0001c0001t0008g0010others(9): Show | 12 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.900+2715A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197333 | ||||||
chr1:12197342
|
C | G | 46 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0147others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.900+2724C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197342 | ||||||
chr1:12197540
|
GGGAGCAT others(16): Show |
G | 2 | a0005c0007t0014g0346a0005c0007t0016g0344 | 2 | HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.900+2923_900+2945d others(25): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197540 | ||||||
chr1:12197599
|
T | C | 10 | a0001c0001t0006g0353a0002c0002t0002g0022a0002c0002t0008g0023others(7): Show | 10 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.900+2981T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197599 | ||||||
chr1:12197708
|
C | T | 1 | a0001c0001t0007g0322 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.900+3090C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197708 | ||||||
chr1:12197712
|
G | A | 5 | a0001c0001t0006g0353a0002c0002t0013g0031a0002c0002t0015g0032others(2): Show | 5 | HG01106.hp2 HG01243.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+3094G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197712 | ||||||
chr1:12197796
|
G | C | 4 | a0002c0002t0002g0022a0002c0002t0008g0351a0002c0002t0011g0324others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+3178G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197796 | ||||||
chr1:12197897
|
G | T | 1 | a0002c0002t0015g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.900+3279G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197897 | ||||||
chr1:12197900
|
C | T | 1 | a0001c0001t0016g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.900+3282C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197900 | ||||||
chr1:12197942
|
A | G | 4 | a0001c0001t0010g0004a0001c0001t0010g0292a0001c0001t0047g0035others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+3324A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197942 | ||||||
chr1:12197953
|
A | G | 2 | a0001c0001t0010g0004a0001c0001t0010g0292 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.900+3335A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197953 | ||||||
chr1:12197998
|
G | A | 1 | a0002c0002t0015g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.900+3380G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197998 | ||||||
chr1:12198036
|
A | G | 1 | a0001c0001t0005g0062 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.900+3418A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198036 | ||||||
chr1:12198046
|
C | T | 2 | a0005c0007t0014g0346a0005c0007t0016g0344 | 2 | HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.900+3428C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198046 | ||||||
chr1:12198117
|
A | G | 64 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0006g0353others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.900+3499A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198117 | ||||||
chr1:12198121
|
C | CA | 15 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0002g0183others(12): Show | 15 | HG00408.hp1 HG01261.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.900+3523dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198121 | |||||
chr1:12198121
|
CA | C | 149 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(146): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.900+3523delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198121 | |||||
chr1:12198121
|
CAA | C | 19 | a0001c0001t0002g0011a0001c0001t0006g0259a0001c0001t0008g0007others(16): Show | 19 | HG01167.hp2 HG01192.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.900+3522_900+3523d others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198121 | |||||
chr1:12198174
|
T | C | 73 | a0001c0001t0002g0224a0001c0001t0002g0326a0001c0001t0002g0327others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.900+3556T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198174 | ||||||
chr1:12198196
|
C | T | 1 | a0001c0001t0043g0274 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.900+3578C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198196 | ||||||
chr1:12198231
|
C | T | 4 | a0001c0001t0006g0353a0002c0002t0013g0031a0002c0002t0017g0033others(1): Show | 4 | HG01106.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+3613C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198231 | ||||||
chr1:12198452
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.901-3515C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198452 | ||||||
chr1:12198517
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0004g0235 | 2 | NA18942.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.901-3450C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198517 | ||||||
chr1:12198659
|
TGCTGGCT others(5): Show |
T | 20 | a0001c0001t0002g0011a0001c0001t0006g0259a0001c0001t0008g0007others(17): Show | 20 | HG01167.hp2 HG01192.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.901-3294_901-3283d others(14): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198659 | |||||
chr1:12198673
|
C | A | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3294C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198673 | ||||||
chr1:12198674
|
T | A | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3293T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198674 | ||||||
chr1:12198675
|
G | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3292G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198675 | ||||||
chr1:12198676
|
G | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3291G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198676 | ||||||
chr1:12198680
|
G | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3287G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198680 | ||||||
chr1:12198681
|
C | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3286C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198681 | ||||||
chr1:12198683
|
G | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3284G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198683 | ||||||
chr1:12198684
|
G | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3283G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198684 | ||||||
chr1:12198685
|
A | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3282A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198685 | ||||||
chr1:12198686
|
A | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3281A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198686 | ||||||
chr1:12198689
|
C | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3278C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198689 | ||||||
chr1:12198691
|
G | GT | 46 | a0001c0001t0001g0142a0001c0001t0001g0223a0001c0001t0001g0240others(43): Show | 46 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.901-3259dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTT | 8 | a0001c0001t0008g0007a0001c0001t0008g0008a0001c0001t0008g0294others(5): Show | 8 | HG00544.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.901-3260_901-3259d others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTGTT others(6): Show |
1 | a0001c0001t0047g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.901-3272_901-3271i others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0013g0037a0002c0002t0011g0324 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.901-3268_901-3259d others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTTTT others(4): Show |
15 | a0001c0001t0001g0297a0001c0001t0002g0120a0001c0001t0002g0171others(12): Show | 15 | HG00323.hp2 HG01255.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.901-3269_901-3259d others(13): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTTTT others(5): Show |
121 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.901-3270_901-3259d others(14): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTTTT others(6): Show |
63 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0098others(60): Show | 63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.901-3271_901-3259d others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTTTT others(7): Show |
10 | a0001c0001t0002g0039a0001c0001t0002g0099a0001c0001t0002g0100others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.901-3272_901-3259d others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0005g0113 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.901-3273_901-3259d others(17): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | |||||
chr1:12198691
|
G | T | 1 | a0002c0002t0038g0358 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3276G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198691 | ||||||
chr1:12198884
|
G | T | 39 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0057g0330others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.901-3083G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198884 | ||||||
chr1:12198972
|
T | G | 11 | a0001c0001t0001g0307a0001c0001t0003g0118a0001c0001t0003g0218others(8): Show | 11 | HG00140.hp2 HG02027.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-2995T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198972 | ||||||
chr1:12198981
|
C | T | 1 | a0001c0001t0011g0291 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.901-2986C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198981 | ||||||
chr1:12199137
|
T | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0074others(7): Show | 11 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.901-2830T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199137 | ||||||
chr1:12199278
|
G | T | 1 | a0001c0001t0002g0303 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.901-2689G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199278 | ||||||
chr1:12199316
|
T | C | 6 | a0001c0001t0008g0009a0001c0001t0008g0010a0002c0002t0002g0022others(3): Show | 6 | HG02055.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-2651T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199316 | ||||||
chr1:12199440
|
G | T | 1 | a0001c0001t0010g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.901-2527G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199440 | ||||||
chr1:12199461
|
G | A | 1 | a0002c0002t0003g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.901-2506G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199461 | ||||||
chr1:12199495
|
G | T | 1 | a0001c0001t0009g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.901-2472G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199495 | ||||||
chr1:12199962
|
G | C | 1 | a0001c0001t0014g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901-2005G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199962 | ||||||
chr1:12199963
|
A | C | 1 | a0001c0001t0014g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901-2004A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199963 | ||||||
chr1:12199964
|
A | AGCCAGTG others(8): Show |
1 | a0001c0001t0014g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901-2003_901-2002i others(17): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199964 | ||||||
chr1:12200167
|
G | C | 3 | a0002c0002t0001g0321a0002c0002t0003g0334a0002c0002t0014g0319 | 3 | HG00140.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.901-1800G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200167 | ||||||
chr1:12200197
|
T | C | 1 | a0002c0002t0032g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.901-1770T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200197 | ||||||
chr1:12200264
|
ATAT | A | 9 | a0002c0002t0001g0151a0002c0002t0001g0321a0002c0002t0002g0030others(6): Show | 9 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.901-1692_901-1690d others(5): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12200264 | |||||
chr1:12200280
|
A | G | 5 | a0001c0001t0006g0353a0002c0002t0008g0023a0002c0002t0013g0031others(2): Show | 5 | HG01106.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-1687A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200280 | ||||||
chr1:12200323
|
C | T | 6 | a0001c0001t0006g0353a0002c0002t0008g0023a0002c0002t0013g0031others(3): Show | 6 | HG01106.hp2 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-1644C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200323 | ||||||
chr1:12200342
|
C | T | 2 | a0005c0007t0014g0346a0005c0007t0016g0344 | 2 | HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.901-1625C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200342 | ||||||
chr1:12200420
|
G | A | 1 | a0002c0002t0015g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.901-1547G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200420 | ||||||
chr1:12200674
|
G | A | 1 | a0001c0001t0010g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.901-1293G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200674 | ||||||
chr1:12200722
|
A | C | 1 | a0001c0001t0003g0192 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.901-1245A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200722 | ||||||
chr1:12200810
|
G | A | 6 | a0001c0001t0006g0353a0002c0002t0008g0023a0002c0002t0013g0031others(3): Show | 6 | HG01106.hp2 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-1157G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200810 | ||||||
chr1:12200811
|
G | A | 1 | a0001c0001t0018g0311 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.901-1156G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200811 | ||||||
chr1:12201260
|
C | CA | 32 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(29): Show | 33 | HG00621.hp2 HG00673.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.901-684dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201260 | |||||
chr1:12201260
|
CA | C | 28 | a0001c0001t0001g0230a0001c0001t0001g0297a0001c0001t0002g0053others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.901-684delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201260 | |||||
chr1:12201282
|
A | G | 1 | a0001c0001t0012g0204 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.901-685A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201282 | ||||||
chr1:12201417
|
A | G | 1 | a0002c0002t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.901-550A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201417 | ||||||
chr1:12201471
|
T | TA | 53 | a0001c0001t0001g0145a0001c0001t0001g0343a0001c0001t0002g0039others(50): Show | 53 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.901-481dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201471 | |||||
chr1:12201471
|
T | TAA | 11 | a0001c0001t0008g0009a0001c0001t0008g0010a0002c0002t0001g0151others(8): Show | 11 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-482_901-481dup others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201471 | |||||
chr1:12201471
|
TA | T | 7 | a0001c0001t0001g0230a0001c0001t0002g0293a0001c0001t0009g0092others(4): Show | 7 | HG02717.hp2 HG03239.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.901-481delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201471 | |||||
chr1:12201556
|
T | C | 3 | a0001c0001t0003g0118a0005c0007t0014g0346a0005c0007t0016g0344 | 3 | HG01358.hp2 HG02129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.901-411T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201556 | ||||||
chr1:12201733
|
T | C | 5 | a0001c0001t0003g0118a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG01358.hp2 HG02129.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-234T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201733 | ||||||
chr1:12201786
|
G | A | 1 | a0002c0002t0002g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.901-181G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201786 | ||||||
chr1:12201915
|
A | G | 42 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0008g0009others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.901-52A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201915 | ||||||
chr1:12201944
|
C | T | 5 | a0001c0001t0001g0189a0001c0001t0002g0116a0001c0001t0002g0349others(2): Show | 5 | HG01256.hp1 NA18960.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-23C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201944 | ||||||
chr1:12202241
|
G | A | 58 | a0001c0001t0002g0011a0001c0001t0002g0326a0001c0001t0002g0327others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1105+70G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202241 | ||||||
chr1:12202369
|
C | T | 44 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(41): Show | 44 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105+198C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202369 | ||||||
chr1:12202619
|
C | T | 8 | a0001c0001t0006g0353a0001c0001t0017g0018a0001c0001t0055g0295others(5): Show | 8 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+448C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202619 | ||||||
chr1:12202632
|
G | A | 46 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(43): Show | 46 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1105+461G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202632 | ||||||
chr1:12202633
|
A | C | 44 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(41): Show | 44 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105+462A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202633 | ||||||
chr1:12202735
|
A | G | 44 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(41): Show | 44 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105+564A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202735 | ||||||
chr1:12202737
|
G | A | 1 | a0001c0001t0066g0250 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1105+566G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202737 | ||||||
chr1:12202817
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1105+646A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202817 | ||||||
chr1:12202830
|
A | G | 1 | a0002c0002t0003g0334 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1105+659A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202830 | ||||||
chr1:12202858
|
C | T | 3 | a0002c0002t0002g0022a0002c0002t0011g0324a0002c0002t0032g0024 | 3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1105+687C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202858 | ||||||
chr1:12203002
|
G | A | 1 | a0002c0002t0005g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1105+831G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203002 | ||||||
chr1:12203345
|
C | T | 1 | a0001c0001t0053g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1105+1174C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203345 | ||||||
chr1:12203403
|
A | T | 2 | a0002c0002t0001g0172a0002c0002t0001g0173 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1105+1232A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203403 | ||||||
chr1:12203460
|
C | A | 5 | a0001c0001t0002g0090a0001c0001t0003g0083a0001c0001t0003g0091others(2): Show | 5 | HG00099.hp1 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+1289C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203460 | ||||||
chr1:12203488
|
C | T | 35 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(32): Show | 35 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1105+1317C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203488 | ||||||
chr1:12203529
|
G | A | 9 | a0001c0001t0006g0353a0001c0001t0017g0018a0001c0001t0055g0295others(6): Show | 9 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1105+1358G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203529 | ||||||
chr1:12203727
|
T | A | 1 | a0002c0002t0001g0143 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1105+1556T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203727 | ||||||
chr1:12203760
|
T | C | 35 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1105+1589T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203760 | ||||||
chr1:12203844
|
C | A | 1 | a0002c0002t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1105+1673C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203844 | ||||||
chr1:12203862
|
C | T | 59 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0289others(56): Show | 59 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1105+1691C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203862 | ||||||
chr1:12203892
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1105+1721G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203892 | ||||||
chr1:12203949
|
C | G | 3 | a0002c0002t0002g0022a0002c0002t0011g0324a0002c0002t0032g0024 | 3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1105+1778C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203949 | ||||||
chr1:12203974
|
T | A | 1 | a0001c0001t0008g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1105+1803T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203974 | ||||||
chr1:12204078
|
C | T | 1 | a0001c0001t0025g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105+1907C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204078 | ||||||
chr1:12204166
|
T | C | 7 | a0002c0002t0001g0151a0002c0002t0001g0321a0002c0002t0002g0030others(4): Show | 7 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105+1995T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204166 | ||||||
chr1:12204265
|
C | G | 1 | a0001c0001t0022g0177 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1105+2094C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204265 | ||||||
chr1:12204298
|
A | G | 350 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1105+2127A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204298 | ||||||
chr1:12204404
|
G | A | 8 | a0001c0001t0002g0071a0002c0002t0001g0151a0002c0002t0001g0321others(5): Show | 8 | HG00140.hp1 HG01168.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+2233G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204404 | ||||||
chr1:12204586
|
A | T | 1 | a0002c0002t0032g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1106-2154A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204586 | ||||||
chr1:12204690
|
C | T | 1 | a0002c0002t0032g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1106-2050C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204690 | ||||||
chr1:12204763
|
T | C | 2 | a0001c0001t0010g0004a0001c0001t0010g0292 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1106-1977T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204763 | ||||||
chr1:12204790
|
TCAC | T | 24 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1106-1926_1106-192 others(7): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12204790 | |||||
chr1:12204808
|
C | CCAA | 11 | a0001c0001t0006g0353a0001c0001t0017g0018a0001c0001t0055g0295others(8): Show | 11 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1106-1930_1106-192 others(7): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12204808 | |||||
chr1:12204811
|
C | A | 21 | a0001c0001t0002g0071a0001c0001t0006g0353a0001c0001t0017g0018others(18): Show | 21 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1106-1929C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204811 | ||||||
chr1:12204814
|
C | A | 28 | a0001c0001t0002g0071a0001c0001t0006g0353a0001c0001t0017g0018others(25): Show | 28 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1106-1926C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204814 | ||||||
chr1:12204818
|
C | CA | 12 | a0001c0001t0008g0007a0001c0001t0008g0008a0001c0001t0008g0256others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1106-1915dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12204818 | |||||
chr1:12204821
|
A | C | 2 | a0005c0007t0014g0346a0005c0007t0016g0344 | 2 | HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1106-1919A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204821 | ||||||
chr1:12204828
|
C | T | 1 | a0002c0002t0015g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1106-1912C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204828 | ||||||
chr1:12205005
|
G | A | 2 | a0001c0001t0006g0353a0001c0001t0055g0295 | 2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1106-1735G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205005 | ||||||
chr1:12205019
|
A | G | 7 | a0002c0002t0001g0151a0002c0002t0001g0321a0002c0002t0002g0030others(4): Show | 7 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106-1721A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205019 | ||||||
chr1:12205235
|
A | G | 2 | a0001c0001t0002g0328a0001c0001t0010g0241 | 2 | HG02080.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1106-1505A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205235 | ||||||
chr1:12205270
|
C | T | 2 | a0002c0002t0001g0143a0002c0002t0005g0141 | 2 | NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1106-1470C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205270 | ||||||
chr1:12205322
|
C | T | 1 | a0001c0001t0053g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1106-1418C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205322 | ||||||
chr1:12205408
|
G | A | 1 | a0002c0002t0001g0321 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1106-1332G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205408 | ||||||
chr1:12205660
|
C | T | 2 | a0001c0001t0005g0073a0001c0001t0005g0079 | 2 | NA18962.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1106-1080C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205660 | ||||||
chr1:12205775
|
C | T | 2 | a0001c0001t0027g0048a0001c0001t0027g0315 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1106-965C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205775 | ||||||
chr1:12205782
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1106-958C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205782 | ||||||
chr1:12205788
|
A | ATT | 17 | a0001c0001t0002g0071a0001c0001t0006g0353a0001c0001t0017g0018others(14): Show | 17 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1106-942_1106-941d others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12205788 | |||||
chr1:12205988
|
G | A | 1 | a0005c0007t0016g0344 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1106-752G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205988 | ||||||
chr1:12206359
|
C | CA | 10 | a0001c0001t0001g0307a0001c0001t0003g0279a0001c0001t0005g0075others(7): Show | 11 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1106-363dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12206359 | |||||
chr1:12206359
|
CA | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0275a0001c0001t0006g0353others(25): Show | 28 | HG00323.hp1 HG00639.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1106-363delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12206359 | |||||
chr1:12206396
|
T | C | 9 | a0001c0001t0006g0353a0001c0001t0011g0291a0001c0001t0017g0018others(6): Show | 9 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106-344T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206396 | ||||||
chr1:12206462
|
A | G | 2 | a0001c0001t0005g0073a0001c0001t0005g0079 | 2 | NA18962.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1106-278A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206462 | ||||||
chr1:12206534
|
A | G | 35 | a0001c0001t0001g0070a0001c0001t0002g0087a0001c0001t0002g0097others(32): Show | 35 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1106-206A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206534 | ||||||
chr1:12206544
|
G | A | 3 | a0002c0002t0001g0321a0002c0002t0003g0334a0002c0002t0014g0319 | 3 | HG00140.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1106-196G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206544 | ||||||
chr1:12206555
|
A | G | 42 | a0001c0001t0001g0070a0001c0001t0002g0071a0001c0001t0002g0087others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1106-185A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206555 | ||||||
chr1:12206585
|
C | A | 1 | a0001c0001t0050g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1106-155C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206585 | ||||||
chr1:12206599
|
G | T | 4 | a0001c0001t0005g0119a0005c0007t0014g0346a0005c0007t0016g0344others(1): Show | 4 | HG01358.hp2 HG02040.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1106-141G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206599 | ||||||
chr1:12206625
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0008a0001c0001t0008g0256others(3): Show | 6 | HG01167.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-115C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206625 |